Department of Urology, Fondazione Policlinico Universitario "A. Gemelli" IRCSS, Largo Agostino Gemelli, 8, 00168, Rome, Italy.
Università Cattolica del Sacro Cuore, L.go A. Gemelli, 8, 00168, Rome, Italy.
BMC Cancer. 2018 Dec 6;18(1):1224. doi: 10.1186/s12885-018-5134-7.
In case of high grade non-muscle invasive bladder cancer (HG-NMIBC), intravesical BCG represents the first-line treatment; despite the "gold" standard therapy, up to 50% of patients relapse, needing radical cystectomy. Hence, alternative therapeutic strategies have been developed. The aim of the study was to evaluate a first-line salvage treatment with EMDA®-MMC in patients with HGNMIBC unresponsive to BCG.
We carried out a prospective, single-center, single-arm Phase II study in order to evaluate the efficacy (in terms of recurrence and progression) and the safety of the EMDA®-MMC treatment in 26 (21 male, 5 female) consecutive patients with "BCG refractory" HGNMIBC on a 3 years follow-up. EMDA®-MMC treatment consisted of 40 mg of MMC diluted in 100 ml of sterile water retained in the bladder for 30 min with 20 mA pulsed electric current. EMDA®-MMC regimen consisted of an induction course of 6 weekly instillations followed by a maintenance course of 6 monthly instillations. Follow-up was performed with systematic mapping biopsies of the bladder (with sampling in the prostatic urethra for men), voiding and washing urinary cytology, radiological study of the upper urinary tract. We performed Survival Kaplan-Meier curves and Log-rank test in order to analyze high grade disease-free survival.
At the end of follow-up, 16 patients (61.5%) preserved their native bladder; 10 patients (38.4%) underwent radical cystectomy, in 6 patients (23.1%) for recurrent HGNMIBC and in 4 patients (15.4%) for progression to muscle-invasive disease. At the end of follow-up, stratifying patients based on TNM classification (TaG3, T1G3, Cis, TaT1G3 + Cis), disease-free rates were 75, 71.4, 50 and 25%, respectively; survival curves showed statistically significant differences (p value < 0.05). Regarding toxicity, we reported severe adverse systemic event of hypersensitivity to the MMC in 3 patients (11.5%), and local side effects in 6 patients (26.1%).
In the field of alternative strategies to radical cystectomy, the EMDA®-MMC could be considered safe and effective in high-risk NMIBC unresponsive to BCG, as a "bladder sparing" therapy in selected patients. Multicenter studies with a larger number of patients and a longer follow-up might confirm our preliminary results.
EudraCT2017-002585-43. 17 June 2017 (retrospectively registered).
对于高级别非肌肉浸润性膀胱癌(HG-NMIBC),膀胱内卡介苗(BCG)是一线治疗方法;尽管这是“金标准”疗法,但仍有多达 50%的患者复发,需要进行根治性膀胱切除术。因此,已经开发了替代治疗策略。本研究旨在评估 EMDA®-MMC 作为一线挽救治疗在对 BCG 无反应的 HG-NMIBC 患者中的疗效(复发和进展方面)和安全性。
我们进行了一项前瞻性、单中心、单臂 II 期研究,以评估 26 例(21 名男性,5 名女性)连续的对 BCG 无反应的 HG-NMIBC 患者的 EMDA®-MMC 治疗的疗效(复发和进展方面)和安全性,随访时间为 3 年。EMDA®-MMC 治疗包括将 40mg 的 MMC 稀释在 100ml 的无菌水中,然后用 20mA 脉冲电流保留在膀胱中 30 分钟。EMDA®-MMC 方案包括 6 周的诱导期和 6 个月的维持期。通过系统膀胱活检(男性进行前列腺尿道采样)、尿排空和冲洗尿液细胞学、上尿路的放射学研究进行随访。我们进行了生存 Kaplan-Meier 曲线和 Log-rank 检验,以分析高级别无病生存率。
随访结束时,16 名患者(61.5%)保留了他们的原膀胱;10 名患者(38.4%)接受了根治性膀胱切除术,其中 6 名患者(23.1%)因复发的 HG-NMIBC 而接受手术,4 名患者(15.4%)因进展为肌层浸润性疾病而接受手术。在随访结束时,根据 TNM 分类(TaG3、T1G3、Cis、TaT1G3+Cis)对患者进行分层,无病生存率分别为 75%、71.4%、50%和 25%;生存曲线显示具有统计学意义的差异(p 值<0.05)。关于毒性,我们报告了 3 名患者(11.5%)对 MMC 发生严重过敏反应,6 名患者(26.1%)发生局部副作用。
在替代根治性膀胱切除术的策略领域中,EMDA®-MMC 可被认为是对 BCG 无反应的高危 NMIBC 安全且有效的治疗方法,是一种可选择的保留膀胱的治疗方法。具有更大数量的患者和更长随访时间的多中心研究可能会证实我们的初步结果。
EudraCT2017-002585-43。2017 年 6 月 17 日(回溯性注册)。