Li Roger, Amrhein John, Cohen Zvi, Champagne Monique, Kamat Ashish M
Department of Urology, The University of Texas MD Anderson Cancer Center , Houston, TX, USA.
McDougall Scientific, Toronto, ON, Canada.
Bladder Cancer. 2017 Jan 27;3(1):65-71. doi: 10.3233/BLC-160084.
We have previously reported the results of a prospective multi-institutional study on the efficacy of MCNA in patients who recurred after intravesical BCG treatment [1]. Since that publication, a new standardized definition for BCG-unresponsiveness has been established [2]. We re-analyzed the oncologic outcomes following intravesical MCNA in patients classified as BCG-unresponsive according to the new definition. For this analysis, we focused on the enrolled patients who satisfied the requirements for BCG Unresponsiveness: i.e. adequate BCG treatment (at least 5/6 induction and 2/3 maintenance instillations) and high grade tumor within 6 months of prior BCG. Treatment course included 6 weekly intravesical instillations of 8 mg MCNA followed by 3 weekly instillations at months 3, 6, 12, 18, and 24. Followup assessments included cystoscopy, urine cytology and biopsy. Patients absent of high grade disease confirmed by central review of biopsy were deemed disease-free. Of the 129 patients enrolled, 94 (68 CIS with/without papillary tumors, 26 papillary only tumors) fit the criteria for the new BCG Unresponsive definition. Overall, disease free survival (DFS) for all BCG unresponsive patients was 48.9% (95% CI 38.0-59.0%) at 6 months, 34.8% (95% CI 24.7-45%) at 1 year and 28.3% (15.7-34.3%) at 2 years post induction. In the group with papillary tumors, DFS measured at months 6, 12, and 24 were: 61.2% (38.2-77.8%), 61.2(38.2-77.8%), and 50.1% (27.5-69%). In the CIS-containing group, the corresponding DFS were: 44.8% (32.3-56.4%), 26.5% (16.3-37.9%), and 16.6% (8.6-26.9%), respectively. For patients who are BCG Unresponsive, MCNA has the potential to render 26.5% of patients with CIS and 61.2% of patients with papillary tumors disease-free for at least 1 year with an intact bladder. The higher efficacy noted in the true BCG-unresponsive cohort than was previously reported with all-comers emphasizes the importance of having clearly defined criteria for clinical trials investigating new intravesical therapies after BCG failure.
我们之前报道了一项关于卡介苗(BCG)膀胱内灌注治疗后复发患者中,丝裂霉素(MCNA)疗效的前瞻性多机构研究结果[1]。自该研究发表以来,已确立了一种新的BCG无反应性标准化定义[2]。我们重新分析了根据新定义被归类为BCG无反应性患者接受膀胱内MCNA治疗后的肿瘤学结局。对于此次分析,我们重点关注符合BCG无反应性要求的入组患者:即充分的BCG治疗(至少5/6次诱导和2/3次维持灌注)以及在先前BCG治疗6个月内出现高级别肿瘤。治疗过程包括每周一次膀胱内灌注8mg MCNA,共6周,随后在第3、6、12、18和24个月每周灌注一次。随访评估包括膀胱镜检查、尿液细胞学检查和活检。经活检中央审查确认无高级别疾病的患者被视为无病。在129名入组患者中,94名(68名伴有/不伴有乳头状肿瘤的原位癌,26名仅为乳头状肿瘤)符合新的BCG无反应性定义标准。总体而言,所有BCG无反应性患者的无病生存率(DFS)在诱导后6个月为48.9%(95%CI 38.0 - 59.0%),1年时为34.8%(95%CI 24.7 - 45%),2年时为28.3%(15.7 - 34.3%)。在伴有乳头状肿瘤的组中,第6、12和24个月时的DFS分别为:61.2%(38.2 - 77.8%)、61.2%(38.2 - 77.8%)和50.1%(27.5 - 69%)。在含有原位癌的组中,相应的DFS分别为:44.8%(32.3 - 56.4%)、26.5%(16.3 - 37.9%)和16.6%(8.6 - 26.9%)。对于BCG无反应性患者,MCNA有可能使26.5%的原位癌患者和61.2%的乳头状肿瘤患者至少1年无病且膀胱完整。在真正的BCG无反应性队列中观察到的更高疗效高于之前报道的所有患者,这强调了在研究BCG失败后新的膀胱内治疗方法的临床试验中,制定明确标准的重要性。