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Long-Term Survival and Clinicopathological Implications of DNA Mismatch Repair Status in Endometrioid Endometrial Cancers in Hong Kong Chinese Women

To investigate the role of DNA mismatch repair status (MMR) in survival of endometrioid endometrial cancer in Hong Kong Chinese women and its correlation to clinical prognostic factors, 238 patients with endometrioid endometrial cancer were included. Tumor MMR status was evaluated by immunohistochem...

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Autores principales: Lee, Jacqueline Ho Sze, Li, Joshua Jing Xi, Chow, Chit, Chan, Ronald Cheong Kin, Kwan, Johnny Sheung Him, Lau, Tat San, To, Ka Fai, Yim, So Fan, Yeung, Suet Ying, Kwong, Joseph
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8533409/
https://www.ncbi.nlm.nih.gov/pubmed/34680502
http://dx.doi.org/10.3390/biomedicines9101385
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author Lee, Jacqueline Ho Sze
Li, Joshua Jing Xi
Chow, Chit
Chan, Ronald Cheong Kin
Kwan, Johnny Sheung Him
Lau, Tat San
To, Ka Fai
Yim, So Fan
Yeung, Suet Ying
Kwong, Joseph
author_facet Lee, Jacqueline Ho Sze
Li, Joshua Jing Xi
Chow, Chit
Chan, Ronald Cheong Kin
Kwan, Johnny Sheung Him
Lau, Tat San
To, Ka Fai
Yim, So Fan
Yeung, Suet Ying
Kwong, Joseph
author_sort Lee, Jacqueline Ho Sze
collection PubMed
description To investigate the role of DNA mismatch repair status (MMR) in survival of endometrioid endometrial cancer in Hong Kong Chinese women and its correlation to clinical prognostic factors, 238 patients with endometrioid endometrial cancer were included. Tumor MMR status was evaluated by immunohistochemistry. Clinical characteristics and survival were determined. Association of MMR with survival and clinicopathological parameters were assessed. MMR deficiency (dMMR) was found in 43 cases (16.5%). dMMR was associated with poor prognostic factors including older age, higher stage, higher grade, larger tumor size and more radiotherapy usage. Long-term survival was worse in dMMR compared to the MMR proficient group. The dMMR group had more deaths, shorter disease-specific survival (DSS), shorter disease-free survival (DFS), less 10-year DSS, less 10-year DFS, and more recurrence. The 5-year DSS and 5-year DFS in the dMMR group only showed a trend of worse survival but did not reach statistical significance. In conclusion, dMMR is present in a significant number of endometrioid endometrial cancers patients and is associated with poorer clinicopathological factors and survival parameters in the long run. dMMR should be considered in the risk stratification of endometrial cancer to guide adjuvant therapy and individualisation for longer follow up plan.
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spelling pubmed-85334092021-10-23 Long-Term Survival and Clinicopathological Implications of DNA Mismatch Repair Status in Endometrioid Endometrial Cancers in Hong Kong Chinese Women Lee, Jacqueline Ho Sze Li, Joshua Jing Xi Chow, Chit Chan, Ronald Cheong Kin Kwan, Johnny Sheung Him Lau, Tat San To, Ka Fai Yim, So Fan Yeung, Suet Ying Kwong, Joseph Biomedicines Article To investigate the role of DNA mismatch repair status (MMR) in survival of endometrioid endometrial cancer in Hong Kong Chinese women and its correlation to clinical prognostic factors, 238 patients with endometrioid endometrial cancer were included. Tumor MMR status was evaluated by immunohistochemistry. Clinical characteristics and survival were determined. Association of MMR with survival and clinicopathological parameters were assessed. MMR deficiency (dMMR) was found in 43 cases (16.5%). dMMR was associated with poor prognostic factors including older age, higher stage, higher grade, larger tumor size and more radiotherapy usage. Long-term survival was worse in dMMR compared to the MMR proficient group. The dMMR group had more deaths, shorter disease-specific survival (DSS), shorter disease-free survival (DFS), less 10-year DSS, less 10-year DFS, and more recurrence. The 5-year DSS and 5-year DFS in the dMMR group only showed a trend of worse survival but did not reach statistical significance. In conclusion, dMMR is present in a significant number of endometrioid endometrial cancers patients and is associated with poorer clinicopathological factors and survival parameters in the long run. dMMR should be considered in the risk stratification of endometrial cancer to guide adjuvant therapy and individualisation for longer follow up plan. MDPI 2021-10-04 /pmc/articles/PMC8533409/ /pubmed/34680502 http://dx.doi.org/10.3390/biomedicines9101385 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Lee, Jacqueline Ho Sze
Li, Joshua Jing Xi
Chow, Chit
Chan, Ronald Cheong Kin
Kwan, Johnny Sheung Him
Lau, Tat San
To, Ka Fai
Yim, So Fan
Yeung, Suet Ying
Kwong, Joseph
Long-Term Survival and Clinicopathological Implications of DNA Mismatch Repair Status in Endometrioid Endometrial Cancers in Hong Kong Chinese Women
title Long-Term Survival and Clinicopathological Implications of DNA Mismatch Repair Status in Endometrioid Endometrial Cancers in Hong Kong Chinese Women
title_full Long-Term Survival and Clinicopathological Implications of DNA Mismatch Repair Status in Endometrioid Endometrial Cancers in Hong Kong Chinese Women
title_fullStr Long-Term Survival and Clinicopathological Implications of DNA Mismatch Repair Status in Endometrioid Endometrial Cancers in Hong Kong Chinese Women
title_full_unstemmed Long-Term Survival and Clinicopathological Implications of DNA Mismatch Repair Status in Endometrioid Endometrial Cancers in Hong Kong Chinese Women
title_short Long-Term Survival and Clinicopathological Implications of DNA Mismatch Repair Status in Endometrioid Endometrial Cancers in Hong Kong Chinese Women
title_sort long-term survival and clinicopathological implications of dna mismatch repair status in endometrioid endometrial cancers in hong kong chinese women
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8533409/
https://www.ncbi.nlm.nih.gov/pubmed/34680502
http://dx.doi.org/10.3390/biomedicines9101385
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