Department of Breast and Endocrine Surgery, Osaka University Graduate School of Medicine, Osaka, Japan.
Lester and Sue Smith Breast Center, Baylor Clinic, Baylor College of Medicine, Houston, TX, USA.
Breast Cancer. 2018 May;25(3):356-364. doi: 10.1007/s12282-018-0838-8. Epub 2018 Feb 15.
The international, phase III FALCON study (NCT01602380) in postmenopausal patients with hormone receptor-positive, locally advanced/metastatic breast cancer (LA/MBC) who had not received prior endocrine therapy, demonstrated statistically significant improvement in progression-free survival (PFS) for patients who received fulvestrant 500 mg vs anastrozole 1 mg. This subgroup analysis evaluated PFS in Asian (randomized in China, Japan, or Taiwan) and non-Asian patients from the FALCON study.
Eligible patients (estrogen receptor- and/or progesterone receptor-positive LA/MBC; World Health Organization performance status 0-2; ≥ 1 measurable/non-measurable lesion[s]) were randomized. PFS was assessed via Response Evaluation Criteria in Solid Tumours version 1.1, surgery/radiotherapy for disease worsening, or death (any cause). Secondary endpoints included: objective response rate, clinical benefit rate, duration of response, and duration of clinical benefit. Consistency of effect across subgroups was assessed via hazard ratios and 95% confidence intervals (CIs) using a log-rank test. Adverse events (AEs) were evaluated.
Of the 462 randomized patients, the Asian and non-Asian subgroups comprised 67 and 395 patients, respectively. In the Asian subgroup, median PFS was 16.6 and 15.9 months with fulvestrant and anastrozole, respectively (hazard ratio 0.81; 95% CI 0.44-1.50). In the non-Asian subgroup, median PFS was 16.5 and 13.8 months, respectively (hazard ratio 0.79; 95% CI 0.62-1.01). Secondary outcomes were numerically improved with fulvestrant vs anastrozole in both subgroups. AE profiles were generally consistent between Asian and non-Asian subgroups.
Results of this subgroup analysis suggest that treatment effects in the Asian patient subgroup are broadly consistent with the non-Asian population.
在未接受过内分泌治疗的激素受体阳性、局部晚期/转移性乳腺癌(LA/MBC)绝经后患者中进行的国际 III 期 FALCON 研究(NCT01602380)表明,与接受 1 毫克阿那曲唑相比,接受 500 毫克氟维司群的患者无进展生存期(PFS)有统计学意义的改善。本亚组分析评估了 FALCON 研究中来自亚洲(在中国、日本或中国台湾随机分组)和非亚洲患者的 PFS。
合格患者(雌激素受体和/或孕激素受体阳性 LA/MBC;世界卫生组织体力状态 0-2;≥1 个可测量/不可测量病灶)被随机分组。PFS 通过实体瘤反应评价标准 1.1 进行评估,疾病进展时手术/放疗,或任何原因导致的死亡。次要终点包括:客观缓解率、临床获益率、缓解持续时间和临床获益持续时间。使用对数秩检验通过风险比和 95%置信区间(CI)评估亚组间效应的一致性。评估了不良事件(AE)。
在 462 名随机患者中,亚洲和非亚洲亚组分别包括 67 名和 395 名患者。在亚洲亚组中,氟维司群和阿那曲唑的中位 PFS 分别为 16.6 个月和 15.9 个月(风险比 0.81;95%CI 0.44-1.50)。在非亚洲亚组中,中位 PFS 分别为 16.5 个月和 13.8 个月(风险比 0.79;95%CI 0.62-1.01)。在两个亚组中,氟维司群治疗的次要结局均有数值改善。AE 谱在亚洲和非亚洲亚组之间基本一致。
本亚组分析的结果表明,亚洲患者亚组的治疗效果与非亚洲人群基本一致。