Lopez M, Di Lauro L, Perno C F, Papaldo P, Barduagni M, Barduagni A
Tumori. 1983 Dec 31;69(6):545-51. doi: 10.1177/030089168306900610.
Seventy-six patients with metastatic breast cancer were treated with fluorouracil, adriamycin (doxorubicin) and cyclophosphamide (FAC) plus high-dose medroxyprogesterone acetate (HD-MPA). MPA was given for 21 days at the dose of 500 mg/day i.m., then on a randomized basis, either 500 mg/week i.m. (FAC+HD-MPA i.m.) or 300 mg/day p.o. (FAC+HD-MPA p.o.). Objective response rates were 79% in 39 patients on FAC+HD-MPA i.m. and 73% in the 37 patients on FAC+HD-MPA p.o. There was no significant difference in the median duration of response and median survival for the 2 regimens (respectively, 17 months and 22 months, and 15 months and 21 months for FAC+HD-MPA i.m. and FAC+HD-MPA p.o.). Toxicity was mild and similar in both groups. Although FAC+HD-MPA was highly effective, at present it is difficult to select which regimen provides the best initial treatment for metastatic breast cancer.
76例转移性乳腺癌患者接受氟尿嘧啶、阿霉素(多柔比星)和环磷酰胺(FAC)联合大剂量醋酸甲羟孕酮(HD-MPA)治疗。甲羟孕酮以500mg/天的剂量肌内注射给药21天,然后随机分为两组,一组以500mg/周的剂量肌内注射(FAC+HD-MPA 肌内注射组),另一组以300mg/天的剂量口服给药(FAC+HD-MPA 口服组)。FAC+HD-MPA肌内注射组的39例患者客观缓解率为79%,FAC+HD-MPA口服组的37例患者客观缓解率为73%。两种治疗方案的中位缓解持续时间和中位生存期无显著差异(FAC+HD-MPA肌内注射组分别为17个月和22个月,FAC+HD-MPA口服组分别为15个月和21个月)。两组的毒性均较轻且相似。虽然FAC+HD-MPA疗效显著,但目前很难选择哪种方案为转移性乳腺癌提供最佳初始治疗。