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The safety of hormone replacement therapy in gynecological cancer survivors

The safety of hormone replacement therapy in gynecological cancer survivors
The safety of hormone replacement therapy in gynecological cancer survivors

Treatment of gynecological cancers often induces a premature menopause. Plus advancing treatments mean more gynecological cancer survivors are living to physiological menopause. Hormone replacement therapy (HRT) has proven substantial long-term benefits in physiological menopause and premature menopause particularly. We aimed to evaluate the current evidence on the safety of HRT in gynecological cancer survivors to help clinicians counsel these patients. HRT is not contraindicated in most gynecological cancer survivors, as evidence available often shows safety or even benefit with HRT use. However, HRT is contraindicated in a few cancers-in low-grade serous ovarian carcinoma, high-risk endometrial carcinoma, and some uterine sarcomas. Caution is advised in high-grade serous, late-stage endometrioid, and granulosa ovarian carcinomas when there is substandard evidence demonstrating safety, but also a theoretical harm present. Due to deficient large randomized controlled trials and methodological biases being present in most studies, HRT use needs to be individualized in most cancers-ovarian carcinomas, endometrial carcinomas, and cervical adenocarcinomas. Justification for HRT use is strong, and HRT is not contraindicated in most gynecological cancers due to largely reassuring evidence. More robust long-term data are needed for further reliable guidance for clinicians and patients.

gynecological cancer, hormone therapy, prognosis
1526-8004
Dodhia, Victoria
f61b84d0-b2b3-4d25-aab9-f592b0138458
Cheong, Ying
4efbba2a-3036-4dce-82f1-8b4017952c83
Dodhia, Victoria
f61b84d0-b2b3-4d25-aab9-f592b0138458
Cheong, Ying
4efbba2a-3036-4dce-82f1-8b4017952c83

Dodhia, Victoria and Cheong, Ying (2025) The safety of hormone replacement therapy in gynecological cancer survivors. Seminars in Reproductive Medicine. (doi:10.1055/s-0045-1802985).

Record type: Review

Abstract

Treatment of gynecological cancers often induces a premature menopause. Plus advancing treatments mean more gynecological cancer survivors are living to physiological menopause. Hormone replacement therapy (HRT) has proven substantial long-term benefits in physiological menopause and premature menopause particularly. We aimed to evaluate the current evidence on the safety of HRT in gynecological cancer survivors to help clinicians counsel these patients. HRT is not contraindicated in most gynecological cancer survivors, as evidence available often shows safety or even benefit with HRT use. However, HRT is contraindicated in a few cancers-in low-grade serous ovarian carcinoma, high-risk endometrial carcinoma, and some uterine sarcomas. Caution is advised in high-grade serous, late-stage endometrioid, and granulosa ovarian carcinomas when there is substandard evidence demonstrating safety, but also a theoretical harm present. Due to deficient large randomized controlled trials and methodological biases being present in most studies, HRT use needs to be individualized in most cancers-ovarian carcinomas, endometrial carcinomas, and cervical adenocarcinomas. Justification for HRT use is strong, and HRT is not contraindicated in most gynecological cancers due to largely reassuring evidence. More robust long-term data are needed for further reliable guidance for clinicians and patients.

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Accepted/In Press date: 22 January 2025
e-pub ahead of print date: 18 March 2025
Keywords: gynecological cancer, hormone therapy, prognosis

Identifiers

Local EPrints ID: 503760
URI: http://eprints.soton.ac.uk/id/eprint/503760
ISSN: 1526-8004
PURE UUID: 88a57ee7-d0d5-4c36-86f6-abf882f2a2ca
ORCID for Victoria Dodhia: ORCID iD orcid.org/0009-0008-7326-8039
ORCID for Ying Cheong: ORCID iD orcid.org/0000-0001-7687-4597

Catalogue record

Date deposited: 12 Aug 2025 17:07
Last modified: 13 Aug 2025 03:02

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Contributors

Author: Victoria Dodhia ORCID iD
Author: Ying Cheong ORCID iD

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