Cargando…
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...
Autores principales: | , , , , , , , , , , , , , |
---|---|
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 |
_version_ | 1784779084961677312 |
---|---|
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. |
format | Online Article Text |
id | pubmed-9428302 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Asian Society of Gynecologic Oncology; Korean Society of Gynecologic Oncology; Japan Society of Gynecologic Oncology |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT tanakatamaki frequencyandclinicalfeaturesofdeficientmismatchrepairinovarianclearcellandendometrioidcarcinoma AT takeharakazuhiro frequencyandclinicalfeaturesofdeficientmismatchrepairinovarianclearcellandendometrioidcarcinoma AT yamashitanatsumi frequencyandclinicalfeaturesofdeficientmismatchrepairinovarianclearcellandendometrioidcarcinoma AT okazawasakaimika frequencyandclinicalfeaturesofdeficientmismatchrepairinovarianclearcellandendometrioidcarcinoma AT kuraokakazuya frequencyandclinicalfeaturesofdeficientmismatchrepairinovarianclearcellandendometrioidcarcinoma AT teramotonorihiro frequencyandclinicalfeaturesofdeficientmismatchrepairinovarianclearcellandendometrioidcarcinoma AT taguchikenichi frequencyandclinicalfeaturesofdeficientmismatchrepairinovarianclearcellandendometrioidcarcinoma AT yamashirokatsushige frequencyandclinicalfeaturesofdeficientmismatchrepairinovarianclearcellandendometrioidcarcinoma AT katohidenori frequencyandclinicalfeaturesofdeficientmismatchrepairinovarianclearcellandendometrioidcarcinoma AT mizunoetomoya frequencyandclinicalfeaturesofdeficientmismatchrepairinovarianclearcellandendometrioidcarcinoma AT suzukirie frequencyandclinicalfeaturesofdeficientmismatchrepairinovarianclearcellandendometrioidcarcinoma AT yamamotodan frequencyandclinicalfeaturesofdeficientmismatchrepairinovarianclearcellandendometrioidcarcinoma AT uekiarisa frequencyandclinicalfeaturesofdeficientmismatchrepairinovarianclearcellandendometrioidcarcinoma AT saitotoshiaki frequencyandclinicalfeaturesofdeficientmismatchrepairinovarianclearcellandendometrioidcarcinoma |