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)

Amor, David

Senter, Leigha

Hoogerbrugge, Nicoline

Rahner, Nils

Duijkers, Floor

Hall, Michael J.

Buchanan, Daniel D.

Le Marchand, Loïc

Win, Aung Ko

Hovig, Eivind

Nakken, Sigve

Hampel, Heather

Williams, Heinric

Rasmussen, Lene J.

Ricciardiello, Luigi

Southey, Melissa

Samadder, N. Jewel

James, Paul

Okkels, Henrik

Lubiński, Jan

Reece, Jeanette

Kalfayan, Pablo

Ngeow, Joanne

Bassaneze, Thiago

Guillem, Jose G.

Ward, Robyn

Ahadova, Aysel

Arnold, Julie

Pai, Rish K.

Jenkins, Mark A.

Wadt, Karin

Ankathil, Ravindran

Burn, John

Holinski Feder, Elke

Monahan, Kevin

Parry, Susan

Evans, D. Gareth

Sampson, Julian R.

Moslein, Gabriela

Bonanni, Bernardo

Lindblom, Annika

Dębniak, Tadeusz

John, Thomas

Büttner, Reinhard

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

Brunet, Joan

Kennelly, Rory

Cavestro, Giulia Martina

Dueñas, Nuria

Greenblatt, Marc

Weitz, Jürgen

Pineda, Marta

Lino Silva, Leonardo S.

Redler, Silke

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 H.

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

Publication date

2022-10-25T14:13:26Z

2022-10-25T14:13:26Z

2022-10-01

2022-10-14T09:48:06Z

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.

Document Type

Article


Published version

Language

English

Publisher

Springer Science and Business Media LLC

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Reproducció del document publicat a: https://doi.org/10.1186/s13053-022-00241-1

Hereditary Cancer in Clinical Practice, 2022, vol. 20, núm. 1

https://doi.org/10.1186/s13053-022-00241-1

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Rights

cc by (c) Møller, Pål et al., 2022

http://creativecommons.org/licenses/by/3.0/es/