肿瘤研究与临床
腫瘤研究與臨床
종류연구여림상
CANCER RESEARCH AND CLINIC
2014年
4期
223-225,234
,共4页
李义慧%王晓红%李玉凤%杨俊泉%胡万宁
李義慧%王曉紅%李玉鳳%楊俊泉%鬍萬寧
리의혜%왕효홍%리옥봉%양준천%호만저
乳腺肿瘤%多西他赛%吡柔比星
乳腺腫瘤%多西他賽%吡柔比星
유선종류%다서타새%필유비성
Breast neoplasms%Docetaxe%THP
目的 观察多西他赛+吡柔比星+环磷酰胺(TAC方案)治疗三阴性乳腺癌患者的疗效和生存情况.方法 乳腺癌患者51例,三阴组:26例三阴性乳腺癌,Ⅱ期16期,Ⅲ期10例,非三阴组:25例非三阴性乳腺癌,Ⅱ期14期,Ⅲ期11例,两组患者均接受多西他赛联合吡柔比星化疗,多西他赛75 mg/m2,静脉滴注,第1天;吡柔比星40 mg/m2,静脉滴注,第1天;环磷酰胺500 mg/m2,第1天,21d重复.51例患者中位治疗周期数为4个周期.分析乳腺癌患者的疗效和生存情况.结果 三阴组术前临床完全缓解(cCR)9例(34.62%),临床部分缓解(cPR) 14例(53.85%),总有效率88.46%.术后病理完全缓解(pCR)7例(26.92%),非三阴组:术前cCR 6例(24.00%),cPR 8例(32.00%),总有效率56.00%,术后pCR 4例(16.00%),两组3年的总生存率分别为73.08%、88.00%,显示三阴性乳腺癌有较差的预后,达pCR的三阴性乳腺癌患者5年生存率(88.89%)高于未达到pCR的三阴性乳腺癌患者(47.06%).结论 TAC方案对局部晚期三阴性乳腺癌有较高缓解率和降期效果,可提高三阴性乳腺癌的疗效,安全性较好.
目的 觀察多西他賽+吡柔比星+環燐酰胺(TAC方案)治療三陰性乳腺癌患者的療效和生存情況.方法 乳腺癌患者51例,三陰組:26例三陰性乳腺癌,Ⅱ期16期,Ⅲ期10例,非三陰組:25例非三陰性乳腺癌,Ⅱ期14期,Ⅲ期11例,兩組患者均接受多西他賽聯閤吡柔比星化療,多西他賽75 mg/m2,靜脈滴註,第1天;吡柔比星40 mg/m2,靜脈滴註,第1天;環燐酰胺500 mg/m2,第1天,21d重複.51例患者中位治療週期數為4箇週期.分析乳腺癌患者的療效和生存情況.結果 三陰組術前臨床完全緩解(cCR)9例(34.62%),臨床部分緩解(cPR) 14例(53.85%),總有效率88.46%.術後病理完全緩解(pCR)7例(26.92%),非三陰組:術前cCR 6例(24.00%),cPR 8例(32.00%),總有效率56.00%,術後pCR 4例(16.00%),兩組3年的總生存率分彆為73.08%、88.00%,顯示三陰性乳腺癌有較差的預後,達pCR的三陰性乳腺癌患者5年生存率(88.89%)高于未達到pCR的三陰性乳腺癌患者(47.06%).結論 TAC方案對跼部晚期三陰性乳腺癌有較高緩解率和降期效果,可提高三陰性乳腺癌的療效,安全性較好.
목적 관찰다서타새+필유비성+배린선알(TAC방안)치료삼음성유선암환자적료효화생존정황.방법 유선암환자51례,삼음조:26례삼음성유선암,Ⅱ기16기,Ⅲ기10례,비삼음조:25례비삼음성유선암,Ⅱ기14기,Ⅲ기11례,량조환자균접수다서타새연합필유비성화료,다서타새75 mg/m2,정맥적주,제1천;필유비성40 mg/m2,정맥적주,제1천;배린선알500 mg/m2,제1천,21d중복.51례환자중위치료주기수위4개주기.분석유선암환자적료효화생존정황.결과 삼음조술전림상완전완해(cCR)9례(34.62%),림상부분완해(cPR) 14례(53.85%),총유효솔88.46%.술후병리완전완해(pCR)7례(26.92%),비삼음조:술전cCR 6례(24.00%),cPR 8례(32.00%),총유효솔56.00%,술후pCR 4례(16.00%),량조3년적총생존솔분별위73.08%、88.00%,현시삼음성유선암유교차적예후,체pCR적삼음성유선암환자5년생존솔(88.89%)고우미체도pCR적삼음성유선암환자(47.06%).결론 TAC방안대국부만기삼음성유선암유교고완해솔화강기효과,가제고삼음성유선암적료효,안전성교호.
Objective To evaluate the efficacy and survival rate of neoadjuvant chemotherapy with docetaxe and pirarubicin in triple negative breast cancer (TNBC).Methods Total 51 breast cancer patients were divided into TNBC group (n =26,including 16 of stage Ⅱ and 10 of stage Ⅲ patients) and non-TNBC group (n =25,including 14 of stage Ⅱ and 11 of stage Ⅲ patients).All patients received a median of 4 treatment cycles with TAC regimen [docetaxe 75 mg/m2 on day 1,pirarubicin 40 mg/m2 on day 1 and cyclophosphamide (CTX) 500 mg/m2 on day 1 of each 21 day cycle].The efficacy of treatment and survival rate of two groups were evaluated.Results In TNBC group,9 out of 26 (34.62 %) patients achieved clinical complete response (cCR),and 14 (53.85 %) had partial response (cPR).Overall,88.46 % of TNBC patients had clinical response and 26.92 % (7/26) showed pathology complete response (pCR).In non-TNBC group,6 (24.00 %) patients reached cCR and 8 (32.00 %) showed cPR.The overall response rate was of 56.00 %,and 4 (16.00 %) patients achieved pCR.The overall 3-year survival rates in TNBC and non-TNBC groups were 73.08 % and 88.00 %,respectively,indicating a poorer prognosis of TNBC.The 5-year survival rates of TNBC patients with and without pCR were 88.89 % and 47.06 %,respectively.Conclusion TAC regimen improves the prognosis for locally advanced TNBC,indicating that the neoadjuvant chemotherapy is effective and safe for TNBC patients.