Department of Urology, Institute of Clinical Medicine, University of Tsukuba, Tsukuba, 1-1-1 Tennoudai, Tsukuba City, Ibaraki, 305-8575 Japan.
Jpn J Clin Oncol. 2013 Aug;43(8):827-34. doi: 10.1093/jjco/hyt086. Epub 2013 Jul 14.
The aim of the study was to investigate the factor of adverse reactions related to compliance with Mycobacterium bovis bacillus Calmette-Guérin maintenance therapy in patients with high-risk non-muscle-invasive bladder cancer.
This study was a post hoc analysis using the database of a randomized controlled trial that examined the efficacy of bacillus Calmette-Guérin (Connaught strain) maintenance therapy. Among the 42 patients assigned to the bacillus Calmette-Guérin maintenance therapy group, six patients dropped out or withdrew consent before the bacillus Calmette-Guérin maintenance therapy. The adverse reactions and clinical backgrounds of the remaining 36 patients who underwent bacillus Calmette-Guérin maintenance therapy were compared between the two groups: the patients who completed the bacillus Calmette-Guérin maintenance therapy (the Completed group), and those who discontinued the bacillus Calmette-Guérin maintenance therapy (the Discontinued group).
Of the 36 patients who underwent bacillus Calmette-Guérin 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-Guérin 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-Guérin induction therapy) was statistically significant (P = 0.0179).
Most patients who completed bacillus Calmette-Guérin maintenance therapy experienced local adverse reactions (≥G2) during the maintenance therapy. Gross hematuria and systemic adverse reactions during bacillus Calmette-Guérin induction therapy might be related to the discontinuation of bacillus Calmette-Guérin maintenance therapy because of severe adverse reactions.
本研究旨在探讨高危非肌层浸润性膀胱癌患者接受卡介苗维持治疗时与依从性相关的不良反应因素。
本研究是对一项卡介苗(康诺特株)维持治疗疗效的随机对照试验数据库的事后分析。在被分配至卡介苗维持治疗组的 42 名患者中,有 6 名患者在卡介苗维持治疗前退出或撤回同意。比较接受卡介苗维持治疗的 36 例患者(卡介苗维持治疗组)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)和停止卡介苗维持治疗的患者(停止组)。
在接受卡介苗维持治疗的 36 例患者中,15 例(41.7%)完成了治疗,21 例(58.3%)停止了治疗。完成组有 86.7%的患者在维持治疗期间出现局部不良反应(≥G2),停止组有 95.2%的患者出现这种情况。至于诱导治疗期间(卡介苗诱导治疗)的不良反应,停止组的肉眼血尿和全身不良反应(任何等级)的频率均高于完成组,尽管差异无统计学意义。在 Cochran-Armitage 趋势检验中,线性 T 趋势(即根据卡介苗诱导治疗时肉眼血尿和全身不良反应的增加率,停药风险的趋势)具有统计学意义(P=0.0179)。
完成卡介苗维持治疗的大多数患者在维持治疗期间出现局部不良反应(≥G2)。卡介苗诱导治疗期间的肉眼血尿和全身不良反应可能与严重不良反应导致的卡介苗维持治疗中断有关。