Maffezzini M, Torelli T, Villa E, Corrada P, Bolognesi A, Leidi G L, Rigatti P, Campo B
Department of Urology, Istituto Scientifico San Raffaele, Milano, Italy.
J Urol. 1991 Apr;145(4):741-3. doi: 10.1016/s0022-5347(17)38440-9.
A total of 44 patients with infiltrating, locally advanced bladder cancer (stages T 3a-b, T 4a-b and N+/N0) were treated with the systemic chemotherapy regimen of cisplatin, methotrexate and vinblastine (CMV) in the neoadjuvant setting, of whom 39 were evaluable for response. After planned radical cystectomy and 2 to 3 cycles of chemotherapy no tumor was found on the pathological specimen of 4 patients (10%), the tumor was downstaged in 19 (49%) and no change was observed in 16 (41%). Toxicity included leukopenia in 29 patients (66%), 1 of whom died of granulocytopenic sepsis, nausea and vomiting in 39 (89%) and mild to moderate mucositis in 18 (41%). Median followup is 12 months with a range of 6 to 39 months. Of 32 patients followed for longer than 6 months 6 (19%) experienced progression or recurrence of disease. We conclude that preoperative CMV chemotherapy is effective in inducing downstaging of the tumor, although systemic toxicity limits its use to cautiously selected patients.
共有44例浸润性局部晚期膀胱癌患者(T 3a - b期、T 4a - b期和N + / N0期)在新辅助治疗中接受了顺铂、甲氨蝶呤和长春碱(CMV)的全身化疗方案,其中39例可评估疗效。在计划进行根治性膀胱切除和2至3个周期化疗后,4例患者(10%)的病理标本未发现肿瘤,19例(49%)肿瘤分期降低,16例(41%)未观察到变化。毒性反应包括29例患者(66%)出现白细胞减少,其中1例死于粒细胞缺乏性败血症,39例(89%)出现恶心和呕吐,18例(41%)出现轻至中度粘膜炎。中位随访时间为12个月,范围为6至39个月。在32例随访时间超过6个月的患者中,6例(19%)出现疾病进展或复发。我们得出结论,术前CMV化疗在诱导肿瘤分期降低方面是有效的,尽管全身毒性限制了其仅适用于谨慎选择的患者。