English
Management of precancerous conditions and lesions in the stomach (MAPS): guideline from the European Society of Gastrointestinal Endoscopy (ESGE), European Helicobacter Study Group (EHSG), European Society of Pathology (ESP), and the Sociedade Portuguesa de Endoscopia Digestiva (SPED)
Atrophic gastritis, intestinal metaplasia, and epithelial dysplasia of the stomach are common and are associated with an increased risk for gastric cancer. In the absence of guidelines, there is wide disparity in the management of patients with these premalignant conditions. The European Society of Gastrointestinal Endoscopy (ESGE), the European Helicobacter Study Group (EHSG), the European Society of Pathology (ESP) and the Sociedade Portuguesa de Endoscopia Digestiva (SPED) have therefore combined efforts to develop evidence-based guidelines on the management of patients with precancerous conditions and lesions of the stomach (termed MAPS). A multidisciplinary group of 63 experts from 24 countries developed these recommendations by means of repeat online voting and a meeting in June 2011 in Porto, Portugal. The recommendations emphasize the increased cancer risk in patients with gastric atrophy and metaplasia, and the need for adequate staging in the case of high grade dysplasia, and they focus on treatment and surveillance indications and methods.
Gastric cancer remains a major problem worldwide. The intestinal type of gastric cancer develops through a cascade of well-defined and recognizable precursors (inflammation–metaplasia–dysplasia–carcinoma sequence) [1]. It has been argued that the identification and surveillance of patients with such precursor conditions and lesions may lead to early diagnosis of gastric cancer. Indeed, this may be an important measure for prevention of death due to gastric cancer both in Western and Asian countries. However, even though such lesions are commonly found in everyday practice, there are no international recommendations to guide clinicians in their care of individuals with these changes. This leads to wide heterogeneity of practice and to failure to diagnose patients with curable forms of cancer. Standardization of management is likely to benefit patients, and may also be cost-effective by focusing resources on patients with the greatest risk.
This consensus project aimed to summarize current evidence on the management of patients with precancerous conditions and lesions, and to propose guidelines for the diagnosis and management of individuals with chronic gastritis, atrophy, intestinal metaplasia, or dysplasia.
This Guideline does not address methodologies for screening these lesions in general populations, or the assessment and management of patients with other precancerous conditions, such as pernicious anemia, Ménétrier disease, or gastric stump, or treatment for gastric adenocarcinoma.
Scope and key questions
We addressed the management, that is, the diagnostic assessment, treatment and follow-up, of individuals with atrophic gastritis, or intestinal metaplasia or dysplasia of the gastric mucosa. Specific issues were included: What is the optimal diagnostic approach for patients with gastric precancerous conditions/lesions? Which patients are at higher risk and would benefit from surveillance to detect early-stage cancer? Should they receive pharmacological interventions to reduce the risk of developing cancer? If so, are such measures cost-effective?
These recommendations were developed according to the process described by the Appraisal of Guidelines for Research and Evaluation (AGREE) Collaboration [2].
2.1 Selection of Working Panel
In May 2010, three authors (M.D.R., E.J.K., and F.C.), on behalf of the European Society of Gastrointestinal Endoscopy (ESGE), the Sociedade Portuguesa de Endoscopia Digestiva (SPED), the European Helicobacter Study Group (EHSG), and the European Society of Pathology (ESP), assembled a panel of European gastroenterologists and pathologists, including clinical experts and young researchers trained in literature search and evidence-based medicine (see Appendix ).
This panel met in October 2010 in Barcelona, and agreed on the methodology to be applied, and on a set of key questions and preliminary statements to guide a literature search. The panel further worked in subgroups ([Table1]) to perform a systematic search for evidence, to review statements on the basis of quality-rated evidence, and to report graded statements and recommendations accordingly. Subsequently representatives from European national societies of digestive endoscopy and pathology, and individual members (see Appendix), considered the applicability of the evidence and draft statements. This was done by means of two online sessions for voting and comments, followed by a second meeting held in June 2011 in Porto, Portugal.
Key questions | Working group |
Which are the precancerous lesions in the stomach? Which outcomes to prevent/avoid? | Fátima Carneiro, Ernst Kuipers, Mário Dinis Ribeiro |
Is there evidence to use endoscopic methods to improve diagnosis? | Miguel Areia, Pedro Pimentel Nunes, AnneMarie de Vries, Bjorn Rembacken, Ernst Kuipers, Mário Dinis Ribeiro, |
Which care should be taken on biopsies (number and sites) for a correct diagnosis and staging? | Ricardo Marcos Pinto, Bjorn Rembacken, Kazumasa Miki, José Carlos Machado, Fátima Carneiro, Ernst Kuipers, Mário Dinis Ribeiro, |
Should other sources of data be added for staging? | Ricardo Marcos Pinto, Carina Pereira, José Carlos Machado, Miguel Areia, AnneMarie de Vries, Fátima Carneiro, Ernst Kuipers, Mário Dinis Ribeiro, Thierry Ponchon, Bjorn Rembacken, Kazumasa Miki |
Is there evidence to use non-invasive methods to improve diagnosis? | Miguel Areia, Ernst Kuipers, Mário Dinis Ribeiro, Kazumasa Miki, |
Should these patients be followed up? | AnneMarie de Vries, Ernst Kuipers, Mário Dinis Ribeiro, Ricardo Marcos Pinto, Carina Pereira |
Does the type, the severity and the extension of the lesion influence the prognosis of these patients? | AnneMarie de Vries, Ernst Kuipers, Mário Dinis Ribeiro, Thierry Ponchon, Bjorn Rembacken, Kazumasa Miki, José Carlos Machado, Ricardo Marcos Pinto, Carina Pereira, Fátima Carneiro |
Is there a role for Helicobacter pylori eradication? | Anthony O’Connor, Pedro Pimentel-Nunes, Ernst Kuipers, Mário Dinis Ribeiro, Peter Malfertheiner, Tamara Matysiak-Budnik, Francis Megraud, Carina Pereira, Ari Ristimaki |
Is there a role for other therapies? | Anthony O’Connor, Carina Pereira, Ernst Kuipers, Mário Dinis Ribeiro, Peter Malfertheiner, Tamara Matysiak-Budnik, Francis Megraud, Pedro Pimentel-Nunes |
May it/these strategies be cost-effective? | Miguel Areia, Richard Peek, Jean-Marc Dumonceau, Ernst Kuipers, Mário Dinis Ribeiro |
A total of 63 participants contributed (all online and 45 in Porto), including participants from Belarus, Belgium, Brazil, China, Chile, Finland, France, Germany, Iraq, Ireland, Italy, Jordan, Latvia, Malta, Portugal, Romania, Russia, Slovakia, Sudan, Switzerland, The Netherlands, Turkey, UK and USA. In addition, nine national societies were represented (Germany, Jordan, Latvia, Portugal, Romania, Russia, Slovakia, Switzerland and The Netherlands).
2.2 Literature search
A literature search using PubMed up to November 2010 was carried out. A small working group from the panel dealt with each question and each string/query, and identified key references which were supplied to the entire panel and participants.
2.3 Grading of evidence
Each working group rated the quality level of the available evidence and the strength of recommendations by using both the Grading of Recommendations, Assessment, Development, and Evaluation (GRADE) process [3][4] and the system of the Scottish Intercollegiate Guidelines Network (SIGN) [5]. Researchers prioritized data from randomized clinical trials (RCTs) when available, and performed meta-analyses when applicable. Each paper was individually assessed by two investigators using a methodological tool that was identical for all topics reviewed in the guidelines. Discrepant assessment results were discussed by the full working group.Tables with the assessment of individual manuscripts are available upon request.
For each question the working group summarized the quantity, quality, and consistency of evidence, and they discussed the external validity of studies and whether the study conclusions were applicable to the target population for the guidelines. The group recorded the overall level of evidence addressing the key question and made a graded recommendation pertaining to the key question (for evidence levels and recommendation grades, see [Table 2]).
Levels | |
1++ | High quality meta-analyses, systematic reviews of RCTs, or RCTs with a very low risk of bias |
1+ | Well conducted meta-analyses, systematic reviews of RCTs, or RCTs with a low risk of bias |
1– | Meta-analyses, systematic reviews or RCTs, or RCTs with a high risk of bias |
2++ | High quality systematic reviews of case–control or cohort studies OR High quality case–control or cohort studies with a very low risk of confounding, bias, or chance and a high probability that the relationship is causal |
2+ | Well conducted case–control or cohort studies with a low risk of confounding, bias, or chance and a moderate probability that the relationship is causal |
2– | Case–control or cohort studies with a high risk of confounding, bias, or chance and a significant risk that the relationship is not causal |
3 | Non-analytic studies, e.g. case reports, case series |
4 | Expert opinion |
Grades | |
A | At least one meta-analysis, systematic review, or RCT rated as 1++, and directly applicable to the target population; OR a systematic review of RCTs OR A body of evidence consisting principally of studies rated as 1+, directly applicable to the target population, and demonstrating overall consistency of results |
B | A body of evidence including studies rated as 2++, directly applicable to the target population, and demonstrating overall consistency of results; OR Extrapolated evidence from studies rated as 1++or 1+ |
C | A body of evidence including studies rated as 2+, directly applicable to the target population and demonstrating overall consistency of results; OR Extrapolated evidence from studies rated as 2++ |
D | Evidence level 3 or 4; OR Extrapolated evidence from studies rated as 2+ |
RCT, randomized controlled trial
It is important to emphasize that the grading does not relate to the importance of the recommendation, but to the strength of the supporting evidence.
Other factors that influenced the grading of a recommendation were taken into account by the participants, including: (i) any evidence of potential harms associated with implementation of a recommendation; (ii) clinical impact on the target population and impact on resource consumption; (iii) whether, and to what extent, any patient populations might be particularly advantaged or disadvantaged by the recommendations; and (iv) opportunities and obstacles regarding implementation in daily clinical practice.
2.4 Consensus process and applicability
A hybrid approach was used to obtain the final version of statements, starting with an online consultation followed by a final meeting in Porto, in June 2011.Online questionnaires (MedQuest) were devised to allow participants to vote anonymously on statements. During the first round the panel members were asked to vote on their agreement with evidence-based statements; and in a second round, all participants, that is, panelists, society representatives, and individual members, were asked to vote on their agreement with statements but also on the level of applicability. At this stage, a collection of summarized references were available to all participants. The final discussion took place in June 2011 in Porto, during a one-day consensus conference, where data were presented and discussed; this was followed by re-voting and attribution of grades to the final statements.
