McElree Ian M, Packiam Vignesh T, Steinberg Ryan L, Hougen Helen Y, Mott Sarah L, Abou Chakra Mohamad, Zakharia Yousef, O'Donnell Michael A
Carver College of Medicine, University of Iowa, Iowa City, IA 52242, USA.
Rutgers Cancer Institute of New Jersey, Division of Urology, Department of Surgery, New Brunswick, NJ 08903, USA.
Cancers (Basel). 2024 Jul 17;16(14):2561. doi: 10.3390/cancers16142561.
Growing evidence suggests that many patients with high-risk non-muscle invasive urothelial carcinoma (NMIUC) can undergo bladder-sparing management with salvage intravesical therapies. However, inherent or developed disease resistance, particularly after multiple lines of prior salvage therapy, implores the continued pursuit of new treatment combinations. Herein, we describe the outcomes of 26 patients (31 treated units; 24 lower tract, 7 upper tract) with high-risk NMIUC treated with sequential intravesical gemcitabine and cabazitaxel with concomitant intravenous pembrolizumab (GCP) at the University of Iowa from August 2020 to February 2023. Median (IQR) follow-up was 30 (IQR: 17-35) months. Treated units had a history of high-risk NMIUC with a median of four prior endoluminal inductions. Overall, 87% of units presented with CIS or positive urine cytology. The 1- and 2-year recurrence-free survival was 77% (CI: 58-88%) and 52% (CI: 30-70%), respectively. The 2-year progression-free and cancer-specific survival was 70% (CI: 44-85%) and 96% (CI: 75-99%), respectively. In total, 22/26 (85%) patients reported any adverse event and 5/26 (19%) reported a grade ≥3 adverse event; however, all patients tolerated a full induction course. These results suggest that GCP is an effective and tolerable treatment option for patients with recurrent high-risk NMIUC.
越来越多的证据表明,许多高危非肌肉浸润性尿路上皮癌(NMIUC)患者可通过挽救性膀胱内治疗进行保膀胱管理。然而,内在的或获得性的疾病耐药性,尤其是在经过多线先前的挽救性治疗后,促使人们继续寻求新的治疗组合。在此,我们描述了2020年8月至2023年2月在爱荷华大学接受序贯膀胱内吉西他滨和卡巴他赛联合静脉注射帕博利珠单抗(GCP)治疗的26例高危NMIUC患者(31个治疗单位;24个下尿路,7个上尿路)的治疗结果。中位(IQR)随访时间为30(IQR:17 - 35)个月。治疗单位有高危NMIUC病史,先前腔内诱导治疗的中位数为4次。总体而言,87%的单位存在原位癌或尿细胞学阳性。1年和2年无复发生存率分别为77%(CI:58 - 88%)和52%(CI:30 - 70%)。2年无进展生存率和癌症特异性生存率分别为70%(CI:44 - 85%)和96%(CI:75 - 99%)。总共有22/26(85%)的患者报告了任何不良事件,5/26(19%)的患者报告了≥3级不良事件;然而,所有患者都耐受了完整的诱导疗程。这些结果表明,GCP是复发性高危NMIUC患者一种有效且可耐受的治疗选择。