Centro Integral Oncológico Clara Campal and START Madrid, Madrid, Spain
Medical Oncology, I.R.C.C.S. San Matteo University Hospital Foundation, Pavia, Italy.
Oncologist. 2019 Mar;24(3):338-348. doi: 10.1634/theoncologist.2018-0267. Epub 2018 Aug 29.
Agents targeting the vascular endothelial growth factor (VEGF) and its receptors (VEGFRs), as well as the mammalian target of rapamycin (mTOR) and immune checkpoint receptor programmed death 1 (PD-1) signaling pathway have improved clinical outcomes for patients with advanced renal cell carcinoma (RCC). The VEGFR tyrosine kinase inhibitors (TKIs) pazopanib and sunitinib are FDA-approved first-line treatment options for advanced RCC; however, other treatment options in this setting are available, including the recently approved combination of nivolumab (anti-PD-1) and ipilimumab (anti-cytotoxic T-lymphocyte-associated protein-4 [CTLA-4]) for patients with intermediate or poor risk. Unfortunately, treatment guideline recommendations provide little guidance to aid first-line treatment choice. In addition, several ongoing randomized phase III trials of investigational first-line regimens may complicate the RCC treatment paradigm if these agents gain approval. This article reviews clinical trial and real-world evidence for currently approved and investigational first-line treatment regimens for advanced RCC and provides clinical evidence to aid first-line treatment selection. IMPLICATIONS FOR PRACTICE: Vascular endothelial growth factor receptor tyrosine kinase inhibitors are approved by the U.S. Food and Drug Administration as first-line treatment options for advanced renal cell carcinoma; however, the treatment paradigm is rapidly evolving. The combination of nivolumab plus ipilimumab was recently approved for intermediate- and poor-risk patients, and other combination strategies and novel first-line agents will likely be introduced soon.
针对血管内皮生长因子 (VEGF) 及其受体 (VEGFRs) 以及哺乳动物雷帕霉素靶蛋白 (mTOR) 和免疫检查点受体程序性死亡 1 (PD-1) 信号通路的药物已改善了晚期肾细胞癌 (RCC) 患者的临床结局。血管内皮生长因子受体酪氨酸激酶抑制剂 (TKI) 帕唑帕尼和舒尼替尼已获美国食品和药物管理局 (FDA) 批准作为晚期 RCC 的一线治疗选择;然而,该治疗环境中还有其他治疗选择,包括最近批准的纳武单抗(抗 PD-1)和伊匹单抗(抗细胞毒性 T 淋巴细胞相关蛋白 4 [CTLA-4])联合用于中危或高危患者。不幸的是,治疗指南建议几乎没有提供指导以帮助进行一线治疗选择。此外,如果这些药物获得批准,几项正在进行的研究性一线治疗方案的随机 III 期临床试验可能会使 RCC 治疗模式复杂化。本文综述了目前批准的和研究性的晚期 RCC 一线治疗方案的临床试验和真实世界证据,并提供了有助于一线治疗选择的临床证据。
血管内皮生长因子受体酪氨酸激酶抑制剂已获 FDA 批准作为晚期肾细胞癌的一线治疗选择;然而,治疗模式正在迅速发展。纳武单抗联合伊匹单抗最近被批准用于中危和高危患者,其他联合治疗策略和新型一线药物可能很快会被引入。