(Voting was on a 6-point scale: a, agree strongly; b agree moderately; c, just agree; d, just disagree; e, disagree moderately; and f, disagree strongly. Prior to the voting process it was defined that a statement would be accepted if more than 75% of the participants voted a, b, or c.
In addition, in the second round, all participants were also specifically queried regarding the level of applicability to their own practice and in their country, when this was relevant.
2.5 Reporting
The present manuscript summarizes the results of this entire process and was reviewed by all participants. Moreover, all ESGE individual members and national societies were asked to send their contributions.
Agreement results are presented as proportions of voters agreeing with the statements. The online voting results are presented for the statements that remained unchanged during the Porto meeting. For those for which a new voting process was conducted during the meeting in Porto, the final results for that meeting are presented. We also present a flow chart of the final results.
3.1 Summary of recommendations
Conventional white light endoscopy cannot accurately differentiate between and diagnose pre-neoplastic gastric conditions/lesions (evidence level 2++, recommendation grade B). Thus, magnification chromoendoscopy or narrow-band imaging (NBI) endoscopy with or without magnification may be offered in these cases as it improves diagnosis of such lesions (evidence level 2++, recommendation grade B). In addition, at least four biopsies of the proximal and distal stomach, on the lesser and greater curvature, are needed for adequate assessment of premalignant gastric conditions (evidence level 2+, recommendation grade C). Systems for histopathological staging (e.g. operative link for gastritis assessment [OLGA] and operative link for gastric intestinal metaplasia [OLGIM] assessment) may be useful for identifying subgroups of patients with different risks of progression to gastric cancer (evidence level 2++, recommendation grade C), namely those with extensive lesions (i.e., atrophy and/or intestinal metaplasia in both antrum and corpus). Although only low potential applicability was reported by participants for this indicator, low serum pepsinogen levels can also predict this phenotype (evidence level 2++, recommendation grade C) and, in such patients, Helicobacter pylori serology may also be useful for further detection of high risk individuals (evidence level 2++, recommendation grade C). Beyond a family history of gastric cancer (evidence level 2++, recommendation grade B), neither age, gender, H. pylori virulence factors, or host genetic variations change these clinical recommendations (evidence level 4, recommendation grade D). Patients with extensive atrophy and/or extensive intestinal metaplasia should be offered endoscopic surveillance (evidence level 2++, recommendation grade B) every 3 years (evidence level 4, recommendation grade D). Further studies are needed however, to accurately estimate the cost–effectiveness of such an approach (evidence level 1, recommendation grade B). Patients with mild to moderate atrophy/intestinal metaplasia only in antrum do not need follow-up (evidence level 4, recommendation grade D). If H. pylori infection is present, eradication should be offered to prevent high grade dysplasia or carcinoma (evidence level 1+, recommendation grade B). Currently, the use of cyclooxygenase-2 (COX-2) inhibitors or the use of dietary supplementation with antioxidants (ascorbic acid and beta-carotene) are not endorsed as approaches to decrease the risk of progression of gastric precancerous lesions (evidence level 1+, recommendation grade B). Patients with dysplasia without a visible endoscopic lesion should be closely followed up, either immediately and 6 to 12 months thereafter, or within 12 months ( evidence level 2+, recommendation grade C), respectively, for those with high grade or low grade dysplasia. Those with dysplasia or cancer within an endoscopically visible lesion should undergo staging and resection.
A flow chart for the proposed management of patients with atrophic gastritis, gastric intestinal metaplasia, or gastric epithelial dysplasia is shown in [Fig.1].
3.2 Definitions and outcomes to prevent
3.2.1 Gastric carcinogenesis
1. Patients with chronic atrophic gastritis or intestinal metaplasia should be considered to be at higher risk for gastric adenocarcinoma. (Agree 96% [vote: a, 68%; b, 18%; c, 10%; d, 2%; e, 2%])
2. High grade dysplasia and invasive carcinoma should be regarded as the outcomes to be prevented when patients with chronic atrophic gastritis or intestinal metaplasia are managed. (Agree 96% [vote: a, 72%; b, 14%; c, 10%; d, 4%])
3. Patients with endoscopically visible high grade dysplasia or carcinoma should undergo staging and adequate management. (Agree 100% [vote: a, 94%; b, 2%; c, 4%])
In most instances, the development of so-called “intestinal” gastric adenocarcinoma represents the culmination of an inflammation–metaplasia–dysplasia–carcinoma sequence, known as the Correa cascade of multistep gastric carcinogenesis, where a progression may occur from normal mucosa through chronic non-atrophic gastritis ([Fig.2a,b]), atrophic gastritis ([Fig.2c,d]), and intestinal metaplasia ([Fig.2e,f]), to dysplasia ([Fig.2g]) and carcinoma [6][7][8]. This model has been consistently confirmed in different studies [9][10].
Fig.2 Morphologic changes in gastric mucosa during gastric carcinogenesis. a,b Non-atrophic gastritis, without gland atrophy and/or intestinal metaplasia: (a ) antrum (hematoxylin and eosin [H&E], ×40); (b ) corpus (H&E, ×100). c,d Moderate atrophy of deep antral glands (gland loss between 30% and 60%), without intestinal metaplasia: (c ) H&E staining, ×40; (d ) Periodic acid–Schiff (PAS)–alcian blue staining, ×40, highlighting gland loss and a single focus of intestinal metaplasia in the superficial part of the gastric mucosa. e,f Severe atrophy of antral mucosa, with loss of more than 60% of original mucous-secreting glands, replaced by intestinal metaplasia: (e ) H&E, ×40; (f ) PAS–alcian blue, ×40. g,h Dysplasia and intramucosal carcinoma: (g ) low grade (left) and high grade (right) dysplasia (H&E, ×100); (h ) intramucosal carcinoma (H&E, ×200).
3.2.2 Precancerous conditions
Mucosal gastric atrophy and intestinal metaplasia confer a high risk for the development of gastric cancer as they constitute the background in which dysplasia and intestinal-type gastric adenocarcinoma develop [7][11][12][13]. Thus, chronic atrophic gastritis and intestinal metaplasia are considered to be precancerous conditions.
Chronic atrophic gastritis should be diagnosed and graded on the basis of the presence of chronic inflammatory cells, including lymphocytes and plasma cells that expand the lamina propria, and the disappearance of the normal glands [14][15][16]. In the gastric body/fundus this is associated with a loss of specialized cells and thus a reduction of gastric secretory functions. The severity of gland loss (atrophy) should be graded although inter- and intraobserver agreement are both poor.
Individuals may develop different phenotypes of chronic gastritis due to different genetic profiles and environmental exposure:
Cases of inflammatory changes limited to the antrum and without gland atrophy and/or intestinal metaplasia are defined as diffuse antral gastritis.
Cases of gland atrophy and/or intestinal metaplasia distributed multifocally including the lesser curvature of the corpus and fundus, are defined as multifocal atrophic gastritis. This phenotype may be described as “extensive,” whereas the term “marked” is used to define a severity grade at a particular site.
The overall background changes in the stomach should therefore be described in terms of the severity and distribution of any premalignant conditions/lesions. Several classification schemes have been developed for chronic gastritis and preneoplastic changes.
At present, the updated Sydney System is generally used both in clinical practice and in research, combining topographic, morphological, and etiological information in reporting systems designed to include both grading and staging of gastritis. In addition, the systems known as OLGA (operative link for gastritis assessment), and OLGIM (operative link on gastric intestinal metaplasia) assessment have been proposed for staging of gastritis (see below). However, most classifications are still difficult to use in clinical practice, and when applied they have the disadvantage of considerable inter- and intraobserver variation.
Nevertheless, these systems seem to be more relevant and easy to apply than subtyping of intestinal metaplasia. Intestinal metaplasia may be classified as “complete” or “incomplete.” Complete intestinal metaplasia (“small-intestinal” or type I) displays goblet and absorptive cells, decreased expression of gastric mucins (MUC1, MUC5AC, and MUC6), and expression of MUC2, an intestinal mucin. Incomplete intestinal metaplasia (“enterocolic” or type IIA/II, and “colonic” or type IIB/III), displays goblet and columnar non-absorptive cells [17][18][19][20], in which gastric mucins (MUC1, MUC5AC, and MUC6) are coexpressed with MUC2 [17][18][19][20]. In Filipe’s classification the typing of intestinal metaplasia (types I, II, and III) was based on the detection of sialomucin and sulphomucin by high iron diamine–alcian blue staining (this approach was discontinued due to toxicity of the reagents). Currently used classifications also take into consideration the presence of Paneth cells (complete metaplasia) or crescent architecture changes, dedifferentiation, and degree of absence of Paneth cells (incomplete metaplasia), as well as the pattern and type of mucin expression [20]. Moreover, some studies indicate a positive correlation between the degree of incomplete intestinal metaplasia and the extent of intestinal metaplasia. However, the use of immunohistochemistry or other special techniques in order to subtype intestinal metaplasia is not widespread in routine diagnostics.
Recently, another pattern of metaplasia, termed spasmolytic polypeptide-expressing metaplasia (SPEM), has been described. This is characterized by the expression of the TFF2 spasmolytic polypeptide that is associated with oxyntic atrophy. SPEM, which characteristically develops in the gastric body and fundus, appears to share some characteristics with pseudopyloric metaplasia, has a strong association with chronic infection with Helicobacter pylori and with gastric adenocarcinoma, and may represent another pathway to gastric neoplasia [21]. At present identification of SPEM is considered an investigational parameter.
3.2.3 Precancerous lesions
Gastric dysplasia represents the penultimate stage of the gastric carcinogenesis sequence, is defined as histologically unequivocal neoplastic epithelium without evidence of tissue invasion, and is thus a direct neoplastic precancerous lesion [22]. It is characterized by cellular atypia reflective of abnormal differentiation, and disorganized glandular architecture [23][24][25][26]. Correct diagnosis and grading of dysplasia are critical, because they predict both the risk of malignant transformation and the risk of metachronous gastric cancer. In fact, the reported progression rates of dysplasia to gastric cancer vary greatly, from 0% to 73% per year [27][28][29][30][31][32][33][34][35][36][37][38][39][40][41][42][43][44][45][46][47][48]. These variations can probably be explained by diverse factors such as differences in study design and populations under study and also differences in definitions and assessment of gastric dysplasia.
There are well-known differences between Japanese and European/North American pathologists in categorizing gastric dysplasia that in some classifications is designated as intraepithelial neoplasia. For instance, in Japan, noninvasive intramucosal neoplastic lesions with high grade cellular and architectural atypia are termed “non-invasive intramucosal carcinoma,” whereas the same lesions are diagnosed as high grade dysplasia by most pathologists in the West [49][50].
