Robertson John F R, Shao Zhimin, Noguchi Shinzaburo, Bondarenko Igor, Panasci Lawrence, Singh Sandeep, Subramaniam Shankar, Ellis Matthew J
Academic of the Unit of Translational Medical Sciences and Graduate Entry Medicine, School of Medicine, University of Nottingham, Royal Derby Hospital, Derby, United Kingdom.
Fudan University Shanghai Cancer Center, Shanghai, China.
J Clin Oncol. 2025 May;43(13):1539-1545. doi: 10.1200/JCO.24.00994. Epub 2025 Jan 7.
The randomized phase III FALCON trial demonstrated significant improvement in progression-free survival (PFS) with fulvestrant versus anastrozole in postmenopausal women with endocrine therapy-naïve, hormone receptor-positive/human epidermal growth factor receptor 2-negative advanced breast cancer. Herein, the prespecified final overall survival (OS) analysis is reported. After the primary PFS analysis, data were collected on survival, serious adverse events, and health-related quality of life. The final OS analysis was triggered at ≥65% maturity and ≥8 years since the last patient was enrolled. Analyses were descriptive with nominal values (one-sided α threshold .01845). At the data cutoff (July 11, 2022), 314 (68.0%) of 462 patients had died (fulvestrant, 157/230 [68.3%], anastrozole, 157/232 [67.7%]). The final OS analysis of FALCON demonstrated no significant difference between fulvestrant and anastrozole (medians, 44.8 and 42.7 months, respectively; hazard ratio [HR], 0.97 [95% CI, 0.77 to 1.21]; = .7579). Among patients with nonvisceral disease (n = 208), a trend showed a 15% reduction in the relative risk of death with fulvestrant versus anastrozole (median OS, 65.2 47.8 months; HR, 0.85 [95% CI, 0.60 to 1.20]). Data from FALCON are consistent with published evidence of long-term clinical benefit with fulvestrant and other endocrine therapies in the subset of patients with nonvisceral disease.
随机III期FALCON试验表明,对于未经内分泌治疗、激素受体阳性/人表皮生长因子受体2阴性的绝经后晚期乳腺癌女性患者,氟维司群对比阿那曲唑可显著改善无进展生存期(PFS)。本文报告了预先设定的最终总生存期(OS)分析结果。在主要PFS分析之后,收集了生存、严重不良事件及健康相关生活质量的数据。最终OS分析在自最后一名患者入组起成熟度≥65%且≥8年时启动。分析采用名义值进行描述性分析(单侧α阈值为0.01845)。在数据截止日期(2022年7月11日),462例患者中有314例(68.0%)死亡(氟维司群组,157/230例[68.3%],阿那曲唑组,157/232例[67.7%])。FALCON试验的最终OS分析显示,氟维司群与阿那曲唑之间无显著差异(中位数分别为44.8个月和42.7个月;风险比[HR]为0.97[95%CI,0.77至1.21];P = 0.7579)。在非内脏疾病患者(n = 208)中,有趋势显示氟维司群对比阿那曲唑死亡相对风险降低15%(OS中位数,65.2对47.8个月;HR,0.85[95%CI,0.60至1.20])。FALCON试验的数据与已发表的证据一致,即氟维司群和其他内分泌疗法对非内脏疾病患者亚组具有长期临床获益。