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Adverse reactions related to treatment compliance during BCG maintenance therapy for non-muscle-invasive bladder cancer

机译:卡介苗维持治疗非肌肉浸润性膀胱癌期间与治疗依从性相关的不良反应

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Objective: The aim of the study was to investigate the factor of adverse reactions related to compliance with Mycobacterium bovis bacillus Calmette-Gué rin maintenance therapy in patients with high-risk non-muscle-invasive bladder cancer. Methods: This study was a post hoc analysis using the database of a randomized controlled trial that examined the efficacy of bacillus Calmette-Gué rin (Connaught strain) maintenance therapy. Among the 42 patients assigned to the bacillus Calmette-Gué rin maintenance therapy group, six patients dropped out or withdrew consent before the bacillus Calmette- Gué rin maintenance therapy. The adverse reactions and clinical backgrounds of the remaining 36 patients who underwent bacillus Calmette-Gué rin maintenance therapy were compared between the two groups: the patients who completed the bacillus Calmette-Gué rin maintenance therapy (the Completed group), and those who discontinued the bacillus Calmette- Gué rin maintenance therapy (the Discontinued group). Results: Of the 36 patients who underwent bacillus Calmette-Gué rin maintenance therapy, 15 (41.7%) were in the Completed group and 21 (58.3%) were in the Discontinued group. Local adverse reactions (≥G2) were observed during maintenance therapy in 86.7% of the Completed group and 95.2% of the Discontinued group. As for adverse reactions during the induction therapy (bacillus Calmette-Gué rin induction therapy), the frequencies of gross hematuria and systemic adverse reactions (any grade) tended to be higher in the Discontinued group than in the Completed group, although not significantly so. In the Cochran-Armitage trend test, the linear T trend (i.e. the trend in the risk of an increased rate of discontinuation according to gross hematuria and systemic adverse reactions with bacillus Calmette-Gué rin induction therapy) was statistically significant (P = 0.0179). Conclusions: Most patients who completed bacillus Calmette-Gué rin maintenance therapy experienced local adverse reactions (≥G2) during the maintenance therapy. Gross hematuria and systemic adverse reactions during bacillus Calmette-Gué rin induction therapy might be related to the discontinuation of bacillus Calmette-Gué rin maintenance therapy because of severe adverse reactions.
机译:目的:本研究的目的是研究高风险非肌肉浸润性膀胱癌患者与牛分枝杆菌卡介苗维持疗法的依从性相关的不良反应因素。方法:本研究是使用一项随机对照试验数据库进行的事后分析,该试验检查了卡介苗(康诺特菌株)维持疗法的功效。在分配给Calmette-Guérin芽孢杆菌维持疗法组的42例患者中,有6名患者在接受Calmette-Guérin芽孢杆菌维持疗法前退出或撤回了同意书。比较两组中其余接受卡介苗维持治疗的36例患者的不良反应和临床背景:完成卡介苗维持治疗的患者(完成组)和停用卡介苗维持治疗的患者(完成组)卡麦特芽孢杆菌-格林疗法维持治疗(停药组)。结果:在接受卡介苗维持治疗的36例患者中,完成组15例(41.7%),停药组21例(58.3%)。维持治疗期间观察到局部不良反应(≥G2),完成组为86.7%,停药组为95.2%。至于诱导疗法(卡介苗-卡林杆菌诱导疗法)期间的不良反应,中止血尿和全身性不良反应(任何等级)的发生率在停药组中比在完成组中高,尽管不明显。在Cochran-Armitage趋势测试中,线性T趋势(即根据严重血尿和卡介苗诱导的全身性不良反应导致停药风险增加的趋势)具有统计学意义(P = 0.0179) 。结论:大多数完成卡介苗维持治疗的患者在维持治疗期间均发生局部不良反应(≥G2)。卡介苗诱导治疗期间的严重血尿和全身不良反应可能与卡介苗维持治疗终止有关,原因是严重的不良反应。

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