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1
Targeting the HIF2-VEGF axis in renal cell carcinoma.靶向肾细胞癌中的 HIF2-VEGF 轴。
Nat Med. 2020 Oct;26(10):1519-1530. doi: 10.1038/s41591-020-1093-z. Epub 2020 Oct 5.
2
Safety and Clinical Activity of MEDI0562, a Humanized OX40 Agonist Monoclonal Antibody, in Adult Patients with Advanced Solid Tumors.在晚期实体瘤成人患者中,人源化 OX40 激动剂单克隆抗体 MEDI0562 的安全性和临床活性。
Clin Cancer Res. 2020 Oct 15;26(20):5358-5367. doi: 10.1158/1078-0432.CCR-19-3070. Epub 2020 Aug 14.
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Survival outcomes and independent response assessment with nivolumab plus ipilimumab versus sunitinib in patients with advanced renal cell carcinoma: 42-month follow-up of a randomized phase 3 clinical trial.纳武利尤单抗联合伊匹单抗对比舒尼替尼用于晚期肾细胞癌患者的生存结局和独立应答评估:一项随机 3 期临床试验的 42 个月随访结果。
J Immunother Cancer. 2020 Jul;8(2). doi: 10.1136/jitc-2020-000891.
4
The PD-1 Pathway Regulates Development and Function of Memory CD8 T Cells following Respiratory Viral Infection.PD-1 通路调节呼吸道病毒感染后记忆性 CD8+T 细胞的发育和功能。
Cell Rep. 2020 Jun 30;31(13):107827. doi: 10.1016/j.celrep.2020.107827.
5
Immunomodulatory Roles of VEGF Pathway Inhibitors in Renal Cell Carcinoma.血管内皮生长因子通路抑制剂在肾细胞癌中的免疫调节作用。
Drugs. 2020 Aug;80(12):1169-1181. doi: 10.1007/s40265-020-01327-7.
6
Salvage Ipilimumab and Nivolumab in Patients With Metastatic Renal Cell Carcinoma After Prior Immune Checkpoint Inhibitors.挽救性依匹单抗和纳武利尤单抗治疗既往免疫检查点抑制剂治疗后转移性肾细胞癌患者。
J Clin Oncol. 2020 Sep 20;38(27):3088-3094. doi: 10.1200/JCO.19.03315. Epub 2020 Jun 3.
7
Safety and efficacy of CDX-014, an antibody-drug conjugate directed against T cell immunoglobulin mucin-1 in advanced renal cell carcinoma.CDX-014,一种针对 T 细胞免疫球蛋白黏蛋白-1 的抗体药物偶联物,在晚期肾细胞癌中的安全性和疗效。
Invest New Drugs. 2020 Dec;38(6):1807-1814. doi: 10.1007/s10637-020-00945-y. Epub 2020 May 29.
8
Interplay of somatic alterations and immune infiltration modulates response to PD-1 blockade in advanced clear cell renal cell carcinoma.体细胞改变与免疫浸润的相互作用调节晚期透明细胞肾细胞癌对 PD-1 阻断的反应。
Nat Med. 2020 Jun;26(6):909-918. doi: 10.1038/s41591-020-0839-y. Epub 2020 May 29.
9
Evaluation of the Safety and Efficacy of Immunotherapy Rechallenge in Patients With Renal Cell Carcinoma.评估免疫治疗再挑战治疗肾细胞癌患者的安全性和疗效。
JAMA Oncol. 2020 Oct 1;6(10):1606-1610. doi: 10.1001/jamaoncol.2020.2169.
10
High systemic and tumor-associated IL-8 correlates with reduced clinical benefit of PD-L1 blockade.高系统和肿瘤相关的白细胞介素 8 与 PD-L1 阻断的临床获益降低相关。
Nat Med. 2020 May;26(5):693-698. doi: 10.1038/s41591-020-0860-1. Epub 2020 May 11.

超越传统免疫检查点抑制——肾细胞癌的新型免疫疗法

Beyond conventional immune-checkpoint inhibition - novel immunotherapies for renal cell carcinoma.

作者信息

Braun David A, Bakouny Ziad, Hirsch Laure, Flippot Ronan, Van Allen Eliezer M, Wu Catherine J, Choueiri Toni K

机构信息

Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.

Harvard Medical School, Boston, MA, USA.

出版信息

Nat Rev Clin Oncol. 2021 Apr;18(4):199-214. doi: 10.1038/s41571-020-00455-z. Epub 2021 Jan 12.

DOI:10.1038/s41571-020-00455-z
PMID:33437048
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8317018/
Abstract

The management of advanced-stage renal cell carcinoma (RCC) has been transformed by the development of immune-checkpoint inhibitors (ICIs). Nonetheless, most patients do not derive durable clinical benefit from these agents. Importantly, unlike other immunotherapy-responsive solid tumours, most RCCs have only a moderate mutational burden, and paradoxically, high levels of tumour CD8 T cell infiltration are associated with a worse prognosis in patients with this disease. Building on the successes of antibodies targeting the PD-1 and CTLA4 immune checkpoints, multiple innovative immunotherapies are now in clinical development for the treatment of patients with RCC, including ICIs with novel targets, co-stimulatory pathway agonists, modified cytokines, metabolic pathway modulators, cell therapies and therapeutic vaccines. However, the successful development of such novel immune-based treatments and of immunotherapy-based combinations will require a disease-specific framework that incorporates a deep understanding of RCC immunobiology. In this Review, using the structure provided by the well-described cancer-immunity cycle, we outline the key steps required for a successful antitumour immune response in the context of RCC, and describe the development of promising new immunotherapies within the context of this framework. With this approach, we summarize and analyse the most encouraging targets of novel immune-based therapies within the RCC microenvironment, and review the landscape of emerging antigen-directed therapies for this disease.

摘要

免疫检查点抑制剂(ICI)的发展改变了晚期肾细胞癌(RCC)的治疗方式。尽管如此,大多数患者并未从这些药物中获得持久的临床益处。重要的是,与其他对免疫疗法有反应的实体瘤不同,大多数RCC的突变负担仅为中等水平,而且矛盾的是,肿瘤CD8 T细胞浸润水平高与该疾病患者的预后较差相关。基于靶向PD-1和CTLA4免疫检查点抗体的成功,多种创新免疫疗法目前正在进行治疗RCC患者的临床开发,包括具有新靶点的ICI、共刺激途径激动剂、修饰细胞因子、代谢途径调节剂、细胞疗法和治疗性疫苗。然而,此类新型免疫疗法以及基于免疫疗法的联合疗法的成功开发将需要一个特定疾病的框架,该框架要深入理解RCC免疫生物学。在本综述中,我们利用描述详尽的癌症-免疫循环提供的结构,概述了RCC背景下成功的抗肿瘤免疫反应所需的关键步骤,并在该框架内描述了有前景的新免疫疗法的发展。通过这种方法,我们总结并分析了RCC微环境中新型免疫疗法最令人鼓舞的靶点,并综述了该疾病新兴的抗原导向疗法的情况。