Bellmunt J, Ribas A, Albanell J, Bermejo B, Vera R, De Torres J A, Morote J, Lopez-Pacios M A, Banus J M, Rovirosa A, Carulla J, Sole L A
Medical Oncology Section, Hospital General Universitari Vall d'Hebron, Universitat Autònoma de Barcelona, Spain.
Am J Clin Oncol. 1996 Aug;19(4):344-8. doi: 10.1097/00000421-199608000-00004.
Carboplatin, methotrexate, and vinblastine (M-CAVI) is an active and well-tolerated regimen for bladder cancer patients ineligible for cisplatin-based regimens. We treated 47 T2-4 N0 M0 bladder cancer patients with M-CAVI in a neoadjuvant phase II trial. These 47 patients are evaluable for clinical response and toxicity. Clinical overall response rate was 34%, for a 95% confidence interval (CI95%) of 21-49%. Pathological response was seen in 40% of the patients (CI95%, 26-56%) with a 26.5% rate of pathological complete response (CI95%, 15-42%). Factors associated with the achievement of a response to therapy were the initial TNM stage (pT3a or lower, greater than pT3a, p = 0.001) and a Karnofsky score greater or equal than 90%, which was marginally significant (p = 0.08). With a median follow-up of 14 months, the disease-specific actuarial survival at 2 years is 42%. No patient has relapsed beyond 21 months of follow-up in a disease-free status. Toxic effects have been moderate. In conclusion, M-CAVI is an active and well-tolerated regimen that should be compared in terms of response rate and survival with a cisplatin-based regimen for invasive bladder cancer.
卡铂、甲氨蝶呤和长春碱(M-CAVI)方案对于不符合基于顺铂方案治疗条件的膀胱癌患者而言,是一种有效的且耐受性良好的治疗方案。在一项新辅助II期试验中,我们采用M-CAVI方案治疗了47例T2-4 N0 M0期膀胱癌患者。这47例患者可评估临床反应和毒性。临床总缓解率为34%,95%置信区间(CI95%)为21%-49%。40%的患者出现病理反应(CI95%,26%-56%),病理完全缓解率为26.5%(CI95%,15%-42%)。与治疗反应相关的因素为初始TNM分期(pT3a及以下、大于pT3a,p = 0.001)以及卡诺夫斯基评分大于或等于90%,此因素具有边缘显著性(p = 0.08)。中位随访14个月,2年的疾病特异性精算生存率为42%。在无病状态下,随访超过21个月没有患者复发。毒性作用为中度。总之,M-CAVI是一种有效的且耐受性良好的方案,在反应率和生存率方面应与基于顺铂的浸润性膀胱癌方案进行比较。