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Updated: Jul 17, 2026

A Syngeneic Mouse Model of Metastatic Renal Cell Carcinoma for Quantitative and Longitudinal Assessment of Preclinical Therapies
Published on: April 12, 2017
Recent advances in the therapy of renal cancer
Guru Sonpavde1, Thomas E Hutson
1US Oncology Research, Houston, Texas, USA
Abstract:
Metastatic clear cell renal cell cancer has traditionally been treated with cytokines (interferon or interleukin-2). Improved understanding of biology has engendered novel targeted therapeutic agents that have radically altered the outlook. Vascular endothelial growth factor, the related receptor and the mTOR signal transduction pathway have particularly been exploited. Sunitinib malate, sorafenib and temsirolimus have improved clinical outcomes compared with interferon in randomized trials. Other multitargeted tyrosine kinase inhibitors (lapatinib, axatinib and pazopanib) and antiangiogenic agents (bevacizumab and lenalidomide) have also demonstrated activity in early studies. Combinations of these agents are being evaluated. The future of the therapy of renal cancer appears promising owing to the efficacy of these novel agents. Clinical trials designed to further assess these and other agents need to be vigorously supported.
Insights
Novel targeted therapies, including tyrosine kinase inhibitors and antiangiogenic agents, show improved outcomes for metastatic clear cell renal cell cancer compared to traditional cytokine treatments. Further clinical trials are essential to support these promising advancements.
Area of Science:
- Oncology
- Pharmacology
Background:
- Metastatic clear cell renal cell cancer was historically treated with cytokines like interferon and interleukin-2.
- Recent advancements in understanding cancer biology have led to the development of novel targeted therapies.
Purpose of the Study:
- To review the impact of novel targeted therapeutic agents on the treatment of metastatic clear cell renal cell cancer.
- To highlight the efficacy of agents targeting vascular endothelial growth factor, its receptor, and the mTOR pathway.
Main Methods:
- Review of clinical outcomes from randomized trials comparing novel agents to interferon.
- Evaluation of early studies on multitargeted tyrosine kinase inhibitors and antiangiogenic agents.
- Assessment of ongoing combination therapy trials.
Main Results:
- Sunitinib malate, sorafenib, and temsirolimus demonstrated improved clinical outcomes versus interferon in randomized trials.
- Other agents like lapatinib, axatinib, pazopanib, bevacizumab, and lenalidomide showed activity in early studies.
- Combination therapies are currently under evaluation.
Conclusions:
- Novel targeted agents have significantly improved the treatment outlook for renal cell cancer.
- The efficacy of these agents suggests a promising future for renal cancer therapy.
- Vigorous support for ongoing and future clinical trials is crucial.
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