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

被引:258
作者
Braun, David A. [1 ,2 ,3 ]
Bakouny, Ziad [1 ]
Hirsch, Laure [1 ,2 ,4 ]
Flippot, Ronan [4 ]
Van Allen, Eliezer M. [1 ,2 ,3 ]
Wu, Catherine J. [1 ,2 ,3 ]
Choueiri, Toni K. [1 ,2 ]
机构
[1] Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
[2] Harvard Med Sch, Boston, MA 02115 USA
[3] Broad Inst MIT & Harvard, Cambridge, MA 02142 USA
[4] Gustave Roussy, Dept Med Oncol, Villejuif, France
关键词
TUMOR-INFILTRATING LYMPHOCYTES; REDUCED CLINICAL BENEFIT; CARBONIC-ANHYDRASE-IX; ENGINEERED T-CELLS; RECOMBINANT INTERLEUKIN-2; MONOCLONAL-ANTIBODY; CANCER REGRESSION; TIM-3; EXPRESSION; 1ST-LINE THERAPY; PATIENTS PTS;
D O I
10.1038/s41571-020-00455-z
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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.
引用
收藏
页码:199 / 214
页数:16
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