Department of Urology, Keio University School of Medicine, Tokyo, Japan.
Department of Urology, Keio University School of Medicine, Tokyo, Japan.
J Urol. 2018 Jun;199(6):1446-1451. doi: 10.1016/j.juro.2017.12.057. Epub 2018 Jan 4.
We investigated the clinical impact of the purified protein derivative skin test prior to bacillus Calmette-Guérin therapy in patients with nonmuscle invasive bladder cancer treated with adjuvant bacillus Calmette-Guérin therapy.
A total of 498 patients with nonmuscle invasive bladder cancer treated with adjuvant bacillus Calmette-Guérin were included in study, of whom 320 underwent the purified protein derivative skin test 1 to 2 weeks prior to therapy. Oncologic outcomes and the rate of bacillus Calmette-Guérin related side effects were statistically evaluated.
The mean ± SD 5-year recurrence-free survival rate in patients who did vs did not undergo the purified protein derivative skin test was 66.6% ± 2.8% and 59.1% ± 4.1%, respectively, which was significantly different (p = 0.048). No significant difference was observed in the progression-free survival rate between patients who did vs did not undergo the test. Multivariate Cox regression analysis revealed that a history of recurrence (HR 1.59, p = 0.02), multiple tumors (HR 1.95, p <0.01), the bacillus Calmette-Guérin Connaught strain (HR 0.71, p = 0.04), 7 or more bacillus Calmette-Guérin instillations (HR 0.70, p = 0.04) and undergoing the purified protein derivative skin test (HR 0.72, p = 0.04) were independently associated with tumor recurrence. Major bacillus Calmette-Guérin related side effects were noted in 77 of the 320 patients (24.1%) who did vs 27 of the 178 (15.2%) who did not undergo the test, which was significantly different (p = 0.02).
The purified protein derivative skin test prior to bacillus Calmette-Guérin treatment enhances the therapeutic effects of this treatment and potentially results in a higher incidence of major bacillus Calmette-Guérin related side effects. Combination therapy with bacillus Calmette-Guérin using the purified protein derivative skin test may improve the oncologic outcomes of that therapy.
我们研究了在接受辅助卡介苗治疗的非肌肉浸润性膀胱癌患者中,卡介苗治疗前纯化蛋白衍生物皮肤试验对卡介苗治疗的临床影响。
共纳入 498 例接受辅助卡介苗治疗的非肌肉浸润性膀胱癌患者,其中 320 例在治疗前 1-2 周进行了纯化蛋白衍生物皮肤试验。统计评估了肿瘤学结果和卡介苗相关不良反应的发生率。
未进行和进行纯化蛋白衍生物皮肤试验的患者 5 年无复发生存率分别为 66.6%±2.8%和 59.1%±4.1%,差异有统计学意义(p=0.048)。未进行和进行该试验的患者无进展生存率差异无统计学意义。多因素 Cox 回归分析显示,复发史(HR 1.59,p=0.02)、多发肿瘤(HR 1.95,p<0.01)、卡介苗康诺特株(HR 0.71,p=0.04)、7 次以上卡介苗灌注(HR 0.70,p=0.04)和进行纯化蛋白衍生物皮肤试验(HR 0.72,p=0.04)与肿瘤复发独立相关。320 例进行纯化蛋白衍生物皮肤试验的患者中,有 77 例(24.1%)出现主要卡介苗相关不良反应,而 178 例未进行该试验的患者中,有 27 例(15.2%)出现主要卡介苗相关不良反应,差异有统计学意义(p=0.02)。
卡介苗治疗前进行纯化蛋白衍生物皮肤试验可增强卡介苗治疗的疗效,并可能导致更高的主要卡介苗相关不良反应发生率。联合使用纯化蛋白衍生物皮肤试验的卡介苗治疗可能改善该治疗的肿瘤学结果。