Breast Center, Mita Hospital, International University of Health and Welfare, Minato-ku, Tokyo 108-8329, Japan.
Cancer Chemother Pharmacol. 2012 Aug;70(2):331-8. doi: 10.1007/s00280-012-1826-x. Epub 2012 Apr 11.
Metronomic combination chemotherapy with the oral fluoropyrimidine doxifluridine/5'-deoxy-5-fluorouridine (5 -DFUR) and oral cyclophosphamide (C) showed promising efficacy in a single-arm study. The oral fluoropyrimidine capecitabine was designed to deliver 5-fluorouracil preferentially to tumors, potentially improving efficacy over doxifluridine. We conducted a phase II multicenter study to evaluate an all-oral XC combination in patients with HER2-negative metastatic breast cancer (MBC).
Patients received capecitabine 828 mg/m(2) twice daily with cyclophosphamide 33 mg/m(2) twice daily, days 1-14 every 3 weeks. The primary endpoint was overall response rate (ORR). Secondary endpoints included progression-free survival (PFS), overall survival (OS), and safety.
Between May 2007 and April 2009, 51 patients were enrolled and 45 were included in the efficacy analysis. The median follow-up was 18.1 months. ORR was 44.4% and stable disease (≥24 weeks) was achieved in 13.4%, resulting in a 57.8% clinical benefit response rate. Median PFS was 12.3 months (95% confidence interval: 8.9-18.9 months). Median PFS was 10.7 months in triple-negative disease and 13.2 months in estrogen-receptor positive, HER2-negative disease. The 1- and 2-year OS rates were 86 and 71%, respectively. Median OS has not been reached. Grade 3 adverse events comprised leukopenia (26%), neutropenia (16%), and decreased hemoglobin (2%). There was no grade 3 hand-foot syndrome.
Oral XC is an effective first- or second-line therapy for MBC, demonstrating high activity in both luminal A and triple-negative disease with few severe side effects. This metronomic oral combination chemotherapy could be beneficial for the treatment of HER2-negative MBC.
口服氟嘧啶类药物多西氟尿苷/5'-去氧-5-氟尿苷(5-DFUR)和环磷酰胺(C)的节拍式联合化疗在一项单臂研究中显示出有希望的疗效。口服氟嘧啶类药物卡培他滨旨在优先向肿瘤输送 5-氟尿嘧啶,可能比多西氟尿苷更有效。我们进行了一项多中心 II 期研究,以评估在 HER2 阴性转移性乳腺癌(MBC)患者中使用全口服 XC 联合治疗。
患者接受卡培他滨 828 mg/m²,每日 2 次,环磷酰胺 33 mg/m²,每日 2 次,每 3 周疗程 14 天。主要终点是总缓解率(ORR)。次要终点包括无进展生存期(PFS)、总生存期(OS)和安全性。
2007 年 5 月至 2009 年 4 月,共招募了 51 例患者,其中 45 例纳入疗效分析。中位随访时间为 18.1 个月。ORR 为 44.4%,稳定疾病(≥24 周)为 13.4%,临床获益反应率为 57.8%。中位 PFS 为 12.3 个月(95%置信区间:8.9-18.9 个月)。三阴性疾病的中位 PFS 为 10.7 个月,雌激素受体阳性、HER2 阴性疾病的中位 PFS 为 13.2 个月。1 年和 2 年的 OS 率分别为 86%和 71%。中位 OS 尚未达到。3 级不良事件包括白细胞减少(26%)、中性粒细胞减少(16%)和血红蛋白减少(2%)。无 3 级手足综合征。
口服 XC 是 MBC 的一种有效一线或二线治疗方法,在 luminal A 和三阴性疾病中均显示出高活性,且副作用较轻。这种节拍式口服联合化疗可能对治疗 HER2 阴性 MBC 有益。