Evidence map›Paper›PMID 31206244›Full record

ArticleThe journal of pathology. Clinical research2019

Prognostic implication of molecular subtypes and response to neoadjuvant chemotherapy in 760 gastric carcinomas: role of Epstein-Barr virus infection and high- and low-microsatellite instability.

Meike Kohlruss, Bianca Grosser, Marie Krenauer, Julia Slotta-Huspenina, Moritz Jesinghaus, Susanne Blank, Alexander Novotny, Magdalena Reiche, Thomas Schmidt, Liridona Ismani and 8 more

Open access · goldAbstract read
In one paragraph

Article in The journal of pathology. Clinical research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed, 2 pooled it
9.4field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

49 citing papers in PubMed, 2 syntheses or guidelines pooled it, 84 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Low microsatellite instability revisited: a review.Virchows Archiv : an international journal of pathology · 2026
    Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Potent therapeutic strategy in gastric cancer with microsatellite instability-high and/or deficient mismatch repair.Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association · 2024
    Review
  9. Review
  10. Article
  11. Article
  12. Stroma AReactive Invasion Front Areas (SARIFA) proves prognostic relevance in gastric carcinoma and is based on a tumor-adipocyte interaction indicating an altered immune response.Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association · 2024
    Article
  13. Article
  14. Low microsatellite instability: A distinct instability type in gastric cancer?Journal of cancer research and clinical oncology · 2023
    Article
  15. Review
  16. Concordance of microsatellite instability and mismatch repair status in paired biopsies and surgical specimens of resectable gastroesophageal adenocarcinoma: time for a call to action.Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association · 2023
    Article
  17. Observational
  18. Observational
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

18 authors at 4 institutions in 1 country.

Meike KohlrussInstitute of Pathology, Technical University of Munich, Munich, Germany.
Bianca GrosserInstitute of Pathology, Technical University of Munich, Munich, Germany.
Marie KrenauerInstitute of Pathology, Technical University of Munich, Munich, Germany.
Julia Slotta-HuspeninaInstitute of Pathology, Technical University of Munich, Munich, Germany.
Moritz JesinghausInstitute of Pathology, Technical University of Munich, Munich, Germany.
Susanne BlankDepartment of Surgery, University of Heidelberg, Heidelberg, Germany.
Alexander NovotnyDepartment of Surgery, Technical University of Munich, Munich, Germany.
Magdalena ReicheInstitute of Pathology, Technical University of Munich, Munich, Germany.
Thomas SchmidtDepartment of Surgery, University of Heidelberg, Heidelberg, Germany.
Liridona IsmaniInstitute of Pathology, Technical University of Munich, Munich, Germany.
Alexander HapfelmeierInstitute of Medical Informatics, Statistics and Epidemiology, Technical University of Munich, Munich, Germany.
Daniel MathiasInstitute of Pathology, Technical University of Munich, Munich, Germany.
Petra MeyerInstitute of Pathology, Technical University of Munich, Munich, Germany.
Matthias M GaidaInstitute of Pathology, University of Heidelberg, Heidelberg, Germany.
Lukas BauerInstitute of Pathology, Technical University of Munich, Munich, Germany.
Katja OttDepartment of Surgery, Klinikum Rosenheim, Rosenheim, Germany.
Wilko WeichertInstitute of Pathology, Technical University of Munich, Munich, Germany.
Gisela KellerInstitute of Pathology, Technical University of Munich, Munich, Germany.ORCID 0000-0003-2886-0371
Technical University of Munich · DEHeidelberg University · DEGerman Cancer Research Center · DERoMed Kliniken · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Epstein-Barr virus positivity (EBV(+)) and high-microsatellite instability (MSI-H) have been identified as molecular subgroups in gastric carcinoma. The aim of our study was to determine the prognostic and predictive relevance of these subgroups in the context of platinum/5-fluorouracil (5-FU) based preoperative chemotherapy (CTx). Additionally, we investigated the clinical relevance of the low-MSI (MSI-L) phenotype. We analysed 760 adenocarcinomas of the stomach or the gastro-oesophageal junction encompassing 143 biopsies before CTx and 617 resected tumours (291 without and 326 after CTx). EBV was determined by PCR and in situ hybridisation for selected cases. MSI was analysed by PCR using five microsatellite markers and classified as MSI-H and MSI-L. Frequencies of EBV(+), MSI-H and MSI-L in the biopsies before CTx were 4.2, 10.5 and 4.9% respectively. EBV(+) or MSI-H did not correlate with response, but MSI-L was associated with better response (p = 0.011). In the resected tumours, frequencies of EBV(+), MSI-H and MSI-L were 3.9, 9.6 and 4.5% respectively. Overall survival (OS) was significantly different in the non-CTx group (p = 0.014). Patients with EBV(+) tumours showed the best OS, followed by MSI-H. MSI-L was significantly associated with worse OS (hazard ratio [HR], 2.21; 95% confidence interval [CI], 1.21-4.04, p = 0.01). In the resected tumours after CTx, MSI-H was also associated with increased OS (HR, 0.54; 95% CI, 0.26-1.09, p = 0.085). In multivariable analysis, molecular classification was an independent prognostic factor in the completely resected (R0) non-CTx group (p = 0.035). In conclusion, MSI-H and EBV(+) are not predictive of response to neoadjuvant platinum/5-FU based CTx, but they are indicative of a good prognosis. In particular, MSI-H indicates a favourable prognosis irrespective of treatment with CTx. MSI-L predicts good response to CTx and its negative prognostic effect for patients treated with surgery alone suggests that MSI-L might help to identify patients with potentially high-benefit from preoperative CTx.

Indexed as

AdenocarcinomaAdultAgedAntineoplastic Combined Chemotherapy ProtocolsChemotherapy, AdjuvantEpstein-Barr Virus InfectionsFemaleHumansMaleMicrosatellite InstabilityMiddle AgedNeoadjuvant TherapyPrognosisStomach NeoplasmsTreatment OutcomeadenocarcinomaEpstein-Barr virusgastricgastro-oesophageal junctionmicrosatellite instabilitymolecular subtypeneoadjuvant chemotherapyoutcomeprognosis

Identifiers

PMID31206244
PMCPMC6817827
OpenAlexW2950041547

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.