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T-cell checkpoint inhibitors in metastatic renal cell carcinoma

机译:转移性肾细胞癌的T细胞检查点抑制剂

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Purpose of reviewThe advent of checkpoint inhibitors has fostered great expectations for long-term outcome in cancer patients. Inhibitors of programmed death -1, programmed death ligand-1 and cytotoxic T-lymphocyte associated protein 4 are targets of contemporary cancer immunotherapy. Current phase III studies are ongoing and may define a novel treatment paradigm in metastatic renal cell carcinoma (mRCC). This review focuses on current clinical data in mRCC.Recent findingsNivolumab and ipilimumab are the most advanced checkpoint inhibitors in the field of mRCC. Current available data include phase I and randomized phase II trials, investigating single agent or combination therapies in mRCC, with objective responses in 20-52% of patients and 19-26 months overall survival in previously treated patients.SummaryImmunotherapies have fostered great expectations on long-term overall survival in mRCC. As seen with previous cytokine treatment, long-term response is a key clinical outcome. Phase III data for previously treated patients are expected later this year and may define a novel standard for treatment. Combinational therapies have generated promising response data, indicating a potential role in treatment intensification in mRCC. Combination treatment is associated with ample toxicity, which might restrict this approach to selected patients. The major task for the future is to tailor immunotherapy for individual patients.
机译:复习目的检查点抑制剂的出现使人们对癌症患者的长期结果抱有很高的期望。程序性死亡-1,程序性死亡配体-1和细胞毒性T淋巴细胞相关蛋白4的抑制剂是当代癌症免疫疗法的目标。当前的第三阶段研究正在进行中,可能会为转移性肾细胞癌(mRCC)定义新的治疗范例。这篇综述着重于mRCC的当前临床数据。最近的发现Nivolumab和ipilimumab是mRCC领域中最先进的检查点抑制剂。目前可用的数据包括I期和II期随机试验,研究mRCC中的单药或联合疗法,对20-52%的患者有客观的反应,以前接受过治疗的患者的总生存期为19-26个月。 mRCC的长期总体生存率。如以前的细胞因子治疗所见,长期反应是关键的临床结果。先前接受治疗的患者的III期数据有望在今年晚些时候发布,并可能定义一种新的治疗标准。组合疗法已产生了令人鼓舞的反应数据,表明在mRCC的治疗强化中有潜在作用。联合治疗与充分的毒性​​相关,这可能会将这种方法限制于特定的患者。未来的主要任务是为个别患者量身定制免疫疗法。

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