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What is the optimal therapy for patients with metastatic renal cell carcinoma who progress on an initial VEGFr-TKI?
Emiliano Calvo1, Alain Ravaud, Joaquim Bellmunt
1Centro Integral Oncológico Clara Campal and START Madrid, Madrid, Spain. emiliano.calvo@start.stoh.com
Abstract:
Sequential treatment with targeted therapies is the current standard of care for patients with metastatic renal cell carcinoma (mRCC). Most patients are initially treated with a first-line vascular endothelial growth factor receptor-tyrosine kinase inhibitor (VEGFr-TKI), but will eventually develop resistance and subsequent disease progression. Patients with mRCC whose disease progresses during initial VEGFr-TKI therapy may continue treatment with a different VEGFr-TKI or they may switch to treatment with a mammalian target of rapamycin (mTOR) inhibitor which has a different mechanism of action. Based on positive results of the phase III RECORD-1 trial, clinical guidelines in the United States and Europe recommend use of everolimus, an mTOR inhibitor, in patients with VEGFr-TKI-refractory mRCC. Positive results of the phase III AXIS trial led to recent approval in the United States of the VEGFr-TKI axitinib for use in patients with mRCC who failed one previous therapy. VEGFr-TKIs and mTOR inhibitors have distinct clinical effects with differing safety profiles, but to date, no head-to-head comparisons in the post-VEGFr-TKI second-line setting are available. This review discusses multiple factors that should be considered when selecting a second-line therapy for patients with VEGFr-TKI-refractory mRCC, including evidence-based guidelines, efficacy, safety, patient profile, and clinician familiarity with available agents.
Insights
For metastatic renal cell carcinoma (mRCC) progressing on vascular endothelial growth factor receptor-tyrosine kinase inhibitors (VEGFr-TKIs), selecting second-line therapy involves considering guidelines, efficacy, and safety. This review aids clinicians in choosing between different VEGFr-TKIs or mammalian target of rapamycin (mTOR) inhibitors.
Area of Science:
- Oncology
- Pharmacology
Background:
- Metastatic renal cell carcinoma (mRCC) treatment typically involves sequential targeted therapies.
- Vascular endothelial growth factor receptor-tyrosine kinase inhibitors (VEGFr-TKIs) are common first-line treatments, but resistance eventually develops.
- Second-line options include alternative VEGFr-TKIs or mammalian target of rapamycin (mTOR) inhibitors.
Purpose of the Study:
- To review factors influencing second-line therapy selection for patients with VEGFr-TKI-refractory mRCC.
- To provide guidance for clinicians managing treatment-resistant mRCC.
Main Methods:
- Review of clinical guidelines and phase III trial data (RECORD-1, AXIS).
- Discussion of efficacy, safety profiles, and patient-specific factors.
- Analysis of distinct clinical effects of VEGFr-TKIs and mTOR inhibitors.
Main Results:
- Everolimus (mTOR inhibitor) is recommended by guidelines for VEGFr-TKI-refractory mRCC.
- Axitinib (VEGFr-TKI) is approved for mRCC after one prior therapy.
- No direct head-to-head comparisons exist for second-line treatments post-VEGFr-TKI therapy.
Conclusions:
- Selection of second-line therapy requires careful consideration of evidence-based guidelines.
- Patient profile, clinician familiarity, efficacy, and safety are critical factors.
- Optimizing treatment for VEGFr-TKI-refractory mRCC necessitates a personalized approach.
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