Hereditary Cancer in Clinical Practice (Feb 2019)
Lack of association between screening interval and cancer stage in Lynch syndrome may be accounted for by over-diagnosis; a prospective Lynch syndrome database report
- Toni T. Seppälä,
- Aysel Ahadova,
- Mev Dominguez-Valentin,
- Finlay Macrae,
- D. Gareth Evans,
- Christina Therkildsen,
- Julian Sampson,
- Rodney Scott,
- John Burn,
- Gabriela Möslein,
- Inge Bernstein,
- Elke Holinski-Feder,
- Kirsi Pylvänäinen,
- Laura Renkonen-Sinisalo,
- Anna Lepistö,
- Charlotte Kvist Lautrup,
- Annika Lindblom,
- John-Paul Plazzer,
- Ingrid Winship,
- Douglas Tjandra,
- Lior H. Katz,
- Stefan Aretz,
- Robert Hüneburg,
- Stefanie Holzapfel,
- Karl Heinimann,
- Adriana Della Valle,
- Florencia Neffa,
- Nathan Gluck,
- Wouter H. de Vos tot Nederveen Cappel,
- Hans Vasen,
- Monika Morak,
- Verena Steinke-Lange,
- Christoph Engel,
- Nils Rahner,
- Wolff Schmiegel,
- Deepak Vangala,
- Huw Thomas,
- Kate Green,
- Fiona Lalloo,
- Emma J. Crosbie,
- James Hill,
- Gabriel Capella,
- Marta Pineda,
- Matilde Navarro,
- Ignacio Blanco,
- Sanne ten Broeke,
- Maartje Nielsen,
- Ken Ljungmann,
- Sigve Nakken,
- Noralane Lindor,
- Ian Frayling,
- Eivind Hovig,
- Lone Sunde,
- Matthias Kloor,
- Jukka-Pekka Mecklin,
- Mette Kalager,
- Pål Møller
Affiliations
- Toni T. Seppälä
- Department of Surgery, Helsinki University Central Hospital
- Aysel Ahadova
- Heidelberg University Hospital and DKFZ
- Mev Dominguez-Valentin
- Department of Tumor Biology, Institute of Cancer Research, The Norwegian Radium Hospital, part of Oslo University Hospital
- Finlay Macrae
- The Royal Melbourne Hospital
- D. Gareth Evans
- University of Manchester & Manchester University Hospitals Foundation Trust
- Christina Therkildsen
- The Danish HNPCC Register, Clinical Research Centre, Copenhagen University Hospital
- Julian Sampson
- Medical Genetics, Cardiff University
- Rodney Scott
- University of Newcastle and the Hunter Medical Research Institute
- John Burn
- University of Newcastle
- Gabriela Möslein
- University Witten-Herdecke
- Inge Bernstein
- Dept. of Surgical Gastroenterology, Aalborg University Hospital
- Elke Holinski-Feder
- Medizinische Klinik und Poliklinik IV, Campus Innenstadt, Klinikum der Universität München
- Kirsi Pylvänäinen
- Central Finland Central Hospital, Education and Research
- Laura Renkonen-Sinisalo
- Department of Surgery, Helsinki University Central Hospital
- Anna Lepistö
- Department of Surgery, Helsinki University Central Hospital
- Charlotte Kvist Lautrup
- Department of Clinical Genetics, Aalborg University Hospital
- Annika Lindblom
- Karolinska Institutet
- John-Paul Plazzer
- The Royal Melbourne Hospital
- Ingrid Winship
- The Royal Melbourne Hospital
- Douglas Tjandra
- The Royal Melbourne Hospital
- Lior H. Katz
- Hadassah Medical Center, Jerusalem, and Sheba Medical Center
- Stefan Aretz
- Institute of Human Genetics, University of Bonn
- Robert Hüneburg
- Department of Internal Medicine I, University Hospital Bonn
- Stefanie Holzapfel
- Department of Internal Medicine I, University Hospital Bonn
- Karl Heinimann
- Institute for Medical Genetics and Pathology, University Hospital Basel
- Adriana Della Valle
- Hospital Fuerzas Armadas, Grupo Colaborativo Uruguayo, Investigación de Afecciones Oncológicas Hereditarias (GCU)
- Florencia Neffa
- Hospital Fuerzas Armadas, Grupo Colaborativo Uruguayo, Investigación de Afecciones Oncológicas Hereditarias (GCU)
- Nathan Gluck
- Tel-Aviv Soursky Medical Center
- Wouter H. de Vos tot Nederveen Cappel
- Department of Gastroenterology and Hepatology, Isala Clinics
- Hans Vasen
- Department of Gastroenterology and Hepatology, Leiden University Medical Centre
- Monika Morak
- Medizinische Klinik und Poliklinik IV, Campus Innenstadt, Klinikum der Universität München
- Verena Steinke-Lange
- Medizinische Klinik und Poliklinik IV, Campus Innenstadt, Klinikum der Universität München
- Christoph Engel
- Institute for Medical Informatics, Statistics and Epidemiology, University of Leipzig
- Nils Rahner
- Medical School, Institute of Human Genetics, Heinrich-Heine-University
- Wolff Schmiegel
- Department of Medicine, Knappschaftskrankenhaus, Ruhr-University Bochum
- Deepak Vangala
- Department of Medicine, Knappschaftskrankenhaus, Ruhr-University Bochum
- Huw Thomas
- St Mark’s Hospital, Department of Surgery and Cancer, Imperial College London
- Kate Green
- University of Manchester & Manchester University Hospitals Foundation Trust
- Fiona Lalloo
- University of Manchester & Manchester University Hospitals Foundation Trust
- Emma J. Crosbie