In an attempt to resolve this issue, several proposals have been made regarding the terminology for the morphological spectrum of lesions, including the Padova and Vienna classifications and more recently, the World Health Organization (WHO) classification.
The WHO recently reiterated the classification of dysplasia/intraepithelial neoplasia. Acknowledging the widespread use of both “dysplasia” and “intraepithelial neoplasia” (IEN), it uses these terms as synonymous (in this paper, dysplasia is the term that will be used from now on). According to the current WHO classification [51], the following diagnostic categories should thus be considered:
1. Negative for intraepithelial neoplasia/dysplasia
2. Indefinite for intraepithelial neoplasia/dysplasia
3. Low grade intraepithelial neoplasia/dysplasia
4. High grade intraepithelial neoplasia/dysplasia
5. Intramucosal invasive neoplasia/intramucosal carcinoma.
In the stomach, and as far as the present guidelines are concerned, category 1, negative for intraepithelial neoplasia/dysplasia, includes chronic atrophic gastritis and intestinal metaplasia. Where there is doubt as to whether a lesion is neoplastic or non-neoplastic (i.e. reactive or regenerative), particularly in small biopsies exhibiting inflammation, the diagnosis should be indefinite for intraepithelial neoplasia/dysplasia. In such cases, the dilemma is usually solved by cutting deeper levels, by obtaining additional biopsies, or after correcting for possible etiologies.
Intraepithelial neoplasia/dysplasia comprises unequivocally epithelial neoplastic proliferations characterized by variable cellular and architectural atypia, but without convincing evidence of invasion. Low grade intraepithelial neoplasia/dysplasia shows minimal architectural disarray and only mild-to-moderate cytological atypia. The nuclei are elongated, polarized, and basally located, and mitotic activity is mild-to-moderate ([Fig.2g], left). High grade intraepithelial neoplasia/dysplasia comprises neoplastic cells that are usually cuboidal, rather than columnar, with a high nucleus-to-cytoplasm ratio, prominent amphophilic nucleoli, more pronounced architectural disarray, and numerous mitoses, which can be atypical. Importantly, the nuclei frequently extend into the luminal aspect of the cell, and nuclear polarity is usually lost ([Fig.2g], right). Most patients harboring lesions classified as high grade dysplasia are at high risk for either synchronous invasive carcinoma or its rapid development [34] (see below).
Intramucosal invasive neoplasia/intramucosal carcinoma defines carcinomas that invade the lamina propria and are distinguished from intraepithelial neoplasia/dysplasia not only by desmoplastic changes that can be minimal or absent, but also by distinct structural anomalies, such as marked glandular crowding, excessive branching, budding, and fused or cribriforming glands ([Fig.2h]). The diagnosis of intramucosal carcinoma indicates that there is an increased risk of lymphatic invasion and lymph-node metastasis. However, endoscopic techniques allow treatment without open surgery, particularly for lesions ≤2cm in size and for those that are well differentiated with no lymphatic invasion. Guidelines for endoscopic treatment of gastric adenocarcinoma are beyond the scope of this manuscript.
3.3 Diagnosis and staging
3.3.1 Endoscopy
4. Conventional white light endoscopy cannot accurately differentiate and diagnose pre-neoplastic gastric conditions. (evidence level2++, recommendation grade B). (Agree 94% [vote: a, 46%; b, 24%; c, 24%; d, 4%; e, 2%])
5. Magnification chromoendoscopy and narrow band imaging (NBI), with or without magnification, improve the diagnosis of gastric preneoplastic conditions/lesions (evidence level 2++, recommendation grade B). (Agree 98% [vote: a, 47%; b, 27%; c, 24%; d, 2%] 83% of voters stated that they would apply this statement; 67% of those representing national societies mentioned that it would also be applicable (63%) or widely applicable (4%) in their countries.)
6. Within this context, diagnostic upper gastrointestinal endoscopy should include gastric biopsies sampling (evidence level 4, recommendation grade D). (Agree 93% [vote: a, 66%; b, 18%; c, 9%; d, 7%])
Some studies have evaluated whether conventional white light (WL) endoscopy can reliably distinguish Helicobacter pylori gastritis and gastric preneoplastic lesions from normal mucosa. In a pioneer study Atkins & Benedict concluded that correlation between endoscopy and histology was poor [52]. This was confirmed in a subsequent prospective study, where Bah et al. concluded that it is not possible to reliably diagnose H. pylori gastritis with endoscopy alone [53]. Antral nodularity appears to be the only endoscopic sign with a high positive predictive value (>90%) for H. pylori infection; however, it is, except in children, only present in a minority of patients with H. pylori gastritis [53][54][55][56]. Absence of rugae and presence of visible vessels in the gastric mucosa predict severe atrophy but with a relatively low sensitivity [57]. Intestinal metaplasia may appear as thin, white mucosal deposits [58]; however, the value of this or other endoscopic signs for the diagnosis of intestinal metaplasia remains unestablished. Taken together, these studies show that conventional endoscopy cannot reliably diagnose H. pylori gastritis, atrophy, or intestinal metaplasia [52][54][55][56][57][58].
There is inconsistent evidence that new high resolution endoscopes are more reliable. Some studies show low accuracy for the diagnosis of gastric mucosal inflammation, atrophy and metaplasia, particularly with patients aged below 50 years and in particular when they have mild atrophy or metaplasia [59], but others suggest a good accuracy [60]. In addition to low accuracy, endoscopy findings were associated with low reproducibility [61] and therefore current evidence suggests that conventional endoscopy cannot be relied upon to correctly identify patients with atrophy or intestinal metaplasia.
Studies have suggested that chromoendoscopy, particularly with magnification, helps to identify lesions of intestinal metaplasia and dysplasia. Dinis-Ribeiro et al. proposed a classification for the diagnosis of these lesions that was reproducible and highly accurate [62]. The accuracy and reproducibility of this chromoendoscopy classification with methylene blue was maintained when it was submitted to external validation [63]. Chromoendoscopy using other solutions, such as indigo carmine, acetic acid, or hematoxylin, was also associated with high accuracy for the diagnosis of these lesions, particularly for dysplasia [64], [65]. Tanaka et al. reported that that the use of acetic acid was superior to that of indigo carmine [65].
However, high resolution magnifying endoscopy without chromoendoscopy also appears superior to standard endoscopy, allowing great accuracy for the diagnosis of H. pylori gastritis, intestinal metaplasia, and dysplasia [66][67]. No comparative study of magnification with or without chromoendoscopy has been made for the diagnosis of these lesions, despite the suggestion of Tanaka et al. that enhanced magnification chromoendoscopy with acetic acid is superior to conventional magnification endoscopy and indigo carmine chromoendoscopy [65].
So, current evidence suggests that magnification chromoendoscopy (MCE) improves accuracy for the detection of preneoplastic gastric lesions. However, this technique lengthens the time of the endoscopic procedure and adds to the workload of gastroenterology departments. Besides, patient tolerance, even with sedation, may be compromised. Taking all these considerations together, routine performance of MCE cannot be recommended, and its use should be restricted to centers experienced in this technique.
The recent technology of narrow band imaging (NBI) has been found to have good sensitivity and specificity for the diagnosis of gastric lesions [68][69][70][71][72][73][74][75][76][77]. However, there is no agreement on which NBI patterns are associated with gastric precancerous lesions. The NBI classification systems varied between studies, there was no external validation, and reproducibility was seldom evaluated. Only two studies used NBI without magnification [76][77]. The latter method, which could be applied in routine clinical practice in contrast to magnification-NBI which is not practicable in an everyday clinical setting, requires some level of expertise and a type of scope that is available in only a few centers. Nevertheless, this indicates that NBI may be useful for the identification of different gastric lesions. However, before this technology can be endorsed, a simple classification system will have to be agreed upon and independently validated in a large prospective multicenter study.
It follows that the best available endoscopic method should be offered to individual patients, but, within the context of optimal identification of patients with precancerous conditions, diagnostic upper gastrointestinal endoscopy should include sampling with gastric biopsies.
3.3.2 Biopsy sampling
7. Atrophic gastritis and intestinal metaplasia are often unevenly distributed throughout the stomach. For adequate staging and grading of gastric precancerous conditions, at least four non-targeted biopsies of two topographic sites (at the lesser and greater curvature, from both the antrum and the corpus) should be taken and clearly labelled in separate vials; additional target biopsies of lesions should be taken (evidence level 2+, recommendation grade C). (Agree 100% [vote: a, 61%; b, 25%; c, 14%]; 90% of voters stated that they would apply this statement; 80% of those representing national societies mentioned that it would also be applicable [60%] or widely applicable [20%] in their countries.)
8. Systems for histopathological staging (e.g. operative link for gastritis assessment [OLGA] and operative link for gastric intestinal metaplasia [OLGIM] assessment) may be useful for categorization of risk of progression to gastric cancer (evidence level 2++, recommendation grade C). (Agree 98% [vote: a, 39%; b, 41%; c, 18%; e, 2%]; 90% of voters stated that they would apply this statement; 70% of those representing national societies mentioned that it would also be applicable in their countries.)
Biopsy specimens of the stomach are essential to the establishment and grading of preneoplastic gastric lesions. The updated Sydney System is the most widely accepted for classification and grading of gastritis [14]. The system was primarily designed to provide standardization for reporting of gastric biopsies. The updated version recommended five biopsies, two from the antrum (3cm from the pylorus, greater and lesser curvatures), one from the incisura, and two from the corpus (one from the lesser curvature, 4cm proximal to the incisura, and one from the middle of the greater curvature); these sites were arbitrarily chosen. Although this biopsy protocol generally correctly establishes H. pylori status and chronic gastritis, the number of biopsies is controversial with regard to adequate staging of premalignant gastric lesions, mainly because of the multifocal nature of these lesions [78][79][80][81][82]. This multifocal nature affects their detectability, in turn affecting decisions regarding the patient’s therapy or future surveillance [1][6].
