Cai Tommaso, Nesi Gabriella, Tinacci Galliano, Zini Enzo, Mondaini Nicola, Boddi Vieri, Mazzoli Sandra, Bartoletti Riccardo
Department of Urology, University of Florence, Florence, Italy.
J Urol. 2008 Jul;180(1):110-5. doi: 10.1016/j.juro.2008.03.038. Epub 2008 May 15.
We evaluated the impact of epirubicin perioperative instillation in improving subsequent bacillus Calmette-Guerin instillation efficacy in high risk patients with nonmuscle invasive bladder cancer.
Between January 2005 and June 2007, 161 patients affected by high risk nonmuscle invasive bladder cancer were enrolled in this prospective, randomized, controlled, double-blind study. A total of 80 patients were assigned to group A (perioperative epirubicin 80 mg/50 ml normal saline) plus delayed bacillus Calmette-Guerin instillations (5 x 108 colony-forming units in 50 ml saline) and 81 to group B (delayed bacillus Calmette-Guerin alone). The main outcome measures were time to first recurrence and recurrence rate. All data obtained from a median followup of 15.3 months in group A and 14.8 months in group B, were analyzed.
At the end of followup 46 of 80 patients in group A (57.5%) had no evidence of disease, just like 41 of 81 in group B (50.6%). No statistical difference was observed between the 2 groups in terms of recurrence rate (p = 0.82) or time to first recurrence (p = 0.095). Kaplan-Meier analysis of recurrence showed no significant differences between group A and group B (p = 0.0952). On multivariate analysis the early single dose instillation of epirubicin was not indicated as an independent prognostic factor (HR 0.50, 95% CI 0.32-1.18).
The present study showed no statistically significant differences in terms of disease-free time and recurrence rate between high risk patients with nonmuscle invasive bladder cancer who had undergone perioperative epirubicin instillation plus delayed bacillus Calmette-Guerin and those who had undergone delayed bacillus Calmette-Guerin alone.
我们评估了表柔比星围手术期灌注对提高高危非肌层浸润性膀胱癌患者后续卡介苗灌注疗效的影响。
2005年1月至2007年6月,161例高危非肌层浸润性膀胱癌患者纳入了这项前瞻性、随机、对照、双盲研究。总共80例患者被分配到A组(围手术期表柔比星80mg/50ml生理盐水)加延迟卡介苗灌注(5×10⁸菌落形成单位于50ml盐水中),81例患者被分配到B组(仅延迟卡介苗灌注)。主要观察指标为首次复发时间和复发率。分析了A组中位随访15.3个月和B组中位随访14.8个月所获得的所有数据。
随访结束时,A组80例患者中有46例(57.5%)无疾病证据,B组81例中有41例(50.6%)。两组在复发率(p = 0.82)或首次复发时间(p = 0.095)方面未观察到统计学差异。复发的Kaplan-Meier分析显示A组和B组之间无显著差异(p = 0.0952)。多因素分析表明,表柔比星早期单剂量灌注未被视为独立的预后因素(HR 0.50,95% CI 0.32 - 1.18)。
本研究表明,围手术期表柔比星灌注加延迟卡介苗灌注的高危非肌层浸润性膀胱癌患者与仅接受延迟卡介苗灌注的患者在无病时间和复发率方面无统计学显著差异。