Eligibility criteria for using menopausal hormone therapy in breast cancer survivors: a safety report based on a systematic review and meta-analysis.

IF 2.8 3区 医学 Q1 OBSTETRICS & GYNECOLOGY
Pluvio J Coronado, Ana Gómez, Eva Iglesias, María Fasero, Laura Baquedano, Sonia Sánchez, Isabel Ramírez-Polo, Esther de la Viuda, Borja Otero, Plácido Llaneza, Nicolás Mendoza, Daniel M Lubián
{"title":"Eligibility criteria for using menopausal hormone therapy in breast cancer survivors: a safety report based on a systematic review and meta-analysis.","authors":"Pluvio J Coronado, Ana Gómez, Eva Iglesias, María Fasero, Laura Baquedano, Sonia Sánchez, Isabel Ramírez-Polo, Esther de la Viuda, Borja Otero, Plácido Llaneza, Nicolás Mendoza, Daniel M Lubián","doi":"10.1097/GME.0000000000002317","DOIUrl":null,"url":null,"abstract":"<p><strong>Importance: </strong>Menopause hormone therapy (MHT) effectively alleviates menopausal symptoms. However, it is generally not recommended for breast cancer survivors, although the scientific evidence is scarce.</p><p><strong>Objective: </strong>This study aimed to establish eligibility criteria for use of the MHT in breast cancer survivors based on a systematic review and meta-analysis of the literature.</p><p><strong>Evidence review: </strong>We conducted exhaustive literature searches until June 2022 in MEDLINE, The Cochrane Library, and EMBASE, using a tailored strategy with a combination of controlled vocabulary and search terms related to breast cancer survivors and MHT. We followed the Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines and assessed the risk of bias using the Cochrane and Risk of Bias in Non-randomized Studies - of Interventions tools. The quality of the evidence was graded according to grading quality of evidence and strength of recommendations criteria (A, high; B, moderate; C, low; and D, very low). We categorized MHT use into four levels: category 1 (no restrictions on use), category 2 (the benefits outweigh the risks), category 3 (the risks generally outweigh the benefits), and category 4 (MHT should not be used).</p><p><strong>Findings: </strong>A total of 12 studies met the eligibility criteria. Analysis of the three randomized clinical trials using combined MHT or tibolone revealed no significant differences concerning tumor recurrence (relative risk [RR], 1.46; 95% CI, 0.99-2.24). A combined analysis of randomized clinical trials, prospective, and retrospective trials found no elevated risk of recurrence (RR, 0.85; 95% CI, 0.54-1.33) or death (RR, 0.91; 95% CI, 0.38-2.19). The eligibility criteria for patients with hormone receptor (HR)-positive tumors fell into categories 3B and 3C for combined MHT or estrogen alone and 4A for tibolone. For HR-negative tumors, the category was 2B and 2C.</p><p><strong>Conclusions and relevance: </strong>Our findings suggest that MHT could be a viable treatment alternative for breast cancer survivors experiencing menopausal symptoms, especially those with HR-negative tumors. Personalized management is recommended for each peri/postmenopausal woman facing a diminished quality of life because of menopause symptoms. Further randomized trials are needed before considering changes to current standards of care.</p>","PeriodicalId":18435,"journal":{"name":"Menopause: The Journal of The North American Menopause Society","volume":null,"pages":null},"PeriodicalIF":2.8000,"publicationDate":"2024-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Menopause: The Journal of The North American Menopause Society","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1097/GME.0000000000002317","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"OBSTETRICS & GYNECOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Importance: Menopause hormone therapy (MHT) effectively alleviates menopausal symptoms. However, it is generally not recommended for breast cancer survivors, although the scientific evidence is scarce.

Objective: This study aimed to establish eligibility criteria for use of the MHT in breast cancer survivors based on a systematic review and meta-analysis of the literature.