Five good quality studies [39][78][79][80][84], in different population settings, addressed the number of biopsies needed for a precise grading of gastritis and intestinal metaplasia. El-Zimaity & Graham [80] concluded that the biopsy protocol recommended by the Sydney System underestimated the presence of intestinal metaplasia and could identify corpus atrophy only when it was extensive; these authors recommended a minimum of eight biopsies. On the other hand, Guarner et al. [79] concluded that the Sydney recommendations for biopsy sites and number were sensitive for identification of H. pylori infection and preneoplastic lesions (in geographic areas with a high prevalence of gastric cancer). The additional value of biopsies from the incisura angularis is unclear and remains insufficiently established. Although this location is considered to be an area of early onset of atrophic–metaplastic transformation [85][86], other studies reported that additional incisura biopsies added little information to those obtained from antrum and corpus [78][83]. On the other hand, deVries et al. [84] in a multicenter study, in a low gastric cancer risk population, evaluated the yield from endoscopic surveillance of premalignant gastric lesions, by standardized biopsy protocols with 12 non-targeted and additional targeted biopsies, in 112 patients with a previous histologically confirmed diagnosis of intestinal metaplasia or dysplasia. The highest prevalence of premalignant lesions was found in the incisura (40%), followed by the antrum (35%) and lesser curvature of the corpus (33%). The non-targeted lesser curvature biopsies had a higher yield compared with those from the greater curvature of the corpus. A biopsy protocol consisting of seven non-targeted biopsies (3 antrum, 1 incisura, 3 from corpus, with 1 from the greater and 2 from the lesser curvature) was able to diagnose intestinal metaplasia in 97% of cases and all cases of dysplasia or cancer. Moreover, despite the low number of cases of gastric dysplasia in this study, it was shown that non-targeted biopsies were important for diagnosing dysplasia or even cancer.
The variability of sampling methods and results obtained is related to the prevalence of premalignant lesions in the studied population. Fewer biopsies are needed for accurate diagnosis and staging in high risk populations where the extent of the lesions is higher [83][87][88]. Even when extensive biopsy protocols are used, the inevitable sampling errors may affect the identification of the premalignant lesions which are frequently patchy [14][80][89][90] and can be missed on follow-up [91]. However, the greater the extent of the lesion, the more likely it is to be found with regular biopsy sampling.
Although the Sydney system and its updated version [14] have contributed to uniformity of reporting of gastric preneoplastic lesions, they are not intended to be gastric cancer risk prediction tools. The aim of the recently established OLGA staging system (operative link for gastritis assessment) is to translate the histopathological data into a standardized report, with information on the gastric condition (topography and extent of the atrophic changes) and subgrouping of patients by cancer risk [92][93]. Initially, two cross-sectional validation studies concluded that OLGA provides relevant clinical information, with identification of a subpopulation of patients (OLGA stage III/IV) with gastric premalignant lesions with high risk for gastric cancer and thus potentially eligible for surveillance of these lesions [94][95]. Recently Rugge et al. [96] described a cohort of patients with premalignant gastric conditions/lesions followed for 12 years. Only two patients with OLGA grade III/IV developed invasive neoplasias (P=0.001; relative risk [RR]=18.56). Because the OLGA system is based on the severity and extent of atrophy, a condition with low interobserver agreement [14][97], Capelle et al. [98] introduced a modified system based on intestinal metaplasia, OLGIM (operative link for gastric intestinal metaplasia), with which there is a high level of interobserver concordance [99]. The agreement between pathologists was moderate for atrophy (k=0.6) and higher for intestinal metaplasia (k=0.9). Application of the OLGIM assessment was associated with categorization of fewer patients into the high risk stages III and IV. This has at least in theory the additional advantage that use of the OLGIM system would select a smaller population for whom surveillance would need to be considered. More studies on feasibility and reproducibility in different epidemiological contexts are needed to validate these classification systems [94].
Amongst these data, we have two good quality studies [96][98] suggesting that for the identification of patients with severe atrophic changes, namely extensive atrophy and/or intestinal metaplasia, which identify patients at risk for dysplasia and/or cancer, biopsies should be taken in the corpus. In addition, other good quality case–control studies provided different conclusions, suggesting a minimum of 4 and a maximum of 8 biopsies for adequate staging and/or surveillance [78][79][80][83][84].
On this basis, the panel concluded that one should sample at least 2 biopsies from the antrum (greater and lesser curvature) and 2 biopsies from the corpus (greater and lesser curvature) to identify patients with atrophy and/or intestinal metaplasia. Biopsy samples should be submitted for pathological examination in different vials labelled according to the site of the sampling [14], [94].
3.3.3 Noninvasive assessment
9. Serum pepsinogen levels can predict extensive atrophic gastritis (evidence level 2++, recommendation grade C). (Agree 92% [vote: a, 30%; b, 28%; c, 34%; d, 4%; e, 4%]; 68% of voters stated that they would apply this statement; only 50% of those representing national societies mentioned that it would be applicable in their countries.)
10. In patients with low pepsinogen test levels, Helicobacter pylori serology may be useful for further detection of high risk individuals (evidence level 2++, recommendation grade C). (Agree 76% [vote: a, 26%; b, 10%; c, 40%; d, 18%; e, 4%; f, 2%]; 77% of voters stated that they would apply this statement; 80% of those representing national societies mentioned that it would also be applicable [70%] or widely applicable [10%] in their countries.)
Serum pepsinogens (PGs) are related to atrophic changes in gastric mucosa and consist of two types: PGI, which is mainly secreted by the fundic mucosa, and PGII secreted by chief cells but also by the pyloric glands and the proximal duodenal mucosa. Inflammation of the gastric mucosa leads to an increase in both PGI and PGII serum levels, usually with a more marked increase of PGII and thus a decrease in the PGI/II ratio. With the development of atrophy and loss of specialized cells, both PGI and PGII may decrease, but PGI usually shows a more marked decrease than PGII, thus there is a further decline in the PGI/II ratio (see review by Kuipers EJ: “In through the out door: serology for atrophic gastritis,” Eur J Gastroenterol Hepatol 2003: 877–879). Thus, a low PGI level, a low PGI/II ratio, or both, are good indicators of atrophic changes in the gastric mucosa.
Many studies have been conducted that compare the levels of the serum pepsinogens with the features of the gastric mucosa as characterized by endoscopy with biopsies, in different countries and populations and using several different cutoff values. The reporting of results in terms of sensitivities and specificities but also as differences in serum pepsinogen mean levels, as correlations, or as odds ratios, makes it difficult to compare or generalize studies.
In a meta-analysis published in 2004, Dinis-Ribeiro et al. [100] combined 42 studies that included 27 population studies (296553 patients) and 15 selected-population studies (4385 patients), and looked for the best cutoff for dysplasia diagnosis. A combination of PGI<50ng/mL and a PGI/PGII ratio 3.0 provided the best results, with a sensitivity of 65%, a specificity of 74%–85% and a negative predictive value >95%. Most of the studies comparing serum pepsinogen levels with the histological assessment of the gastric mucosa were cross-sectional studies, from screening populations to selected high risk patients. Usually in these studies the gastroenterologist and the pathologist were blinded to each other’s findings and both tests were done simultaneously.
When the study outcome was the extent of atrophy of the gastric corpus, values ranged between sensitivities of 9.4% to 92.3% and specificities of 9.9% to 100% [101][102][103][104][105][106][107][108][109][110][111][112][113][114][115][116][117][118][119], but other methods of reporting results found statistically significantly lower mean values of serum pepsinogen in extensive atrophic gastritis [105][110][120][121][122][123], significant correlations between atrophy extent and serum pepsinogen values [101][124][125], or significant odds/likelihood ratios for progression of atrophy to the corpus [112][126][127].
When the study outcome was the presence or extent of intestinal metaplasia, results presented sensitivity values of 15%–75% and specificity values of 92.2%–97.8% [102][115][128], or significant odds ratios [126][127][129].
When the study outcome was dysplasia/gastric cancer, some well-designed cohort studies were found reporting large numbers of patients followed-up for many years, together with several other case series reports or case–control studies.
The best evidence on the risk associated with premalignant gastric lesions comes from well-designed cohort studies, preferably with long follow-up times, including a large number of patients, and with small numbers lost to follow-up.At least six cohort studies fulfilling these criteria have been published to date. Watabe et al. [130] conducted a cohort study of 6983 patients for 4.7 years and found that H. pylori-positive patients with a PGI <70ng/mL and a PGI/II ratio <3.0 had a hazard ratio (HR) for gastric cancer of 6.0 (95% confidence intervals [95%CI] 2.4–14.5); in H. pylori-negative patients with the same pepsinogen profile the HR increased to 8.2 (3.2–21.5). Yamaji et al. [131], in a study with 6158 patients followed for 4.7 years, found an HR of 6.2 (2.9–13.0), whilst Yanaoka et al. [132][133], in 5209 patients followed for 10 years, obtained a HR of 2.77 (1.46–5.26). Ohata et al. [134] studied a cohort of 4655 patients for 7.7 years after collecting serum for pepsinogen and H. pylori antibodies; they concluded that in patients who were H. pylori-positive, with chronic atrophic gastritis by pepsinogen definition, the HR was 14.85 (1.96–107.7), whilst for patients who were H. pylori-negative with severe chronic atrophic gastritis the HR increased to 61.85 (5.6–682.64). Oishi et al. [135] followed 2466 patients for 12 years and found that a PGI level <70ng/mL with a PGI/II ratio <3.0 was linked with an HR for gastric cancer of 3.42 (1.92–6.11), and a PGI <30ng/mL with a PGI/II ratio <2.0 related to an HR of 4.43 (2.18–7.82). Finally, Dinis-Ribeiro et al., in a cohort of 100 patients followed for 3 years, found that the combination of incomplete intestinal metaplasia and a PGI/PGII ratio <3 was significantly associated with progression to dysplasia, with an HR of 13.9 (1.6–122.1) when compared with patients with only chronic atrophic gastritis or complete intestinal metaplasia [136].
Some of these studies also evaluated the presence of H. pylori and found that the most advanced and severe cases of gastric atrophy judged by the pepsinogen assessment, when combined with a negative H. pylori serology, probably due to a spontaneous disappearance of H. pylori antibody, were associated with an even greater progression to dysplasia and cancer. The values of hazard ratios of severely atrophic H. pylori-negative cases versus less atrophic H. pylori-positive cases were: 8.2 (3.2–21.5) vs. 6.0 in the study of Watabe et al. [130], 131.98 (11.95–1457.36) vs. 2.77 in that of Yanaoka et al. [132][133], and 61.85 (5.6–682.64) vs. 14.85 in that of Ohata et al. [134]. Yamaji et al. also found an increased incidence of gastric cancer, from 0.37% cases per year for the less atrophic H. pylori-positive cases to 0.53% cases per year in the severely atrophic H. pylori-negative cases [131].
On the issue of acceptability of examinations to patients, Miki et al. conducted a screening by serum pepsinogen in 101892 patients. This indicated 21178 endoscopies, of which 13789 were effectively done (65%): 125 cancers were diagnosed, 80% of them at an early stage [137].
