中国基层医药
中國基層醫藥
중국기층의약
Chinese Journal of Primary Medicine and Pharmacy
2015年
21期
3207-3210
,共4页
刘庆华%张明英%刘春娟%于文军%张传涛
劉慶華%張明英%劉春娟%于文軍%張傳濤
류경화%장명영%류춘연%우문군%장전도
乳腺肿瘤%多西他赛%卡铂
乳腺腫瘤%多西他賽%卡鉑
유선종류%다서타새%잡박
Breast cancer%Docetaxel%Carboplatin
目的:观察多西他赛联合卡铂21 d 方案(TC 方案)二、三线治疗转移性三阴乳腺癌(ATNBC)患者的疗效和不良反应。方法37例蒽环类耐药的晚期 ATNBC 患者,多西他赛70 mg/m2,第1天静脉滴注;卡铂曲线下面积(AUC)=5,第1天静脉滴注,21 d 为1个疗程,直到疾病进展或无法耐受或最多接受6个周期化疗。结果37例患者共完成147个周期化疗,中位化疗周期为4个周期。均可评价疗效和不良反应。其中完全缓解(CR)0例,部分缓解(PR)12例(32.43%),稳定(SD)11例(29.73%),进展14例(PD)(41.18%)。有效率(RR =CR +PR)为32.43%,疾病控制率(CR +PR +SD)为62.15%,中位疾病进展时间(TTP)3.9个月(95%CI:4~8个月),中位总生存时间(OS)10.0个月,至随访结束,仍有3例患者无进展生存。治疗后主要不良反应为血液学毒性(白细胞减少51.53%)和消化道反应(56.76%)。结论TC 方案治疗晚期 ATNBC 患者安全有效,不良反应可以耐受。
目的:觀察多西他賽聯閤卡鉑21 d 方案(TC 方案)二、三線治療轉移性三陰乳腺癌(ATNBC)患者的療效和不良反應。方法37例蒽環類耐藥的晚期 ATNBC 患者,多西他賽70 mg/m2,第1天靜脈滴註;卡鉑麯線下麵積(AUC)=5,第1天靜脈滴註,21 d 為1箇療程,直到疾病進展或無法耐受或最多接受6箇週期化療。結果37例患者共完成147箇週期化療,中位化療週期為4箇週期。均可評價療效和不良反應。其中完全緩解(CR)0例,部分緩解(PR)12例(32.43%),穩定(SD)11例(29.73%),進展14例(PD)(41.18%)。有效率(RR =CR +PR)為32.43%,疾病控製率(CR +PR +SD)為62.15%,中位疾病進展時間(TTP)3.9箇月(95%CI:4~8箇月),中位總生存時間(OS)10.0箇月,至隨訪結束,仍有3例患者無進展生存。治療後主要不良反應為血液學毒性(白細胞減少51.53%)和消化道反應(56.76%)。結論TC 方案治療晚期 ATNBC 患者安全有效,不良反應可以耐受。
목적:관찰다서타새연합잡박21 d 방안(TC 방안)이、삼선치료전이성삼음유선암(ATNBC)환자적료효화불량반응。방법37례은배류내약적만기 ATNBC 환자,다서타새70 mg/m2,제1천정맥적주;잡박곡선하면적(AUC)=5,제1천정맥적주,21 d 위1개료정,직도질병진전혹무법내수혹최다접수6개주기화료。결과37례환자공완성147개주기화료,중위화료주기위4개주기。균가평개료효화불량반응。기중완전완해(CR)0례,부분완해(PR)12례(32.43%),은정(SD)11례(29.73%),진전14례(PD)(41.18%)。유효솔(RR =CR +PR)위32.43%,질병공제솔(CR +PR +SD)위62.15%,중위질병진전시간(TTP)3.9개월(95%CI:4~8개월),중위총생존시간(OS)10.0개월,지수방결속,잉유3례환자무진전생존。치료후주요불량반응위혈액학독성(백세포감소51.53%)화소화도반응(56.76%)。결론TC 방안치료만기 ATNBC 환자안전유효,불량반응가이내수。
Objective To observe the clinical efficacy and adverse reactions of docetaxel and carboplatin 21 day regimen (TC)as second -or third -line in treatment of patients with advanced triple -negative breast cancer (ATNBC).Methods 37 ATNBC patients with anthracyclines resistance were given docetaxel 70mg/m2 ,the first day of intravenous drip,carboplatin AUC =5,through intravenous drip on the first day,21 days for a course of treatment, until disease progression or not tolerated or most received six cycles of chemotherapy.Results 147 cycles of chemo-therapy were completed in 37 patients,and the median chemotherapy cycle was 4 cycles.The efficacy and adverse reactions could be evaluated in all patients.Among them,complete remission (CR)in 0 patient,partial remission (PR)in 12 patients (32.43%),stable (SD)in 11 patients (29.73%),and progression (PD)in 14 patients (41.18%).The effective rate(CR +PR)was 32.43%.The disease control rate (CR +PR +SD)was 62.15%,median TTP was 3.9 months (95%CI:4 -8months),and median OS was 10 months.Until the end of follow -up,there were 3 patients with no progress.The main adverse reactions were hematological toxicity (51.53%)and gastrointestinal reaction (56.76%).Conclusion TC regimen is effective and safe in the treatment of patients with ATNBC.