Evidence review: We conducted exhaustive literature searches until June 2022 in MEDLINE, The Cochrane Library, and EMBASE, using a tailored strategy with a combination of controlled vocabulary and search terms related to breast cancer survivors and MHT. We followed the Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines and assessed the risk of bias using the Cochrane and Risk of Bias in Non-randomized Studies - of Interventions tools. The quality of the evidence was graded according to grading quality of evidence and strength of recommendations criteria (A, high; B, moderate; C, low; and D, very low). We categorized MHT use into four levels: category 1 (no restrictions on use), category 2 (the benefits outweigh the risks), category 3 (the risks generally outweigh the benefits), and category 4 (MHT should not be used).

Findings: A total of 12 studies met the eligibility criteria. Analysis of the three randomized clinical trials using combined MHT or tibolone revealed no significant differences concerning tumor recurrence (relative risk [RR], 1.46; 95% CI, 0.99-2.24). A combined analysis of randomized clinical trials, prospective, and retrospective trials found no elevated risk of recurrence (RR, 0.85; 95% CI, 0.54-1.33) or death (RR, 0.91; 95% CI, 0.38-2.19). The eligibility criteria for patients with hormone receptor (HR)-positive tumors fell into categories 3B and 3C for combined MHT or estrogen alone and 4A for tibolone. For HR-negative tumors, the category was 2B and 2C.

Conclusions and relevance: Our findings suggest that MHT could be a viable treatment alternative for breast cancer survivors experiencing menopausal symptoms, especially those with HR-negative tumors. Personalized management is recommended for each peri/postmenopausal woman facing a diminished quality of life because of menopause symptoms. Further randomized trials are needed before considering changes to current standards of care.

乳腺癌幸存者使用绝经激素疗法的资格标准:基于系统回顾和荟萃分析的安全报告。
重要性:更年期激素疗法(MHT)可有效缓解更年期症状。然而,尽管科学证据很少,但一般不建议乳腺癌幸存者使用这种疗法:本研究旨在通过对文献进行系统回顾和荟萃分析,确定乳腺癌幸存者使用更年期激素疗法的资格标准:截至 2022 年 6 月,我们在 MEDLINE、The Cochrane Library 和 EMBASE 中进行了详尽的文献检索,采用了有针对性的策略,结合了与乳腺癌幸存者和 MHT 相关的控制词汇和检索词。我们遵循《系统综述和元分析首选报告项目》指南,并使用 Cochrane 和《干预措施非随机研究中的偏倚风险》工具评估偏倚风险。根据证据质量分级和建议力度标准(A,高;B,中等;C,低;D,极低)对证据质量进行分级。我们将MHT的使用分为四个等级:第1类(不限制使用)、第2类(益处大于风险)、第3类(风险一般大于益处)和第4类(不应使用MHT):共有 12 项研究符合资格标准。对联合使用MHT或替勃龙的三项随机临床试验进行分析后发现,两者在肿瘤复发方面没有显著差异(相对风险[RR],1.46;95% CI,0.99-2.24)。对随机临床试验、前瞻性试验和回顾性试验进行综合分析后发现,复发风险(RR,0.85;95% CI,0.54-1.33)或死亡风险(RR,0.91;95% CI,0.38-2.19)均未升高。激素受体(HR)阳性肿瘤患者的资格标准为:联合 MHT 或单独使用雌激素为 3B 类和 3C 类,替勃龙为 4A 类。HR阴性肿瘤患者的类别为2B和2C:我们的研究结果表明,对于出现更年期症状的乳腺癌幸存者,尤其是那些HR阴性肿瘤患者,MHT可能是一种可行的替代治疗方法。建议对每一位因绝经症状而导致生活质量下降的围绝经期/绝经后妇女进行个性化管理。在考虑改变目前的治疗标准之前,还需要进行更多的随机试验。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
5.40
自引率
7.40%
发文量
330
审稿时长
3-8 weeks
期刊介绍: ​Menopause, published monthly, provides a forum for new research, applied basic science, and clinical guidelines on all aspects of menopause. The scope and usefulness of the journal extend beyond gynecology, encompassing many varied biomedical areas, including internal medicine, family practice, medical subspecialties such as cardiology and geriatrics, epidemiology, pathology, sociology, psychology, anthropology, and pharmacology. This forum is essential to help integrate these areas, highlight needs for future research, and enhance health care.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信