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Tamoxifen use in recurrent ovarian cancer in a Chinese population: A 15 ‐year clinical experience in a tertiary referral center

AIM: To review the clinical use and the effectiveness of tamoxifen in patients with advanced or recurrent ovarian cancer. METHODS: A retrospective review of clinical records was conducted in patients who received tamoxifen for the treatment of ovarian cancer between 2002 and 2016. We reviewed the cl...

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Autores principales: Chan, Karen Kar Loen, Ngu, Siew Fei, Chu, Mandy Man Yee, Tse, Ka Yu, Ngan, Hextan Yuen Sheung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8359459/
https://www.ncbi.nlm.nih.gov/pubmed/33079469
http://dx.doi.org/10.1111/ajco.13478
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author Chan, Karen Kar Loen
Ngu, Siew Fei
Chu, Mandy Man Yee
Tse, Ka Yu
Ngan, Hextan Yuen Sheung
author_facet Chan, Karen Kar Loen
Ngu, Siew Fei
Chu, Mandy Man Yee
Tse, Ka Yu
Ngan, Hextan Yuen Sheung
author_sort Chan, Karen Kar Loen
collection PubMed
description AIM: To review the clinical use and the effectiveness of tamoxifen in patients with advanced or recurrent ovarian cancer. METHODS: A retrospective review of clinical records was conducted in patients who received tamoxifen for the treatment of ovarian cancer between 2002 and 2016. We reviewed the clinical setting that it was given, duration of use, patients' tolerability, clinical benefit and progression‐free survival. We also attempted to identify predictive markers for response. RESULTS: A total of 92 patients received tamoxifen during this 15‐year period. The patients received a median of 2.5 lines of chemotherapy before switching to tamoxifen, and they remained on tamoxifen for a median of 5.6 months (range 0–85 months), with 24 patients receiving it for more than 12 months. Seventy‐six patients continued on tamoxifen for more than 2 months. In this group, 75 patients had an evaluable response, either by CA 125 or clinically and clinical benefit rate (defined as complete, partial response and static disease) was seen in 42 patients (56%), with majority of patients having static disease. The median progression‐free survival was 5.3 months (95% confidence interval, 2.6–8.1). Tamoxifen was well tolerated. Hormone receptor status was not demonstrated to predict response. CONCLUSION: Patients with advanced ovarian cancer who have failed previous lines of chemotherapy may achieve static disease with tamoxifen with minimal side effects. Tamoxifen may still have a role in the era of molecular target therapy.
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spelling pubmed-83594592021-08-17 Tamoxifen use in recurrent ovarian cancer in a Chinese population: A 15 ‐year clinical experience in a tertiary referral center Chan, Karen Kar Loen Ngu, Siew Fei Chu, Mandy Man Yee Tse, Ka Yu Ngan, Hextan Yuen Sheung Asia Pac J Clin Oncol Original Articles AIM: To review the clinical use and the effectiveness of tamoxifen in patients with advanced or recurrent ovarian cancer. METHODS: A retrospective review of clinical records was conducted in patients who received tamoxifen for the treatment of ovarian cancer between 2002 and 2016. We reviewed the clinical setting that it was given, duration of use, patients' tolerability, clinical benefit and progression‐free survival. We also attempted to identify predictive markers for response. RESULTS: A total of 92 patients received tamoxifen during this 15‐year period. The patients received a median of 2.5 lines of chemotherapy before switching to tamoxifen, and they remained on tamoxifen for a median of 5.6 months (range 0–85 months), with 24 patients receiving it for more than 12 months. Seventy‐six patients continued on tamoxifen for more than 2 months. In this group, 75 patients had an evaluable response, either by CA 125 or clinically and clinical benefit rate (defined as complete, partial response and static disease) was seen in 42 patients (56%), with majority of patients having static disease. The median progression‐free survival was 5.3 months (95% confidence interval, 2.6–8.1). Tamoxifen was well tolerated. Hormone receptor status was not demonstrated to predict response. CONCLUSION: Patients with advanced ovarian cancer who have failed previous lines of chemotherapy may achieve static disease with tamoxifen with minimal side effects. Tamoxifen may still have a role in the era of molecular target therapy. John Wiley and Sons Inc. 2020-10-20 2021-08 /pmc/articles/PMC8359459/ /pubmed/33079469 http://dx.doi.org/10.1111/ajco.13478 Text en © 2020 The Authors. Asia‐Pacific Journal of Clinical Oncology Published by John Wiley & Sons Australia, Ltd https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Original Articles
Chan, Karen Kar Loen
Ngu, Siew Fei
Chu, Mandy Man Yee
Tse, Ka Yu
Ngan, Hextan Yuen Sheung
Tamoxifen use in recurrent ovarian cancer in a Chinese population: A 15 ‐year clinical experience in a tertiary referral center
title Tamoxifen use in recurrent ovarian cancer in a Chinese population: A 15 ‐year clinical experience in a tertiary referral center
title_full Tamoxifen use in recurrent ovarian cancer in a Chinese population: A 15 ‐year clinical experience in a tertiary referral center
title_fullStr Tamoxifen use in recurrent ovarian cancer in a Chinese population: A 15 ‐year clinical experience in a tertiary referral center
title_full_unstemmed Tamoxifen use in recurrent ovarian cancer in a Chinese population: A 15 ‐year clinical experience in a tertiary referral center
title_short Tamoxifen use in recurrent ovarian cancer in a Chinese population: A 15 ‐year clinical experience in a tertiary referral center
title_sort tamoxifen use in recurrent ovarian cancer in a chinese population: a 15 ‐year clinical experience in a tertiary referral center
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8359459/
https://www.ncbi.nlm.nih.gov/pubmed/33079469
http://dx.doi.org/10.1111/ajco.13478
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