Mead G M, Russell M, Clark P, Harland S J, Harper P G, Cowan R, Roberts J T, Uscinska B M, Griffiths G O, Parmar M K
Royal South Hants Hospital, Brintons Terrace, Southampton, UK.
Br J Cancer. 1998 Oct;78(8):1067-75. doi: 10.1038/bjc.1998.629.
Transitional cell carcinomas may arise at any site within the urinary tract and are a source of considerable morbidity and mortality. In particular, patients with metastatic disease have a poor prognosis, with less than 5% alive at 5 years. A multicentre randomized trial comparing methotrexate and vinblastine (MV) with cisplatin, methotrexate and vinblastine (CMV) in advanced or metastatic transitional cell carcinoma was conducted in the UK. From April 1991 to June 1995, 214 patients were entered by 16 centres, 108 randomized to CMV and 106 to MV. A total of 204 patients have died. The hazard ratio (relative risk of dying) was 0.68 (95% CI 0.51-0.90, P-value = 0.0065) in favour of CMV. This translates to an absolute improvement in 1-year survival of 13%, 16% in MV and 29% in CMV. The median survival for CMV and MV was 7 months and 4.5 months respectively. Two hundred and eight patients objectively progressed or died. The hazard ratio was 0.55 (95% CI 0.41-0.73, P-value = 0.0001) in favour of CMV. Two hundred and nine patients symptomatically progressed or died. The hazard ratio was 0.48 (95% CI 0.36-0.64, P-value = 0.0001) in favour of CMV. The most important pretreatment factors influencing overall survival were WHO performance status and extent of disease. These two factors were used to derive a prognostic index which could be used to categorize patients into three prognostic groups. We conclude that the addition of cisplatin to methotrexate and vinblastine should be considered in patients with transitional cell carcinoma, taking into account the increased toxicity.
移行细胞癌可发生于尿路的任何部位,是导致相当高发病率和死亡率的一个原因。特别是转移性疾病患者预后较差,5年生存率低于5%。在英国进行了一项多中心随机试验,比较甲氨蝶呤和长春碱(MV)与顺铂、甲氨蝶呤和长春碱(CMV)用于晚期或转移性移行细胞癌的疗效。从1991年4月至1995年6月,16个中心纳入了214例患者,108例随机分配至CMV组,106例随机分配至MV组。共有204例患者死亡。风险比(死亡相对风险)为0.68(95%置信区间0.51 - 0.90,P值 = 0.0065),支持CMV组。这意味着1年生存率的绝对改善为13%,MV组为16%,CMV组为29%。CMV组和MV组的中位生存期分别为7个月和4.5个月。208例患者出现客观进展或死亡。风险比为0.55(95%置信区间0.41 - 0.73,P值 = 0.0001),支持CMV组。209例患者出现症状性进展或死亡。风险比为0.48(95%置信区间0.36 - 0.64,P值 = 0.0001),支持CMV组。影响总生存期的最重要预处理因素是世界卫生组织的体能状态和疾病范围。利用这两个因素得出一个预后指数,可用于将患者分为三个预后组。我们得出结论,对于移行细胞癌患者,考虑到毒性增加,应考虑在甲氨蝶呤和长春碱中加入顺铂。