Clinical outcomes of nivolumab plus ipilimumab in patients with metastatic non‐clear cell renal cell carcinoma: Real‐world data from a Japanese multicenter retrospective study

医学 易普利姆玛 无容量 内科学 肾透明细胞癌 肿瘤科 肾细胞癌 养生 实体瘤疗效评价标准 不利影响 泌尿科 胃肠病学 进行性疾病 化疗 免疫疗法 癌症
作者
Keita Izumi,Masaharu Inoue,Satoshi Washino,Suguru Shirotake,Makoto Kagawa,Hideki Takeshita,Yuji Miura,Yoji Hyodo,Masafumi Oyama,Satoru Kawakami,Tomoaki Miyagawa,Kazutaka Saito,Yukio Kageyama
出处
期刊:International Journal of Urology [Wiley]
卷期号:30 (9): 714-721 被引量:14
标识
DOI:10.1111/iju.15128
摘要

Objectives Although nivolumab plus ipilimumab has become a standard treatment regimen for metastatic clear cell renal cell carcinoma (ccRCC), its efficacy in non‐clear cell carcinoma (nccRCC) has not been fully examined. In the current study, we evaluated the clinical outcomes of nivolumab plus ipilimumab in nccRCC compared with ccRCC. Methods We retrospectively analyzed 22 patients with metastatic and/or locally advanced unresectable nccRCC who received nivolumab plus ipilimumab as a first‐line therapy and compared them with 107 patients with ccRCC. Objective response rate (ORR), progression‐free survival (PFS), overall survival (OS), and toxicity were compared between the nccRCC and ccRCC groups. Results The histology of nccRCC included eight papillary, six unclassified, three chromophobe, two collecting duct carcinoma, and three other subtypes. Best objective response in nccRCC patients included three complete responses and five partial responses, resulting in an ORR of 36%, while that in ccRCC patients was 50% ( p = 0.22). With a median follow‐up of 11.9 months, OS was significantly shorter in patients with nccRCC than in those with ccRCC (median 20.8 months vs. not reached, p = 0.04), while there was no significant difference in PFS (median 6.3 vs. 10.8 months, p = 0.21). Treatment‐related adverse events occurred in 14 (64%) nccRCC patients and 81 (76%) ccRCC patients. Conclusions Combination treatment with nivolumab and ipilimumab demonstrated modest clinical efficacy in patients with nccRCC compared with patients with ccRCC, suggesting it could be a therapeutic option for metastatic nccRCC patients.
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