Department of Oncology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.
J Breast Cancer. 2011 Jun;14(2):135-9. doi: 10.4048/jbc.2011.14.2.135. Epub 2011 Jun 18.
Fulvestrant, a potent estrogen receptor (ER) antagonist with a novel mechanism of action, has shown efficacy in pretreated patients with advanced breast cancer. We assessed the efficacy and tolerability of fulvestrant in Korean postmenopausal women.
Of the 25 candidates identified at Asan Medical Center, Seoul, Korea, six were deemed ineligible due to inadequate baseline and follow-up imaging. The 19 patients included in this retrospective analysis received the approved dose of fulvestrant (250 mg intramuscular injection, once per month) as second- (n=8), third- (n=7), or fourth-line (n=4) endocrine therapy.
At a median follow-up of 7.4 months (range, 1.2-34.8 months), the 19 patients received a median of four cycles (range, 1-34 cycles) of fulvestrant. Median time to progression was 5.5 months (95% confidence interval [CI], 0.4-10.7 months), and median overall survival was 17.9 months (95% CI, 2.7-33.1 months). Among 17 evaluable patients, one (5.3%) achieved a partial response, 10 (52.6%) showed stable disease, and six (31.6%) showed progressive disease. The clinical benefit rate was 26.3%. Four patients (21.1%) reported adverse events, but all were grade 1 or 2.
Fulvestrant was effective and well tolerated in patients with advanced breast cancer who had been previously treated with several lines of endocrine and chemotherapeutic agents.
氟维司群是一种作用机制新颖的强效雌激素受体(ER)拮抗剂,已被证实对预处理的晚期乳腺癌患者有效。我们评估了氟维司群在韩国绝经后妇女中的疗效和耐受性。
在韩国首尔的 Asan 医疗中心确定的 25 名候选者中,有 6 名因基线和随访影像学不足而被认为不符合条件。这项回顾性分析包括的 19 名患者接受了批准剂量的氟维司群(250mg 肌肉注射,每月一次)治疗,作为二线(n=8)、三线(n=7)或四线(n=4)内分泌治疗。
中位随访时间为 7.4 个月(范围 1.2-34.8 个月),19 名患者接受了中位数为 4 个周期(范围 1-34 个周期)的氟维司群治疗。中位无进展生存期为 5.5 个月(95%置信区间 [CI],0.4-10.7 个月),中位总生存期为 17.9 个月(95%CI,2.7-33.1 个月)。在 17 名可评估的患者中,1 名(5.3%)患者达到部分缓解,10 名(52.6%)患者疾病稳定,6 名(31.6%)患者疾病进展。临床获益率为 26.3%。4 名患者(21.1%)报告了不良反应,但均为 1 级或 2 级。
氟维司群在先前接受过多种内分泌和化疗药物治疗的晚期乳腺癌患者中是有效且耐受良好的。