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卡介苗维持治疗Ta T1期膀胱肿瘤与毒性增加无关:欧洲癌症研究与治疗组织泌尿生殖组III期试验结果

Maintenance Bacillus Calmette-Guerin for Ta T1 bladder tumors is not associated with increased toxicity: results from a European Organisation for Research and Treatment of Cancer Genito-Urinary Group Phase III Trial.

作者信息

van der Meijden Adrian P M, Sylvester Richard J, Oosterlinck Wim, Hoeltl Wolfgang, Bono Aldo V

机构信息

Department of Urology, Jeroen Bosch Hospital, P.O. Box 90153, 5200 ME, 's Hertogenbosch, The Netherlands

出版信息

Eur Urol. 2003 Oct;44(4):429-34. doi: 10.1016/s0302-2838(03)00357-9.

Abstract

OBJECTIVES

After transurethral resection, the local and systemic side effects of Bacillus Calmette-Guerin (BCG) instillations were assessed during a 6-week induction course followed by 3 weekly maintenance instillations at 3, 6, 12, 18, 24, 30 and 36 months to determine if BCG toxicity increases over time.

METHODS

487 patients who received BCG in a multicenter phase III trial were included. Side effects were divided into 5 different treatment periods: the first 6 weeks induction, months 3 and 6, month 12, the second year, and the third year.

RESULTS

99 (20.3%) patients stopped BCG due to side effects. 72 (14.8%) stopped due to local side effects, including 59 for BCG induced cystitis, 33 during the first 6 months. 46 (9.4%) stopped due to systemic side effects: 23 due to fever, 19 within 6 months, and 15 due to general malaise, 12 within 6 months. 68% who stopped due to side effects did so during the first 6 months. The percent stopping after 6 months due to local side effects does not increase and actually decreases for systemic side effects.

CONCLUSIONS

The majority of local and systemic side effects are seen already during the induction and the first half-year of maintenance. During further maintenance BCG toxicity does not increase and instillations are generally well tolerated.

摘要

目的

经尿道切除术后,在为期6周的诱导疗程期间评估卡介苗(BCG)膀胱灌注的局部和全身副作用,随后在3、6、12、18、24、30和36个月进行每周一次的维持灌注,以确定BCG毒性是否随时间增加。

方法

纳入多中心III期试验中接受BCG治疗的487例患者。副作用分为5个不同的治疗阶段:前6周的诱导期、第3和6个月、第12个月、第二年和第三年。

结果

99例(20.3%)患者因副作用停止BCG治疗。72例(14.8%)因局部副作用停止治疗,其中59例因BCG诱导的膀胱炎,33例发生在最初6个月内。46例(9.4%)因全身副作用停止治疗:23例因发热,19例在6个月内,15例因全身不适,12例在6个月内。因副作用停止治疗的患者中,68%在最初6个月内停止。6个月后因局部副作用停止治疗的百分比没有增加,而因全身副作用停止治疗的百分比实际上有所下降。

结论

大多数局部和全身副作用在诱导期和维持治疗的前半年就已出现。在进一步维持治疗期间,BCG毒性没有增加,灌注通常耐受性良好。

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