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Updated: Apr 21, 2026

A Syngeneic Mouse Model of Metastatic Renal Cell Carcinoma for Quantitative and Longitudinal Assessment of Preclinical Therapies
Published on: April 12, 2017
Optimal first-line and second-line treatments for metastatic renal cell carcinoma: current evidence
Maxine Sun1, Alessandro Larcher2, Pierre I Karakiewicz1
1Cancer Prognostics and Health Outcomes Unit, University of Montreal Health Center, Montreal, QC, Canada.
Abstract:
Since 2005, an abundance of targeted agents has been approved for the treatment of metastatic renal cell carcinoma (mRCC), without any specification as to what may be the most optimal first-line and second-line sequence. Hence, our objective was to critically examine the evidence supporting the use of first-line and second-line agents in the management of mRCC. Our review suggests that in first line, sunitinib and pazopanib represent treatment options for patients with favorable or intermediate-risk features and clear cell histology. Unfortunately, the Phase III trial cannot conclusively prove the noninferiority of pazopanib relative to sunitinib. Hence, the use of sunitinib as first-line standard of care remains justified. Pazopanib represents an option for specific patients in whom sunitinib might not be tolerated. In patients with poor-risk features, temsirolimus represents the only option supported with level 1 evidence. Less optimal alternatives include sunitinib and bevacizumab combined with interferon, based on the minimal inclusion of poor-risk patients in pivotal Phase III studies of these two molecules. In patients with non-clear cell mRCC, the use of temsirolimus is supported by Phase III data, unlike for any other molecule. In second line, the options consist of everolimus and axitinib. However, the axitinib data are substantially more robust given the inclusion of more patients considered as true second-line, and validly justify the choice of axitinib over everolimus. Nonetheless, the Phase III trial of everolimus may be considered as level 1 evidence for use as third-line or subsequent lines of therapy.
Insights
For metastatic renal cell carcinoma (mRCC), sunitinib is a justified first-line treatment. Axitinib shows more robust data for second-line therapy compared to everolimus in mRCC patients.
Area of Science:
- Oncology
- Pharmacology
- Clinical Trial Analysis
Background:
- Numerous targeted therapies for metastatic renal cell carcinoma (mRCC) approved since 2005 lack defined optimal sequencing.
- Uncertainty exists regarding the best first-line and second-line treatment strategies for mRCC management.
Purpose of the Study:
- To critically evaluate the evidence base for first-line and second-line targeted agents in metastatic renal cell carcinoma (mRCC).
- To provide guidance on optimal sequencing of therapies for mRCC based on current clinical trial data.
Main Methods:
- Systematic review and critical appraisal of Phase III clinical trial data for targeted agents in mRCC.
- Analysis of treatment efficacy and safety profiles based on patient risk stratification and histology.
Main Results:
- First-line: Sunitinib and pazopanib are options for favorable/intermediate-risk clear cell mRCC; sunitinib is the justified standard due to non-inferiority trial limitations for pazopanib.
- First-line: Temsirolimus is the sole option with Level 1 evidence for poor-risk mRCC; sunitinib and bevacizumab/interferon are less optimal.
- Second-line: Axitinib demonstrates more robust data than everolimus; everolimus has Level 1 evidence for third-line or subsequent therapy.
Conclusions:
- Sunitinib remains a preferred first-line standard for specific mRCC patient groups.
- Axitinib is a more robust choice for second-line treatment in mRCC.
- Temsirolimus is indicated for poor-risk and non-clear cell mRCC, and everolimus for later lines of therapy.
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