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Frequency and clinical features of deficient mismatch repair in ovarian clear cell and endometrioid carcinoma.

Authors :
Tamaki Tanaka
Kazuhiro Takehara
Natsumi Yamashita
Mika Okazawa-Sakai
Kazuya Kuraoka
Norihiro Teramoto
Kenichi Taguchi
Katsushige Yamashiro
Hidenori Kato
Tomoya Mizunoe
Rie Suzuki
Dan Yamamoto
Arisa Ueki
Toshiaki Saito
Source :
Journal of Gynecologic Oncology. Sep2022, Vol. 33 Issue 5, p1-13. 13p.
Publication Year :
2022

Abstract

Objective: To clarify the frequency of deficient mismatch repair (dMMR) in Japanese ovarian cancer patients, we examined microsatellite instability (MSI) status and immunohistochemistry (IHC) subtypes, including endometrioid carcinoma (EMC), clear cell carcinoma (CCC), or a mixture of both (Mix). Methods: We registered 390 patients who were diagnosed with EMC/CCC/Mix between 2006 and 2015 and treated at seven participating facilities. For 339 patients confirmed eligible by the Central Pathological Review Board, MSI, IHC, and MutL homolog 1 methylation analyses were conducted. The tissues of patients with Lynch syndrome (LS)-related cancer histories, such as colorectal and endometrial cancer, were also investigated. Results: MSI-high (MSI-H) status was observed in 2/217 CCC (0.9%), 10/115 EMC (8.7%), and 1/4 Mix (25%). Additionally, loss of MMR protein expression (LoE-MMR) was observed in 5/219 (2.3%), 16/115 (14.0%), and 1/4 (25%) patients with CCC, EMC, and Mix, respectively. Both MSI-H and LoE-MMR were found significantly more often in EMC (p<0.001). The median (range) ages of patients with MMR expression and LoE-MMR were 54 (30-90) and 46 (22-76) (p=0.002), respectively. In the multivariate analysis, advanced stage and histological type were identified as prognostic factors. Conclusion: The dMMR rate for EMC/CCC was similar to that reported in Western countries. In Japan, it is assumed that the dMMR frequency is higher because of the increased proportion of CCC. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
20050380
Volume :
33
Issue :
5
Database :
Academic Search Index
Journal :
Journal of Gynecologic Oncology
Publication Type :
Academic Journal
Accession number :
158882334
Full Text :
https://doi.org/10.3802/jgo.2022.33.e67