Occurrence of High Microsatellite-Instability/Mismatch Repair Deficiency in Nearly 2,000 Human Adenocarcinomas of the Gastrointestinal Tract, Pancreas, and Bile Ducts: A Study From a Large German Comprehensive Cancer Center.

Union for International Cancer Control (UICC) stage 4 esophageal adenocarcinoma gastric carcinoma high microsatellite-instability (MSI-H) microsatellite-instability

Journal

Frontiers in oncology
ISSN: 2234-943X
Titre abrégé: Front Oncol
Pays: Switzerland
ID NLM: 101568867

Informations de publication

Date de publication:
2021
Historique:
received: 04 06 2020
accepted: 02 07 2021
entrez: 9 8 2021
pubmed: 10 8 2021
medline: 10 8 2021
Statut: epublish

Résumé

Knowledge of the high microsatellite-instability (MSI-H)/mismatch repair deficiency (MMRd) status is of increasing interest for personalized neoadjuvant or adjuvant therapy planning. Only a few studies are available on MSI-H distribution in the Northern European Caucasian patient population. In this study, we focused on a large cohort of tumors of the upper gastrointestinal tract. Surgical material from a total of 1,965 patients was analyzed for MSI-H/MMRd status (including 1,267 carcinomas of the esophagus or stomach). All tumors were analyzed with an internationally recommended immunohistochemical panel consisting of four antibodies (MLH1, MSH2, PMS2, and MSH6). The results were molecularly objectified. Adenocarcinomas with MSI-H/MMRd were detected with the following distribution: esophagus (1.4%), stomach (8.3%), small intestine (18.2%), large intestine (8.5%), intrahepatic bile ducts (1.9%), and pancreas (0%). In case of gastric tumors with MSI-H/MMRd, neoadjuvant therapy did not influence the prognosis of patients (p = 0.94). Within all tumor entities with MSI-H/MMRd, patients with a UICC stage 4 were also represented. In this advanced stage, 11.7% of patients with MSS tumors were diagnosed compared to 0.5% of patients with MSI-H tumors relative to the entire tumor collective. In this study, the proportion of MSI-H/MMRd tumors in the stomach is smaller than would have been expected in knowledge of the data published by TCGA or AGRC. Negative prognostic effects regarding MSI-H status and neoadjuvant therapy as described by the MAGIC study group were not seen in our cohort. The extent to which the MSI-H/MMRd status should be known for neoadjuvant therapy planning must be clarified in prospective studies in the future. At present, there is no convincing data to dispense the neoadjuvant therapy for gastric carcinoma. Due to the very convincing, positive data regarding the response rates of MSI-H tumors to treatment with PD1/PD-L1 inhibitors, every metastatic carcinoma of the gastrointestinal tract should be tested for its MSI-H status.

Identifiants

pubmed: 34367937
doi: 10.3389/fonc.2021.569475
pmc: PMC8343401
doi:

Types de publication

Journal Article

Langues

eng

Pagination

569475

Informations de copyright

Copyright © 2021 Quaas, Rehkaemper, Rueschoff, Pamuk, Zander, Hillmer, Siemanowski, Wittig, Buettner, Plum, Popp, Gebauer, Bruns, Loeser, Alakus and Schoemig-Markiefka.

Déclaration de conflit d'intérêts

Author JR was employed by company Nordhessen and Targos Molecular Pathology GmbH. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Alexander Quaas (A)

Institute of Pathology, University Hospital Cologne, Cologne, Germany.

Jan Rehkaemper (J)

Institute of Pathology, University Hospital Cologne, Cologne, Germany.

Josef Rueschoff (J)

Institute of Pathology, Nordhessen and Targos Molecular Pathology GmbH, Kassel, Germany.

Aylin Pamuk (A)

Department of General, Visceral and Cancer Surgery, University Hospital Cologne, Cologne, Germany.

Thomas Zander (T)

Department of Internal Medicine I, University Hospital Cologne, Cologne, Germany.

Axel Hillmer (A)

Institute of Pathology, University Hospital Cologne, Cologne, Germany.

Janna Siemanowski (J)

Institute of Pathology, University Hospital Cologne, Cologne, Germany.

Jana Wittig (J)

Institute of Pathology, University Hospital Cologne, Cologne, Germany.

Reinhard Buettner (R)

Institute of Pathology, University Hospital Cologne, Cologne, Germany.

Patrick Plum (P)

Department of General, Visceral and Cancer Surgery, University Hospital Cologne, Cologne, Germany.

Felix Popp (F)

Department of General, Visceral and Cancer Surgery, University Hospital Cologne, Cologne, Germany.

Florian Gebauer (F)

Department of General, Visceral and Cancer Surgery, University Hospital Cologne, Cologne, Germany.

Christiane Josephine Bruns (CJ)

Department of General, Visceral and Cancer Surgery, University Hospital Cologne, Cologne, Germany.

Heike Loeser (H)

Institute of Pathology, University Hospital Cologne, Cologne, Germany.

Hakan Alakus (H)

Department of General, Visceral and Cancer Surgery, University Hospital Cologne, Cologne, Germany.

Birgid Schoemig-Markiefka (B)

Institute of Pathology, University Hospital Cologne, Cologne, Germany.

Classifications MeSH