Real-world effectiveness of aromatase inhibitors and fulvestrant in HR+/HER2- advanced breast cancer: a snapshot of the last two years before conventional use of CDK 4/6 inhibitors in a Portuguese institution.

IF 3.3 Q1 HEALTH POLICY & SERVICES Journal of Pharmaceutical Policy and Practice Pub Date : 2024-01-17 eCollection Date: 2024-01-01 DOI:10.1080/20523211.2023.2296551
Maria Inês Teodoro, Alexandra Mayer, Ana da Costa Miranda, Hugo Nunes, Filipa Alves da Costa, António Lourenço
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Abstract

Background: Monotherapy with aromatase inhibitors and fulvestrant were the standard-of-care for hormone receptor-positive (HR+)/human epidermal growth factor receptor-type2 negative (HER2-) advanced breast cancer, before integration of cyclin-dependent kinase 4/6 inhibitors. Effectiveness data is essential for regulatory action, but little is known about real-world use of aromatase inhibitors and fulvestrant.

Methods: A retrospective cohort study was conducted resorting to data from a cancer registry to identify adult women with HR+/HER- advanced breast cancer exposed to aromatase inhibitors or fulvestrant (31 May 2017-31 March 2019) at the main oncology hospital in Portugal. Cases were updated with follow-up until death or cut-off (31 March 2021) and pseudoanonymized data extracted. Primary outcome was overall survival (OS) and secondary time to treatment failure (TTF), estimated using survival analysis and compared with published trials.

Results: 192 patients were distributed by subgroups according to the medicine. Letrozole: OS 30.8 (95% confidence interval (CI) 20.6-41.4); TTF 11.2 (95%CI 8.7-13.7). Exemestane: OS 22.1 (95%CI 9.7-34.6); TTF 6.0 (95%CI 4.1-7.8). Fulvestrant: OS 21.6 (95%CI 16.5-26.7); TTF 5.6 (95%CI 4.5-6.6).

Conclusions: Estimated effectiveness (OS) of letrozole and fulvestrant was, respectively, 3.2-3.5 months lower than reported. The clinical meaning seems uncertain and may be explained a higher proportion of worse prognostic characteristics in patients treated in the real-world.

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芳香化酶抑制剂和氟维司群在HR+/HER2-晚期乳腺癌中的实际疗效:葡萄牙一家机构在常规使用CDK 4/6抑制剂前两年的快照。
背景:在整合细胞周期依赖性激酶4/6抑制剂之前,芳香化酶抑制剂和氟维司群单药疗法是激素受体阳性(HR+)/人表皮生长因子受体2型阴性(HER2-)晚期乳腺癌的标准疗法。疗效数据对监管行动至关重要,但人们对芳香化酶抑制剂和氟维司群的实际使用情况知之甚少:利用癌症登记处的数据开展了一项回顾性队列研究,以确定葡萄牙主要肿瘤医院中接触过芳香化酶抑制剂或氟维司群的HR+/HER-晚期乳腺癌成年女性(2017年5月31日至2019年3月31日)。对病例进行更新,随访至死亡或截止日期(2021 年 3 月 31 日),并提取假匿名数据。主要结果为总生存期(OS),次要结果为治疗失败时间(TTF),采用生存分析进行估算,并与已发表的试验进行比较:192名患者根据药物进行了分组。来曲唑OS为30.8(95%置信区间(CI)为20.6-41.4);TTF为11.2(95%CI为8.7-13.7)。依西美坦OS:22.1(95%CI 9.7-34.6);TTF:6.0(95%CI 4.1-7.8)。氟维司群OS为21.6(95%CI为16.5-26.7);TTF为5.6(95%CI为4.5-6.6):结论:来曲唑和氟维司群的估计疗效(OS)分别比报告的低3.2-3.5个月。结论:来曲唑和氟维司群的估计有效期(OS)分别比报告的低3.2-3.5个月,其临床意义似乎并不确定,可能是因为在真实世界中接受治疗的患者中预后特征较差的比例较高。
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来源期刊
Journal of Pharmaceutical Policy and Practice
Journal of Pharmaceutical Policy and Practice Health Professions-Pharmacy
CiteScore
4.70
自引率
9.50%
发文量
81
审稿时长
14 weeks
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