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Modeling Spontaneous Metastatic Renal Cell Carcinoma (mRCC) in Mice Following Nephrectomy
Published on: April 29, 2014
Advanced renal cell carcinoma: what to do after first line antiangiogenic therapy?
1Hematologist and Medical Oncologist, Centre Hospitalier de l'Université de Montréal, Montreal, Quebec, Canada. Denis.soulieres.chum@ssss.gouv.qc.ca
Purpose Of Review:
Antiangiogenic therapy is now a standard in first line for metastatic renal cell carcinoma. Among the different options, sunitinib is particularly proposed by most guidelines, as well as a combination of bevacizumab and interferon-alfa. Defining second line therapy after these agents is dependent on indirect data since no phase III trial has specifically addressed that question.
Recent Findings:
The most relevant data point to everolimus that has been proven to improve PFS with acceptable toxicity compared with best supportive care in a phase III trial. Most studies on the use of antiangiogenic therapies after failure of a first one seem to demonstrate, more than anything else, that the most effective antiangiogenic therapy should be used up front since limited benefit is expected in second line.
Summary:
This paper presents some relevant data to help recommend the most appropriate second-line therapy. The quality of data on everolimus is sufficient to propose its use for most patients in the second line setting after failure of a vascular endothelial growth factor receptor-tyrosine kinase inhibitor (VEGFR-TKI). Studies on a second line of antiangiogenic therapy demonstrate limited efficacy that does not lead to a recommendation of adequacy for most patients.
Insights
For metastatic renal cell carcinoma, everolimus shows promise as a second-line therapy after initial antiangiogenic treatment failure. Limited benefit is observed with subsequent antiangiogenic therapies, suggesting upfront use of the most effective agents.
Area of Science:
- Oncology
- Medical Research
- Clinical Trials
Background:
- Antiangiogenic therapy is a standard first-line treatment for metastatic renal cell carcinoma (mRCC).
- Sunitinib and bevacizumab with interferon-alfa are common first-line options.
- Limited phase III data exists for second-line therapy after these agents.
Purpose of the Study:
- To review data and recommend appropriate second-line therapy for mRCC.
- To evaluate the efficacy of treatments following first-line antiangiogenic therapy failure.
Main Methods:
- Review of existing clinical trial data, including phase III trials.
- Analysis of treatment outcomes for second-line therapies in mRCC.
Main Results:
- Everolimus demonstrated improved progression-free survival (PFS) with acceptable toxicity in a phase III trial.
- Subsequent antiangiogenic therapies show limited efficacy in the second-line setting.
- Data suggests prioritizing the most effective antiangiogenic therapy in the first line.
Conclusions:
- Everolimus is a viable option for second-line treatment after vascular endothelial growth factor receptor-tyrosine kinase inhibitor (VEGFR-TKI) failure.
- Second-line antiangiogenic therapy generally offers limited benefit.
- Current data supports everolimus for most patients in the second-line setting.
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