TY - JOUR
T1 - Survival by colon cancer stage and screening interval in Lynch syndrome
T2 - A prospective Lynch syndrome database report
AU - Dominguez-Valentin, Mev
AU - Seppälä, Toni T.
AU - Sampson, Julian R.
AU - MacRae, Finlay
AU - Winship, Ingrid
AU - Evans, D. Gareth
AU - Scott, Rodney J.
AU - Burn, John
AU - Möslein, Gabriela
AU - Bernstein, Inge
AU - Pylvänäinen, Kirsi
AU - Renkonen-Sinisalo, Laura
AU - Lepistö, Anna
AU - Lindblom, Annika
AU - Plazzer, John Paul
AU - Tjandra, Douglas
AU - Thomas, Huw
AU - Green, Kate
AU - Lalloo, Fiona
AU - Crosbie, Emma J.
AU - Hill, James
AU - Capella, Gabriel
AU - Pineda, Marta
AU - Navarro, Matilde
AU - Vidal, Joan Brunet
AU - Rønlund, Karina
AU - Nielsen, Randi Thyregaard
AU - Yilmaz, Mette
AU - Elvang, Louise Laurberg
AU - Katz, Lior
AU - Nielsen, Maartje
AU - Ten Broeke, Sanne W.
AU - Nakken, Sigve
AU - Hovig, Eivind
AU - Sunde, Lone
AU - Kloor, Matthias
AU - Knebel Doeberitz, Magnus V.
AU - Ahadova, Aysel
AU - Lindor, Noralane
AU - Steinke-Lange, Verena
AU - Holinski-Feder, Elke
AU - Mecklin, Jukka Pekka
AU - Møller, Pål
N1 - Funding Information:
We would like to express our gratitude to Heikki Järvinen, Beatriz Alcala-Repo and Marianne Haeusler for their efforts during the years. TTS and J-PM are supported by the Emil Aaltonen Foundation, the Finnish Medical Foundation, the Instrumentarium Science Foundation, Sigrid Juselius Foundation, The Finnish Cancer Foundation, Jane and Aatos Erkko foundation and State Research Funding. DGE and EJC are both supported through the National Institute for Health Research Manchester Biomedical Research Centre (IS-BRC-1215-20007). The Spanish contribution: GC and MP were funded by the Spanish Ministry of Economy and Competitiveness and cofunded by FEDER funds -a way to build Europe- (grant SAF2015-68016-R) and the CIBERONC, 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 Norwegian contribution: Norwegian Cancer Society, contract 194751- 2017 for funding. Work relevant for the German contribution was funded in part by Wilhelm Sander Foundation (2016.056.1) and German Research Foundation (Deutsche Forschungsgemeinschaft, DFG; KFO227, KL2354). 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:
© 2019 The Author(s).
PY - 2019/10/14
Y1 - 2019/10/14
N2 - Background: We previously reported that in pathogenic mismatch repair (path-MMR) variant carriers, the incidence of colorectal cancer (CRC) was not reduced when colonoscopy was undertaken more frequently than once every 3 years, and that CRC stage and interval since last colonoscopy were not correlated. Methods: The Prospective Lynch Syndrome Database (PLSD) that records outcomes of surveillance was examined to determine survival after colon cancer in relation to the time since previous colonoscopy and pathological stage. Only path-MMR variants scored by the InSiGHT variant database as class 4 or 5 (clinically actionable) were included in the analysis. Results: Ninety-nine path-MMR carriers had no cancer prior to or at first colonoscopy, but subsequently developed colon cancer. Among these, 96 were 65 years of age or younger at diagnosis, and included 77 path-MLH1, 17 path-MSH2, and 2 path-MSH6 carriers. The number of cancers detected within < 1.5, 1.5-2.5, 2.5-3.5 and at > 3.5 years after previous colonoscopy were 9, 43, 31 and 13, respectively. Of these, 2, 8, 4 and 3 were stage III, respectively, and only one stage IV (interval 2.5-3.5 years) disease. Ten-year crude survival after colon cancer were 93, 94 and 82% for stage I, II and III disease, respectively (p < 0.001). Ten-year crude survival when the last colonoscopy had been < 1.5, 1.5-2.5, 2.5-3.5 or > 3.5 years before diagnosis, was 89, 90, 90 and 92%, respectively (p = 0.91). Conclusions: In path-MLH1 and path-MSH2 carriers, more advanced colon cancer stage was associated with poorer survival, whereas time since previous colonoscopy was not. Although the numbers are limited, together with our previously reported findings, these results may be in conflict with the view that follow-up of path-MMR variant carriers with colonoscopy intervals of less than 3 years provides significant benefit.
AB - Background: We previously reported that in pathogenic mismatch repair (path-MMR) variant carriers, the incidence of colorectal cancer (CRC) was not reduced when colonoscopy was undertaken more frequently than once every 3 years, and that CRC stage and interval since last colonoscopy were not correlated. Methods: The Prospective Lynch Syndrome Database (PLSD) that records outcomes of surveillance was examined to determine survival after colon cancer in relation to the time since previous colonoscopy and pathological stage. Only path-MMR variants scored by the InSiGHT variant database as class 4 or 5 (clinically actionable) were included in the analysis. Results: Ninety-nine path-MMR carriers had no cancer prior to or at first colonoscopy, but subsequently developed colon cancer. Among these, 96 were 65 years of age or younger at diagnosis, and included 77 path-MLH1, 17 path-MSH2, and 2 path-MSH6 carriers. The number of cancers detected within < 1.5, 1.5-2.5, 2.5-3.5 and at > 3.5 years after previous colonoscopy were 9, 43, 31 and 13, respectively. Of these, 2, 8, 4 and 3 were stage III, respectively, and only one stage IV (interval 2.5-3.5 years) disease. Ten-year crude survival after colon cancer were 93, 94 and 82% for stage I, II and III disease, respectively (p < 0.001). Ten-year crude survival when the last colonoscopy had been < 1.5, 1.5-2.5, 2.5-3.5 or > 3.5 years before diagnosis, was 89, 90, 90 and 92%, respectively (p = 0.91). Conclusions: In path-MLH1 and path-MSH2 carriers, more advanced colon cancer stage was associated with poorer survival, whereas time since previous colonoscopy was not. Although the numbers are limited, together with our previously reported findings, these results may be in conflict with the view that follow-up of path-MMR variant carriers with colonoscopy intervals of less than 3 years provides significant benefit.
KW - Cancer stage
KW - Colon cancer
KW - Colonoscopy
KW - Lynch syndrome
KW - Surveillance
KW - Survival
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U2 - 10.1186/s13053-019-0127-3
DO - 10.1186/s13053-019-0127-3
M3 - Article
AN - SCOPUS:85075119347
SN - 1731-2302
VL - 17
JO - Hereditary Cancer in Clinical Practice
JF - Hereditary Cancer in Clinical Practice
IS - 1
M1 - 28
ER -