Evidence map›Paper›PMID 36765729›Full record

ArticleCancers2023

Significant Tumor Regression after Neoadjuvant Chemotherapy in Gastric Cancer, but Poor Survival of the Patient? Role of MHC Class I Alterations.

Theresa Hiltner, Noémi Szörenyi, Meike Kohlruss, Alexander Hapfelmeier, Anna-Lina Herz, Julia Slotta-Huspenina, Moritz Jesinghaus, Alexander Novotny, Sebastian Lange, Katja Ott and 2 more

Abstract read
In one paragraph

Article in Cancers, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. 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

12 authors.

Theresa HiltnerInstitute of Pathology, TUM School of Medicine, Technical University of Munich, 81675 Munich, Germany.ORCID 0000-0001-7933-0966
Noémi SzörenyiInstitute of Pathology, TUM School of Medicine, Technical University of Munich, 81675 Munich, Germany.
Meike KohlrussInstitute of Pathology, TUM School of Medicine, Technical University of Munich, 81675 Munich, Germany.
Alexander HapfelmeierInstitute of Medical Informatics, Statistics and Epidemiology, Technical University of Munich, 81675 Munich, Germany.
Anna-Lina HerzInstitute of Pathology, TUM School of Medicine, Technical University of Munich, 81675 Munich, Germany.
Julia Slotta-HuspeninaInstitute of Pathology, TUM School of Medicine, Technical University of Munich, 81675 Munich, Germany.
Moritz JesinghausInstitute of Pathology, TUM School of Medicine, Technical University of Munich, 81675 Munich, Germany.
Alexander NovotnyDepartment of Surgery, TUM School of Medicine, Technical University of Munich, 81675 Munich, Germany.ORCID 0000-0002-8029-5958
Sebastian LangeII. Medizinische Klinik, Klinikum rechts der Isar, Technical University of Munich, 81675 Munich, Germany.
Katja OttDepartment of Surgery, Klinikum Rosenheim, 83022 Rosenheim, Germany.
Wilko WeichertInstitute of Pathology, TUM School of Medicine, Technical University of Munich, 81675 Munich, Germany.
Gisela KellerInstitute of Pathology, TUM School of Medicine, Technical University of Munich, 81675 Munich, Germany.ORCID 0000-0003-2886-0371

Funding

German Cancer Aid 70112177Wilhelm-Sander-Stiftung 2019.156.1
6 · The paper itself

Abstract

We aimed to determine the clinical and prognostic relevance of allelic imbalance (AI) of the major histocompatibility complex (MHC) class I genes, encompassing the human leukocyte antigen (HLA) class I and beta-2 microglobulin (B2M) genes, in the context of neoadjuvant platinum/fluoropyrimidine chemotherapy (CTx). Biopsies before CTx were studied in 158 patients with adenocarcinoma of the stomach or gastroesophageal junction. The response was histopathologically evaluated. AI was detected by multiplex PCRs analysis of four or five microsatellite markers in HLA and B2M regions, respectively. AI with no marker was significantly associated with response or survival. However, subgroup analysis revealed differences. AI at marker D6S265, close to the HLA-A gene, was associated with an obvious increased risk in responding (HR, 3.62; 95% CI, 0.96-13.68,

Indexed as

adenocarcinomaallelic imbalanceB2Mgastricgastroesophageal junctionHLAloss of heterozygosityneoadjuvant chemotherapyprognosistumor regression

Identifiers

PMID36765729
PMCPMC9913563

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.