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

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). ME...

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Autores principales: Tanaka, Tamaki, Takehara, Kazuhiro, Yamashita, Natsumi, Okazawa-Sakai, Mika, Kuraoka, Kazuya, Teramoto, Norihiro, Taguchi, Kenichi, Yamashiro, Katsushige, Kato, Hidenori, Mizunoe, Tomoya, Suzuki, Rie, Yamamoto, Dan, Ueki, Arisa, Saito, Toshiaki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Asian Society of Gynecologic Oncology; Korean Society of Gynecologic Oncology; Japan Society of Gynecologic Oncology 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9428302/
https://www.ncbi.nlm.nih.gov/pubmed/36032025
http://dx.doi.org/10.3802/jgo.2022.33.e67
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author Tanaka, Tamaki
Takehara, Kazuhiro
Yamashita, Natsumi
Okazawa-Sakai, Mika
Kuraoka, Kazuya
Teramoto, Norihiro
Taguchi, Kenichi
Yamashiro, Katsushige
Kato, Hidenori
Mizunoe, Tomoya
Suzuki, Rie
Yamamoto, Dan
Ueki, Arisa
Saito, Toshiaki
author_facet Tanaka, Tamaki
Takehara, Kazuhiro
Yamashita, Natsumi
Okazawa-Sakai, Mika
Kuraoka, Kazuya
Teramoto, Norihiro
Taguchi, Kenichi
Yamashiro, Katsushige
Kato, Hidenori
Mizunoe, Tomoya
Suzuki, Rie
Yamamoto, Dan
Ueki, Arisa
Saito, Toshiaki
author_sort Tanaka, Tamaki
collection PubMed
description 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.
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spelling pubmed-94283022022-09-07 Frequency and clinical features of deficient mismatch repair in ovarian clear cell and endometrioid carcinoma Tanaka, Tamaki Takehara, Kazuhiro Yamashita, Natsumi Okazawa-Sakai, Mika Kuraoka, Kazuya Teramoto, Norihiro Taguchi, Kenichi Yamashiro, Katsushige Kato, Hidenori Mizunoe, Tomoya Suzuki, Rie Yamamoto, Dan Ueki, Arisa Saito, Toshiaki J Gynecol Oncol Original Article 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. Asian Society of Gynecologic Oncology; Korean Society of Gynecologic Oncology; Japan Society of Gynecologic Oncology 2022-07-25 /pmc/articles/PMC9428302/ /pubmed/36032025 http://dx.doi.org/10.3802/jgo.2022.33.e67 Text en © 2022. Asian Society of Gynecologic Oncology, Korean Society of Gynecologic Oncology, and Japan Society of Gynecologic Oncology https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Tanaka, Tamaki
Takehara, Kazuhiro
Yamashita, Natsumi
Okazawa-Sakai, Mika
Kuraoka, Kazuya
Teramoto, Norihiro
Taguchi, Kenichi
Yamashiro, Katsushige
Kato, Hidenori
Mizunoe, Tomoya
Suzuki, Rie
Yamamoto, Dan
Ueki, Arisa
Saito, Toshiaki
Frequency and clinical features of deficient mismatch repair in ovarian clear cell and endometrioid carcinoma
title Frequency and clinical features of deficient mismatch repair in ovarian clear cell and endometrioid carcinoma
title_full Frequency and clinical features of deficient mismatch repair in ovarian clear cell and endometrioid carcinoma
title_fullStr Frequency and clinical features of deficient mismatch repair in ovarian clear cell and endometrioid carcinoma
title_full_unstemmed Frequency and clinical features of deficient mismatch repair in ovarian clear cell and endometrioid carcinoma
title_short Frequency and clinical features of deficient mismatch repair in ovarian clear cell and endometrioid carcinoma
title_sort frequency and clinical features of deficient mismatch repair in ovarian clear cell and endometrioid carcinoma
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9428302/
https://www.ncbi.nlm.nih.gov/pubmed/36032025
http://dx.doi.org/10.3802/jgo.2022.33.e67
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