Altman S J, Metter G E, Nealon T F, Weiss A J, Ramirez G, Madden R E, Fletcher W S, Strawitz J G, Multhauf P M
Cancer Treat Rep. 1978 Mar;62(3):389-95.
Two hundred and eight acceptable patients were treated with Yoshi 864 (2 mg/kg/day by iv push X 5 days repeated once every 6 weeks). Toxicity was minimal. There was an overall response rate of 11%. Cross resistance with other alkylating agents may not be present. Because of its lack of toxicity, Yoshi 864 should be further evaluated in chronic myelocytic leukemia, lymphomas, and carcinomas of the ovary and bladder where significant responses were seen. It should also be evaluated in combinations as a replacement for other alkylating agents which cause more nausea and vomiting.
208名符合条件的患者接受了Yoshi 864治疗(静脉推注,2毫克/千克/天,共5天,每6周重复一次)。毒性极小。总体缓解率为11%。可能不存在与其他烷化剂的交叉耐药性。由于其毒性低,Yoshi 864应在慢性粒细胞白血病、淋巴瘤以及卵巢癌和膀胱癌中进一步评估,这些疾病中已观察到显著疗效。它还应作为其他导致更多恶心和呕吐的烷化剂的替代品进行联合评估。