Colozza M, Gori S, Mosconi A M, Belsanti V, Basurto C, Rossetti R, Di Costanzo F, Buzzi F, Bacchi M, Davis S
Division of Medical Oncology, Ospedale Policlinico, Perugia, Italy.
Am J Clin Oncol. 1989 Apr;12(2):137-41. doi: 10.1097/00000421-198904000-00010.
Thirty-three evaluable patients with metastatic breast cancer (12 previously treated with adjuvant chemotherapy) were treated with a combination of cis-platin, doxorubicin, and cyclophosphamide (CAP). cis-Platin was given intravenously, 20 mg/m2, on days 1-3, doxorubicin, 40 mg/m2 i.v., on day 1, and cyclophosphamide, 200 mg/m2 i.v., on days 1-3. Cycles were repeated every 3 weeks. A complete response (CR) was obtained in 3 patients (9%) and a partial response (PR) in 18 (54%). The highest response rate was observed in soft tissue and in liver metastases. Median response duration was 48 weeks and median survival 93 weeks. Toxicity was moderate and consisted of alopecia (100%), gastrointestinal toxicity (86%), and myelosuppression (60%). We conclude that this regimen is active in the treatment of advanced breast carcinoma, with a generally acceptable tolerance, but further evaluations in Phase III studies are required.
33例可评估的转移性乳腺癌患者(其中12例曾接受辅助化疗)接受了顺铂、阿霉素和环磷酰胺(CAP)联合治疗。顺铂在第1 - 3天静脉注射,剂量为20mg/m²;阿霉素在第1天静脉注射,剂量为40mg/m²;环磷酰胺在第1 - 3天静脉注射,剂量为200mg/m²。每3周重复一个周期。3例患者(9%)获得完全缓解(CR),18例(54%)获得部分缓解(PR)。在软组织和肝转移灶中观察到最高缓解率。中位缓解持续时间为48周,中位生存期为93周。毒性为中度,包括脱发(100%)、胃肠道毒性(86%)和骨髓抑制(60%)。我们得出结论,该方案在晚期乳腺癌治疗中有效,耐受性总体可接受,但需要在III期研究中进一步评估。