临床肿瘤学杂志

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EC序贯P剂量密集方案与TEC方案在乳腺癌新辅助化疗中的疗效比较

胡赛男1,俞乔2,胡亦钦2,袁渊1,高津1,张莉莉1   

  1. 1 210009 南京江苏省肿瘤医院肿瘤内科 2 210009江苏省肿瘤医院乳腺外科
  • 收稿日期:2014-10-07 修回日期:2014-11-08 出版日期:2015-04-30 发布日期:2015-04-30
  • 通讯作者: 张莉莉

Efficacy and safety of dose-dense EC followed by P regimen in neoadjuvant chemotherapy for breast cancer:a retrospective comparison with the TEC regimen

HU Sainan,YU Qiao,HU Yiqing,YUAN Yuan,GAO Jing,ZHANG Lili.   

  1. Department of Medical Oncology, Jiangsu Provincial Cancer Hospital, Nanjing 210009, China
  • Received:2014-10-07 Revised:2014-11-08 Online:2015-04-30 Published:2015-04-30
  • Contact: ZHANG Lili

摘要: 目的 比较EC序贯P剂量密集方案与TEC方案在乳腺癌新辅助化疗中的疗效和不良反应。 方法 对2011年2月至2012年8月收治的64例Ⅱa期~Ⅲc期乳腺癌新辅助化疗患者进行回顾性分析,根据化疗方案分为剂量密集组(31例)和TEC组(33例),术前分别接受3~8个周期EC序贯P剂量密集方案和2~6个周期TEC方案新辅助化疗。密集方案:E(表阿霉素)90 mg/m2 d1,联合C(环磷酰胺)600 mg/m2 d1,每14天为1周期,共4个周期,序贯至P(紫杉醇)175 mg/m2d1,每14天为1周期,共4个周期。TEC方案:T(多西紫杉醇)75 mg/m2d1,E 70 mg/m2 d1,C 600 mg/m2d1,每21天为1周期。按照实体瘤的疗效评价标准(RECIST)1.1和术后病理组织学 结果 评定疗效,按照不良事件常用术语评定标准4.0版(CTCAE 4.0)评价不良反应。 结果 全组64例患者均可评价疗效。剂量密集组和TEC组的病理完全缓解率分别为16.1%和12.1%,有效率分别为80.6%和66.7%,两组的病理完全缓解率和有效率的差异无统计学差异(P>0.05);剂量密集组和TEC组的1、2年无病生存率分别为93.5%、86.7%和93.9%、81.8%, 1、2年总生存率分别为100.0%、90.3%和100.0%、85.8%,且两组无病生存率和总生存率的差异均无统计学差异(P>0.05);TEC组3~4级中性粒细胞下降的发生率高于剂量密集组(6.4% vs. 33.3%,P=0.012),剂量密集组1~2级神经毒性(80.6% vs. 36.4%,P<0.001)和肌肉关节酸痛(67.7% vs. 30.3%,P=0.005)的发生率均高于TEC组。 结论 剂量密集EC序贯P新辅助化疗方案与TEC方案疗效相似,毒副反应可以耐受,但安全性更好,有延长无病生存期和总生存期的趋势,是新辅助化疗的优选方案。

Abstract: Objective To compare the efficacy and safety of dose-dense EC followed by P regimen versus TEC regimen in neoadjuvant chemotherapy for breast cancer. Methods In a retrospective comparison, the clinical data of 64 breast cancer patients with stage Ⅱa-Ⅲc in our hospital from February 2011 to August 2012 were analyzed. According to the chemotherapy regimen,31 cases received dose-dense EC followed by P regimen for 3-8 cycles before surgery(dose-dense group), and 33 cases received TEC regimen for 2-6 cycles before surgery(TEC group). Dose-dense regimen was as follows: epirubicin(90 mg/m2, d1) plus cyclophosphamide(600 mg/m2, d1) every two weeks for four cycles followed by paclitaxel(175 mg/m2, d1) every two weeks for four cycles. TEC regimen was as follows: docetaxel(75 mg/m2, d1), epirubicin(70 mg/m2, d1) and cyclophosphamide(600 mg/m2, d1) every 21 days. Response to chemotherapy was assessed by RECIST criteria 1.1 and histopathological reaction after surgery. The toxicity was evaluated according to Common Terminology Criteria Adverse Events(CTCAE) 4.0. Results All patients were evaluable for efficacy and toxicity. The assessments of 64 patients were available. The pathologic complete response rates were 16.1% and 12.1%, and the response rates were 80.6% and 66.7% in dose-dense group and TEC group, respectively. No difference was observed on the pathologic complete response rate and response rate between both groups. The 1-, 2-year disease free survival rates were 93.5% and 86.7% in dose-dense group and 93.9% and 81.8% in TEC group, and the 1-, 2-year overall survival rates were 100.0% and 90.3% in dose-dense group and 100% and 85.8% in TEC group without significant difference(P>0.05). There were higher incidences of grade 1-2 neurotoxicity(80.6% vs. 36.4%) and muscle arthrosis ache(67.7% vs. 30.3%) but a lower incidence of grade 3-4 neutropenia(6.4% vs. 33.3%) in dose-dense group versus TEC group(P<0.05). Conclusion The efficacy of dose-dense and TEC neoadjuvant chemotherapy regimens are similar. The dose-dense regimen is well tolerated and more secure, which showed a non-significant trend toward better disease free survival and overall survival when compared with the TEC regimen. It is a preferred regimen in neoadjuvant chemotherapy.

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