- University of Manchester and St Mary’s Hospital
- James Hill
- University of Manchester & Manchester University Hospitals Foundation Trust
- Gabriel Capella
- Hereditary Cancer Program, Catalan Institute of Oncology, Insititut d’Investigació Biomèdica de Bellvitge (IDIBELL), ONCOBELL Program, L’Hospitalet de Llobregat
- Marta Pineda
- Hereditary Cancer Program, Catalan Institute of Oncology, Insititut d’Investigació Biomèdica de Bellvitge (IDIBELL), ONCOBELL Program, L’Hospitalet de Llobregat
- Matilde Navarro
- Hereditary Cancer Program, Catalan Institute of Oncology, Insititut d’Investigació Biomèdica de Bellvitge (IDIBELL), ONCOBELL Program, L’Hospitalet de Llobregat
- Ignacio Blanco
- Hereditary Cancer Program, Catalan Institute of Oncology, Insititut d’Investigació Biomèdica de Bellvitge (IDIBELL), ONCOBELL Program, L’Hospitalet de Llobregat
- Sanne ten Broeke
- University Medical Center Groningen
- Maartje Nielsen
- Leids Universitair Medisch Centrum
- Ken Ljungmann
- Department of Surgical Gastroenterology, Aarhus University Hospital
- Sigve Nakken
- Department of Tumor Biology, Institute of Cancer Research, The Norwegian Radium Hospital, part of Oslo University Hospital
- Noralane Lindor
- Department of Health Sciences Research, Mayo Clinic
- Ian Frayling
- Medical Genetics, Cardiff University
- Eivind Hovig
- Department of Tumor Biology, Institute of Cancer Research, The Norwegian Radium Hospital, part of Oslo University Hospital
- Lone Sunde
- Department of Medical Genetics, Aarhus University Hospital
- Matthias Kloor
- Heidelberg University Hospital and DKFZ
- Jukka-Pekka Mecklin
- Department of Surgery, Central Finland Central Hospital
- Mette Kalager
- Department of Tumor Biology, Institute of Cancer Research, The Norwegian Radium Hospital, part of Oslo University Hospital
- Pål Møller
- Department of Tumor Biology, Institute of Cancer Research, The Norwegian Radium Hospital, part of Oslo University Hospital
- DOI
- https://doi.org/10.1186/s13053-019-0106-8
- Journal volume & issue
-
Vol. 17,
no. 1
pp. 1 – 8
Abstract
Abstract Background Recent epidemiological evidence shows that colorectal cancer (CRC) continues to occur in carriers of pathogenic mismatch repair (path_MMR) variants despite frequent colonoscopy surveillance in expert centres. This observation conflicts with the paradigm that removal of all visible polyps should prevent the vast majority of CRC in path_MMR carriers, provided the screening interval is sufficiently short and colonoscopic practice is optimal. Methods To inform the debate, we examined, in the Prospective Lynch Syndrome Database (PLSD), whether the time since last colonoscopy was associated with the pathological stage at which CRC was diagnosed during prospective surveillance. Path_MMR carriers were recruited for prospective surveillance by colonoscopy. Only variants scored by the InSiGHT Variant Interpretation Committee as class 4 and 5 (clinically actionable) were included. CRCs detected at the first planned colonoscopy, or within one year of this, were excluded as prevalent cancers. Results Stage at diagnosis and interval between last prospective surveillance colonoscopy and diagnosis were available for 209 patients with 218 CRCs, including 162 path_MLH1, 45 path_MSH2, 10 path_MSH6 and 1 path_PMS2 carriers. The numbers of cancers detected within 3.5 years since last colonoscopy were 36, 93, 56 and 33, respectively. Among these, 16.7, 19.4, 9.9 and 15.1% were stage III–IV, respectively (p = 0.34). The cancers detected more than 2.5 years after the last colonoscopy were not more advanced than those diagnosed earlier (p = 0.14). Conclusions The CRC stage and interval since last colonoscopy were not correlated, which is in conflict with the accelerated adenoma-carcinoma paradigm. We have previously reported that more frequent colonoscopy is not associated with lower incidence of CRC in path_MMR carriers as was expected. In contrast, point estimates showed a higher incidence with shorter intervals between examinations, a situation that may parallel to over-diagnosis in breast cancer screening. Our findings raise the possibility that some CRCs in path_MMR carriers may spontaneously disappear: the host immune response may not only remove CRC precursor lesions in path_MMR carriers, but may remove infiltrating cancers as well. If confirmed, our suggested interpretation will have a bearing on surveillance policy for path_MMR carriers.
Keywords
- Mismatch repair
- Microsatellite instability
- Lynch syndrome
- Hereditary cancer
- Colorectal cancer
- Hereditary nonpolyposis colorectal cancer