Eto H, Oka Y, Ueno K, Nakamura I, Yoshimura K, Arakawa S, Kamidono S, Obe S, Ogawa T, Hamami G
Department of Urology, Kobe University, School of Medicine, Japan.
Cancer Chemother Pharmacol. 1994;35 Suppl:S46-51. doi: 10.1007/BF00686919.
A multicentric randomized trial was conducted for the purpose of investigating the prophylactic efficacy of intravesical epirubicin instillation following transurethral resection of superficial bladder cancer in comparison with the efficacy of doxorubicin. The patients were centrally randomized into 2 groups and received 19 intravesical instillations of epirubicin or doxorubicin at 30 mg/30 ml physiological saline twice a week for 4 weeks and then once monthly for 11 months. A total of 150 patients with Ta and T1 superficial bladder cancer were entered in the trial, and 114 were evaluable. The nonrecurrence rates determined for each group at 1 and 2 years by the Kaplan-Meier method were 92.8% and 88.6%, respectively, for the epirubicin group and 86.4% and 81.7%, respectively, for the doxorubicin group. The differences between the two groups were not statistically significant. The main side effects encountered in this study were symptoms of bladder irritation such as micturitional pain, pollakisuria, and hematuria. The respective frequencies of those symptoms were 10%, 15.0%, and 5.0% in the epirubicin group and 14.8%, 14.8%, and 0 in the doxorubicin group. These results suggest that epirubicin is a useful drug, comparable with doxorubicin, for intravesical instillation chemotherapy in the prophylactic treatment of superficial bladder cancer.
开展了一项多中心随机试验,旨在研究经尿道浅表性膀胱癌切除术后膀胱内灌注表柔比星与阿霉素相比的预防效果。患者被集中随机分为两组,接受19次膀胱内灌注表柔比星或阿霉素,剂量为30mg/30ml生理盐水,每周两次,共4周,然后每月一次,共11个月。共有150例Ta和T1期浅表性膀胱癌患者进入试验,114例可评估。采用Kaplan-Meier法确定,表柔比星组1年和2年的无复发率分别为92.8%和88.6%,阿霉素组分别为86.4%和81.7%。两组之间的差异无统计学意义。本研究中遇到的主要副作用是膀胱刺激症状,如排尿疼痛、尿频和血尿。表柔比星组这些症状的发生率分别为10%、15.0%和5.0%,阿霉素组分别为14.8%、14.8%和0。这些结果表明,在浅表性膀胱癌的预防性治疗中,表柔比星是一种与阿霉素相当的有用的膀胱内灌注化疗药物。