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Updated: May 20, 2026

A Syngeneic Mouse Model of Metastatic Renal Cell Carcinoma for Quantitative and Longitudinal Assessment of Preclinical Therapies
Published on: April 12, 2017
Novel agents and approaches for advanced renal cell carcinoma
Robert Figlin1, Cora Sternberg, Christopher G Wood
1Department of Medicine, Samuel Oschin Comprehensive Cancer Institute, Cedars-Sinai Medical Center, Los Angeles, California 90048, USA. robert.figlin@cshs.org
Purpose:
Targeted agents have changed the treatment paradigm for advanced renal cell carcinoma. Approved agents with demonstrated efficacy are sunitinib, sorafenib, pazopanib, bevacizumab, temsirolimus and everolimus. However, there is an unmet need for new agents to improve the clinical outcome in treatment naïve patients and in those who are disease refractory or intolerant to traditional and targeted therapies. Many novel targeted agents, of which some have different mechanisms of action than approved agents, and immunomodulatory agents are currently in development for renal cell carcinoma.
Materials And Methods:
We searched ClinicalTrials.gov to identify novel agents for advanced renal cell carcinoma in ongoing phase II/III clinical trials. Using the relevant agents as search terms we reviewed the medical literature for mechanisms of action and efficacy, and safety results to date, including data from recent major oncology meetings.
Results:
A total of 11 novel targeted agents, including next generation tyrosine kinase inhibitors, and inhibitors of vascular endothelial growth factor ligand binding, Akt and endothelial cell proliferation, and 3 novel immunomodulatory agents, are under evaluation for renal cell carcinoma. In addition to ongoing phase II/III trials of emerging agents, head-to-head, crossover and combination trials of approved targeted agents are under way.
Conclusions:
Although many agents are approved or in development for renal cell carcinoma, comparative effectiveness data are lacking. Ongoing and future head-to-head trials using appropriate comparators are essential to update renal cell carcinoma treatment guidelines. Future research should be aimed at identifying agents that improve patient outcomes and have decreased toxicity compared with currently approved agents with the goal of complete remission.
Insights
New targeted and immunomodulatory agents show promise for advanced renal cell carcinoma (RCC). Further head-to-head trials are needed to compare effectiveness and reduce toxicity in RCC treatment.
Area of Science:
- Oncology
- Pharmacology
- Clinical Trials
Background:
- Advanced renal cell carcinoma (RCC) treatment has been transformed by targeted agents.
- Approved therapies include sunitinib, sorafenib, pazopanib, bevacizumab, temsirolimus, and everolimus.
- An unmet need exists for improved outcomes in treatment-naïve, refractory, or intolerant RCC patients.
Purpose of the Study:
- To identify novel agents for advanced renal cell carcinoma (RCC) in ongoing phase II/III clinical trials.
- To review mechanisms of action, efficacy, and safety data of emerging RCC therapies.
- To assess the current landscape of novel targeted and immunomodulatory agents in RCC development.
Main Methods:
- Searched ClinicalTrials.gov for novel agents in advanced RCC.
- Reviewed medical literature for mechanisms, efficacy, and safety of identified agents.
- Included data from recent major oncology meetings for comprehensive review.
Main Results:
- Eleven novel targeted agents, including next-generation tyrosine kinase inhibitors and pathway inhibitors, are under evaluation for advanced RCC.
- Three novel immunomodulatory agents are also being investigated for RCC.
- Ongoing phase II/III trials include emerging agents and head-to-head, crossover, and combination trials of approved targeted agents.
Conclusions:
- Despite numerous agents approved or in development for advanced RCC, comparative effectiveness data are limited.
- Head-to-head trials with appropriate comparators are crucial for updating RCC treatment guidelines.
- Future research should focus on identifying agents with improved patient outcomes and reduced toxicity for complete remission in RCC.
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