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序贯卡介苗与表柔比星联合应用与单独使用卡介苗治疗浅表性膀胱肿瘤的随机前瞻性研究。

Sequential bacillus Calmette-Guerin and epirubicin versus bacillus Calmette-Guerin alone for superficial bladder tumors: a randomized prospective study.

作者信息

Ali-El-Dein B, Nabeeh A, Ismail E H, Ghoneim M A

机构信息

Urology & Nephrology Center, Mansoura University, Egypt.

出版信息

J Urol. 1999 Aug;162(2):339-42.

Abstract

PURPOSE

This study was designed to find a new therapeutic modality that may have the same efficacy and lower toxicity than bacillus Calmette-Guerin (BCG) for the treatment of superficial transitional cell carcinoma of the bladder.

MATERIALS AND METHODS

Between January 1993 and July 1997 a prospective randomized trial was conducted on 139 patients with stages pTa and pT1 bladder transitional cell carcinoma to compare the prophylactic efficacy and toxicity of sequential BCG and epirubicin (group 1) versus BCG alone (group 2). Group 1 comprised 69 patients who received alternating doses of 150 mg. BCG and 50 mg. epirubicin (1 drug at a time), while 70 patients in group 2 received 150 mg. BCG at each instillation. Treatment was continued for 6 weeks followed by 10 monthly instillations.

RESULTS

Therapy was discontinued permanently in 3 group 1 and 12 group 2 patients due to severe side effects, and they were excluded from the study. Among the 124 evaluable patients (96 men and 28 women, mean age 58.2 years) mean followup was 30.4 months (range 12 to 50). Recurrence and progression rates were statistically comparable in both groups. Interval to first recurrence with or without progression was longer in group 1 than in group 2 (log rank p = 0.05). Toxicity and complications were significantly lower with sequential treatment than with BCG alone at rates of 27.3% (18 patients) and 70.7% (41), respectively (p = 0.001).

CONCLUSIONS

Sequential BCG and epirubicin are comparable to BCG alone in efficacy and superior in terms of toxicity.

摘要

目的

本研究旨在寻找一种新的治疗方式,其在治疗膀胱浅表性移行细胞癌时可能具有与卡介苗(BCG)相同的疗效且毒性更低。

材料与方法

1993年1月至1997年7月,对139例pTa和pT1期膀胱移行细胞癌患者进行了一项前瞻性随机试验,以比较序贯使用BCG和表柔比星(第1组)与单独使用BCG(第2组)的预防疗效和毒性。第1组包括69例患者,他们交替接受150毫克BCG和50毫克表柔比星(每次一种药物),而第2组的70例患者每次灌注接受150毫克BCG。治疗持续6周,随后每月灌注10次。

结果

由于严重副作用,第1组3例和第2组12例患者永久停止治疗,并被排除在研究之外。在124例可评估患者(96例男性和28例女性,平均年龄58.2岁)中,平均随访时间为30.4个月(范围12至50个月)。两组的复发率和进展率在统计学上具有可比性。第1组有或无进展的首次复发间隔时间比第2组长(对数秩检验p = 0.05)。序贯治疗的毒性和并发症明显低于单独使用BCG,发生率分别为27.3%(18例患者)和70.7%(41例)(p = 0.001)。

结论

序贯使用BCG和表柔比星在疗效上与单独使用BCG相当,在毒性方面更具优势。

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