Several case–control studies comparing gastric cancer patients with healthy controls, including a range of 84 to 511 cases per study, found statistically significant odds ratios (ORs) for cancer, ranging from 2.24–12.0 for a PGI level <50ng/mL to an OR of 2.78–10.92 for a PGI/PGII ratio <3 [138][139][140][141][142][143][144][145][146][147][148][149][150][151][152][153][154].
In diagnostic studies, detection of cancer by serum pepsinogen presented sensitivities of 66.7%–84.6% and specificities of 73.5%–81.5% [155][156][157], lower mean pepsinogen values compared with non-cancer patients [120][121][158], and a positive correlation with lower PGI/PGII ratio values [159]. Comparative studies of serum pepsinogen and gastric X-ray concluded that the positive predictive value was superior for serum pepsinogen (1.4% vs. 0.8%) especially before the age of 50 years [160][161].
Nevertheless, it was noted that most studies came from Japan, and that different laboratory methodologies and different population settings may require cutoff adjustment. Therefore, the term “low level of pepsinogens” was preferred over a defined cutoff value.
3.3.4 Additional diagnostic factors
11. Family history of gastric cancer should be taken into account in the follow-up of precancerous conditions (evidence level 2++, recommendation grade B). (Agree 96% [vote: a, 58%; b, 22%; c, 16%; d, 4%]; 98% voters stated that they would apply this statement; 100% of those representing national societies mentioned that it would also be applicable [90%] or widely applicable [10%] in their countries.)
12. Even though diverse studies assessed age, gender, and Helicobacter pylori virulence factors as well as host genetic variations, no clinical recommendations can be made for targeted management based on these factors with regard to diagnosis and surveillance (evidence level 4, recommendation grade D). (Agree 82% [vote: a, 42%; b, 4%; c, 36%; d, 14%; e,2%; f, 2%])
It has long been recognized that 10% of cases of gastric cancer exhibit some kind of familial aggregation. Of these, only 1%–3% are clearly vertically inherited familial syndromes, such as hereditary diffuse gastric gancer [162][163], Lynch syndrome [164][165], Peutz–Jeghers syndrome [166][167], and familial adenomatous polyposis [168], in which the risk of gastric cancer and carcinogenesis is well established. For the remainder, the significance of family history and familial clustering of gastric cancer is not clearly determined. Having a first-degree relative with gastric cancer is a risk factor for gastric cancer with an odds ratio (OR) varying from 2 to 10 in relation to geographic region and ethnicity [169]. A large study from Turkey reported an OR of 10.1 for siblings of gastric cancer patients, although these results were not adjusted for environmental factors [170]. Other European (OR 1.8–3.5), American (OR 2.2) and Asian (OR 1.5–9.9) case–control studies consistently provided corroboration that having a family history of gastric cancer is a risk factor [171][172][173][174][175][176][177][178]. Adjustment for environmental factors did not alter the risk. Interestingly, the Lauren intestinal type of gastric cancer was more strongly associated with family history of gastric cancer than the diffuse type [176][179]. It is believed that this familial clustering of gastric cancer is due to an inherited genetic susceptibility, shared environmental or lifestyle factors, or a combination of these in different populations. A recent meta-analysis [180] of 11 studies addressed Helicobacter pylori infection and prevalence of premalignant conditions/lesions in first-degree relatives of gastric cancer patients. For the total of 1500 cases and 2638 controls, the pooled OR for cases to have H. pylori gastritis was 1.93 (95% confidence interval [CI] 1.41–2.61), and it was 2.20 (1.27–3.82) for atrophy, and 1.98 (1.36–2.88) for intestinal metaplasia. Altogether, these data show that first-degree relatives of gastric cancer patients have an increased prevalence of H. pylori infection and premalignant conditions/lesions, as well as an increased risk for gastric cancer. To the best of our knowledge, there are no studies aiming to assess whether the premalignant conditions/lesions in relatives of a gastric cancer patient progress more rapidly through the carcinogenic cascade to gastric cancer than similar lesions in matched controls in a general population.
Assuming the gene–environment interaction for gastric cancer, multiple risk factors have been linked to the multistep progression from chronic non-atrophic gastritis to atrophic gastritis, intestinal metaplasia, dysplasia, and finally cancer [6].
H. pylori plays a pivotal role in this progression and has been classified as a type 1 carcinogen in 1994 by the World Health Organization (WHO) [181]. It is believed that the combination of a virulent organism in a genetically susceptible host is associated with more severe chronic inflammation and more rapid progression to gastric cancer, at least for Lauren’s intestinal type [182][183][184]. Different strains of H. pylori vary in their carcinogenic potential, with those containing virulence factor CagA inducing a high degree of inflammation. A meta-analysis of 16 case–control studies showed that among H. pylori-infected individuals, infection with CagA-positive strains further increases the risk for gastric cancer by 1.64 fold [185]. Other bacterial virulence factors, such as the CagA forms encoding multiple EPIYA-C type segments, and strains that harbor VacA signal region type s1 and mid-region m1 [186] have also been related to an increased risk for gastric cancer. Nevertheless there are no studies addressing the clinical usefulness of genotyping H. pylori strains with regard to the management and surveillance of gastric premalignant conditions/lesions.
An immense number of studies have addressed the issue of genes and genetic variations and their implications for gastric carcinogenesis, although their relevance has not always been clear. In the last few years, the role of host genetic interleukin polymorphisms has been widely studied in relation to gastric carcinogenesis. The best characterized are those that play a role in the inflammatory response to H. pylori infection and inflammation of the gastric mucosa, leading to mucosal atrophy and progression to gastric cancer. These in particular include IL-1B, IL1-receptor antagonist (IL-1RN), IL8, IL10 and TNF-α. Early studies by El-Omar et al. [187] showed an association of gastric cancer risk with the interleukin 1 genotypes IL-1B-511T, IL-1B-31T, and the IL1-receptor antagonist type *2/*2, with ORs of 2.5, 2.6 and 3.7 for development of gastric cancer among homozygotic carriers of these alleles compared with non-carriers. Results from other studies were inconsistent because of variations in allele frequencies in different ethnic groups, tumor type and location, H. pylori infection, methodologies, and quality of studies [188][189]. Three powered meta-analyses found an association of IL-1B and IL-1RN*2 risk in Caucasians but not in Asians [190][191][192] and another study found a null association in both populations [193]. Another recent meta-analysis [189] found an increased cancer risk for IL-RN*2 carriers, a risk that was specific to non-Asian populations and for distal cancers; the analysis restricted for high quality studies or H. pylori-positive cases and controls disclosed an association with the carrier and the homozygosity status. Regarding Asian populations, reduced risk was observed with IL-1B-31C carrier status (in high quality studies). Caucasian carriers of TNF-α-308A were found to be at an increased risk for gastric cancer in a recent meta-analysis [194]. At present, the heterogeneity of results makes it difficult to translate them into recommendations for daily clinical practice.
3.4 Surveillance
3.4.1 Dysplasia
13. Patients with low grade dysplasia in the absence of an endoscopically defined lesion should receive follow-up within 1 year after diagnosis. In the presence of an endoscopically defined lesion, endoscopic resection should be considered, to obtain a more accurate histological diagnosis (evidence level 2+, recommendation grade C). (Agree 98% [vote: a, 60%; b, 26%; c, 13%; d, 2%]; 96% of voters stated that they would apply this statement; 90% of those representing national societies mentioned that it would be applicable [80%] or widely applicable [10%] in their countries.)
14. For patients with high grade dysplasia in the absence of endoscopically defined lesions, immediate endoscopic reassessment with extensive biopsy sampling and surveillance at 6-month to 1–year intervals is indicated (evidence level 2+, recommendation grade C). (Agree 98% [vote: a, 69%; b, 17%; c, 12%; d, 2%]; 100% of voters stated that they would apply this statement; 100% of those representing national societies mentioned that it would be applicable [70%] or widely applicable [30%] in their countries.)
As mentioned above, differences exist between studies from the West and from Asia in reported progression rate of severe dysplasia. A large prospective study in China included 546 patients with dysplasia: within 5 years of follow-up, progression rates to gastric cancer were 0.6% per year for mild dysplasia (now generally called low grade dysplasia), and 1.4% for severe dysplasia (now generally called high grade dysplasia) [32]. The largest Western study included 7,616 patients with mild to moderate dysplasia, and 562 with severe dysplasia: within 5 years’ follow-up, the annual incidence of gastric cancer was 0.6% for mild to moderate dysplasia, and 6% for severe dysplasia [28].
High grade dysplasia-associated risk. Most patients harboring lesions classified as high grade dysplasia are at high risk for either synchronous invasive carcinoma or its rapid development [34]. In a cohort of patients with premalignant gastric lesions, approximately 25% of patients with high grade dysplasia received a diagnosis of gastric cancer within 1 year of follow-up [28]. This finding implies that thorough endoscopic and histological re-evaluation shortly after initial diagnosis is indicated, and resection needs to be considered in the case of endoscopically defined lesions, either through endoscopy (endoscopic mucosal resection) or surgery [45][195][196][197].
Low grade dysplasia-associated risk. Gastric cancer risk in patients with low grade dysplasia is similar to or even considerably higher than the risk of cancer after removal of colonic adenomas, or in patients with Barrett’s esophagus, or in those with long-standing inflammatory bowel disease [198][199][200]. In comparison with patients harboring high grade dysplasia, patients with low grade dysplasia seem to show a smaller risk to progress to invasive carcinoma of 7% (95%CI 6%–8%) [28][29][33][34][35][36][37][42][43][45][201][202][203].
Thus, at least endoscopic surveillance at regular intervals seems to be indicated, although cost–effectiveness requires further evaluation. When repeated endoscopy with surveillance biopsy sampling confirms the presence of low grade dysplasia, continued surveillance is warranted. When low grade dysplasia cannot be confirmed during re-evaluation endoscopy, it is unclear for how long surveillance should be continued.
Of major importance is the fact that low grade and high grade dysplasia may present as endoscopically visible, depressed or elevated lesions [34][200], but may also present as minute or flat lesions, that may be isolated or multifocal [7]. Thus, the disappearance of dysplasia or its assumed disappearance, as evaluated by successive current videoendoscopy biopsies during follow-up procedures, does not rule out the possible progression to invasive cancer [37][44][196][204].
