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Modeling Spontaneous Metastatic Renal Cell Carcinoma (mRCC) in Mice Following Nephrectomy
Published on: April 29, 2014
How to carry out retrospective studies in metastatic renal cell cancer: two caveats that should be avoided
Giuseppe Di Lorenzo1, Matteo Ferro, Carlo Buonerba
1Dipartimento di Endocrinologia e Oncologia Clinica e Molecolare, Università Federico II, Napoli, Italy. giuseppedilorenzoncol@hotmail.com
Abstract:
The results achieved with targeted therapy have changed the natural course of kidney cancer not amenable to local therapy. Sunitinib, bevacizumab and pazopanib are approved in the first-line setting for patients at good/intermediate prognosis, while temsirolimus should be the first-line agent to be used in patients at poor prognosis. The oncology community has been eagerly awaiting results as far as second-line treatment is concerned. The RECORD-1 and AXIS trials provided evidence in favor of everolimus and axitinib, respectively, in patients pretreated with VEGF-directed agents. As the number of available agents grows, so does the possibility of using multiple lines of therapy with a potential benefit in overall survival. The third-line setting has been poorly investigated, and no comparative prospective trials are presently available. Retreatment with VEGF-directed therapy may be an option in everolimus-pretreated patients, with the possibility that mTOR inhibitors may reverse resistance to VEGF-directed therapy. Grunwald et al. presented retrospective data showing that retreatment with VEGF-directed targeted agents, including sunitinib, bevacizumab/interferon, dovitinib and sorafenib, was associated with a progression-free survival time of approximately 5 months. Although the evidence provided by retrospective studies is weak, their role in highlighting matters of clinical relevance deserving investigation is undoubtful, as demonstrated by the retrospective study discussed in this paper.
Insights
Targeted therapies have transformed kidney cancer treatment. Retreatment with vascular endothelial growth factor (VEGF)-directed agents shows promise in later lines of therapy, particularly after mTOR inhibitor treatment.
Area of Science:
- Oncology
- Nephrology
- Pharmacology
Background:
- Targeted therapies have significantly altered the treatment landscape for advanced kidney cancer.
- First-line treatment options like sunitinib, bevacizumab, and pazopanib are established for good/intermediate prognosis, while temsirolimus is indicated for poor prognosis.
Discussion:
- Second-line treatments such as everolimus and axitinib are effective after vascular endothelial growth factor (VEGF)-directed therapy.
- The third-line setting remains under-investigated, with limited prospective comparative trials.
- Retreatment with VEGF-directed agents, even after mTOR inhibitor therapy, is a potential strategy.
Key Insights:
- Retrospective data suggest retreatment with VEGF-targeted agents can yield approximately 5 months of progression-free survival.
- mTOR inhibitors might potentially reverse resistance to VEGF-directed therapy.
- Retrospective studies, despite limitations, identify clinically relevant areas for future research.
Outlook:
- Further prospective trials are needed to validate third-line treatment strategies and retreatment options.
- Investigating the sequence and combination of targeted agents may optimize overall survival benefits.
- Understanding mechanisms of resistance and cross-talk between targeted pathways is crucial for future drug development.
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