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ACT-FASTER, a Prospective Cohort Study Exploring Treatment Patterns with Fulvestrant and Exemestane in Postmenopausal Patients with Advanced Hormone Receptor-Positive Breast Cancer under Real-Life Conditions in Germany

机译:德国先进激素受体阳性乳腺癌晚期患者在绝经后患者中探索治疗模式,探索治疗模式。

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Background: Endocrine therapy is recommended for the treatment of postmenopausal women with hormone receptor-positive (HR+) advanced breast cancer (ABC). Methods: ACT-FASTER was a German prospective non-interventional cohort study in postmenopausal women with HR+ ABC receiving fulvestrant 500 mg as first line (1 L), second line (2 L) or third line (3 L), or exemestane (any line) in the real-world palliative setting. Primary study objectives included the effectiveness of fulvestrant according to line of palliative treatment measured by time to progression (TTP), and real-life data on the epidemiology and management of these patients. Results: Of 498 evaluable patients (mean age 67.5 years), 99% were estrogen receptor-positive. On study, 86.7% of patients received fulvestrant 500 mg and 13.3% exemestane. Median TTP was 9.7 months in patients receiving fulvestrant 1 L; 6.8 months for 2 L; and 6.7 months for 3 L. The comparison between fulvestrant 1 L palliative treatment and 2 L or 3 L showed that early initiation of treatment prolonged TTP (hazard ratio 1.26; 95% confidence interval 1.08-1.48). Treatments were well tolerated. Conclusion: Fulvestrant 500 mg was administered successfully to patients under daily practice conditions, and both medications were well tolerated. TTP was longest in patients treated with fulvestrant 500 mg 1 L compared with 2 L and 3 L in the palliative care setting.
机译:背景:建议对患有激素受体阳性(HR +)晚期乳腺癌(ABC)治疗绝经后妇女的内分泌治疗。方法:作品较快是德国预期非介入队列在绝经后妇女的德国预期非介入队列研究,HR + ABC接受500mg作为第一线(1L),第二线(2L)或第三线(3L)或Exemestans(任何线)在真实世界的姑息设置。初级研究目标包括根据随着时间的推移(TTP)的姑息治疗和这些患者的流行病学和管理的现实生活数据来氟斯特提的有效性。结果:498名可评估患者(平均67.5岁),99%是雌激素受体阳性。在研究中,86.7%的患者接受氟斯特提500毫克和13.3%的大使。在接受富士驯鹿1 L的患者中,中位TTP为9.7个月; 6.8个月2升; 3 L.PL.PLETRANT 1 L姑息治疗和2L或3L之间的比较显示,早期启动治疗延长TTP(危险比1.26; 95%置信区间1.08-1.48)。治疗耐受良好。结论:在日常实践条件下成功向患者施用500mg,两种药物耐受良好。在姑息治疗环境中,用氟斯特语500mg11处理的患者中TTP最长。

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