Department of Urology, Hirosaki University Graduate School of Medicine, Hirosaki, Japan.
Department of Urology, Hirosaki University Graduate School of Medicine, Hirosaki, Japan.
Urol Oncol. 2020 Aug;38(8):684.e17-684.e24. doi: 10.1016/j.urolonc.2020.03.009. Epub 2020 Apr 9.
To evaluate the safety and efficacy of intensive intravesical instillation of low-dose pirarubicin (THP) for 6 times vs. bacillus Calmette-Guérin (BCG) without maintenance therapy after transurethral resection of bladder tumor (TURBT) in patients with primary high-risk non-muscle-invasive bladder cancer (NMIBC).
We retrospectively evaluated 370 patients with primary high-risk NMIBC who underwent TURBT from November 1993 to April 2019. The patients were divided into 2 groups: patients treated with intravesical instillation of BCG without maintenance therapy (BCG group) and intensive intravesical instillation of low-dose (20 mg) THP for 6 times within 10 days after TURBT (THP group). Safety was assessed using the Common Terminology Criteria for Adverse Events version 5.0. Background-adjusted multivariate analyses were performed to evaluate the effect of intensive intravesical instillation of low-dose THP on oncological outcomes, including intravesical recurrence-free survival (RFS), upper urinary tract RFS, muscle-invasive bladder cancer-free survival, metastasis-free survival, cancer-specific survival, and overall survival.
Of the 370 patients with primary high-risk NMIBC, 180 (49%) and 190 (51%) were stratified into the BCG and THP groups, respectively. The incidence rate of adverse events of any grade in the BCG group was significantly higher than that in the THP group (P < 0.001). In the background-adjusted multivariate analyses, no significant differences were observed in oncological outcomes between the BCG and THP groups.
Intensive intravesical instillation of low-dose THP for 6 times may be one of the treatment options in view of safety and efficacy after TURBT in patients with primary high-risk NMIBC.
评估经尿道膀胱肿瘤切除术(TURBT)后 6 次密集膀胱内低剂量吡柔比星(THP)灌注与不维持治疗卡介苗(BCG)治疗初发高危非肌层浸润性膀胱癌(NMIBC)患者的安全性和疗效。
我们回顾性评估了 1993 年 11 月至 2019 年 4 月期间接受 TURBT 的 370 例初发高危 NMIBC 患者。患者分为两组:接受膀胱内灌注 BCG 且不维持治疗(BCG 组)和 TURBT 后 10 天内接受 6 次密集膀胱内低剂量(20mg)THP 灌注(THP 组)。使用通用不良事件术语标准 5.0 评估安全性。进行背景调整的多变量分析,以评估密集膀胱内低剂量 THP 灌注对肿瘤学结局的影响,包括膀胱内无复发生存(RFS)、上尿路 RFS、肌层浸润性膀胱癌无复发生存、无转移生存、癌症特异性生存和总生存。
在 370 例初发高危 NMIBC 患者中,180 例(49%)和 190 例(51%)分别分为 BCG 组和 THP 组。BCG 组任何级别的不良事件发生率明显高于 THP 组(P<0.001)。在背景调整的多变量分析中,BCG 组和 THP 组的肿瘤学结局无显著差异。
考虑到 TURBT 后初发高危 NMIBC 患者的安全性和疗效,密集膀胱内低剂量 THP 灌注 6 次可能是一种治疗选择。