The roaring 2020s: a new decade of systemic therapy for renal cell carcinoma

被引:17
|
作者
Srivastava, Arnav [1 ]
Doppalapudi, Sai K. [1 ]
Patel, Hiren, V [1 ]
Srinivasan, Ramaprasad [2 ]
Singer, Eric A. [1 ]
机构
[1] Rutgers Canc Inst New Jersey, Sect Urol Oncol, New Brunswick, NJ 08903 USA
[2] NCI, Urol Oncol Branch, Ctr Canc Res, NIH, Bethesda, MD USA
基金
美国国家卫生研究院;
关键词
clear cell renal cell carcinoma; hypoxia inducible factor inhibitor; immune checkpoint inhibitors; nonclear cell renal cell carcinoma; systemic therapy; ENDOTHELIAL GROWTH-FACTOR; TARGETED THERAPY; OPEN-LABEL; PHASE-II; SUNITINIB; CABOZANTINIB; SURVIVAL; PEMBROLIZUMAB; NEPHRECTOMY; CHECKPOINT;
D O I
10.1097/CCO.0000000000000831
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose of review The genomic and immunologic profiling of renal cell carcinoma (RCC) has provided the impetus for advancements in systemic treatments using combination therapy - either with immune check point inhibitor (ICI) + ICI or with ICI + targeted therapy. This approach has been examined in several landmark trials, treating both clear cell (ccRCC) and nonclear cell (nccRCC) histologies. In this review, we highlight systemic therapy advancements made in this new decade, the 2020s. Recent findings Targeting the programmed death receptor 1/PD-L1 pathway has created more tolerable and effective immunotherapy regimens, expanding the applications of ICIs. These new applications, paired with trial data, include ICI monotherapy in nccRCC and adjuvant pembrolizumab in resected, high-risk RCC. In addition, ICI + ICI and ICI + TKI combination therapy have demonstrated oncologic efficacy in advanced ccRCC and sarcomatoid RCC. Similar progress has been noted regarding new targeted therapies. Along the hypoxia inducible factor pathway, belzutifan has received FDA approval in von Hippel-Lindau-associated RCC. In addition, in papillary RCC, agents such as cabozantinib target the MET proto-oncogene pathway and have demonstrated impressive oncologic outcomes. The 2020s utilize the molecular profiling of advanced RCC as a scaffold for recent trials in immunotherapy and targeted therapies. Going forward, emphasizing patient-reported outcomes and careful clinical trial construction remain critical to improve systemic therapy in RCC.
引用
收藏
页码:234 / 242
页数:9
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