Martin M, Villar A, Sole-Calvo A, Gonzalez R, Massuti B, Lizon J, Camps C, Carrato A, Casado A, Candel M T, Albanell J, Aranda J, Munarriz B, Campbell J, Diaz-Rubio E
Hospital Universitario San Carlos, Madrid, Spain.
Ann Oncol. 2003 Jun;14(6):833-42. doi: 10.1093/annonc/mdg260.
The purpose of this study was to determine the relative efficacy of doxorubicin versus methotrexate in combination with intravenous cyclophosphamide and 5-fluorouracil (FAC versus CMF) as adjuvant chemotherapy for operable breast cancer.
Over a 4-year period, 985 women undergoing curative surgery for breast cancer (T1-3 N0-2 M0, stage I-IIIA, UICC) from nine hospitals were stratified with respect to axillary node involvement (node positive versus node negative) and randomized to receive either FAC (500/50/500/m(2)) every 3 weeks for six cycles or CMF (600/60/600/m(2)) every 3 weeks for six cycles.
The relative dose intensities of FAC and CMF were 87% and 85% of planned doses, respectively. Unadjusted data indicated a non-significant trend towards better results with FAC. In the prospectively formed subset of node-negative patients, disease-free survival and overall survival were statistically superior in the FAC treatment arm (P = 0.041 and 0.034, respectively), but this advantage was not seen in the subset of node-positive patients, probably because of a difference in the percentage of patients with four or more positive nodes. Adjusting data for size of treatment effect and potential interactions (number of positive nodes, tumor size, treatment center), the overall relative risk (RR) of disease recurrence and death were significantly lower with FAC treatment (RR 1.2, P = 0.03, and RR 1.3, P = 0.05, respectively). This result was mainly due to the difference observed in the node-negative patient population. Toxicity was mild: FAC induced more alopecia, emesis, mucositis and cardiotoxicity; this last was of clinical concern, but was infrequent and manageable. CMF induced more conjunctivitis and weight gain. There were no toxic deaths.
Doxorubicin in combination with day 1 i.v. cyclophosphamide and 5-fluorouracil is superior to methotrexate in combination with day 1 i.v. cyclophosphamide and 5-fluorouracil as adjuvant chemotherapy for operable breast cancer. A treatment effect is particularly evident in the node-negative patients. Although the clinical toxicity of FAC is greater than that of CMF, the levels were manageable and clinically acceptable.
本研究旨在确定多柔比星与甲氨蝶呤联合静脉注射环磷酰胺和5-氟尿嘧啶(FAC方案与CMF方案)作为可手术乳腺癌辅助化疗的相对疗效。
在4年期间,来自9家医院的985例接受乳腺癌根治性手术(T1-3 N0-2 M0,I-IIIA期,国际抗癌联盟分期)的女性,根据腋窝淋巴结受累情况(淋巴结阳性与阴性)进行分层,并随机分为每3周接受FAC方案(500/50/500/m²)共6个周期或CMF方案(600/60/600/m²)共6个周期。
FAC方案和CMF方案的相对剂量强度分别为计划剂量的87%和85%。未经调整的数据显示FAC方案有取得更好结果的非显著趋势。在前瞻性形成的淋巴结阴性患者亚组中,FAC治疗组的无病生存率和总生存率在统计学上更优(分别为P = 0.041和0.034),但在淋巴结阳性患者亚组中未观察到这一优势,可能是因为有四个或更多阳性淋巴结的患者百分比存在差异。对治疗效果大小和潜在相互作用(阳性淋巴结数量、肿瘤大小、治疗中心)的数据进行调整后,FAC治疗组疾病复发和死亡的总体相对风险(RR)显著更低(RR分别为1.2,P = 0.03;RR为1.3,P = 0.05)。这一结果主要归因于在淋巴结阴性患者群体中观察到的差异。毒性较轻:FAC方案导致更多脱发、呕吐、黏膜炎和心脏毒性;最后一项具有临床相关性,但发生率低且可处理。CMF方案导致更多结膜炎和体重增加。无毒性死亡病例。
多柔比星联合第1天静脉注射环磷酰胺和5-氟尿嘧啶作为可手术乳腺癌的辅助化疗优于甲氨蝶呤联合第1天静脉注射环磷酰胺和5-氟尿嘧啶。治疗效果在淋巴结阴性患者中尤为明显。虽然FAC方案的临床毒性大于CMF方案,但毒性水平可处理且临床可接受。