Brambilla C, Valagussa P, Bonadonna G
Cancer Chemother Pharmacol. 1978;1(1):35-9. doi: 10.1007/BF00253144.
The results of a prospective controlled study with alternating cycles of two effective non-cross resistant combinations in advanced breast cancer are reported. The two combinations consisted of adriamycin plus vincristine (AV) and cyclophosphamide, methotrexate and fluorouracil (CMF). The study was carried out with the main intent to obtain a higher incidence and a longer duration of response compared to that obtained with either combination alone. A total of 110 evaluable patients (55 for each treatment group) not previously treated with chemotherapy were randomly allocated to receive either Therapy A (2 AV followed by 2 CMF) or Therapy B (2 CMF followed by 2 AV). Complete plus partial response (53% vs 60%) as well as duration of remission (11 vs 12 months) were similar in both treatment groups. At the time of present analysis, 20 patients died from cancer (Therapy A: 9; Therapy B: 11) and in 9 of them death occurred during the first 12 months. The administration of sequential combinations was no more toxic than the administration of either combination alone.
本文报告了一项前瞻性对照研究的结果,该研究针对晚期乳腺癌采用两种有效的非交叉耐药联合方案交替循环治疗。这两种联合方案分别为阿霉素加长春新碱(AV)以及环磷酰胺、甲氨蝶呤和氟尿嘧啶(CMF)。该研究的主要目的是,相比于单独使用任一联合方案,获得更高的缓解率和更长的缓解持续时间。共有110例此前未接受过化疗的可评估患者(每个治疗组55例)被随机分配接受治疗A(2个周期的AV方案后接2个周期的CMF方案)或治疗B(2个周期的CMF方案后接2个周期的AV方案)。两个治疗组的完全缓解加部分缓解率(分别为53%和60%)以及缓解持续时间(分别为11个月和12个月)相似。在本次分析时,20例患者死于癌症(治疗A组:9例;治疗B组:11例),其中9例在最初12个月内死亡。序贯联合方案的毒性并不高于单独使用任一联合方案。