TY - JOUR
T1 - No Difference in Colorectal Cancer Incidence or Stage at Detection by Colonoscopy Among 3 Countries With Different Lynch Syndrome Surveillance Policies
AU - Engel, Christoph
AU - Vasen, Hans F.
AU - Seppälä, Toni
AU - Aretz, Stefan
AU - Bigirwamungu-Bargeman, Marloes
AU - de Boer, Sybrand Y.
AU - Bucksch, Karolin
AU - Büttner, Reinhard
AU - Holinski-Feder, Elke
AU - Holzapfel, Stefanie
AU - Hüneburg, Robert
AU - Jacobs, Maarten A. J. M.
AU - Järvinen, Heikki
AU - Kloor, Matthias
AU - von Knebel Doeberitz, Magnus
AU - Koornstra, Jan J.
AU - van Kouwen, Mariette
AU - Langers, Alexandra M.
AU - van de Meeberg, Paul C.
AU - Morak, Monika
AU - Möslein, Gabriela
AU - Nagengast, Fokko M.
AU - Pylvänäinen, Kirsi
AU - Rahner, Nils
AU - Renkonen-Sinisalo, Laura
AU - Sanduleanu, Silvia
AU - Schackert, Hans K.
AU - Schmiegel, Wolff
AU - Schulmann, Karsten
AU - Steinke-Lange, Verena
AU - Strassburg, Christian P.
AU - Vecht, Juda
AU - Verhulst, Marie-Louise
AU - de Vos tot Nederveen Cappel, Wouter
AU - Zachariae, Silke
AU - Mecklin, Jukka-Pekka
AU - Loeffler, Markus
AU - German HNPCC Consortium, the Dutch Lynch Syndrome Collaborative Group, and the Finnish Lynch Syndrome Registry
PY - 2018
Y1 - 2018
N2 - Background & Aims: Patients with Lynch syndrome are at high risk for developing colorectal cancer (CRC). Regular colonoscopic surveillance is recommended, but there is no international consensus on the appropriate interval. We investigated whether shorter intervals are associated with lower CRC incidence and detection at earlier stages by comparing the surveillance policies in Germany, which evaluates patients by colonoscopy annually, in the Netherlands (patients evaluated at 1–2-year intervals), and Finland (patients evaluated at 2–3-year intervals). Methods: We collected data from 16,327 colonoscopic examinations (conducted from 1984 through 2015) of 2747 patients with Lynch syndrome (pathogenic variants in the MLH1, MSH2, or MSH6 genes) from the German HNPCC Consortium, the Dutch Lynch Syndrome Registry, and the Finnish Lynch Syndrome Registry. Our analysis included 23,309 person-years of cumulative observation time. Time from the index colonoscopy to incident CRC or adenoma was analyzed using the Kaplan-Meier method; groups were compared using the log-rank test. We performed multivariable Cox regression analyses to identify factors associated with CRC risk (diagnosis of CRC before the index colonoscopy, sex, mutation, age, and presence of adenoma at the index colonoscopy). Results: The 10-year cumulative CRC incidence ranged from 4.1% to 18.4% in patients with low- and high-risk profiles, respectively, and varied with age, sex, mutation, and prior detection of CRC or adenoma. Observed colonoscopy intervals were largely in accordance with the country-specific recommendations. We found no significant differences in cumulative CRC incidence or CRC stage at detection among countries. There was no significant association between CRC stage and time since last colonoscopy. Conclusions: We did not find a significant reduction in CRC incidence or stage of detection in Germany (annual colonoscopic surveillance) than in countries with longer surveillance intervals (the Netherlands, with 1–2-year intervals, and Finland, with 2–3-year intervals). Overall, we did not find a significant association of the interval with CRC risk, although age, sex, mutation, and prior neoplasia were used to individually modify colonoscopy intervals. Studies are needed to develop and validate risk-adapted surveillance strategies and to identify patients who benefit from shorter surveillance intervals.
AB - Background & Aims: Patients with Lynch syndrome are at high risk for developing colorectal cancer (CRC). Regular colonoscopic surveillance is recommended, but there is no international consensus on the appropriate interval. We investigated whether shorter intervals are associated with lower CRC incidence and detection at earlier stages by comparing the surveillance policies in Germany, which evaluates patients by colonoscopy annually, in the Netherlands (patients evaluated at 1–2-year intervals), and Finland (patients evaluated at 2–3-year intervals). Methods: We collected data from 16,327 colonoscopic examinations (conducted from 1984 through 2015) of 2747 patients with Lynch syndrome (pathogenic variants in the MLH1, MSH2, or MSH6 genes) from the German HNPCC Consortium, the Dutch Lynch Syndrome Registry, and the Finnish Lynch Syndrome Registry. Our analysis included 23,309 person-years of cumulative observation time. Time from the index colonoscopy to incident CRC or adenoma was analyzed using the Kaplan-Meier method; groups were compared using the log-rank test. We performed multivariable Cox regression analyses to identify factors associated with CRC risk (diagnosis of CRC before the index colonoscopy, sex, mutation, age, and presence of adenoma at the index colonoscopy). Results: The 10-year cumulative CRC incidence ranged from 4.1% to 18.4% in patients with low- and high-risk profiles, respectively, and varied with age, sex, mutation, and prior detection of CRC or adenoma. Observed colonoscopy intervals were largely in accordance with the country-specific recommendations. We found no significant differences in cumulative CRC incidence or CRC stage at detection among countries. There was no significant association between CRC stage and time since last colonoscopy. Conclusions: We did not find a significant reduction in CRC incidence or stage of detection in Germany (annual colonoscopic surveillance) than in countries with longer surveillance intervals (the Netherlands, with 1–2-year intervals, and Finland, with 2–3-year intervals). Overall, we did not find a significant association of the interval with CRC risk, although age, sex, mutation, and prior neoplasia were used to individually modify colonoscopy intervals. Studies are needed to develop and validate risk-adapted surveillance strategies and to identify patients who benefit from shorter surveillance intervals.
UR - https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85055885341&origin=inward
UR - https://www.ncbi.nlm.nih.gov/pubmed/30063918
U2 - 10.1053/j.gastro.2018.07.030
DO - 10.1053/j.gastro.2018.07.030
M3 - Article
C2 - 30063918
VL - 155
SP - 1400-1409.e2
JO - Gastroenterology
JF - Gastroenterology
SN - 0016-5085
IS - 5
ER -