It seems therefore reasonable to propose high quality endoscopic follow-up for patients with low grade dysplasia [33][37][201][205], expanding this to endoscopic resection of the most severe lesions in some patients [196][202][206]. In fact, a histological diagnosis of low grade dysplasia in forceps biopsies, obtained from an endoscopically defined lesion, may be upgraded to a diagnosis of high grade dysplasia or even adenocarcinoma after endoscopic mucosal resection (EMR) [207][208]. In a Korean patient series such an upgraded diagnosis after EMR occurred in up to 19% of low grade dysplasia diagnoses on biopsy forceps specimens [208]. However, previously mentioned progression rates of low grade dysplasia in large series seem discrepant with these findings. Moreover, in 3% to 5% of gastric neoplasia diagnoses on forceps biopsy tissue, EMR does not confirm this diagnosis [208][209]. Nevertheless, EMR may be considered in patients with low grade dysplasia with an endoscopically defined lesion, in order to obtain a more accurate histological diagnosis.
3.4.2 Atrophy or intestinal metaplasia
15. Endoscopic surveillance should be offered to patients with extensive atrophy and/or intestinal metaplasia (i.e., atrophy and/or intestinal metaplasia in the antrum and corpus) (evidence level 2++, recommendation grade B). (Agree 94% [vote: a, 60%; b, 15%; c, 19%; d, 4%; f, 2%]; 91% of voters stated that they would apply this statement; 80% of those representing national societies mentioned that it would be applicable in their countries.)
16. Patients with extensive atrophy and/or intestinal metaplasia should receive follow-up every 3 years after diagnosis (evidence level 4, recommendation grade D). (Agree 86% [vote: a, 43%; b, 20%; c, 23%; d, 12%; f, 2%]; 90% of voters stated that they would apply this statement; 80% of those representing national societies mentioned that it would be applicable [70%] or widely applicable [10%] in their countries.)
17. For those patients with mild to moderate atrophy/intestinal metaplasia restricted to the antrum there is no evidence to recommend surveillance (evidence level 4, recommendation grade D). (Agree 99% [vote: a, 87%; b, 13%; c, 9%; d, 1%])
As early detection of gastric cancer leads to improved survival, surveillance of premalignant gastric conditions/lesions may be important, as shown in several studies. Rates of progression in patients with atrophic gastritis, and intestinal metaplasia vary between respectively 0% to 1.8%, and 0% to 10% per year. Overall, gastric cancer risk is too low to justify endoscopic surveillance in all patients with atrophic gastritis and intestinal metaplasia. Therefore, additional risk factors for progression towards gastric cancer need to be identified in these categories of patients.
First, the intragastric distribution and extent of intestinal metaplasia has been identified as a risk factor for gastric cancer. Atrophic gastritis tends to show a diffuse intragastric pattern, whereas intestinal metaplasia tends to be multifocal [44]. Several studies have shown that gastric cancer risk increases in patients with extensive intragastric lesions [210][211][212][213]. Two forms of extensive intestinal metaplasia have been identified. In the so-called “magenstrasse” or “transitional zones” distribution, intestinal metaplasia is found over the lesser curvature from cardia to pylorus and is especially common in the transitional zones (from cardia to corpus, from corpus to antrum), and in the “diffuse distribution” the gastric mucosa is diffusely replaced by intestinal-type mucosa, except for in the fundic region [214]. These topographical patterns of intestinalization show an increased risk for cancer (odds ratio [OR]=5.7 [95%CI 1.3–26] and OR=12.2 [2.0–72.9], respectively). To establish the extent of atrophic gastritis and intestinal metaplasia, three methods can be used: endoscopic assessment, histological assessment of biopsy specimens, and serology. In Asian countries the presence and extent of premalignant gastric conditions/lesions are frequently established at endoscopy. For the presence of atrophic gastritis the Kimura classification is used [215]. However, this method requires considerable experience on the part of endoscopists. In addition, biopsy sampling can be used to estimate the intragastric extent of lesions and the severity of atrophic gastritis and intestinal metaplasia can be assessed according to the Sydney System. As has been suggested by the OLGA (operative link for gastritis assessment) and OLGIM (operative link for gastric intestinal metaplasia) classifications, both the intragastric extent and severity of atrophic gastritis and intestinal metaplasia within biopsy samples determines gastric cancer risk. Finally, serologic testing for pepsinogens, gastrin, and H. pylori antibodies has great potential for establishing the intragastric extent of atrophic gastritis. Serology identifies individuals at increased risk of progression towards dysplasia and gastric cancer, and is currently used in certain Japanese gastric cancer screening programs to identify patients to whom follow-up should be offered [100].
Secondly, individuals with a positive family history of gastric cancer carry an increased risk of premalignant gastric conditions/lesions, and gastric cancer. The risk of atrophic gastritis in these individuals is approximately seven times higher compared with that of controls [187].
Thirdly, the type of intestinal metaplasia has been suggested as a risk factor for gastric cancer development. In a few studies, type III or incomplete intestinal metaplasia was associated with an increased risk for development of gastric cancer [19][216][217]. However, these observations have not been confirmed in other studies [218][219]. Therefore, subtyping of intestinal metaplasia is not recommended for clinical practice.
3.5 Therapy
3.5.1 Eradication of Helicobacter pylori
18. Helicobacter pylori eradication heals nonatrophic chronic gastritis and it may lead to partial regression of atrophic gastritis (evidence level 1+, recommendation grade B). (Agree 96% [vote: a, 70%; b, 16%; c, 10%; d, 4%]; 98% of voters stated they would apply this statement; 90% of those representing national societies mentioned that it would be applicable [40%] or widely applicable [50%] in their countries.)
19. In patients with intestinal metaplasia, H. pylori eradication does not appear to reverse intestinal metaplasia but it may slow progression to neoplasia, and therefore it is recommended (evidence level 1+, recommendation grade B). (Agree 96% [vote: a, 50%; b, 24%; c, 22%; d, 4%]; 100% of voters stated they would apply this statement; 90% of those representing national societies mentioned that it would be applicable or widely applicable [30%] in their countries.)
20. H. pylori eradication is recommended for patients with previous neoplasia after endoscopic or surgical therapy (evidence level 1++, recommendation grade A). (Agree 96% [vote: a, 80%; b, 8%; c, 8%; d, 4%]; 96% of voters stated they would apply this statement; 100% of those representing national societies mentioned that it would be applicable or widely applicable [50%] in their countries.)
In rodent models, Helicobacter pylori eradication has been shown to have a prophylactic effect on gastric cancer [220][221][222].
However, studies on H. pylori eradication in humans have shown less consistent results. There is no dispute that H. pylori eradication leads to healing of non-atrophic gastritis, but the evidence is not so clear for gastric atrophy and intestinal metaplasia.
A recent randomized study and a meta-analysis showed that in early stages of disease such as chronic gastritis and gastric atrophy without metaplasia, H. pylori eradication markedly improves gastric histology towards normal [223][224]. Another systematic review also concluded that atrophic gastritis can regress within 1–2 years after H. pylori eradication [225].
A more recent meta-analysis on this subject suggests that gastric atrophy, however, may be reversible only in the corpus and not in the antrum [226]. The probability of reversal of gastric atrophy appears to be dependent on the extent and topographic location of atrophy [226]; however it is unclear whether the effects of H. pylori eradication vary with the location and extent of atrophy.
In contrast to gastritis and atrophy, the effect of H. pylori eradication on gastric intestinal metaplasia is controversial. Some authors completely refute the idea of reversibility of intestinal metaplasia after H. pylori eradication [227][228]. A lower H. pylori colonization of metaplastic areas may indicate a limited benefit for eradication. Two meta-analyses on this subject also concluded that there is no significant improvement in intestinal metaplasia after H. pylori eradication [224][226]. Nevertheless, in a randomized trial, after 6 years of follow-up, Correa et al. showed that in patients with preneoplastic lesions, effective anti-H. pylori treatment and dietary supplementation with antioxidant micronutrients may interfere with the precancerous process, mostly by increasing the rate of regression of cancer precursor conditions/lesions including intestinal metaplasia [229]. This regression of atrophy and intestinal metaplasia was further confirmed after 12 years of follow-up [230].
Nevertheless, it remains to be proven whether eradication at these stages reduces the risk of cancer.
A large-scale randomized trial in China failed to demonstrate that H. pylori eradication led to a significant decrease in the rate of gastric cancer [231]. However, in the same study, considering only the group of patients without preneoplasic conditions/lesions at baseline, the risk of cancer in a period of 7.5 years was reduced after H. pylori eradication (0 vs. 6 cases, P=0.02). A subsequent meta-analysis, including four randomized intervention studies with a follow-up ranging from 5 to 12 years comparing H. pylori eradication versus placebo for prevention of gastric cancer, showed a non-statistically significant trend in favor of eradication therapy. Further analysis with inclusion of non-randomized studies with follow-up of 3–8.5 years showed a significant reduction in cancer incidence after eradication [232]. The same authors recently updated their meta-analysis and, in a pooled analysis of 6 studies with a total of 6695 participants followed from 4 to 10 years, they found that the relative risk for gastric cancer following H. pylori eradication was 0.65 (95%CI 0.43–0.98) [233]. These authors concluded that while H. pylori eradication seems to reduce gastric cancer, however, that might be relevant in only a subset of participants, probably in the early stages of gastritis (non-atrophic) [232][233]. Another systematic review also concluded that there is sufficient clinical evidence that H. pylori eradication has a role in the prevention of gastric cancer in patients with chronic non-atrophic gastritis and with atrophic gastritis [225]. Indeed, a large prospective study (mean follow-up of 9.4 years) also suggested that H. pylori eradication before the development of intestinal metaplasia is probably more effective in reducing gastric cancer incidence [234].
Moreover, four prospective trials (follow-up range 3–8.5 years) that evaluated the effect of H. pylori eradication in patients with premalignant conditions/lesions to the end point of gastric cancer failed to show a significant reduction in cancer risk [230][231][235][236]. And, one non-randomized prospective study (mean follow-up 8.6 years) demonstrated a significant reduction of gastric cancer development after successful H. pylori eradication in comparison with those with persistent H. pylori infection [237]. However, in the same cohort, cancer still developed after 14 years of follow-up in some H. pylori-negative patients, suggesting that even after cure of infection, cancer can still develop [238]. Nevertheless, in studies involving patients who had previously undergone endoscopic resection of cancer, the majority of whom had extensive intestinal metaplasia, the risk of cancer was significantly reduced after successful H. pylori eradication and in a short period of time (3 years) [239][240].
Indeed, at least, H. pylori eradication seems to decrease the progression of gastric intestinal metaplasia [235][241][242]. However, even after successful H. pylori eradication, gastric cancer still develops in the context of intestinal metaplasia [234][238]. Therefore, the evidence is not clear regarding whether H. pylori eradication will reduce the risk of cancer in patients with extensive intestinal metaplasia, although there is some evidence that it slows progression.
