Using a multistep approach with multidisciplinary team to increase the diagnosis rate of Lynch syndrome- associated colorectal cancer after universal screening: A single-center study in Japan

Author:

Tatsuta Kyota1,Sakata Mayu1,Iwaizumi Moriya1,Kojima Risa1,Yamanaka Katsumasa1,Baba Satoshi1,Suzuki Katusnori1,Morita Yoshifumi1,Kikuchi Hirotoshi1,Hiramatsu Yoshihiro1,Kurachi Kiyotaka1,Takeuchi Hiroya1

Affiliation:

1. Hamamatsu University School of Medicine

Abstract

Abstract Backgrounds: This study aimed to evaluate the changes in the rates of genetic counseling and genetic testing as well as the diagnosis rate of Lynch syndrome (LS)-associated colorectal cancer before and after multistep approach with multidisciplinary team in Japanese. Methods: In September 2016, we started universal screening for LS by mismatch repair protein immunohistochemistry and prospectively collected the records. Following patient interviews, we started multistep approach with multidisciplinary team (MA) in January 2020. MA consistsof several surgeons, one genetic counselor, one medical geneticist, and several pathologists. MA is set upto compensate for patients’lack of knowledge about geneticdiseases and make case selection for elderly colorectal cancer patients with deficient mismatch repair (dMMR). MA isdesigned as a system that could be performed by a small number of medical genetic specialists. A total of 522 patients were included during the study duration, 323 and 199 patients in the pre-MA (P-MA) and MA groups, respectively. Results: The frequency of dMMR in all patients was 10.0%. The patient interview results indicated a significant lack of patient education regarding genetic diseases. Therates of genetic counseling and genetic testing wassignificantly higher in MA group than in P-MA group (genetic counseling: MA 34.6% vs P-MA 7.7%, p = 0.04;genetic testing: MA 30.8% vs P-MA 3.8%, p = 0.02). Moreover, the diagnosis rate of LS-associated colorectal cancer was significantly higher in MA group (2.5%) than in P-MA group (0.3%) (P = 0.03). In addition, MA could be performed without problems despite the small number of medical and human genetics specialists. Conclusions: MA has achieved appropriate pickup of suspected hereditary colorectal cancer patients and complemented the lack of knowledge about genetic diseases. The introduction of MA increased LS-associated colorectal cancer after universal screening. MA is an appropriate LS screening protocol for Japanese who lag behind in medical and human genetics education.

Publisher

Research Square Platform LLC

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