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卡介苗与表柔比星预防多发性浅表性膀胱肿瘤的比较:采用改良治疗方案的前瞻性随机研究结果

BCG versus epirubicin in the prophylaxis of multiple superficial bladder tumours: results of a prospective randomized study using modified treatment schemes.

作者信息

Melekos M D, Zarakovitis I, Dandinis K, Fokaefs E, Chionis H, Dauaher H, Barbalias G

机构信息

Department of Urology, University of Patras School of Medicine, Greece.

出版信息

Int Urol Nephrol. 1996;28(4):499-509. doi: 10.1007/BF02550957.

Abstract

A prospective randomized trial on 94 eligible patients evaluated and compared the efficacy of adjuvant intravesical epirubicin and bacillus Calmette-Guérin (BCG) after complete resection of multifocal superficial bladder cancer. BCG treatment schedule consisted of an induction 6-week course of instillations (150 mg Pasteur BCG per instillation) and single maintenance doses to patients who remained free of recurrences at follow-up examinations for a total treatment period of 2 years. These initial responders received additionally a separate 4-week course of therapy 6 months after the start of treatment. Chemoprophylaxis included an early (on the second postoperative day) instillation followed by 4 weekly treatments with epirubicin (50 mg per instillation) and then by 10 monthly treatments for the initial responders during the first year of follow-up and at every follow-up examination for a total treatment period of 2 years. The overall treatment results did not differ significantly between the 2 arms (54% of patients of the epirubicin group remained free of recurrences compared to 65% of those treated with BCG) for an identical mean follow-up of 35.1 months. However, a significant benefit in favour of BCG when compared with epirubicin was shown in patients who had stage T1 and grade 3 tumours and in terms of relative risk of recurrences, disease-free interval and recurrence rate per 100 patient-months. Both drugs were proved to be safe with manageable toxicity.

摘要

一项针对94例符合条件患者的前瞻性随机试验,评估并比较了多灶性浅表膀胱癌完全切除术后辅助膀胱内注射表柔比星和卡介苗(BCG)的疗效。BCG治疗方案包括一个为期6周的诱导灌注疗程(每次灌注150mg巴斯德BCG),对于随访检查中无复发的患者给予单次维持剂量,总治疗期为2年。这些初始缓解者在治疗开始6个月后额外接受一个单独的为期4周的治疗疗程。化学预防包括术后早期(术后第二天)灌注,随后每周用表柔比星(每次灌注50mg)治疗4次,然后在随访的第一年对初始缓解者每月治疗10次,并在每次随访检查时进行,总治疗期为2年。在平均随访35.1个月相同的情况下,两组的总体治疗结果无显著差异(表柔比星组54%的患者无复发,而BCG治疗组为65%)。然而,在T1期和3级肿瘤患者中,与表柔比星相比,BCG在复发相对风险、无病间期和每100患者月复发率方面显示出显著优势。两种药物均被证明安全,毒性可控。

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