Department of Medical Oncology, Integrated Centers of Oncology (ICO) Paul Papin, Angers, France.
Department of Medical Oncology, Hôpital Saint-André, University of Bordeaux-CHU, Bordeaux, France.
Eur J Cancer. 2020 Sep;136:76-83. doi: 10.1016/j.ejca.2020.02.019. Epub 2020 Jul 9.
Papillary renal cell carcinoma (pRCC) is the most common non-clear cell RCC (nccRCC). Pivotal studies evaluating immune checkpoint inhibitors mostly excluded nccRCC. The aim of this retrospective and multicentre study was to evaluate the activity of programmed death-1 (PD-1)/ programmed death-ligand 1 (PD-L1) inhibitors specifically in metastatic pRCC.
The primary end-point was time to treatment failure (TTF). Secondary endpoints included objective response rate (ORR), overall survival (OS) and treatment-related adverse events (TRAEs).
From 02/2016 to 01/2019, 57 patients with pRCC were included. Histology included 16 (28%) type 1 pRCC, 34 (60%) type 2 pRCC and 7 (12%) unclassified pRCC. Treatment with immune checkpoint inhibitors was used in the first-line setting in 4 patients (7%), in the second-line setting in 32 patients (56%) and in the third-line setting or more in 21 patients (37%). With a median follow-up of 12 months (95% confidence interval [CI]: 9.9-21.0), the median TTF was 3.1 months (95% CI: 2.7-5.0). Among the 55 patients evaluable for ORR, best response was complete response/partial response in 6 patients (11%), stable disease in 18 patients (33%) and progressive disease in 31 patients (56%). The median OS was 14.6 months (95% CI: 9.0- not reached). TRAEs of grade III-IV were noted in 6 patients (10%) leading to treatment discontinuation, and no grade V TRAEs were observed.
PD-1/PD-L1 inhibitors exhibit limited activity as monotherapy in this pRCC population, which remains an unmet need. Our findings underline the need for further prospective clinical trials evaluating immune checkpoint inhibitor combinations in patients with pRCC.
乳头状肾细胞癌(pRCC)是最常见的非透明细胞肾细胞癌(nccRCC)。评估免疫检查点抑制剂的关键研究大多排除了 nccRCC。本回顾性多中心研究的目的是专门评估程序性死亡-1(PD-1)/程序性死亡配体 1(PD-L1)抑制剂在转移性 pRCC 中的活性。
主要终点是治疗失败时间(TTF)。次要终点包括客观缓解率(ORR)、总生存期(OS)和治疗相关不良事件(TRAEs)。
从 2016 年 2 月至 2019 年 1 月,共纳入 57 例 pRCC 患者。组织学包括 16 例(28%)1 型 pRCC、34 例(60%)2 型 pRCC 和 7 例(12%)未分类 pRCC。4 例(7%)患者一线使用免疫检查点抑制剂,32 例(56%)患者二线使用,21 例(37%)患者三线及以上使用。中位随访 12 个月(95%置信区间[CI]:9.9-21.0),中位 TTF 为 3.1 个月(95%CI:2.7-5.0)。在 55 例可评估 ORR 的患者中,最佳缓解为完全缓解/部分缓解 6 例(11%),稳定疾病 18 例(33%),进展疾病 31 例(56%)。中位 OS 为 14.6 个月(95%CI:9.0-未达到)。3 级-4 级 TRAEs 见于 6 例(10%)患者,导致治疗中止,未观察到 5 级 TRAEs。
PD-1/PD-L1 抑制剂在该 pRCC 人群中单药治疗活性有限,这仍然是一个未满足的需求。我们的研究结果强调了需要进一步进行前瞻性临床试验,评估免疫检查点抑制剂联合治疗 pRCC 患者的疗效。