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机构地区:[1]平顶山市第一人民医院,河南平顶山467000
出 处:《现代肿瘤医学》2018年第8期1222-1224,共3页Journal of Modern Oncology
摘 要:目的:观察依维莫司联合依西美坦治疗非甾体类芳香化酶抑制剂(NSAIs)耐药的激素受体阳性、HER2阴性绝经后晚期乳腺癌的安全性及疗效。方法:2014年8月10日至2016年9月20日收治的绝经后激素受体阳性、HER2阴性,NSAIs治疗后进展的晚期乳腺癌患者46例,随机进入研究组和对照组。研究组23例口服依维莫司10 mg/d及依西美坦2.5 mg/d;对照组23例口服依西美坦单药2.5 mg/d,分析两组患者的肿瘤控制率(DCR)、不良反应发生率、无进展生存期(PFS)。结果:中位随访时间9.5个月,研究组和对照组的DCR率分别为65.2%和34.8%,差异具有统计学意义(P=0.038)。研究组最常见的不良反应为口腔炎(65.2%)和乏力(47.8%)与对照组差异具有统计学意义(P<0.05)。研究组和对照组的中位PFS分别为6.5个月(95%CI=4.8~8.2)和3.5个月(95%CI=2.7~4.3),差异有统计学意义(P=0.02)。结论:依维莫司联合依西美坦治疗绝经后NSAIs耐药的激素受体阳性、HER2阴性晚期乳腺癌的不良反应可控,可显著提高DCR率及PFS。Objective:To observe the safety and efficacy of everolimus plus exemestane in postmenopausal hormone receptor-positive,HER2-negative locally advanced or metastatic breast cancer progressing on prior nonsteroidal aromatase inhibitors (NSAIs).Methods:From 10th August,2014 to 20th September,2016,46 eligible patients were randomly assigned to experimental group(23 cases) and control group(23 cases).Patients in the experimental group received everolimus 10 mg/d plus exemestane 2.5 mg/d,and in the control group all patients received exemestane 2.5 mg/d.The primary end point was progression-free survival(PFS).Results:The disease control rate(DCR) in the experimental group and control group were 65.2% and 34.8% respectively,with statistical difference (P=0.038).There were more stomatitis (65.2%) and fatigue (47.8%) in the experimental group,with statistical difference compared with control (P〈0.05).The median PFS were 6.5 months (95%CI=4.8-8.2) and 3.5 months (95%CI=2.7-4.3)respectively in the two group,with statistically difference(P=0.02).Conclusion:Everolimus plus exemestane can be delivered safely with careful monitor in hormone receptor-positive,HER2-negative locally advanced or metastatic breast cancer progressing on prior NSAIs,can significantly improve the DCR and PFS.
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