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Real‐world effectiveness of fulvestrant monotherapy as first endocrine treatment in patients with metastatic breast cancer

机译:氟斯特语单药治疗作为转移乳腺癌患者的第一内分泌治疗的现实世界效力

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Abstract Fulvestrant monotherapy is approved for postmenopausal women with hormone receptor‐positive, metastatic breast cancer (MBC) who progressed following antiendocrine therapy, or those with hormone receptor‐positive, human epidermal receptor 2‐negative advanced breast cancer (BC) not previously treated with endocrine therapy (ET). However, real‐world data are lacking. Retrospective reviews of 10 United States community oncology practices identified patients diagnosed with MBC between 1 January 2011 and 31 December 2015 who received fulvestrant as the first ET, either as initial therapy for metastatic disease or after progression following one line of chemotherapy. Endpoints were progression‐free survival (PFS) and overall survival (OS). Patients were classified as ET‐na?ve or by relapse status following adjuvant ET (“early” recurrence during or ≤12?months of completing adjuvant ET, or “late” 12?months after completing adjuvant ET). Outcomes were evaluated using Kaplan‐Meier methods. Among 121 patients, median PFS (95% confidence interval) was 8.3?months (4.8‐12.3) for early relapse, 15.4?months (10.2‐21.2) for late relapse, and 18.7?months (10.1‐20.8) among ET‐na?ve patients ( P ?=?.018). Median OS was 39.8?months (25.0‐55.1) for early relapse and 61.4?months (47.1‐61.4) for late relapse, but was not reached (NR; 55.6–NR) for ET‐na?ve patients ( P ?=?.002). Fulvestrant monotherapy as the first ET after MBC diagnosis demonstrates PFS comparable to clinical study results; outcomes appeared better in patients without prior ET exposure and in patients with disease recurrence 12?months following adjuvant ET. These findings support fulvestrant monotherapy in patients with hormone receptor‐positive MBC.
机译:摘要氟斯特朗单疗法被批准用于患有激素受体阳性,转移性乳腺癌(MBC)的绝经后妇女,他们在抗抗脑处理治疗之后,或具有激素受体阳性的人表皮受体2阴性晚期乳腺癌(BC)的那些未治疗内分泌治疗(ET)。但是,缺乏现实世界的数据。回顾美国社区肿瘤学实践的鉴定鉴定2011年1月1日至2015年12月31日患有MBC的患者,他们将氟斯特提作为前提ET作为转移性疾病的初始治疗或在一系列化疗后的进展之后。终点是无进展的存活(PFS)和总存活(OS)。患者被归类为ET-Naαve或通过复发状态(“早期”复发或≤12Ω患者或≤12Ω患者,完成佐剂等,或“晚期”& 12?完成佐剂ET)。使用Kaplan-Meier方法评估结果。在121名患者中,早期复发的中位数PFS(95%置信区间)为8.3?月(4.8-12.3),15.4个月(10.2-21.2)为晚复发,18.7个月(10.1-20.8)在et-na中ve患者(p?= 018)。 Median OS是39.8个月(25.0-55.1)的早期复发和61.4个月(47.1-61.4),用于迟到复发,但没有达到(NR; 55.6-NR)对Et-Na?ve患者(p?=? .002)。 MBC诊断后的氟氯雌肽作为第一个等,证明了与临床研究结果相当的PFS;在没有先前的ET暴露和疾病复发患者的患者中,结果表现出更好的结果。佐剂等疾病患者。这些发现支持激素受体阳性MBC患者的氟斯特朗单疗法。

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