Kim Sun Hye, Park In Hae, Lee Hyewon, Lee Keun Seok, Nam Byung-Ho, Ro Jungsil
National Cancer Center, Goyang, Korea.
Asian Pac J Cancer Prev. 2012;13(3):979-83. doi: 10.7314/apjcp.2012.13.3.979.
Previous studies have suggested a lack of complete cross-resistance between steroidal (exemestane) and non-steroidal aromatase inhibitors (nSAI).
Eighty-eight metastatic breast cancer (MBC) patients who received 25 mg of exemestane orally once a day at the National Cancer Center, Korea, between 2003 and 2009, were reviewed retrospectively. All patients had received nSAI for metastatic disease prior to exemestane therapy.
The median age was 52 years (range, 33-79), and 13 (14.8%) patients were premenopausal who concomitantly received GnRH agonist. Exemestane was given as a second- (80.7%) or third-line (19.3%) hormone therapy. The clinical benefit (CB) rate (complete response + partial response + stable disease ≥ 24 weeks) was 30.7%, with a median CB duration of 10.0 months (range, 6.3-78.7). The median progression-free survival (PFS) was 3.0 months (95% confidence interval [CI], 1.99-4.01) and the overall survival (OS) 21.5 months (95% CI, 17.96-25.04), with a median follow-up of 50.3 months. Patients who achieved CB had longer OS than those patients who did not (29.6 vs 17.9 months; P = 0.002). On univariate analysis of predictive factors, patients who had achieved CB from previous nSAI tended to show lower CB rate (24.6% vs 44.4%, respectively; P = 0.063) and shorter PFS (2.8 vs 4.8 months, respectively; p = 0.233) than patients who had not. Achieving CB from previous nSAI became independent predictive factor for CBR to exemestane on multivariable analysis (Odds ratio = 2.852, P = 0.040).
Exemestane after nSAI failure was effective in prolonging CB duration. The drug's efficacy seemed to be inferior in patients who had benefit from previous nSAI use.
既往研究提示甾体类(依西美坦)与非甾体类芳香化酶抑制剂(nSAI)之间不存在完全交叉耐药。
对2003年至2009年期间在韩国国立癌症中心接受每日一次口服25 mg依西美坦治疗的88例转移性乳腺癌(MBC)患者进行回顾性分析。所有患者在接受依西美坦治疗前均已接受过nSAI治疗转移性疾病。
中位年龄为52岁(范围33 - 79岁),13例(14.8%)患者为绝经前患者,同时接受GnRH激动剂治疗。依西美坦作为二线(80.7%)或三线(19.3%)激素治疗。临床获益(CB)率(完全缓解 + 部分缓解 + 疾病稳定≥24周)为30.7%,中位CB持续时间为10.0个月(范围6.3 - 78.7个月)。中位无进展生存期(PFS)为3.0个月(95%置信区间[CI],1.99 - 4.01),总生存期(OS)为21.5个月(95% CI,17.96 - 25.04),中位随访时间为50.3个月。达到CB的患者OS长于未达到CB的患者(29.6个月对17.9个月;P = 0.002)。在对预测因素的单因素分析中,既往从nSAI获得CB疗效的患者,其CB率(分别为24.6%对44.4%;P = 0.063)和PFS(分别为2.8个月对4.8个月;P = 0.233)往往低于未获得CB疗效的患者。在多因素分析中,既往从nSAI获得CB疗效成为依西美坦治疗CB反应的独立预测因素(比值比 = 2.852,P = 0.040)。
nSAI治疗失败后使用依西美坦可有效延长CB持续时间。对于既往从nSAI治疗中获益的患者,该药物的疗效似乎较差。