Oncology Department, Hospital Universitario Clínico San Cecilio and Medicine Department, Granada University, Avenida del Conocimiento s/n, 18006, Granada, Spain.
Oncology Department, Hospital Universitario Fundación Alcorcón, Calle Budapest, 1, 28922, Alcorcón, Madrid, Spain.
Sci Rep. 2021 Feb 19;11(1):4274. doi: 10.1038/s41598-021-83622-1.
Goals of endocrine therapy for advanced breast cancer (ABC) include prolonging survival rates, maintaining the quality of life, and delaying the initiation of chemotherapy. We evaluated the effectiveness of fulvestrant as first-line in patients with estrogen receptor (ER)-positive ABC with relapse during or after adjuvant anti-estrogenic therapy in real-world settings. Retrospective, observational study involving 171 postmenopausal women with ER-positive ABC who received fulvestrant as first-line between January 2011 and May 2018 in Spanish hospitals. With a median follow-up of 31.4 months, the progression-free survival (PFS) with fulvestrant was 14.6 months. No differences were seen in the visceral metastatic (14.3 months) versus non-visceral (14.6 months) metastatic subgroup for PFS. Overall response rate and clinical benefit rate were 35.2% and 82.8%. Overall survival was 43.1 months. The duration of the clinical benefit was 19.2 months. Patients with ECOG performance status 0 at the start of treatment showed a significant greater clinical benefit rate and overall survival than with ECOG 1-2. Results in real-world settings are in concordance with randomized clinical trials. Fulvestrant continues to demonstrate clinical benefits in real-world settings and appears be well tolerated as first-line for the treatment of postmenopausal women with ER-positive ABC.
晚期乳腺癌(ABC)内分泌治疗的目标包括延长生存率、保持生活质量和延迟化疗的开始。我们评估了氟维司群作为一线治疗在辅助抗雌激素治疗期间或之后复发的雌激素受体(ER)阳性 ABC 患者中的疗效,这是在真实环境下进行的。这是一项回顾性、观察性研究,涉及 171 名接受氟维司群作为一线治疗的绝经后 ER 阳性 ABC 患者,他们于 2011 年 1 月至 2018 年 5 月在西班牙医院接受治疗。中位随访 31.4 个月,氟维司群的无进展生存期(PFS)为 14.6 个月。在无内脏转移(14.3 个月)和有内脏转移(14.6 个月)亚组中,PFS 无差异。总体缓解率和临床获益率分别为 35.2%和 82.8%。总生存期为 43.1 个月。临床获益的持续时间为 19.2 个月。治疗开始时 ECOG 体能状态为 0 的患者的临床获益率和总生存率显著高于 ECOG 1-2 的患者。真实环境下的结果与随机临床试验一致。氟维司群在真实环境下继续显示出临床获益,并且似乎作为一线治疗 ER 阳性 ABC 绝经后妇女的治疗药物具有良好的耐受性。