Based on these literature data, the consensus panel came to the view that H. pylori eradication should be considered in a case-by-case approach in patients with intestinal metaplasia, taking into account the extent of metaplasia and the degree of H. pylori colonization.
H. pylori eradication is recommended by several societies and guidelines for gastric cancer patients who undergo subtotal gastrectomy [243][244][245][246]. Indeed, eradication of H. pylori in patients with previous endoscopic resection of tumors decreases the rate of occurrence of new tumors and the severity of intestinal metaplasia [240]. These results were confirmed in a multicenter randomized control trial [239]. In this open-label study, 272 patients were allocated for eradication or no eradication, with similar baseline characteristics in both groups; after 3 years of follow-up, 24 metachronous lesions had developed in the non-eradication group compared with 9 new lesions in the eradication group (P <0.01). Another study showed that H. pylori eradication in this high risk population was a cost-effective strategy [247]. All these studies showed this protective effect after a short period of time (3 years).
Concerning the effect of H. pylori eradication on the progression of gastric dysplasia, the data are scarce and contradictory [229][230][236]. So far, most of the evidence suggests that dysplastic lesions are not affected by eradication. However, patients with dysplasia may benefit from eradication because of a decreased incidence of metachronous lesions.
Taking these considerations together, in patients with a previous history of gastric cancer, including dysplasia, H. pylori eradication is strongly recommended.
3.5.2 Additional measures
21. Currently, the use of cyclooxgenase-2 (COX-2) inhibitors cannot be supported as an approach to decrease the risk of progression of gastric precancerous lesions (evidence level 1+, recommendation grade B). (Agree 96% [vote: a, 50%; b, 20%; c, 26%; d, 2%; e, 2%])
22. The use of dietary supplementation with antioxidants (ascorbic acid and beta-carotene) cannot be supported as a therapy to reduce the prevalence of atrophy or intestinal metaplasia (evidence level 1+, recommendation grade B). (Agree 96% [vote: a, 63%; b, 14%; c, 19%; d, 4%])
Meta-analyses of observational studies demonstrated that long-term non-selective inhibition of cyclooxygenase (COX), through the use of non-steroidal anti-inflammatory drugs (NSAIDs), is an effective chemopreventive strategy for gastric cancer development [248][249].
The available literature on the efficacy of the use of COX-2 inhibitors to prevent the progression of gastric precancerous lesions is restricted to five clinical studies conducted exclusively in Asian populations. The overall evidence regardless of type of drug used is inconsistent. Apart from one well-designed placebo-controlled randomized controlled trial (RCT) [250] the evidence suggesting a preventive effect of these chemopreventive agents on precancerous lesions outcome is drawn from low quality studies, comprising one small RCT [251], one pilot study [252] and two prospective cohorts [253][254]. These were conducted in very heterogeneous populations (first-degree relatives of gastric cancer patients, dyspeptic patients with rheumatologic diseases, early gastric cancer patients, etc) that compromise the generalizability and interpretation of data.
Three selective COX-2 inhibitors were considered: rofecoxib, etodolac, and celecoxib. Rofecoxib for 2 years in an RCT did not have a significant benefit in terms of intestinal metaplasia regression after Helicobacter pylori eradication [250]. Yanaoka et al. reported a higher metachronous cancer incidence in patients treated with 300mg/day of etodolac, after a mean follow-up period of 4.2 years. Interestingly, no significant change in the extent of precancerous conditions/lesions was observed despite etodolac treatment [253].
Most studies focused on whether celecoxib, a selective COX-2, could decrease the severity of gastric precancerous conditions/lesions following H. pylori eradication. In patients receiving celecoxib in a small randomized trial, a 67% improvement in gastric precancerous lesion histology was observed (P<0.001, vs. 16.1% in the placebo group) after 12 weeks [251]. In a pilot study, following 8 weeks of intervention, in 29% of patients a complete regression of persistent intestinal metaplasia was noticed in those with confirmed H. pylori eradication [252]. Furthermore, in those patients without complete regression an improvement in intestinal metaplasia severity was noticed (P<0.007) [252]. Additionally, Yang et al. [254], observed that dyspeptic chronic users of celecoxib for rheumatologic diseases presented a higher regression rate of intestinal metaplasia than non-NSAID users (42% vs. 20%; relative risk [RR]=2.9, 95%CI 1.88–6.91) but only after H. pylori eradication.
Therefore, there is some evidence supporting the involvement of celecoxib in the regression of gastric precancerous conditions/lesions, namely intestinal metaplasia, that could motivate the design of larger RCTs with longer follow-up.Furthermore, regular use of non-selective NSAIDs, including aspirin, has been associated with a decreased risk for gastric cancer development, as observed in a recent large retrospective cohort [255] and meta-analyses [249]. Further prospective clinical trials are needed to address the effects of these non-specific COX inhibitors on the progression of gastric lesions.
Three chemoprevention trials specifically designed to evaluate the effects of antioxidant vitamin supplementation on gastric precancerous lesions, have been reported [136][156][229]. These randomized double-blind placebo-ontrolled trials, conducted in populations at high risk for gastric cancer, presented conflicting results and their quality is compromised by significant loss to follow-up/withdrawal observed in two of the studies [229][256].
Correa et al. [229] reported that patients randomized to single active intervention with ascorbic acid (1g twice daily), beta-carotene (30mg/day) or anti-H. pylori therapy were three times more likely to show an improvement in the histology of their lesions after a 6-year follow-up period. However, this antioxidant benefit disappeared after a further 6 years with no vitamin supplementation, as shown in a re-evaluation at 12 years after the inception of the study [230].
In contrast, a long-term trial in Linqu County, Shandong, China reported no favorable effect on the prevalence of gastric precancerous conditions/lesions after 7.2 years of intervention with vitamin supplements (capsule with 250mg ascorbic acid, 100IU vitamin E, and 37.5µL selenium, twice daily) [236]. Similarly, Plummer et al. [256], in a study involving patients randomized to receive either vitamins (capsule with 250mg ascorbic acid, 200mg vitamin E, and 6mg beta-carotene/thrice daily) or placebo for 3 years, did not observe any significant association between vitamin supplementation and the progression/regression of gastric precancerous conditions/lesions.
These studies were carried out in populations with a high incidence of gastric cancer, in Columbia, Venezuela and China [229][236][256]. It is as yet unclear to what extent these results can be generalized to populations with a low incidence of gastric cancer.
3.6 Cost–effectiveness
23. After endoscopic resection of early gastric cancer, Helicobacter pylori eradication is cost-effective (evidence level 1+, recommendation grade B). (Agree 100% [vote: a, 79%; b, 14%; c, 7%])
24. Currently available evidence does not allow an accurate estimation of the cost–effectiveness of surveillance for premalignant gastric conditions worldwide (evidence level 2+, recommendation grade C). (Agree 98% [vote: a, 41%; b, 16%; c, 41%; d, 2%])
Most of the studies on cost–effectiveness of Helicobacter pylori eradication for gastric cancer prevention report on models with a population screening scenario, which is outside the scope of this manuscript. Only a few studies dealt with the issue of surveillance after an incidental diagnosis of a gastric premalignant condition/lesion. Most of these studies compared strategies of screening for and treating H. pylori versus no screening from the public healthcare provider’s perspective; used estimates from systematic reviews of the literature; and conducted sensitivity analyses with results that were consistent in most strategies. Despite involving populations with very different gastric cancer risks, and also the use of diverse models, all studies concluded that the screening option is cost-effective compared with no screening [257][258][259][260][261][262][263][264][265][266][267][268][269].
Concerning the possibility of H. pylori eradication after endoscopic mucosal resection (EMR) of a gastric precancerous lesion, Shin et al. [247] developed a Markov model based on a randomized clinical trial conducted by Fukase et al. [239] precisely on this topic. They used a very wide set of clinical health estimates derived from an extensive search of the literature, and costs were based on the perspective of the Korean public healthcare provider. The results showed that in the base-case assumptions, H. pylori eradication was less costly than no eradication (US$ 29 780 versus 30 594) and also provided more benefits (mean life expectancy of 13.60 versus 13.55). Thus, treatment of 10000 persons would lead to a net saving of US$ 814 200 and around 50 life-years saved (LYS) would be gained. This strategy was dominant (less costly and more effective) but the usual calculation of the ICER (incremental cost–effectiveness ratio) value was not performed. By conducting one-way and three-way sensitivity analyses, the authors confirmed the robustness of the model, with a dominant ICER conclusion for the strategy of eradication in almost every scenario or providing very cost-effective values (always below US$ 3852 per LYS).
Concerning the cost–effectiveness of secondary surveillance of incidentally detected precancerous conditions/lesions, studies in the published literature provide conflicting results, mainly due to different estimates for lesion progression to dysplasia or cancer. Yeh et al. [270] compared several strategies, from neither surveillance nor treatment to surveillance of various precancerous gastric conditions/lesions at several frequencies followed by treatment with endoscopic mucosal resection (EMR) or surgery. The model was cost-effective for men over 50 years with dysplasia treated by EMR with annual surveillance (cost per quality-adjusted life-year [QALY] US$ 39 800), but not for patients with intestinal metaplasia (cost per QALY US$ 544 500 for surveillance every 10 years). Hassan et al. [271], using a model for the American population, revealed an incremental cost-effectiveness ratio above $70 000 per life-year saved for an yearly endoscopy versus no surveillance in patients with intestinal metaplasia, while in a model derived from a Portuguese cohort, Dinis-Ribeiro et al. [136] obtained a cost of only €1868 per QALY in a protocol of yearly magnification chromoendoscopy and pepsinogen measurement.
These conflicting results might arise from very different estimates of the yearly rates for progression of conditions (0.00–0.012% per year for dysplasia to invasive cancer in the study of Yeh et al. [270]; 0.18% for intestinal metaplasia to cancer in Hassan et al. [271]; and 12.8%–56.0% for intestinal metaplasia to dysplasia in the study by Dinis-Ribeiro et al. [136]), and might also arise from the differing cost estimates included in the models (cost per endoscopy of US$ 871 versus US$ 358 in the studies by Yeh at al. and Hassan et al., respectively [270][271]). Moreover, no study except that of Dinis-Ribeiro et al. [136] considered different stages of premalignant gastric conditions/lesions.
The extensive examination of the literature and the discussion within the consensus panel led to the research agenda described below, with the possibility of a review in 3 to 5 years.
