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The Immunotherapy Landscape in Renal Cell Carcinoma.

Publication ,  Journal Article
Brown, LC; Desai, K; Zhang, T; Ornstein, MC
Published in: BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy
December 2020

The past 30 years have borne witness to a gradual evolution in the treatment landscape of advanced renal cell carcinoma (aRCC). Early immunotherapy approaches such as interferon-α and high-dose interleukin-2 (IL-2) therapy in this immunogenic tumor provided durable responses in only a minority of patients and came with toxic side effects. A growing understanding of the tumor biology elucidated pathways of tumorigenesis, which in turn revealed novel targets amenable to targeted therapies. Inhibition of angiogenesis and cell signaling emerged as cornerstones of treatment with the approval of bevacizumab and several pan-kinase and tyrosine kinase inhibitors. Though effective, their use has been limited by low rates of durable response, resistance, and side effects. The immunotherapy revolution of the past decade has led to immunotherapy-based combination regimens such as ipilimumab plus nivolumab, pembrolizumab plus axitinib, and avelumab plus axitinib, displacing single agent anti-angiogenic therapy in the first-line setting by demonstrating durable responses and improved survival over sunitinib. These immunotherapy-based combinations define first-line standard of care for aRCC today. The pipeline of second-line agents for consideration in patients who have disease progression despite immunotherapy regimens is robust but still in early stages of development.

Duke Scholars

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Published In

BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy

DOI

EISSN

1179-190X

ISSN

1173-8804

Publication Date

December 2020

Volume

34

Issue

6

Start / End Page

733 / 748

Related Subject Headings

  • Sunitinib
  • Kidney Neoplasms
  • Immunotherapy
  • Immunology
  • Humans
  • Carcinoma, Renal Cell
  • Axitinib
  • 3214 Pharmacology and pharmaceutical sciences
  • 1115 Pharmacology and Pharmaceutical Sciences
 

Citation

APA
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ICMJE
MLA
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Brown, L. C., Desai, K., Zhang, T., & Ornstein, M. C. (2020). The Immunotherapy Landscape in Renal Cell Carcinoma. BioDrugs : Clinical Immunotherapeutics, Biopharmaceuticals and Gene Therapy, 34(6), 733–748. https://doi.org/10.1007/s40259-020-00449-4
Brown, Landon C., Kunal Desai, Tian Zhang, and Moshe C. Ornstein. “The Immunotherapy Landscape in Renal Cell Carcinoma.BioDrugs : Clinical Immunotherapeutics, Biopharmaceuticals and Gene Therapy 34, no. 6 (December 2020): 733–48. https://doi.org/10.1007/s40259-020-00449-4.
Brown LC, Desai K, Zhang T, Ornstein MC. The Immunotherapy Landscape in Renal Cell Carcinoma. BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy. 2020 Dec;34(6):733–48.
Brown, Landon C., et al. “The Immunotherapy Landscape in Renal Cell Carcinoma.BioDrugs : Clinical Immunotherapeutics, Biopharmaceuticals and Gene Therapy, vol. 34, no. 6, Dec. 2020, pp. 733–48. Epmc, doi:10.1007/s40259-020-00449-4.
Brown LC, Desai K, Zhang T, Ornstein MC. The Immunotherapy Landscape in Renal Cell Carcinoma. BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy. 2020 Dec;34(6):733–748.
Journal cover image

Published In

BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy

DOI

EISSN

1179-190X

ISSN

1173-8804

Publication Date

December 2020

Volume

34

Issue

6

Start / End Page

733 / 748

Related Subject Headings

  • Sunitinib
  • Kidney Neoplasms
  • Immunotherapy
  • Immunology
  • Humans
  • Carcinoma, Renal Cell
  • Axitinib
  • 3214 Pharmacology and pharmaceutical sciences
  • 1115 Pharmacology and Pharmaceutical Sciences