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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 treatment of metastatic renal cell carcinoma
1Department of Urology, Dokkyo Medical University, Mibu, Tochigi, Japan.
Abstract:
In the past 5 years, the treatment of patients with metastatic renal cell carcinoma has changed dramatically from being largely cytokine-based with the emergence of targeted therapy. Following the elucidation of various molecular pathways in renal cell carcinoma, targeted agents (particularly vascular endothelial growth factor-targeting antiangiogenic agents) now form the backbone of most therapeutic strategies for patients with metastatic renal cell carcinoma and the outcome of treatment has improved. However, many tumors eventually develop resistance to targeted therapy due to secondary mutation of the target protein or compensatory changes within the target pathway that bypass the site of inhibition. On the other hand, there are new forms of immunotherapy that hold the promise of improving the outcome for patients with metastatic renal cell carcinoma. In this article, we describe some of these new therapies, including the anti-vascular endothelial growth factor monoclonal antibody bevacizumab, several receptor tyrosine kinase inhibitors (sorafenib, sunitinib, pazopanib, axitinib, and tivozanib), the mammalian target of rapamycin inhibitors temsirolimus and everolimus, and new immunotherapy modalities, such as anti-cytotoxic T-lymphocyte-associated antigen 4 antibody and anti-programmed cell death 1/programmed cell death-ligand 1 antibody. We also discuss their role in the current management of patients with metastatic renal cell carcinoma.
Insights
Targeted therapies have improved outcomes for metastatic renal cell carcinoma (mRCC) but resistance is common. New immunotherapies offer promise for better mRCC treatment outcomes.
Area of Science:
- Oncology
- Pharmacology
Background:
- Metastatic renal cell carcinoma (mRCC) treatment has shifted from cytokine-based therapies to targeted agents.
- Targeted therapies, especially anti-angiogenic agents, are now standard for mRCC, improving outcomes.
- Tumor resistance to targeted therapy develops through secondary mutations or pathway bypass.
Purpose of the Study:
- To review emerging targeted therapies and immunotherapies for metastatic renal cell carcinoma.
- To discuss the role of these novel agents in current mRCC management.
Main Methods:
- Review of anti-vascular endothelial growth factor monoclonal antibody (bevacizumab).
- Summary of receptor tyrosine kinase inhibitors (sorafenib, sunitinib, pazopanib, axitinib, tivozanib).
- Overview of mammalian target of rapamycin (mTOR) inhibitors (temsirolimus, everolimus) and immunotherapies (anti-CTLA-4, anti-PD-1/PD-L1 antibodies).
Main Results:
- Targeted agents form the backbone of mRCC treatment, improving outcomes.
- Resistance to targeted therapy is a significant clinical challenge.
- New immunotherapies show promise for enhancing patient outcomes in mRCC.
Conclusions:
- Despite advances, resistance to targeted therapies necessitates exploration of novel treatment strategies.
- Emerging immunotherapies represent a promising frontier for improving metastatic renal cell carcinoma management.
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