TY - JOUR
T1 - Colorectal cancer incidence in path_MLH1 carriers subjected to different follow-up protocols
T2 - A Prospective Lynch Syndrome Database report
AU - in collaboration with The Mallorca Group
AU - Seppälä, Toni
AU - Pylvänäinen, Kirsi
AU - Evans, Dafydd Gareth
AU - Järvinen, Heikki
AU - Renkonen-Sinisalo, Laura
AU - Bernstein, Inge
AU - Holinski-Feder, Elke
AU - Sala, Paola
AU - Lindblom, Annika
AU - Macrae, Finlay
AU - Blanco, Ignacio
AU - Sijmons, Rolf
AU - Jeffries, Jacqueline
AU - Vasen, Hans
AU - Burn, John
AU - Nakken, Sigve
AU - Hovig, Eivind
AU - Rødland, Einar Andreas
AU - Tharmaratnam, Kukatharmini
AU - de Vos tot Nederveen Cappel, Wouter H.
AU - Hill, James
AU - Wijnen, Juul
AU - Jenkins, Mark
AU - Genuardi, Maurizio
AU - Green, Kate
AU - Lalloo, Fiona
AU - Sunde, Lone
AU - Mints, Miriam
AU - Bertario, Lucio
AU - Pineda, Marta
AU - Navarro, Matilde
AU - Morak, Monika
AU - Frayling, Ian M.
AU - Plazzer, John Paul
AU - Sampson, Julian R.
AU - Capella, Gabriel
AU - Möslein, Gabriela
AU - Mecklin, Jukka Pekka
AU - Møller, Pål
N1 - Funding Information:
The Finnish contribution: The Finnish Cancer Foundation, The Sigrid Juselius Foundation, Mary and Georg C. Ehrnrooth foundation, Jane and Aatos Erkko foundation and State Research Funding. The Spanish contribution: Spanish Ministry of Economy and Competitiveness, the Carlos III Health Institute, the Scientific Foundation Asociación Española Contra el Cáncer and the Government of Catalonia. The Welsh Contribution: Wales Gene Park. The study sponsors did not have a role in planning the study design; in the collection, analysis, or interpretation of data; in the writing of the report; or in the decision to submit the paper for publication.
Publisher Copyright:
© 2017 The Author(s).
PY - 2017/10/10
Y1 - 2017/10/10
N2 - Background: We have previously reported a high incidence of colorectal cancer (CRC) in carriers of pathogenic MLH1 variants (path_MLH1) despite follow-up with colonoscopy including polypectomy. Methods: The cohort included Finnish carriers enrolled in 3-yearly colonoscopy (n = 505; 4625 observation years) and carriers from other countries enrolled in colonoscopy 2-yearly or more frequently (n = 439; 3299 observation years). We examined whether the longer interval between colonoscopies in Finland could explain the high incidence of CRC and whether disease expression correlated with differences in population CRC incidence. Results: Cumulative CRC incidences in carriers of path_MLH1 at 70-years of age were 41% for males and 36% for females in the Finnish series and 58% and 55% in the non-Finnish series, respectively (p > 0.05). Mean time from last colonoscopy to CRC was 32.7 months in the Finnish compared to 31.0 months in the non-Finnish (p > 0.05) and was therefore unaffected by the recommended colonoscopy interval. Differences in population incidence of CRC could not explain the lower point estimates for CRC in the Finnish series. Ten-year overall survival after CRC was similar for the Finnish and non-Finnish series (88% and 91%, respectively; p > 0.05). Conclusions: The hypothesis that the high incidence of CRC in path_MLH1 carriers was caused by a higher incidence in the Finnish series was not valid. We discuss whether the results were influenced by methodological shortcomings in our study or whether the assumption that a shorter interval between colonoscopies leads to a lower CRC incidence may be wrong. This second possibility is intriguing, because it suggests the dogma that CRC in path_MLH1 carriers develops from polyps that can be detected at colonoscopy and removed to prevent CRC may be erroneous. In view of the excellent 10-year overall survival in the Finnish and non-Finnish series we remain strong advocates of current surveillance practices for those with LS pending studies that will inform new recommendations on the best surveillance interval.
AB - Background: We have previously reported a high incidence of colorectal cancer (CRC) in carriers of pathogenic MLH1 variants (path_MLH1) despite follow-up with colonoscopy including polypectomy. Methods: The cohort included Finnish carriers enrolled in 3-yearly colonoscopy (n = 505; 4625 observation years) and carriers from other countries enrolled in colonoscopy 2-yearly or more frequently (n = 439; 3299 observation years). We examined whether the longer interval between colonoscopies in Finland could explain the high incidence of CRC and whether disease expression correlated with differences in population CRC incidence. Results: Cumulative CRC incidences in carriers of path_MLH1 at 70-years of age were 41% for males and 36% for females in the Finnish series and 58% and 55% in the non-Finnish series, respectively (p > 0.05). Mean time from last colonoscopy to CRC was 32.7 months in the Finnish compared to 31.0 months in the non-Finnish (p > 0.05) and was therefore unaffected by the recommended colonoscopy interval. Differences in population incidence of CRC could not explain the lower point estimates for CRC in the Finnish series. Ten-year overall survival after CRC was similar for the Finnish and non-Finnish series (88% and 91%, respectively; p > 0.05). Conclusions: The hypothesis that the high incidence of CRC in path_MLH1 carriers was caused by a higher incidence in the Finnish series was not valid. We discuss whether the results were influenced by methodological shortcomings in our study or whether the assumption that a shorter interval between colonoscopies leads to a lower CRC incidence may be wrong. This second possibility is intriguing, because it suggests the dogma that CRC in path_MLH1 carriers develops from polyps that can be detected at colonoscopy and removed to prevent CRC may be erroneous. In view of the excellent 10-year overall survival in the Finnish and non-Finnish series we remain strong advocates of current surveillance practices for those with LS pending studies that will inform new recommendations on the best surveillance interval.
KW - Colorectal cancer
KW - Hereditary non-polyposis colorectal cancer
KW - Lynch syndrome
KW - Microsatellite instability
U2 - 10.1186/s13053-017-0078-5
DO - 10.1186/s13053-017-0078-5
M3 - Article
AN - SCOPUS:85030831455
SN - 1731-2302
VL - 15
JO - HEREDITARY CANCER IN CLINICAL PRACTICE
JF - HEREDITARY CANCER IN CLINICAL PRACTICE
IS - 1
M1 - 18
ER -