Kyriakakis Z, Dimopoulos M A, Kostakopoulos A, Karayiannis A, Sofras F, Zervas A, Giannopoulos A, Dimopoulos C
Department of Urology, University of Athens School of Medicine, Greece.
J Urol. 1997 Aug;158(2):408-11.
We investigated the activity of combination chemotherapy consisting of cisplatin, ifosfamide, methotrexate and vinblastine in patients with metastatic urothelial cancer.
A total of 32 consecutive patients was treated with 30 mg./m.2 cisplatin on days 1 through 3, 1.5 gm./m.2 ifosfamide with mesna on days 1 through 3, 30 mg./m.2 methotrexate and 3 mg./m.2 vinblastine on day 1 plus 5 micrograms./kg. granulocyte colonystimulating factor on days 7 through 11. Courses were repeated every 21 days for a maximum of 6 cycles.
Major toxicity was granulocytopenia in 56% of patients, including 11 episodes of granulocytopenic fever. Anemia and thrombocytopenia developed in a third of the cases. No other significant toxicity or treatment related death was noted. An objective response was achieved in 20 patients (62.5%, 95% confidence interval 44 to 79). Median time to progression was 7 months and median survival was 13 months.
The cisplatin, ifosfamide, methotrexate and vinblastine regimen appeared active in patients with metastatic urothelial carcinoma. This regimen was associated with significant but manageable hematological toxicity and the incidence of mucositis or renal impairment was low. Prospective randomized studies are needed to assess whether the addition of ifosfamide to other active agents will improve the survival of patients with this disease.
我们研究了顺铂、异环磷酰胺、甲氨蝶呤和长春碱联合化疗对转移性尿路上皮癌患者的疗效。
连续32例患者接受治疗,第1至3天给予顺铂30mg/m²,第1至3天给予异环磷酰胺1.5g/m²并同时给予美司钠,第1天给予甲氨蝶呤30mg/m²和长春碱3mg/m²,第7至11天给予粒细胞集落刺激因子5μg/kg。每21天重复一个疗程,最多6个周期。
主要毒性为56%的患者出现粒细胞减少,其中包括11次粒细胞减少性发热。三分之一的病例出现贫血和血小板减少。未发现其他显著毒性或与治疗相关的死亡。20例患者(62.5%,95%置信区间44%至79%)获得客观缓解。中位进展时间为7个月,中位生存期为13个月。
顺铂、异环磷酰胺、甲氨蝶呤和长春碱方案对转移性尿路上皮癌患者似乎有效。该方案与显著但可控的血液学毒性相关,且粘膜炎或肾功能损害的发生率较低。需要进行前瞻性随机研究以评估在其他活性药物中加入异环磷酰胺是否会改善该疾病患者的生存率。