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Fulvestrant: A Review in Advanced Breast Cancer Not Previously Treated with Endocrine Therapy

机译:Fulvestrant:在先前未治疗内分泌治疗的晚期乳腺癌中的综述

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摘要

Fulvestrant (Faslodex(A (R))), a selective estrogen receptor (ER) degrader, is now indicated for the treatment of ER+ or hormone-receptor positive (HR+)/HER2- advanced breast cancer in postmenopausal women previously untreated with endocrine therapy. In the phase 3 FALCON trial conducted in this setting, intramuscular fulvestrant 500 mg/month (plus an additional dose at 2 weeks) was significantly more effective in prolonging progression-free survival (PFS) than oral anastrozole 1 mg/day (particularly in patients with non-visceral disease), with this benefit seemingly driven by fulvestrant recipients responding significantly longer to treatment. Other efficacy measures, including objective response rate, did not significantly or markedly differ between the two regimens and median overall survival was not yet calculable. Fulvestrant was generally well tolerated in this trial, displaying an overall tolerability profile consistent with its known tolerability in other breast cancer settings. Thus, monotherapy with intramuscular fulvestrant is a generally well tolerated and more effective treatment option than standard-of-care anastrozole for ER+ or HR+/HER2- advanced breast cancer in postmenopausal women not previously treated with endocrine therapy.
机译:氟斯特朗(Faslodex(A(R))),一种选择性雌激素受体(ER)降解剂现在表明用于治疗ER +或激素受体阳性(HR +)/海拔乳腺癌,以前未治疗内分泌治疗。在该阶段进行的第3阶段进行Falcon试验中,肌内氟斯特朗特500毫克/月(加上2周的额外剂量)在延长无流动的存活率(PFS)比口服Anstrozole 1mg /天(特别是患者含有非内脏疾病),这种福利受到普瑞斯受者似乎驱动的效果明显更长的治疗。其他疗效措施,包括客观反应率,两种方案和中位数的整体生存率尚未显着或显着不同。在该试验中,氟斯特将富含富含耐受性,显示总体耐受性曲线,其具有其它乳腺癌环境中的已知耐受性。因此,具有肌内富氯雌雌性的单药治疗是一种普遍良好的耐受性和更有效的治疗方法,比在未治疗内分泌治疗之前未治疗的绝经后妇女的ER +或HR + / HER2-先进的乳腺癌。

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