Evidence map›Paper›PMID 42490032›Full record

ArticleGastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association2026

Therapeutic management of resectable mismatch-repair deficient/microsatellite instability-high gastroesophageal adenocarcinoma: a real-world analysis from Austria.

Martin Korpan, Daniel Nothdurfter, Bernhard Doleschal, Lukas Weiss, Sophie Roider-Schur, Leopold Öhler, Ewald Wöll, Julia M Berger, Elisabeth S Bergen, Gerald W Prager and 6 more

Abstract readMulticenter Study
In one paragraph

Article in Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

16 authors.

Martin KorpanDivision of Oncology, Department of Medicine I, Medical University of Vienna, Vienna, Austria.
Daniel NothdurfterDepartment of Internal Medicine I for Hematology With Stem Cell Transplantation, Hemostaseology, and Medical Oncology, Ordensklinikum Linz, Linz, Austria.
Bernhard DoleschalDepartment of Internal Medicine I for Hematology With Stem Cell Transplantation, Hemostaseology, and Medical Oncology, Ordensklinikum Linz, Linz, Austria.
Lukas WeissDepartment of Internal Medicine III With Hematology, Medical Oncology, Hemostaseology, Infectiology and Rheumatology, Oncologic Center, Paracelsus Medical University, Salzburg, Austria.
Sophie Roider-SchurDepartment of Medicine I, Oncology, St. Josef Krankenhaus, Vienna, Austria.
Leopold ÖhlerDepartment of Medicine I, Oncology, St. Josef Krankenhaus, Vienna, Austria.
Ewald WöllDepartment of Internal Medicine, St. Vinzenz Hospital Zams, Zams, Tyrol, Austria.
Julia M BergerDivision of Oncology, Department of Medicine I, Medical University of Vienna, Vienna, Austria.
Elisabeth S BergenDivision of Oncology, Department of Medicine I, Medical University of Vienna, Vienna, Austria.
Gerald W PragerDivision of Oncology, Department of Medicine I, Medical University of Vienna, Vienna, Austria.
Behrang MozayaniDepartment of Pathology, Medical University of Vienna, Vienna, Austria.
Anna S BerghoffDivision of Oncology, Department of Medicine I, Medical University of Vienna, Vienna, Austria.
Matthias PreusserDivision of Oncology, Department of Medicine I, Medical University of Vienna, Vienna, Austria.
Hannah C PuhrDivision of Oncology, Department of Medicine I, Medical University of Vienna, Vienna, Austria.
Florian Huemer *Department of Internal Medicine III With Hematology, Medical Oncology, Hemostaseology, Infectiology and Rheumatology, Oncologic Center, Paracelsus Medical University, Salzburg, Austria.
Aysegül Ilhan-Mutlu *Division of Oncology, Department of Medicine I, Medical University of Vienna, Vienna, Austria. aysegul.ilhan@meduniwien.ac.at.ORCID http://orcid.org/0000-0001-8291-0873

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMismatch-repair deficient (dMMR)/microsatellite instability-high (MSI-H) gastroesophageal adenocarcinoma (GEA) is associated with favorable prognosis but limited benefit from perioperative chemotherapy. Although immune checkpoint inhibition (ICI)-based approaches have shown promising activity in early-phase studies, the optimal therapeutic combinations and the feasibility of non-operative management (NOM) in resectable disease remain unclear.

methodsThis exploratory, retrospective, multicenter, real-world study included 55 patients with resectable dMMR/MSI-H GEA, who were divided into subgroups, characterized and compared according to treatment strategy (chemotherapy, chemoimmunotherapy, immunotherapy and initial resection). Pathological and clinical complete response (pCR, cCR), progression-free (PFS) and overall survival (OS) were evaluated.

resultsPatients received chemotherapy (n=10), chemoimmunotherapy (n=16), immunotherapy (n=13), or initial resection without subsequent systemic treatment (n=16). Forty five (82%) patients had surgical resection. The pCR rate was 22% (n=2/9) in the chemotherapy, 27% (n=4/15) in the chemoimmunotherapy, and 100% (n=5/5) in the immunotherapy (i.e., doublet ICI) subgroup, respectively. The overall cCR rate in NOM patients was 33% (n=3/9), with rates of 37.5% (n=3/8) in the immunotherapy subgroup and 0% (n=0/1) in the chemoimmunotherapy subgroup. Complete response rates (pCR/cCR) were significantly associated with PD-L1 CPS ≥10 (p=0.027).

conclusionThis real-world study is, to our knowledge, the first to evaluate a broad spectrum of therapeutic combinations in patients with resectable MSI-H/dMMR GEA, showing meaningful antitumor activity, particularly with doublet ICI. Given the challenges of conducting randomized prospective trials in this setting, such real world data may support clinicians in guiding therapeutic decision-making.

Indexed as

AdenocarcinomaDNA Mismatch RepairEsophageal NeoplasmsMicrosatellite InstabilityStomach NeoplasmsAdultAgedAustriaFemaleHumansImmunotherapyMaleMiddle AgedPathologic Complete ResponsePrognosisRetrospective StudiesGastroesophageal adenocarcinomaImmune checkpoint inhibitionMicrosatellite instability-highMismatch repair deficiencyNon-operative management

Identifiers

PMID42490032
PMCPMC13525024

What OpenQuestion holds

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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.