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检查点抑制剂免疫疗法在肾癌中的应用。

Checkpoint inhibitor immunotherapy in kidney cancer.

机构信息

Beth Israel Deaconess Medical Center, Boston, MA, USA.

MedStar Georgetown University Hospital, Washington, DC, USA.

出版信息

Nat Rev Urol. 2020 Mar;17(3):137-150. doi: 10.1038/s41585-020-0282-3. Epub 2020 Feb 4.

Abstract

Kidney cancer has unique features that make this malignancy attractive for therapeutic approaches that target components of the immune system. Immune checkpoint inhibition is a well-established part of kidney cancer treatment, and rapid advances continue to be made in this field. Initial preclinical studies that elucidated the biology of the programmed cell death 1 (PD-1), programmed cell death 1 ligand 1 (PD-L1) and cytotoxic T lymphocyte antigen 4 (CTLA-4) immune checkpoints led to a series of clinical trials that resulted in regulatory approval of nivolumab and the combination of ipilimumab plus nivolumab for the treatment of advanced renal cell carcinoma. Subsequent data led to approvals of combination strategies of immune checkpoint inhibition plus agents that target the vascular endothelial growth factor receptor and a shift in the current standard of renal cell carcinoma care. However, controversies remain regarding the optimal therapy selection and treatment strategy for individual patients, which might be eventually overcome by current intensive efforts in biomarker research. That work includes evaluation of tumour cell PD-L1 expression, gene expression signatures, CD8 T cell density and others. In the future, further advances in the understanding of immune checkpoint biology might reveal new therapeutic targets beyond PD-1, PD-L1 and CTLA-4, as well as new combination approaches.

摘要

肾癌具有独特的特征,使其成为针对免疫系统成分的治疗方法的理想选择。免疫检查点抑制是肾癌治疗的一个成熟部分,该领域的进展仍在迅速推进。最初阐明程序性细胞死亡蛋白 1(PD-1)、程序性细胞死亡蛋白配体 1(PD-L1)和细胞毒性 T 淋巴细胞抗原 4(CTLA-4)免疫检查点生物学的临床前研究,导致了一系列临床试验,从而监管部门批准了纳武单抗和伊匹单抗联合纳武单抗用于治疗晚期肾细胞癌。随后的数据导致了免疫检查点抑制联合靶向血管内皮生长因子受体的药物的联合治疗策略的批准,并改变了当前肾细胞癌治疗的标准。然而,对于个体患者的最佳治疗选择和治疗策略仍存在争议,这可能最终会被当前在生物标志物研究方面的密集努力所克服。这项工作包括评估肿瘤细胞 PD-L1 表达、基因表达谱、CD8 T 细胞密度等。未来,对免疫检查点生物学的进一步了解可能会揭示除 PD-1、PD-L1 和 CTLA-4 之外的新的治疗靶点,以及新的联合治疗方法。

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