Lopez R, Karakousis C P, Didolkar M S, Holyoke E D
Cancer Treat Rep. 1978 Sep;62(9):1329-32.
Twenty-six patients (14 men and 12 women) with histologically proven advanced malignant melanoma, who previously had not responded to DTIC, methyl-CCNU, and procarbazine, received estramustine phosphate (estracyt) (15 mg/m2) in daily divided doses. All patients had measurable disease. One patient developed a complete remission and one patient had improvement in liver function without measurable regression in the tumor. In three other patients (11%), the disease remained static for a period of 3--5 months. The mean survival time from the beginning of therapy was 16.8 months for the patients with a response or static disease and 2.18 months for those who had no response. Gastrointestinal toxicity was minimal; no hematologic toxicity was observed. It appears that estramustine phosphate used as a single agent for treating advanced malignant melanoma after patients failed to respond to DTIC and to the combination of methyl-CCNU and procarbazine has a poor response rate.
26例经组织学证实的晚期恶性黑色素瘤患者(14例男性,12例女性),之前对达卡巴嗪、甲环亚硝脲和丙卡巴肼无反应,接受了磷酸雌莫司汀(癌腺治)(15mg/m²)每日分次给药。所有患者均有可测量的病灶。1例患者完全缓解,1例患者肝功能改善但肿瘤无明显缩小。另外3例患者(11%)病情稳定3至5个月。治疗开始后的平均生存时间,有反应或病情稳定的患者为16.8个月,无反应的患者为2.18个月。胃肠道毒性极小;未观察到血液学毒性。对于达卡巴嗪以及甲环亚硝脲和丙卡巴肼联合治疗无效的晚期恶性黑色素瘤患者,使用磷酸雌莫司汀单药治疗似乎缓解率较低。