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Updated: Jun 27, 2026

A Syngeneic Mouse Model of Metastatic Renal Cell Carcinoma for Quantitative and Longitudinal Assessment of Preclinical Therapies
Published on: April 12, 2017
Sequential therapy with sorafenib and sunitinib in renal cell carcinoma
Arkadiusz Z Dudek1, Jakub Zolnierek, Anu Dham
1Department of Medicine, Division of Hematology, Oncology and Transplantation, University of Minnesota, Minneapolis, Minnesota 55455, USA. dudek002@umn.edu
Background:
Sunitinib and sorafenib are small-molecule tyrosine kinase inhibitors (TKI) with antitumor activity in advanced renal cell carcinoma. A retrospective study was conducted to assess the response of renal cell carcinoma to sequential treatment with these two agents.
Methods:
Tumor response was evaluated by using Response Evaluation Criteria In Solid Tumors (RECIST) criteria in patients failing first-line therapy with either sunitinib or sorafenib and subsequently receiving second-line therapy with the other TKI agent.
Results:
Twenty-nine patients received sorafenib followed by sunitinib (Group A), and 20 patients received sunitinib followed by sorafenib (Group B). TKI drugs were terminated in 6 (12%) patients in Group A and 4 (8%) in Group B because of toxicity. Median duration of stable disease for Groups A and B was 20 and 9.5 weeks, respectively. Median time from starting first TKI to disease progression after second TKI (time to progression) in Groups A and B was 78 and 37 weeks, respectively. Multivariate analysis revealed that Group B had a shorter time to progression than Group A (risk ratio [RR] 3.0; P=.016). Median overall survival was 102 and 45 weeks in Groups A and B, respectively (P=.061).
Conclusions:
The longer duration of disease control in patients who received sorafenib followed by sunitinib warrants further investigation.
Insights
Sequential treatment with sorafenib then sunitinib demonstrated superior disease control in advanced renal cell carcinoma patients compared to sunitinib then sorafenib. Further investigation is warranted for this treatment sequence.
Area of Science:
- Oncology
- Pharmacology
Background:
- Sunitinib and sorafenib are tyrosine kinase inhibitors (TKIs) used for advanced renal cell carcinoma.
- Sequential TKI therapy is an emerging treatment strategy.
Purpose of the Study:
- To evaluate the efficacy of sequential sunitinib and sorafenib treatment in advanced renal cell carcinoma.
- To compare the outcomes of sorafenib followed by sunitinib versus sunitinib followed by sorafenib.
Main Methods:
- Retrospective study of 49 advanced renal cell carcinoma patients.
- Patients received either sorafenib then sunitinib (Group A) or sunitinib then sorafenib (Group B).
- Tumor response assessed by RECIST criteria; toxicity and survival data collected.
Main Results:
- Group A (sorafenib-sunitinib) had longer median stable disease duration (20 weeks) and time to progression (78 weeks) than Group B (sunitinib-sorafenib).
- Multivariate analysis showed Group B had a significantly shorter time to progression (RR 3.0; P=.016).
- Median overall survival was longer in Group A (102 weeks) versus Group B (45 weeks), though not statistically significant (P=.061).
Conclusions:
- Sequential treatment with sorafenib followed by sunitinib resulted in longer disease control.
- This sequence warrants further investigation for advanced renal cell carcinoma management.
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