Value of upper gastrointestinal endoscopy for gastric cancer surveillance in patients with Lynch syndrome.


Journal

International journal of cancer
ISSN: 1097-0215
Titre abrégé: Int J Cancer
Pays: United States
ID NLM: 0042124

Informations de publication

Date de publication:
01 01 2021
Historique:
received: 10 05 2020
revised: 04 08 2020
accepted: 05 08 2020
pubmed: 16 9 2020
medline: 11 6 2021
entrez: 15 9 2020
Statut: ppublish

Résumé

In our study, we evaluated the effectiveness of upper gastrointestinal (GI) endoscopy as an instrument for early gastric cancer (GC) detection in Lynch syndrome (LS) patients by analyzing data from the registry of the German Consortium for Familial Intestinal Cancer. In a prospective, multicenter cohort study, 1128 out of 2009 registered individuals with confirmed LS underwent 5176 upper GI endoscopies. Compliance was good since 77.6% of upper GI endoscopies were completed within the recommended interval of 1 to 3 years. Forty-nine GC events were observed in 47 patients. MLH1 (n = 21) and MSH2 (n = 24) mutations were the most prevalent. GCs in patients undergoing regular surveillance were diagnosed significantly more often in an early-stage disease (UICC I) than GCs detected through symptoms (83% vs 25%; P = .0231). Thirty-two (68%) patients had a negative family history of GC. The median age at diagnosis was 51 years (range 28-66). Of all GC patients, 13 were diagnosed at an age younger than 45. Our study supports the recommendation of regular upper GI endoscopy surveillance for LS patients beginning no later than at the age of 30.

Identifiants

pubmed: 32930401
doi: 10.1002/ijc.33294
doi:

Substances chimiques

MLH1 protein, human 0
MSH2 protein, human EC 3.6.1.3
MutL Protein Homolog 1 EC 3.6.1.3
MutS Homolog 2 Protein EC 3.6.1.3

Types de publication

Journal Article Multicenter Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

106-114

Informations de copyright

© 2020 The Authors. International Journal of Cancer published by John Wiley & Sons Ltd on behalf of Union for International Cancer Control.

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Auteurs

Swetlana Ladigan-Badura (S)

Department of Internal Medicine, Knappschaftskrankenhaus, Ruhr University, Bochum, Germany.

Deepak B Vangala (DB)

Department of Internal Medicine, Knappschaftskrankenhaus, Ruhr University, Bochum, Germany.

Christoph Engel (C)

Institute for Medical Informatics, Statistics and Epidemiology, University of Leipzig, Leipzig, Germany.

Karolin Bucksch (K)

Institute for Medical Informatics, Statistics and Epidemiology, University of Leipzig, Leipzig, Germany.

Robert Hueneburg (R)

Department of Internal Medicine I, University Hospital of Bonn, Bonn, Germany.
Center for Hereditary Tumor Syndromes, University Hospital of Bonn, Bonn, Germany.

Claudia Perne (C)

Center for Hereditary Tumor Syndromes, University Hospital of Bonn, Bonn, Germany.
Institute of Human Genetics, University of Bonn, Bonn, Germany.

Jacob Nattermann (J)

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

Verena Steinke-Lange (V)

Medizinische Klinik und Poliklinik IV, Campus Innenstadt, Klinikum der Universität München, Munich, Germany.
MGZ - Medizinisch Genetisches Zentrum, Munich, Germany.

Nils Rahner (N)

Institute of Human Genetics, Medical School, Heinrich Heine University, Duesseldorf, Germany.

Hans K Schackert (HK)

Department of Surgery, Technische Universität, Dresden, Germany.

Jürgen Weitz (J)

Department of Surgery, Technische Universität, Dresden, Germany.

Matthias Kloor (M)

Department of Applied Tumor Biology, Institute of Pathology, University Hospital Heidelberg, Germany; and Cooperation Unit Applied Tumor Biology, German Cancer Research Center (DKFZ), Heidelberg, Germany.

Judith Kuhlkamp (J)

Department of Internal Medicine, Knappschaftskrankenhaus, Ruhr University, Bochum, Germany.

Huu Phuc Nguyen (HP)

Institute for Human Genetics, Ruhr-University, Bochum, Germany.

Gabriela Moeslein (G)

Ev. BETHESDA Krankenhaus Duisburg, Center for Hereditary Tumors, Duisburg, Germany.

Christian Strassburg (C)

Department of Internal Medicine I, University Hospital of Bonn, Bonn, Germany.
Center for Hereditary Tumor Syndromes, University Hospital of Bonn, Bonn, Germany.

Monika Morak (M)

Medizinische Klinik und Poliklinik IV, Campus Innenstadt, Klinikum der Universität München, Munich, Germany.
MGZ - Medizinisch Genetisches Zentrum, Munich, Germany.

Elke Holinski-Feder (E)

Medizinische Klinik und Poliklinik IV, Campus Innenstadt, Klinikum der Universität München, Munich, Germany.
MGZ - Medizinisch Genetisches Zentrum, Munich, Germany.

Reinhard Buettner (R)

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

Stefan Aretz (S)

Center for Hereditary Tumor Syndromes, University Hospital of Bonn, Bonn, Germany.
Institute of Human Genetics, University of Bonn, Bonn, Germany.

Markus Loeffler (M)

Institute for Medical Informatics, Statistics and Epidemiology, University of Leipzig, Leipzig, Germany.

Wolff Schmiegel (W)

Department of Internal Medicine, Knappschaftskrankenhaus, Ruhr University, Bochum, Germany.

Christian Pox (C)

Department of Medicine, Hospital St. Joseph-Stift, Bremen, Germany.

Karsten Schulmann (K)

Department of Hematology and Oncology, Klinikum Hochsauerland, Meschede, Germany.
Praxis fuer Haematologie & Onkologie, MVZ Arnsberg, Germany.

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