Your browser doesn't support javascript.
loading
Early detection of duodenal cancer by upper gastrointestinal-endoscopy in Lynch syndrome.
Vangala, Deepak B; Ladigan-Badura, Swetlana; Engel, Christoph; Hüneburg, Robert; Perne, Claudia; Bucksch, Karolin; Nattermann, Jacob; Steinke-Lange, Verena; Rahner, Nils; Weitz, Jürgen; Kloor, Matthias; Tomann, Judith; Canbay, Ali; Nguyen, Huu-Phuc; Strassburg, Christian; Möslein, Gabriele; Morak, Monika; Holinski-Feder, Elke; Büttner, Reinhard; Aretz, Stefan; Löffler, Markus; Schmiegel, Wolff; Pox, Christian; Schulmann, Karsten.
Afiliación
  • Vangala DB; Department of Medicine, Knappschaftskrankenhaus, Ruhr-University Bochum, Bochum, Germany.
  • Ladigan-Badura S; Molecular GI-Oncology, Ruhr-University Bochum, Bochum, Germany.
  • Engel C; Department of Medicine, Knappschaftskrankenhaus, Ruhr-University Bochum, Bochum, Germany.
  • Hüneburg R; Molecular GI-Oncology, Ruhr-University Bochum, Bochum, Germany.
  • Perne C; Institute for Medical Informatics, Statistics and Epidemiology, University of Leipzig, Leipzig, Germany.
  • Bucksch K; Department of Internal Medicine I, University Hospital Bonn, Bonn, Germany.
  • Nattermann J; National Center for Hereditary Tumor Syndromes, University Hospital Bonn, Bonn, Germany.
  • Steinke-Lange V; National Center for Hereditary Tumor Syndromes, University Hospital Bonn, Bonn, Germany.
  • Rahner N; Institute of Human Genetics, University of Bonn, Bonn, Germany.
  • Weitz J; Institute for Medical Informatics, Statistics and Epidemiology, University of Leipzig, Leipzig, Germany.
  • Kloor M; Department of Internal Medicine I, University Hospital Bonn, Bonn, Germany.
  • Tomann J; National Center for Hereditary Tumor Syndromes, University Hospital Bonn, Bonn, Germany.
  • Canbay A; Medizinische Klinik und Poliklinik IV, Campus Innenstadt, Klinikum der Universität München, Munich, Germany.
  • Nguyen HP; Medical Genetics Center Munich, Munich, Germany.
  • Strassburg C; Institute of Human Genetics, Medical School, Heinrich Heine University, Düsseldorf, Germany.
  • Möslein G; Department of Surgery, Technische Universitaet Dresden, Dresden, Germany.
  • Morak M; Department of Applied Tumour Biology, Institute of Pathology, University Hospital Heidelberg, Heidelberg, Germany.
  • Holinski-Feder E; Cooperation Unit Applied Tumour Biology, German Cancer Research Center (DKFZ), Heidelberg, Germany.
  • Büttner R; Department of Medicine, Knappschaftskrankenhaus, Ruhr-University Bochum, Bochum, Germany.
  • Aretz S; Department of Medicine, Knappschaftskrankenhaus, Ruhr-University Bochum, Bochum, Germany.
  • Löffler M; Department for Human Genetics, Ruhr-University Bochum, Bochum, Germany.
  • Schmiegel W; Department of Internal Medicine I, University Hospital Bonn, Bonn, Germany.
  • Pox C; National Center for Hereditary Tumor Syndromes, University Hospital Bonn, Bonn, Germany.
  • Schulmann K; Surgical Center for Hereditary Tumors, Evangelisches Bethesda Krankenhaus, Duisburg, Germany.
Int J Cancer ; 149(12): 2052-2062, 2021 12 15.
Article en En | MEDLINE | ID: mdl-34331771
ABSTRACT
Small bowel cancer (SBC) is the malignancy with the highest standardized incidence ratio in Lynch syndrome (LS) patients. Of all SBCs, about 50% are duodenal cancers (DCs), therefore being accessible by esophago-gastro-duodenoscopy (EGD) for surveillance. We asked whether early detection of DC is possible for LS patients undergoing surveillance by EGD and if surveillance should be limited to specific subgroups. Data for LS patients with DC were retrieved from the registry of the German Consortium for Familial Intestinal Cancer. Patients undergoing active surveillance by EGDs (surveillance group) were compared to those who did not (nonsurveillance group) regarding tumor stage at diagnosis. Union for International Cancer Control stages I-IIA were defined as early stage disease and IIB-IV as advanced stage disease. Statistical analysis was performed using Fisher's exact test. Among 2015 patients with pathogenic variants in any mismatch-repair-gene, 47 patients with 49 DCs were identified. In 10% of cases, patients were under 35 years at diagnosis; family and personal tumor history did not correlate with DC diagnosis. Pathogenic germline variants in MSH6, PMS2 or EPCAM were present in 10% of patients. Statistical analysis could be performed on 13 DC patients in the surveillance group and 14 in the nonsurveillance group. Early detection was possible for 71% of patients in the surveillance group and 29% of patients in the nonsurveillance group (P = .021). Early detection of DC by EGD in LS patients is feasible regardless of family history, mutational status and should start no later than 25 years of age.
Asunto(s)
Palabras clave

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Neoplasias Colorrectales Hereditarias sin Poliposis / Biomarcadores de Tumor / Duodenoscopía / Neoplasias Duodenales / Detección Precoz del Cáncer Tipo de estudio: Diagnostic_studies / Guideline / Observational_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Límite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Int J Cancer Año: 2021 Tipo del documento: Article País de afiliación: Alemania

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Neoplasias Colorrectales Hereditarias sin Poliposis / Biomarcadores de Tumor / Duodenoscopía / Neoplasias Duodenales / Detección Precoz del Cáncer Tipo de estudio: Diagnostic_studies / Guideline / Observational_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Límite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Int J Cancer Año: 2021 Tipo del documento: Article País de afiliación: Alemania