Hwang W S, Hsiung C A, Ko W S, Wang C C, Chang J Y, Lai G M, Hsieh R K, Tsao C J, Chen L T, Law C K, Cheng A L, Fan S F, Tzeng C H, Chiou T J, Whang-Peng J
Chi-Mei Foundation Hospital, Taiwan Cooperative Oncology Group, Tainan, Taiwan, ROC.
Oncology. 1997 Jul-Aug;54(4):293-7. doi: 10.1159/000227706.
In a prospective phase II study, 102 women with advanced breast cancer were treated with low doses of cyclophosphamide, Adriamycin and 5-fluorouracil (CAF) at weekly intervals by intravenous injection. Seventy-five patients were evaluable for treatment response and the overall response rate was 52% (95% confidence interval, 41-63%). Of the evaluable patients, 15% had complete response and 37% had partial response. The median survival after therapy was 15.6 months, the median time to progression was 6.8 months and the median duration of response was 9.1 months. The main toxicities were mild vomiting and moderate myelosuppression. There was only 1 patient who experienced heart failure. Weekly CAF appears to have an efficacy with tolerable side effects comparable to standard CAF with an every-3-week schedule.
在一项前瞻性II期研究中,102例晚期乳腺癌女性患者接受了低剂量的环磷酰胺、阿霉素和5-氟尿嘧啶(CAF)治疗,通过静脉注射,每周一次。75例患者可评估治疗反应,总体反应率为52%(95%置信区间,41-63%)。在可评估的患者中,15%完全缓解,37%部分缓解。治疗后的中位生存期为15.6个月,中位进展时间为6.8个月,中位反应持续时间为9.1个月。主要毒性为轻度呕吐和中度骨髓抑制。只有1例患者发生心力衰竭。每周一次的CAF似乎具有与每三周一次的标准CAF相当的疗效且副作用可耐受。