Medical Research Council Clinical Trials Unit, London, United Kingdom.
J Clin Oncol. 2011 Jun 1;29(16):2171-7. doi: 10.1200/JCO.2010.32.3139. Epub 2011 Apr 18.
This article presents the long-term results of the international multicenter randomized trial that investigated the use of neoadjuvant cisplatin, methotrexate, and vinblastine (CMV) chemotherapy in patients with muscle-invasive urothelial cancer of the bladder treated by cystectomy and/or radiotherapy. Nine hundred seventy-six patients were recruited between 1989 and 1995, and median follow-up is now 8.0 years.
This was a randomized phase III trial of either no neoadjuvant chemotherapy or three cycles of CMV.
The previously reported possible survival advantage of CMV is now statistically significant at the 5% level. Results show a statistically significant 16% reduction in the risk of death (hazard ratio, 0.84; 95% CI, 0.72 to 0.99; P = .037, corresponding to an increase in 10-year survival from 30% to 36%) after CMV.
We conclude that CMV chemotherapy improves outcome as first-line adjunctive treatment for invasive bladder cancer. Two large randomized trials (by the Medical Research Council/European Organisation for Research and Treatment of Cancer and Southwest Oncology Group) have confirmed a statistically significant and clinically relevant survival benefit, and neoadjuvant chemotherapy followed by definitive local therapy should be viewed as state of the art, as compared with cystectomy or radiotherapy alone, for deeply invasive bladder cancer.
本文介绍了一项国际多中心随机试验的长期结果,该试验研究了新辅助顺铂、甲氨蝶呤和长春碱(CMV)化疗在接受膀胱根治性切除术和/或放疗的肌层浸润性膀胱癌患者中的应用。1989 年至 1995 年间共招募了 976 名患者,目前的中位随访时间为 8.0 年。
这是一项随机 III 期试验,比较了无新辅助化疗和接受 3 个周期 CMV 化疗的疗效。
先前报告的 CMV 可能的生存优势现在在统计学上具有显著意义(P =.037),风险比为 0.84(95%可信区间为 0.72 至 0.99),这表明接受 CMV 化疗的患者死亡风险降低了 16%(10 年生存率从 30%提高到 36%)。
我们得出结论,CMV 化疗作为浸润性膀胱癌的一线辅助治疗可改善预后。两项大型随机试验(由英国医学研究理事会/欧洲癌症研究与治疗组织和美国西南肿瘤协作组进行)已经证实了具有统计学意义和临床相关的生存获益,与单独接受膀胱根治性切除术或放疗相比,新辅助化疗后行确定性局部治疗应被视为肌层浸润性膀胱癌的标准治疗方法。