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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.

Authors :
Tatsuta, Kyota
Sakata, Mayu
Iwaizumi, Moriya
Kojima, Risa
Yamanaka, Katsumasa
Baba, Satoshi
Suzuki, Katsunori
Morita, Yoshifumi
Kikuchi, Hirotoshi
Hiramatsu, Yoshihiro
Kurachi, Kiyotaka
Takeuchi, Hiroya
Source :
Hereditary Cancer in Clinical Practice. 7/17/2023, Vol. 21 Issue 1, p1-8. 8p.
Publication Year :
2023

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 consists of six surgeons, one genetic counselor, one medical geneticist, and six pathologists. MA is set up to compensate for patients' lack of knowledge about genetic diseases and make case selection for elderly colorectal cancer patients with deficient mismatch repair (dMMR). MA is designed 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. The rates of genetic counseling and genetic testing was significantly 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 patients who lag behind in medical and human genetics education. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
17312302
Volume :
21
Issue :
1
Database :
Academic Search Index
Journal :
Hereditary Cancer in Clinical Practice
Publication Type :
Academic Journal
Accession number :
164982454
Full Text :
https://doi.org/10.1186/s13053-023-00258-0