J Clin Oncol. 2001 Feb 1;19(3):602-11. doi: 10.1200/JCO.2001.19.3.602.
To determine the influence of the epirubicin dose in operable node-positive breast cancer patients with factors of poor prognosis.
Between April 1990 and July 1993, 565 operable breast cancer patients with either more than three positive nodes or between one and three positive nodes with Scarff Bloom Richardson grade > or = 2 and hormone receptor negativity were randomized after surgery to receive either fluorouracil 500 mg/m(2), epirubicin 50 mg/m(2), and cyclophosphamide 500 mg/m(2) every 21 days for six cycles (FEC 50) or the same regimen except with epirubicin dose of 100 mg/m(2) (FEC 100). Postmenopausal patients received tamoxifen 30 mg/d for 3 years at the beginning of chemotherapy. Radiotherapy was delivered at the end of chemotherapy in both groups.
The median follow-up was 67 months. The 5-year disease-free survival (DFS) was 54.8% with FEC 50 and 66.3% with FEC 100 (P =.03). The 5-year overall survival (OS) was 65.3% and 77.4%, respectively (P =.007). The mean relative dose-intensity was similar in the two groups (90.3% and 86.1%, respectively). Neutropenia and anemia were significantly more frequent in FEC 100 (P < 10(-3)), as were nausea-vomiting (P =.008) and stomatitis and alopecia (P < 10(-3)). Nine cases of grade 3 infection occurred only with FEC 100, and no toxic deaths occurred. Three cases of acute cardiac toxicity were observed (FEC50 = 1, FEC100 = 2) and 10 patients (FEC50 = 6, FEC100 = 4) presented delayed cardiac dysfunctions. Two cases of secondary leukemia were observed (acute lymphatic leukemia with FEC 50 and acute myelogenous leukemia with FEC 100).
After 5 years of follow-up, the increased epirubicin dose led to a significant benefit in terms of DFS and OS, with a high survival rate among patients with poor-prognosis breast cancer.
确定表柔比星剂量对具有预后不良因素的可手术的淋巴结阳性乳腺癌患者的影响。
1990年4月至1993年7月期间,565例可手术的乳腺癌患者,有三个以上阳性淋巴结或一至三个阳性淋巴结且斯卡夫-布卢姆-理查森分级≥2级以及激素受体阴性,术后随机分组,分别接受每21天一次氟尿嘧啶500mg/m²、表柔比星50mg/m²和环磷酰胺500mg/m²,共六个周期(FEC 50),或相同方案但表柔比星剂量为100mg/m²(FEC 100)。绝经后患者在化疗开始时接受他莫昔芬30mg/d,共3年。两组均在化疗结束时进行放疗。
中位随访时间为67个月。FEC 50组的5年无病生存率(DFS)为54.8%,FEC 100组为66.3%(P = 0.03)。5年总生存率(OS)分别为65.3%和77.4%(P = 0.007)。两组的平均相对剂量强度相似(分别为90.3%和86.1%)。FEC 100组中性粒细胞减少和贫血明显更常见(P < 10⁻³),恶心呕吐(P = 0.008)、口腔炎和脱发(P < 10⁻³)也是如此。仅FEC 100组发生9例3级感染,无毒性死亡发生。观察到3例急性心脏毒性(FEC50 = 1,FEC100 = 2),10例患者(FEC50 = 6,FEC100 = 4)出现延迟性心脏功能障碍。观察到2例继发性白血病(FEC 50为急性淋巴细胞白血病,FEC 100为急性髓细胞白血病)。
经过5年随访,表柔比星剂量增加在DFS和OS方面带来显著益处,预后不良的乳腺癌患者生存率较高。