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Updated: May 5, 2026

Pre-clinical Evaluation of Tyrosine Kinase Inhibitors for Treatment of Acute Leukemia
Published on: September 18, 2013
Novel tyrosine kinase inhibitors for renal cell carcinoma
Tanya B Dorff1, Sumanta K Pal, David I Quinn
1Department of Medicine, USC Keck School of Medicine, USC Norris Comprehensive Cancer Center, 1441 Eastlake Ave. #3440, Los Angeles, CA 90033, USA.
Abstract:
Although targeted therapy against VEGF and mTOR have revolutionized the treatment of advanced renal cell carcinoma (RCC), additional agents are required due to toxicity and resistance to currently available drugs. Some next-generation tyrosine kinase inhibitors have focused on VEGF, narrowing the spectrum of receptors which are inhibited and enhancing binding affinity. However, targeting novel receptors with tyrosine kinase inhibition of additional receptor targets has also emerged as an important future therapeutic strategy for RCC, both clear cell and variant histology. New pathways being targeted include FGF, angiopoietin and MET. In this review, we highlight five novel tyrosine kinase inhibitors in development for RCC: tivozanib; dovitinib; regorafenib; cabozantinib; and tivantinib.
Insights
New tyrosine kinase inhibitors targeting novel pathways like FGF, angiopoietin, and MET are in development for advanced renal cell carcinoma (RCC). These agents aim to overcome resistance and toxicity associated with current VEGF and mTOR therapies.
Area of Science:
- Oncology
- Pharmacology
- Urology
Background:
- Advanced renal cell carcinoma (RCC) treatment has been improved by targeted therapies against vascular endothelial growth factor (VEGF) and mammalian target of rapamycin (mTOR).
- However, drug resistance and toxicity necessitate the development of novel therapeutic agents for RCC.
- Next-generation tyrosine kinase inhibitors (TKIs) are being developed with improved specificity and broader receptor inhibition.
Purpose of the Study:
- To review emerging tyrosine kinase inhibitors (TKIs) for advanced renal cell carcinoma (RCC).
- To highlight novel therapeutic strategies targeting pathways beyond VEGF and mTOR.
- To discuss five specific TKIs under development for RCC treatment.
Main Methods:
- Review of current literature on tyrosine kinase inhibitors in renal cell carcinoma (RCC) research.
- Identification of novel receptor targets and pathways being investigated for RCC therapy.
- Summary of five investigational TKIs: tivozanib, dovitinib, regorafenib, cabozantinib, and tivantinib.
Main Results:
- Several novel TKIs are in development, targeting a wider range of receptors.
- New pathways such as fibroblast growth factor (FGF), angiopoietin, and MET are being explored.
- These agents aim to offer improved efficacy and safety profiles for advanced RCC.
Conclusions:
- Targeting novel receptors and pathways with TKIs represents a promising future strategy for advanced RCC.
- Investigational agents like tivozanib, dovitinib, regorafenib, cabozantinib, and tivantinib show potential.
- Further research and clinical trials are essential to establish the role of these novel TKIs in RCC management.
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