Related Experiment Video
Updated: May 16, 2026

A Syngeneic Mouse Model of Metastatic Renal Cell Carcinoma for Quantitative and Longitudinal Assessment of Preclinical Therapies
Published on: April 12, 2017
Sunitinib in advanced metastatic non-clear cell renal cell carcinoma: a single institution retrospective study
Chiara Paglino1, Ilaria Imarisio, Carlo Ganini
1Medical Oncology, IRCCS San Matteo University Hospital Foundation, Piazzale C. Golgi 19, Pavia, I-27100 Pavia, Italy.
Aim:
Sunitinib is an orally active multi-targeted tyrosine kinase inhibitor that exerts its antitumor effects primarily through the selective inhibition of VEGF. Novel targeted therapies such as sunitinib have transformed the treatment of advanced metastatic renal cell carcinomas, particularly those with clear cell histology. Here, our experience in patients with non-clear cell kidney cancer treated as part of the sunitinib Expanded Access Program is reported.
Materials & Methods:
This was a retrospective assessment of 21 patients with non-clear cell renal cell carcinoma who were treated with oral sunitinib 50 mg/day in repeated 6 weekly cycles (4 weeks on and 2 weeks off). Disease assessment and physical examination were recorded at baseline and tumor assessments were performed every 3 months, according to Response Evaluation Criteria In Solid Tumors. The primary outcome measure was progression-free survival.
Results:
Patients received an average of 6.38 cycles of sunitinib; one patient was classified as a complete responder and two as partial responders. The overall response rate was 14.3% and clinical benefit was attained by 52.4%. The median progression-free survival was 4.1 months while median overall survival was 14.6 months. In general, sunitinib was well tolerated and only three patients experienced a grade 3 toxicity, which resolved with dosage reduction.
Conclusion:
As expected, sunitinib exerted lower antitumor activity in patients with non-clear cell renal cell carcinoma than was achieved in the general population with metastatic kidney cancer. However, responses (one complete and two partial) were documented and clinical benefit was observed in more than half of all patients.
Insights
Sunitinib showed some antitumor activity in non-clear cell kidney cancer patients, with a 14.3% response rate and clinical benefit in over half. While less effective than in clear cell types, it was generally well-tolerated.
Area of Science:
- Oncology
- Pharmacology
Background:
- Sunitinib, a multi-targeted tyrosine kinase inhibitor, is a key therapy for advanced metastatic renal cell carcinoma, especially clear cell histology.
- Targeted therapies like sunitinib have significantly improved outcomes in renal cell carcinoma treatment.
Purpose of the Study:
- To report the experience and outcomes of using sunitinib in patients with non-clear cell renal cell carcinoma.
- To evaluate the efficacy and tolerability of sunitinib in a specific, less-studied subtype of kidney cancer.
Main Methods:
- Retrospective analysis of 21 patients with non-clear cell renal cell carcinoma treated with sunitinib.
- Sunitinib administered at 50 mg/day in 6-week cycles (4 weeks on, 2 weeks off).
- Disease and tumor assessments conducted every 3 months using Response Evaluation Criteria In Solid Tumors (RECIST); progression-free survival was the primary outcome.
Main Results:
- Median progression-free survival was 4.1 months; median overall survival was 14.6 months.
- Overall response rate was 14.3% (1 complete response, 2 partial responses).
- Clinical benefit observed in 52.4% of patients; sunitinib was generally well-tolerated with manageable toxicity.
Conclusions:
- Sunitinib demonstrated antitumor activity and provided clinical benefit in a subset of patients with non-clear cell renal cell carcinoma.
- The observed antitumor activity was lower compared to that typically seen in clear cell renal cell carcinoma.
- Sunitinib was generally well-tolerated in this patient population, with manageable side effects.
More Related Videos
13:19Quantifying Antibody-Dependent Cellular Cytotoxicity in a Tumor Spheroid Model: Application for Drug Discovery
Published on: April 26, 2024
06:43Robotic Duodenal Sleeve Resection for Gastrointestinal Stromal Tumor with Rare Exon 8 KIT Mutation Following Neoadjuvant Imatinib
Published on: April 3, 2026