Colorectal cancer incidences in Lynch syndrome: a comparison of results from the prospective lynch syndrome database and the international mismatch repair consortium

dc.contributor.author
Møller, Pål
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Seppälä, Toni T.
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Dowty, James G.
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Haupt, Saskia
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Dominguez Valentin, Mev
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Sunde, Lone
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Bernstein, Inge
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Engel, Christoph
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Aretz, Stefan
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Nielsen, Maartje
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Capellá, G. (Gabriel)
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Amor, David
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Senter, Leigha
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Hoogerbrugge, Nicoline
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Rahner, Nils
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Duijkers, Floor
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Hall, Michael J.
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Buchanan, Daniel D.
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Le Marchand, Loïc
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Win, Aung Ko
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Hovig, Eivind
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Nakken, Sigve
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Hampel, Heather
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Williams, Heinric
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Rasmussen, Lene J.
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Ricciardiello, Luigi
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Southey, Melissa
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Samadder, N. Jewel
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James, Paul
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Okkels, Henrik
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Lubiński, Jan
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Reece, Jeanette
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Kalfayan, Pablo
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Ngeow, Joanne
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Bassaneze, Thiago
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Guillem, Jose G.
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Ward, Robyn
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Ahadova, Aysel
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Arnold, Julie
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Pai, Rish K.
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Jenkins, Mark A.
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Wadt, Karin
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Ankathil, Ravindran
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Burn, John
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Holinski Feder, Elke
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Monahan, Kevin
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Parry, Susan
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Evans, D. Gareth
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Sampson, Julian R.
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Moslein, Gabriela
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Bonanni, Bernardo
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Lindblom, Annika
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Dębniak, Tadeusz
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John, Thomas
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Büttner, Reinhard
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Hopper, John L.
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Gallinger, Steven
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Figueiredo, Jane
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Ten Broeke, Sanne W.
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Van Overeem Hansen, Thomas
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Caldés, Trinidad
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Yamaguchi, Tatsuro
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Barca Tierno, Verónica
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Gluck, Nathan
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Garre, Pilar
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Brunet, Joan
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Kennelly, Rory
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Cavestro, Giulia Martina
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Dueñas, Nuria
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Greenblatt, Marc
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Weitz, Jürgen
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Pineda, Marta
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Lino Silva, Leonardo S.
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Redler, Silke
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Green, Kate
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Sheth, Harsh
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Rossi, Benedito Mauro
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Stakelum, Aine
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Portenkirchner, Carmen
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Nascimento, Ivana
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Lalloo, Fiona
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Newton, Katie
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Torrezan, Giovana Tardin
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Martin, Claudia
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Kloor, Matthias
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The European Hereditary Tumour Group (ehtg) And The International Mismatch Repair Consortium (imrc)
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Bertario, Lucio
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Crosbie, Emma J.
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Mints, Miriam
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Tjandra, Douglas
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Steinke-Lange, Verena
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Neffa, Florencia
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Perne, Claudia
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Esperon, Patricia
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Winship, Ingrid
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Latchford, Andrew
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Kariv, Revital
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Macrae, Finlay
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Guillén Ponce, Carmen
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Rosner, Guy
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Levi, Zohar
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Vaccaro, Carlos Alberto
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Tibiletti, Maria Grazia
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Pavicic, Walter Hernán
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Plazzer, John-Paul
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Sijmons, Rolf H.
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Backman, Ann Sofie
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De Vargas, Aída Falcón
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Vangala, Deepak
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Lautrup, Charlotte K.
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Laghi, Luigi
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Valle, Adriana Della
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Carraro, Dirce Maria
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Abu Freha, Naim
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Winter, Des
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Bohorquez, Mabel
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Horisberger, Karoline
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Heinimann, Karl
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Half, Elizabeth
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Lopez Köstner, Francisco
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Alvarez Valenzuela, Karin
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Van Hest, Liselotte P.
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Scott, Rodney J.
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Thomas, Huw
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Ligtenberg, Marjolijn J. L.
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Katz, Lior
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Da Silva, Leandro Apolinário
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Zahary, Mohd N.
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Laish, Ido
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Rossi, Norma Teresa
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Morrison, Patrick J.
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Vainer, Elez
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Zaránd, Attila
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Poplawski, Nicola
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Aronson, Melyssa
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Kohonen Corish, Maija R. J.
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Lee, Grant
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Chen Shtoyerman, Rakefet
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Mecklin, Jukka Pekka
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Pylvänäinen, Kirsi
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Schmiegel, Wolff
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Hüneburg, Robert
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Gerdes, Anne Marie
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Snyder, Carrie
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Renkonen Sinisalo, Laura
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Lepisto, Anna
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Peltomäki, Päivi
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Therkildsen, Christina
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Heuveline, Vincent
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Lindberg, Lars Joachim
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Lindor, Noralane
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Thorlacius Ussing, Ole
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Stoffel, Elena
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Newcomb, Polly A.
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Von Knebel Doeberitz, Magnus
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Palmero, Edenir
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Thibodeau, Stephen N.
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Loeffler, Markus
dc.date.issued
2022-10-25T14:13:26Z
dc.date.issued
2022-10-25T14:13:26Z
dc.date.issued
2022-10-01
dc.date.issued
2022-10-14T09:48:06Z
dc.identifier
1897-4287
dc.identifier
https://hdl.handle.net/2445/190189
dc.identifier
36182917
dc.description.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.
dc.format
11 p.
dc.format
application/pdf
dc.language
eng
dc.publisher
Springer Science and Business Media LLC
dc.relation
Reproducció del document publicat a: https://doi.org/10.1186/s13053-022-00241-1
dc.relation
Hereditary Cancer in Clinical Practice, 2022, vol. 20, núm. 1
dc.relation
https://doi.org/10.1186/s13053-022-00241-1
dc.rights
cc by (c) Møller, Pål et al., 2022
dc.rights
http://creativecommons.org/licenses/by/3.0/es/
dc.rights
info:eu-repo/semantics/openAccess
dc.source
Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))
dc.subject
Colonoscòpia
dc.subject
Epidemiologia
dc.subject
Colonoscopy
dc.subject
Epidemiology
dc.title
Colorectal cancer incidences in Lynch syndrome: a comparison of results from the prospective lynch syndrome database and the international mismatch repair consortium
dc.type
info:eu-repo/semantics/article
dc.type
info:eu-repo/semantics/publishedVersion


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