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低剂量膀胱内卡介苗(东京株)治疗浅表性膀胱癌的评估

Evaluation of a low-dose intravesical bacillus Calmette-Guérin (Tokyo strain) therapy for superficial bladder cancer.

作者信息

Takashi M, Wakai K, Ohno Y, Murase T, Miyake K

机构信息

Department of Urology Nagoya University School of Medicine, Japan.

出版信息

Int Urol Nephrol. 1995;27(6):723-33. doi: 10.1007/BF02552138.

Abstract

To examine whether intravesical instillation of low-dose bacillus Calmette-Guérin (BCG) therapy is effective with low toxicity, we reviewed data for 111 patients with superficial bladder cancer (stages Ta and T1). Among them, 74 received the BCG treatment for prophylaxis of intravesical recurrence after transurethral resection, and the remaining 37 therapeutically for Ta or T1 tumours. The patients were divided into two groups by instillation dose of BCG (Tokyo 172 strain): 40 mg (n = 55) and 80 mg (n = 56), and statistically compared for recurrence, antitumour effect and toxicity. The mean instillations were done 8.4 times in the 40 mg dose group and 8.6 times in the 80 mg dose group. Among the 74 patients with BCG therapy for prophylaxis those with a previous episode of bladder cancer treatment (n = 47) experienced a significantly (p = 0.006) shorter recurrence-free interval than those with no episode (n = 27). Among 47 patients with a previous treatment episode, those receiving the 80 mg dose demonstrated a significantly longer recurrence-free interval than those given the 40 mg dose (p = 0.03). Among the 27 patients without previous treatment no significant difference in recurrence-free intervals was found between the two dose groups. Univariate and multivariate analyses using Cox's proportional hazards model confirmed the above findings. The recurrence index was also significantly reduced after BCG therapy in the 80 mg and 40 mg groups and similar antitumour effects for Ta or T1 tumours were observed in the two dose groups. The degree of toxicity due to BCG therapy was significantly (p = 0.02) lower with the 40 mg dose. The present study suggests that (1) a 40 mg BCG low-dose (Tokyo 172 strain) regimen is useful for preventing recurrence, with sufficient therapeutic efficacy and low frequency of toxicity, among patients without a previous treatment, and (2) prophylactic effects with the 80 mg dose regimen are much superior for previous treatment cases.

摘要

为了研究膀胱内灌注低剂量卡介苗(BCG)疗法是否疗效显著且毒性较低,我们回顾了111例浅表性膀胱癌(Ta期和T1期)患者的数据。其中,74例在经尿道切除术后接受BCG治疗以预防膀胱内复发,其余37例针对Ta或T1期肿瘤进行治疗。根据BCG(东京172株)的灌注剂量将患者分为两组:40毫克(n = 55)和80毫克(n = 56),并对复发率、抗肿瘤效果和毒性进行统计学比较。40毫克剂量组的平均灌注次数为8.4次,80毫克剂量组为8.6次。在74例接受BCG预防治疗的患者中,既往有膀胱癌治疗史的患者(n = 47)的无复发间期明显短于无治疗史的患者(n = 27)(p = 0.006)。在47例有既往治疗史的患者中,接受80毫克剂量的患者的无复发间期明显长于接受40毫克剂量的患者(p = 0.03)。在27例无既往治疗史的患者中,两个剂量组的无复发间期无显著差异。使用Cox比例风险模型进行的单因素和多因素分析证实了上述发现。80毫克和40毫克组在BCG治疗后复发指数也显著降低,且两个剂量组对Ta或T1期肿瘤的抗肿瘤效果相似。40毫克剂量的BCG治疗导致的毒性程度显著较低(p = 0.02)。本研究表明:(1)40毫克BCG低剂量(东京172株)方案对于无既往治疗史的患者预防复发有效,具有足够的治疗效果且毒性发生率低;(2)80毫克剂量方案对既往有治疗史的病例预防效果更佳。

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