Department of Medical Oncology, Cancer Institute & Hospital, Chinese Academy of Medical Sciences, Peking Union Medical College, Beijing, 100021, China.
Endocr J. 2011;58(6):509-16. doi: 10.1507/endocrj.k11e-020. Epub 2011 Apr 29.
A promising new option as the treatment of choice for premenopausal patients with metastatic breast cancer (MBC) could be the combination of a luteinising hormone-releasing hormone analog and an aromatase inhibitor. Very little data about the use of goserelin with anastrozole in advanced breast cancer are available, and no cohort studies on the efficacy of goserelin with letrozole in advanced premenopausal breast cancer patients have been reported. We present the single-centre, retrospective, experience of goserelin plus letrozole in a total of 52 premenopausal women with MBC. All patients received goserelin 3.6 mg by subcutaneous injection every 4 weeks along with letrozole 2.5 mg daily as first-line (n=36) and second-line (n=16) hormonal treatment. The median duration of goserelin with letrozole treatment was 11 (range, 2-61) months, and the median duration of overall follow-up was 31 (range, 3-66) months. The objective response rate (ORR) was 21.1%, with two complete response (CR) (3.8%) and nine partial response (PR) (17.3%). Stable disease (SD) lasting more than 6 months was achieved by 26 patients (50.0%). Thus, goserelin with letrozole conferred clinical benefit (CB) in 37 women (71.1%). The progression-free survival (PFS) was 10 months. CR was exclusively observed in hormone receptor-double-positive patients. Drug therapy was well tolerated; no grade 3/4 toxicities were reported. Goserelin plus letrozole appears to be an efficacious and well-tolerated regimen in women with advanced breast cancer. Further prospectively randomized studies involving more patients and longer follow-up are indicated.
作为治疗选择,对于患有转移性乳腺癌(MBC)的绝经前患者,促黄体生成素释放激素类似物和芳香化酶抑制剂的联合治疗可能是一种很有前景的新选择。关于晚期乳腺癌中戈舍瑞林联合阿那曲唑的应用数据很少,也没有关于戈舍瑞林联合来曲唑治疗晚期绝经前乳腺癌患者的疗效的队列研究。我们报告了戈舍瑞林联合来曲唑治疗 52 例 MBC 绝经前妇女的单中心回顾性经验。所有患者均接受戈舍瑞林 3.6 mg 皮下注射,每 4 周 1 次,同时接受来曲唑 2.5 mg 每日 1 次的治疗,作为一线(n=36)和二线(n=16)激素治疗。戈舍瑞林联合来曲唑治疗的中位时间为 11 个月(范围,2-61 个月),总随访中位时间为 31 个月(范围,3-66 个月)。客观缓解率(ORR)为 21.1%,其中完全缓解(CR)2 例(3.8%),部分缓解(PR)9 例(17.3%)。26 例(50.0%)患者达到了持续时间超过 6 个月的疾病稳定(SD)。因此,戈舍瑞林联合来曲唑使 37 名妇女(71.1%)获得了临床获益(CB)。无进展生存期(PFS)为 10 个月。CR 仅见于激素受体双阳性患者。药物治疗耐受性良好;未报告 3/4 级毒性。戈舍瑞林联合来曲唑似乎是一种有效且耐受良好的方案,适用于晚期乳腺癌患者。需要进一步进行涉及更多患者和更长随访时间的前瞻性随机研究。