Reliability studies for histopathological staging systems for precancerous conditions and for endoscopic features
Large multicenter cohort studies to derive and validate clinical decision rules addressing the value of variables other than the phenotype of lesion extent, such as age, gender, Helicobacter pylori virulence factors, and genetic profiles
Large multicenter cohort studies to further clarify stages involved in gastric carcinogenesis, such as the elucidation of the role of spasmolytic polypeptide-expressing metaplasia (SPEM)
Standardization and validation of endoscopic features with new endoscopic technologies, and randomized trials to address the benefit per-patient in this setting (diagnosis of intestinal metaplasia and atrophy in corpus; and diagnosis of superficial lesions)
Further clarification of the role of H. pylori eradication and other therapies in prevention of gastric cancer
Observational and/or decision-analysis studies addressing follow-up intervals and cost–benefit of these strategies
Studies to address methodologies and target populations for the screening of these lesions in Western countries.
These guidelines were made possible through the financial support of the European Society of Gastrointestinal Endoscopy (ESGE) and the Sociedade Portuguesa de Endoscopia Digestiva (SPED). Olympus (Europe), Casen-Fleet (Portugal) and Angelini (Portugal) gave educational grants to ESGE and SPED. We would also like to acknowledge Eng. Jorge Jacome for his support through MedQuest development; and the Secretariats of ESGE (Hilary Hamilton and Nicola Oremus) and SPED (Maria José Ilharco).
All contributors are listed below in alphabetic order, according to their role (Working Group, as national representative, or as an individual), and their participation in the Porto meeting (* indicates those who voted online only, and not at the Porto meeting).
Panel of Experts or Young Investigators (Working Group)
Miguel Areia, Gastroenterology Department, Portuguese Oncology Institute; Fátima Carneiro, European Society of Pathology, Porto Faculty of Medicine, Serviço de Anatomia Patológica, Porto ,Portugal; Annemarie de Vries, Erasmus MC University Medical Center Rotterdam, Gastroenterology and Hepatology, Rotterdam, The Netherlands; Mário Dinis-Ribeiro, Servico de Gastrenterologia, Instituto Portugues de Oncologia Francisco Gentil, Porto, Portugal; Jean-Marc Dumonceau, Départment de Gastroénterologie et d’Hépatopancréatologie, H.U.G. Hôpital Cantonal, Geneve, Switzerland; *Arzu Ensari, Department of Pathology, Ankara University Medical School, Turkey; Ernst J. Kuipers, Department of Gastroenterology and Hepatology, Erasmus MC, Rotterdam, The Netherlands; Guilherme Macedo, IPATIMUP, Porto, Portugal; Jose Carlos Machado, Department of Gastroenterology, Hospital de S.João/Porto Faculty of Medicine, Portugal; Peter Malfertheiner, Klinik der Gasroenterologie, Hepatologie und Infektologie, Otto von Guericke Universität Magdeburg, Germany; Ricardo Marcos-Pinto, Gastroenterology Department, Centro Hospitalar do Porto, Portugal; Tamara Matysiak-Budnik, Service d’Hépato-Gastroentérologie, Hôtel Dieu, CHU de Nantes, France; Francis Megraud, Inserm U853 and Université Bordeaux, Laboratoire de Bacteriologie, Bordeaux, France; Kazumasa Miki, Japan Research Foundation of Prediction, Diagnosis and Therapy for Gastric Cancer (JRF PDT GC), Tokyo, Japan; Matilde Monteiro-Soares CINTESIS, Porto Faculty of Medicine, Portugal; Anthony O’Connor, AMNCH/TCD, Adelaide and Meath Hospital/Trinity College, Dublin Tallagh, Ireland; Colm O’Morain, Department of Gastroenterology, Adelaide and Meath Hospital, Dublin, Ireland; Richard Peek, Division of Gastroenterology, Vanderbilt University School of Medicine, Nashville, USA; Carina Pereira, Grupo de Oncologia Molecular, Instituto Português de Oncologia do Porto FG, EPE, Porto, Portugal; Pedro Pimentel-Nunes, Servico de Gastrenterologia, IPO-Porto, Portugal, and Department of Physiology, Cardiovascular Research and Development Unit, Medical Faculty, Porto, Portugal; Thierry Ponchon, Hopital Edouard Herriot, Department of Digestive Diseases, Lyon, France; Björn Rembacken, Centre for Digestive Diseases, The General Infirmary at Leeds, UK; Ari Ristimaki, Department of Pathology, HUSLAB and Haartman Institute, Helsinki University Central Hospital and University of Helsinki, Helsinki, Finland.
National representatives
Gieri Cathomas (Switzerland, pathology), Head of the Cantonal Institute for Pathology, President Swiss Society of Gastrointestinal Pathology, Cantonal Institute for Pathology, Liestal, Switzerland; Evgeny D. Fedorov (Russia), Russia State Medical University, Moscow University Hospital; Pedro Manuel Narra de Figueiredo (Portugal), Hospitais da Universidade de Coimbra, Serviço de Gastrenterologia, Coimbra, Portugal; Adrian Goldis (Romania), Clinic of Gastroenterology Algomed, Timisoara, Romania; Marcis Leja (Latvia), University of Latvia, Latvian Society of Gastroenterology, Hospital Linezers, Riga, Latvia; Markus Moehler (Germany), 1.Medizinische Klinik und Poliklinik der Johannes-Gutenberg Universität Mainz, Germany; Emil Plesea (Romania, pathology), Department of Pathology, University of Medicine and Pharmacy, Craiova, Romania; *Jacques Bergman (The Netherlands), Department of Gastroenterology and Hepatology, Academic Medical Center Amsterdam, The Netherlands; *Waseem Hamoudi (Jordan), Jordanian Society of Gastroenterology, Amman, Jordan.
As individuals
Raquel Almeida, IPATIMUP, Porto, Portugal; Bruno Annibale, Dipartimento Medico-chirurgico di scienze cliniche, Tecnobiomediche e medicina traslazionale, Section of Gastroenterology, Rome, Italy; Luís Azevedo Lobo, Gastroenterology Department, Pedro Hispano Hospital, ULS Matosinhos, Senhora da Hora, Portugal; Yasemin Hatice Balaban, Hacettepe University, Gastroenterology Unit, Ankara, Turkey; Alina Boeriu, Gastroenterology Department, University of Medicine, Targu Mures, Romania; Alain Burette, Gastroenterology Department, CHIREC, Brussels, Belgium; Anne Courillon Mallet, Service Hépato-gastroentérologie, Centre Hospitalier de Villeneuve St Georges, Villeneuve St Georges, France; Leonor David, IPATIMUP, Porto, Portugal; Jean-Charles Delchier, Service d’hépatogastroentérologie, Hôpital Henri Mondor, Créteil, France; Ecaterina Daniela Dobru, Gastroenterology Department, University of Medicine and Pharmacy, TG. Mures, Romania; Carlos Fernandes, C. H. Vila Nova de Gaia/Espinho, Portugal; Michel Kahaleh, Division of Gastroenterology/Hepatology, University of Virginia Health System, Charlottesville, USA; Sergey Kashin, Yaroslavl Regional Cancer Hospital, Yaroslavl, Russia; Rafael Lomba-Viana, Porto, Portugal; Nuno Lunet, University of Porto Medical School, Department of Clinical Epidemiology, Predictive Medicine and Public Health, Porto, Portugal; Kirill Marakhouski, Minsk, Belarus; Luis Moreira-Dias, Instituto Português De Oncologia Do Porto, Serviço De Gastrenterologia, Porto, Portugal; Carlos Noronha Ferreira, Serviço de Gastrenterologia e Hepatologia, Hospital de Santa Maria-Centro Hospitalar Lisboa Norte, Lisbon, Portugal; Teresa Pinto Pais, Portugal; Antonio Rollán, Gastroenterology Department, Clinica Alemana, Santiago, Chile; Ana Sadio, IPATIMUP, Porto, Portugal; Carlos Figueiredo Costa Santos, Casa Saude Boavista, Porto, Portugal; *Joao Santos Barbosa, Lisbon, Portugal; *Kent-Man Chu, Department of Surgery, The University of Hong Kong, Queen Mary Hospital, Pokfulam, Hong Kong; *Giancarlo D’Ambra, Rome, Italy; *Pierre Ellul, Mater Dei Hospital, Sliema, Malta; *Nicole van Grieken, Department of Pathology, VU University Medical Center, Amsterdam, The Netherlands; *Dominique Lamarque, Service Hépato-Gastroentérologie, Oncologie digestive, Hôpital Ambroise Paré, Boulogne-Billancourt, France; *Akram Ajeel Najeeb, Medical City, Bab Al-Mudhaam, Baghdad, Iraq.
These guidelines represent a consensus of best practice based on the available evidence at the time of preparation. They may not apply in all situations and should be interpreted in the light of specific clinical situations and resource availability. Further controlled clinical studies may be needed to clarify aspects of these statements, and revision may be necessary as new data appear. Clinical consideration may justify a course of action at variance to these recommendations. These guidelines are intended to be an educational device to provide information that may assist endoscopists in providing care to patients. They are not rules and should not be construed as establishing a legal standard of care or as encouraging, advocating, requiring, or discouraging any particular treatment.
Competing interests: None.
* Chairman, ESGE Educational Committee, and Chairman, SPED Research Committee
† Chairperson, ESP Digestive Pathology Working Group
‡ Chairman, ESGE Guidelines Committee
§ President, Portuguese Society of Digestive Endoscopy
¶ ESP Digestive Pathology Working Group
** on behalf of MAPS Participants. Including: Cathomas G (Switzerland), Fedorov ED (Russia), Figueiredo P (Portugal), Goldis A (Romania), Leja M (Latvia), Moehler M (Germany), Plesea E (Romania), Bergman J (The Netherlands), Hamoudi W (Jordan), Almeida R, Annibale B, Lobo LA, Balaban YH, Boeriu A, Burette A, Mallet AC, David L, Delchier J-C, Dobru ED, Fernandes C, Kahaleh M, Kashin S, Lomba-Viana R, Lunet N, Marakhouski K, Moreira-Dias L, Ferreira CF, Pais TP, Rollán A, Sadio A, Santos C, Chu K-M, D'Ambra G, Ellul P, van Grieken N, Lamarque D, Najeeb AA
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Korrespondenzadresse
M. Dinis-Ribeiro, MD PhD
Gastroenterology Department
Portuguese Oncology Institute of Porto
Rua Dr. Bernardino de Almeida
4200–072 Porto
Portugal
+351–22–5084055
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