Beom Seung Hoon, Oh Jisu, Kim Tae-Yong, Lee Kyung-Hun, Yang Yaewon, Suh Koung Jin, Moon Hyeong-Gon, Han Sae-Won, Oh Do-Youn, Han Wonshik, Kim Tae-You, Noh Dong-Young, Im Seock-Ah
Department of Internal Medicine, Yonsei University College of Medicine, Seoul, Korea.
Department of Internal Medicine, CHA Bundang Medical Center, CHA University, Seongnam, Korea.
Cancer Res Treat. 2017 Apr;49(2):454-463. doi: 10.4143/crt.2016.259. Epub 2016 Aug 23.
Letrozole showed efficacy and generally favorable toxicities, along with the convenience of oral administration in postmenopausal patients with hormone receptor (HR)-positive metastatic breast cancer (MBC). To the best of our knowledge, there have been no reports of the clinical outcomes in Korean patients, although letrozole is widely used in practice. Therefore, this studywas conducted to affirm the efficacy and toxicities of letrozole in Korean patients.
This study retrospectively analyzed 84 HR-positive MBC patients who had been treated with letrozole from January 2001 to December 2012. Clinicopathological characteristics and treatment history were extracted from medicalrecords. All patients received 2.5 mg letrozole once a day until there were disease progressions or unacceptable toxicity. Progression-free survival (PFS) was the primary endpoint, and secondary endpoints were overall survival (OS), objective response rate (ORR), and toxicity.
The median age of the subjects was 59.3 years. Letrozole treatment resulted in a median PFS of 16.8 months (95% confidence interval [CI], 9.8 to 23.8) and a median OS of 56.4 months (95% CI, 38.1 to 74.7). The ORR was 36.9% for the 84 patients with measurable lesions. Multivariate analysis revealed symptomatic visceral disease (hazard ratio, 3.437; 95% CI, 1.576 to 7.495; p=0.002) and a disease-free interval ≤ 2 years (hazard ratio, 2.697; 95% CI, 1.262 to 5.762; p=0.010) were independently associated with shorter PFS. However, sensitivity to adjuvant hormone treatment was not related to PFS. Letrozole was generally well tolerated.
Letrozole showed considerable efficacy and tolerability as a first-line treatment in postmenopausal patients with HR-positive MBC.
来曲唑在激素受体(HR)阳性转移性乳腺癌(MBC)的绝经后患者中显示出疗效且总体毒性良好,同时口服给药方便。据我们所知,尽管来曲唑在实际中广泛使用,但尚无关于韩国患者临床结局的报道。因此,本研究旨在确认来曲唑在韩国患者中的疗效和毒性。
本研究回顾性分析了2001年1月至2012年12月期间接受来曲唑治疗的84例HR阳性MBC患者。从病历中提取临床病理特征和治疗史。所有患者每天服用2.5mg来曲唑一次,直至出现疾病进展或不可接受的毒性。无进展生存期(PFS)是主要终点,次要终点是总生存期(OS)、客观缓解率(ORR)和毒性。
受试者的中位年龄为59.3岁。来曲唑治疗导致中位PFS为16.8个月(95%置信区间[CI],9.8至23.8),中位OS为56.4个月(95%CI,38.1至74.7)。84例有可测量病灶的患者的ORR为36.9%。多变量分析显示,有症状的内脏疾病(风险比,3.437;95%CI,1.576至7.495;p=0.002)和无病间期≤2年(风险比,2.697;95%CI,1.262至5.762;p=0.010)与较短的PFS独立相关。然而,对辅助激素治疗的敏感性与PFS无关。来曲唑总体耐受性良好。
来曲唑作为HR阳性MBC绝经后患者的一线治疗显示出相当的疗效和耐受性。