摘要
目的:探讨他莫昔芬治疗芳香化酶抑制剂(AIs)耐药的激素受体阳性(HR+)绝经后转移性乳腺癌(MBC)患者的疗效和安全性。方法:回顾性分析他莫昔芬治疗AIs耐药的30例HR+绝经后MBC患者的临床资料,观察终点为缓解率(RR)、临床获益率(CBR)、疾病进展时间(TTP)和安全性。结果:30例患者中,CR1例,PR 9例,SD 15例,RR为33.3%,CBR为50%,中位TTP 6.1个月。23例骨和/或软组织转移患者中,RR为34.8%,CBR为52.2%,中位TTP 7.3个月;7例肝脏和/或肺部转移患者中,RR为28.6%,CBR为42.8%,中位TTP 4.8个月(P=0.019)。不良反应多为面部潮红、阴道干燥、白带增多、阴道出血、恶心、呕吐、腹泻等,均为I、II级。结论:他莫昔芬治疗AIs耐药的HR+绝经后MBC患者安全有效,可改善患者预后。
Objective: To investigate the curative effect and safety of tamoxifen in hormone receptor- positive( HR+) postmenopausal patients with metastatic breast cancer( MBC) failing to Aromatase inhibitors( AIs). Methods: Retrospectively analyzed clinical data of 30 patients with HR+postmenopausal MBC treated with tamoxifen after AIs resistance. The endpoints were response rate( RR),clinical benefit rate( CBR),time of tumor progression( TTP)and safety. Results: In 30 patients,the patients who acquired CR,PR and SD were 1,9 and 15. The RR and CBR were33. 3% and 50%. The median TTP was 6. 1 months. The RR and CBR in 23 cases with bone and / or soft tissue metastasis and 7 cases of liver and / or pulmonary metastasis were 34. 8%,52. 2% and 28. 6%,42. 8%. The median TTP were 7. 3 and 4. 8 months in two groups( P = 0. 019). The most common adverse reactions were hot flashes,vaginal dryness,vaginal discharge,vaginal bleeding,nausea,vomiting,diarrhea and so on. Most side effects were grade Ⅰ orⅡ on the WHO scale. Conclusion: Treatment with tamoxifen in AIs resistant HR+postmenopausal patients with MBC is safe and effective,can improve prognosis of patients.
出处
《现代肿瘤医学》
CAS
2015年第7期966-968,共3页
Journal of Modern Oncology
基金
深圳市卫生计生系统科研项目(编号:201402025)