Henderson I C, Gelman R, Canellos G P, Frei E
Cancer Treat Rep. 1981;65 Suppl 1:67-75.
Sixty-six patients were treated with the combination "super-CMF" as follows: cyclophosphamide 100 mg/m2 po days 2 through 14; methotrexate 3.0 g/m2 iv days 1 and 8; 5-fluorouracil 600 m g/m2 iv days 1 and 8; citrovorum factor rescue 10 mg/m2 iv days 2 and 9 and po days 2 through 4 and 9 through 11; and Adriamycin 70 to 90 mg/m2 iv day 29. This cycle was repeated at 49-day intervals. The single-agent activity of high-dose methotrexate with rescue was first evaluated in breast cancer patients in a truncated phase II study; 3 of 19 had a partial response (greater than 50% regression of measurable lesions) after 2 to 6 weekly courses and another 6 to 19 had some objective evidence of response (greater than 25%, less than 50%). The response rate to the combination "super-CMF" was: complete response (CR) 15 of 55 evaluable patients (27%) and partial response (PR) 28 of 55 (51%). The median duration of response was 24.5 months and the median time to treatment failure was 21.6 months. Nineteen of these patients have completed 12 to 18 months of drug treatment and have been followed in continuing remission for 1 to 28 months without further therapy. The total response rate and the CR rate achieved with this regimen are substantial, and the durability of the responses appears to be considerably greater than that obtained with other drug combinations.
66例患者接受了如下“超级CMF”联合治疗方案:环磷酰胺100mg/m²,口服,第2至14天;甲氨蝶呤3.0g/m²,静脉注射,第1天和第8天;5-氟尿嘧啶600mg/m²,静脉注射,第1天和第8天;亚叶酸解救,10mg/m²,静脉注射,第2天和第9天,口服,第2至4天以及第9至11天;阿霉素70至90mg/m²,静脉注射,第29天。此疗程每49天重复一次。高剂量甲氨蝶呤联合解救治疗的单药活性首先在一项截短的II期研究中的乳腺癌患者中进行评估;19例患者中有3例在2至6个每周疗程后出现部分缓解(可测量病灶消退大于50%),另有6至19例有一些客观缓解证据(大于25%,小于50%)。“超级CMF”联合治疗方案的缓解率为:55例可评估患者中,完全缓解(CR)15例(27%),部分缓解(PR)28例(51%)。缓解的中位持续时间为24.5个月,治疗失败的中位时间为21.6个月。其中19例患者已完成12至18个月的药物治疗,在未接受进一步治疗的情况下持续缓解1至28个月。该方案所达到的总缓解率和CR率相当可观,且缓解的持续时间似乎明显长于其他药物联合方案。