School of Medicine, New York University, New York, NY.
Department of Population Health, New York University, New York, NY.
Clin Genitourin Cancer. 2020 Jun;18(3):e209-e216. doi: 10.1016/j.clgc.2019.10.001. Epub 2019 Oct 16.
First-line PD-inhibition in cisplatin-ineligible patients with locally advanced or metastatic urothelial cancer represents a novel clinical setting, with uncertainty concerning second-line outcomes. Specifying second-line treatment and outcomes will provide guidance in this new sequence. We performed a retrospective chart review to document the outcomes of these patients treated at our institution.
Our cohort consisted of 43 patients with advanced urothelial cancer receiving first-line checkpoint inhibition. Baseline factors, programmed death-ligand 1 (PD-L1) status, treatments, and outcomes during and beyond the first line were obtained. Response was scored using Response Evaluation Criteria in Solid Tumors, version 1.1 criteria. Log rank tests were used to compare outcomes in prognostic subgroups, and outcome associations with PD-L1 status were analyzed with Fisher exact tests.
A total of 43 patients received first-line atezolizumab or pembrolizumab from June 2014 until June 2018. The median age was 76.8 years, and the population was 74% male, with 60% having visceral metastases. Reasons for cisplatin ineligibility were Eastern Cooperative Oncology Group performance status 2%, 30%; renal insufficiency, 44%, and both, 21%. First-line objective response rate (ORR) was 30%, and complete response was 14%. The median overall survival was 11.7 months. Of 29 patients progressing, 17 received second-line treatment (most commonly, gemcitabine/carboplatin [10 patients]). The second-line response rate was 33%, and the ORR was 11%. The second-line median overall survival was 6.2 months. No association was found between PD-L1 status and outcomes.
Outcomes with first-line immunotherapy are consistent with historical outcomes. The ORR after first-line checkpoint inhibition falls short of historical comparators; however, the response rate compares favorably to those of chemotherapies used in previous second-line regimens. The older age and poorer performance status may have contributed to second-line outcomes.
在不适合顺铂治疗的局部晚期或转移性尿路上皮癌患者中,一线 PD 抑制治疗代表了一种新的临床环境,二线治疗结果存在不确定性。明确二线治疗和结果将为这一新方案提供指导。我们进行了回顾性病历审查,以记录在我院接受治疗的这些患者的结果。
我们的队列包括 43 名接受一线检查点抑制治疗的晚期尿路上皮癌患者。获取了基线因素、程序性死亡配体 1(PD-L1)状态、一线治疗期间和之后的治疗方法和结果。使用实体瘤反应评估标准 1.1 版(Response Evaluation Criteria in Solid Tumors,version 1.1 criteria)对反应进行评分。对数秩检验用于比较预后亚组的结果,Fisher 精确检验用于分析 PD-L1 状态与结果的相关性。
共有 43 名患者于 2014 年 6 月至 2018 年 6 月期间接受了一线阿特珠单抗或帕博利珠单抗治疗。中位年龄为 76.8 岁,人群中 74%为男性,60%有内脏转移。不适合顺铂治疗的原因包括东部肿瘤协作组(Eastern Cooperative Oncology Group)体能状态 2%,30%;肾功能不全,44%,两者兼有,21%。一线客观缓解率(ORR)为 30%,完全缓解率为 14%。中位总生存期为 11.7 个月。在 29 名进展的患者中,17 名接受了二线治疗(最常见的是吉西他滨/卡铂[10 名患者])。二线缓解率为 33%,ORR 为 11%。二线中位总生存期为 6.2 个月。未发现 PD-L1 状态与结果之间存在关联。
一线免疫治疗的结果与历史结果一致。一线检查点抑制治疗后的 ORR 低于历史对照,但与之前二线治疗方案中使用的化疗相比,反应率更有利。年龄较大和体能状态较差可能导致二线结果不佳。