Title: | Colorectal cancer incidences in Lynch syndrome: a comparison of results from the prospective lynch syndrome database and the international mismatch repair consortium |
Author: | Møller, Pål Seppälä, Toni T. Dowty, James G. Haupt, Saskia Dominguez Valentin, Mev Sunde, Lone Bernstein, Inge Engel, Christoph Aretz, Stefan Nielsen, Maartje Capellá, G. (Gabriel) Nakken, Sigve Kalfayan, Pablo Burn, John Büttner, Reinhard Brunet, Joan Green, Kate Sheth, Harsh Rossi, Benedito Mauro Stakelum, Aine Portenkirchner, Carmen Nascimento, Ivana Lalloo, Fiona Newton, Katie Torrezan, Giovana Tardin Martin, Claudia Kloor, Matthias The European Hereditary Tumour Group (ehtg) And The International Mismatch Repair Consortium (imrc) Bertario, Lucio Crosbie, Emma J. Mints, Miriam Tjandra, Douglas Steinke Lange, Verena Neffa, Florencia Perne, Claudia Esperon, Patricia Winship, Ingrid Latchford, Andrew Kariv, Revital Macrae, Finlay Guillén Ponce, Carmen Rosner, Guy Levi, Zohar Vaccaro, Carlos Alberto Tibiletti, Maria Grazia Pavicic, Walter Hernán Plazzer, John-Paul Sijmons, Rolf Backman, Ann Sofie De Vargas, Aída Falcón Vangala, Deepak Lautrup, Charlotte K. Laghi, Luigi Valle, Adriana Della Carraro, Dirce Maria Abu Freha, Naim Winter, Des Bohorquez, Mabel Horisberger, Karoline Heinimann, Karl Half, Elizabeth Lopez Köstner, Francisco Alvarez Valenzuela, Karin Van Hest, Liselotte P. Scott, Rodney J. Thomas, Huw Ligtenberg, Marjolijn J. L. Katz, Lior Da Silva, Leandro Apolinário Zahary, Mohd N. Laish, Ido Rossi, Norma Teresa Morrison, Patrick J. Vainer, Elez Zaránd, Attila Poplawski, Nicola Aronson, Melyssa Kohonen Corish, Maija R. J. Lee, Grant Chen Shtoyerman, Rakefet Mecklin, Jukka Pekka Pylvänäinen, Kirsi Schmiegel, Wolff Hüneburg, Robert Gerdes, Anne Marie Snyder, Carrie Renkonen Sinisalo, Laura Lepisto, Anna Peltomäki, Päivi Therkildsen, Christina Heuveline, Vincent Lindberg, Lars Joachim Lindor, Noralane Thorlacius Ussing, Ole Stoffel, Elena Newcomb, Polly A. Von Knebel Doeberitz, Magnus Palmero, Edenir Thibodeau, Stephen N. Loeffler, Markus Amor, David Senter, Leigha Hoogerbrugge, Nicoline Rahner, Nils Duijkers, Floor Hall, Michael J. Buchanan, Daniel D. Le Marchand, Loïc Win, Aung Ko Hovig, Eivind Hampel, Heather Williams, Heinric Rasmussen, Lene J. Ricciardiello, Luigi Southey, Melissa Samadder, N. Jewel James, Paul Okkels, Henrik Lubiński, Jan Reece, Jeanette Ngeow, Joanne Bassaneze, Thiago Guillem, Jose G. Ward, Robyn Ahadova, Aysel Arnold, Julie Pai, Rish K. Jenkins, Mark A. Wadt, Karin Ankathil, Ravindran Holinski Feder, Elke Monahan, Kevin Parry, Susan Evans, D. Gareth Sampson, Julian R. Moslein, Gabriela Bonanni, Bernardo Lindblom, Annika Dębniak, Tadeusz John, Thomas Hopper, John L. Gallinger, Steven Figueiredo, Jane Ten Broeke, Sanne W. Van Overeem Hansen, Thomas Caldés, Trinidad Yamaguchi, Tatsuro Barca Tierno, Verónica Gluck, Nathan Garre, Pilar Kennelly, Rory Cavestro, Giulia Martina Dueñas, Nuria Greenblatt, Marc Weitz, Jürgen Pineda, Marta Lino Silva, Leonardo S. Redler, Silke |
Keywords: | Colonoscòpia Epidemiologia Colonoscopy Epidemiology |
Issue Date: | 1-Oct-2022 |
Publisher: | Springer Science and Business Media LLC |
Abstract: | Objective To compare colorectal cancer (CRC) incidences in carriers of pathogenic variants of the MMR genes in the PLSD and IMRC cohorts, of which only the former included mandatory colonoscopy surveillance for all participants. Methods CRC incidences were calculated in an intervention group comprising a cohort of confirmed carriers of pathogenic or likely pathogenic variants in mismatch repair genes (path_MMR) followed prospectively by the Prospective Lynch Syndrome Database (PLSD). All had colonoscopy surveillance, with polypectomy when polyps were identified. Comparison was made with a retrospective cohort reported by the International Mismatch Repair Consortium (IMRC). This comprised confirmed and inferred path_MMR carriers who were first- or second-degree relatives of Lynch syndrome probands. Results In the PLSD, 8,153 subjects had follow-up colonoscopy surveillance for a total of 67,604 years and 578 carriers had CRC diagnosed. Average cumulative incidences of CRC in path_MLH1 carriers at 70 years of age were 52% in males and 41% in females; for path_MSH2 50% and 39%; for path_MSH6 13% and 17% and for path_PMS2 11% and 8%. In contrast, in the IMRC cohort, corresponding cumulative incidences were 40% and 27%; 34% and 23%; 16% and 8% and 7% and 6%. Comparing just the European carriers in the two series gave similar findings. Numbers in the PLSD series did not allow comparisons of carriers from other continents separately. Cumulative incidences at 25 years were < 1% in all retrospective groups. Conclusions Prospectively observed CRC incidences (PLSD) in path_MLH1 and path_MSH2 carriers undergoing colonoscopy surveillance and polypectomy were higher than in the retrospective (IMRC) series, and were not reduced in path_MSH6 carriers. These findings were the opposite to those expected. CRC point incidence before 50 years of age was reduced in path_PMS2 carriers subjected to colonoscopy, but not significantly so. |
Note: | Reproducció del document publicat a: https://doi.org/10.1186/s13053-022-00241-1 |
It is part of: | Hereditary Cancer in Clinical Practice, 2022, vol. 20, núm. 1 |
URI: | https://hdl.handle.net/2445/190189 |
Related resource: | https://doi.org/10.1186/s13053-022-00241-1 |
ISSN: | 1897-4287 |
Appears in Collections: | Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))
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