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卡介苗与表柔比星治疗原发性、继发性或同时性膀胱原位癌:欧洲癌症研究与治疗组织-泌尿生殖组III期试验(30906)的结果

Bacillus Calmette-Guerin versus epirubicin for primary, secondary or concurrent carcinoma in situ of the bladder: results of a European Organization for the Research and Treatment of Cancer--Genito-Urinary Group Phase III Trial (30906).

作者信息

de Reijke Theo M, Kurth Karl Heinz, Sylvester Richard J, Hall Reg R, Brausi Maurizio, van de Beek Kees, Landsoght K E J, Carpentier Paul

机构信息

Academic Medical Center, Amsterdam, The Netherlands.

出版信息

J Urol. 2005 Feb;173(2):405-9. doi: 10.1097/01.ju.0000150425.09317.67.

Abstract

PURPOSE

We compared the efficacy and side effects of intravesical instillations of bacillus Calmette-Guerin (BCG) and epirubicin in patients with carcinoma in situ (CIS) of the bladder.

MATERIALS AND METHODS

Patients with primary, secondary or concurrent CIS of the bladder were randomized to 81 mg BCG-Connaught (6 weekly instillations) or 50 mg epirubicin (8 weekly instillations). When a complete response (CR), defined as no Ta/T1 or CIS on biopsy and negative cytology, was obtained, patients in the 2 groups received maintenance instillations at months 3, 6, 12, 18, 24, 30 and 36. When no complete response was observed, the original treatment was repeated, followed again by cystoscopy and biopsies plus cytology.

RESULTS

A total of 168 patients were randomized between March 1993 and April 1999 to receive BCG (84) or epirubicin (84), while 4 on epirubicin and 3 on BCG were ineligible. The majority (52%) had concurrent CIS. Primary and secondary CIS was found in 23% and 24% of cases, respectively. The overall CR rate was 56% for epirubicin and 65% for BCG (p = 0.21, 90% CI 21.5 to -2.9). When tumor was found following 2 instillation courses, further treatment was left to the investigator (BCG in 29 cases and epirubicin in 37). Time to bladder tumor recurrence after CR was longer in patients treated with BCG vs epirubicin (median 5.1 vs 1.4 years). CIS recurrences were more frequently observed in complete responders to epirubicin (45% vs 16%). No differences in time to progression or duration of survival were observed. Side effects were more frequently seen in patients on BCG with 26 on BCG and 8 on epirubicin stopping treatment due to side effects.

CONCLUSIONS

No significant difference in CR rates could be demonstrated with intravesical instillations of epirubicin or BCG. Time to recurrence was significantly longer in patients treated with BCG after having achieved a CR. More CIS recurrences were found in patients treated with epirubicin. For time to progression and survival longer followup is warranted. Side effects were more frequent in patients on BCG.

摘要

目的

我们比较了膀胱内灌注卡介苗(BCG)和表柔比星对膀胱原位癌(CIS)患者的疗效和副作用。

材料与方法

原发性、继发性或合并性膀胱CIS患者被随机分为两组,一组接受81mg康诺特BCG(每周灌注6次),另一组接受50mg表柔比星(每周灌注8次)。当获得完全缓解(CR)时,即活检时无Ta/T1或CIS且细胞学检查为阴性,两组患者在第3、6、12、18、24、30和36个月接受维持灌注。若未观察。若未观察到完全缓解,则重复原治疗,随后再次进行膀胱镜检查、活检及细胞学检查。

结果

1993年3月至1999年4月,共有168例患者被随机分组,其中84例接受BCG治疗,84例接受表柔比星治疗,另有4例接受表柔比星治疗和3例接受BCG治疗的患者不符合纳入标准。大多数患者(52%)合并CIS。原发性和继发性CIS分别占病例的23%和24%。表柔比星组的总体CR率为56%,BCG组为65%(p = 0.21,90%置信区间为21.5至 -2.9)。在两个疗程灌注后发现肿瘤的患者,后续治疗由研究者决定(29例接受BCG治疗,37例接受表柔比星治疗)。CR后膀胱肿瘤复发时间,接受BCG治疗的患者比接受表柔比星治疗的患者更长(中位数分别为5.1年和1.4年)。表柔比星完全缓解患者中CIS复发更常见(45%对16%)。在疾病进展时间或生存持续时间方面未观察到差异。BCG治疗患者的副作用更常见,有26例接受BCG治疗和8例接受表柔比星治疗的患者因副作用停止治疗。

结论

膀胱内灌注表柔比星或BCG的CR率无显著差异。达到CR后,接受BCG治疗的患者复发时间显著更长。表柔比星治疗的患者中CIS复发更多。对于疾病进展时间和生存情况,需要更长时间的随访观察。BCG治疗患者的副作用更频繁。

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