Prospective Clinical Trial of Preoperative Sunitinib in Patients With Renal Cell Carcinoma
Purpose
Sunitinib is an approved treatment for metastatic renal cell carcinoma. We performed a prospective clinical trial to evaluate the safety and clinical response to sunitinib administered before nephrectomy in patients with localized or metastatic clear cell renal cell carcinoma.
Materials and Methods
Patients with biopsy proven clear cell renal cell carcinoma were enrolled in the study and treated with 37.5 mg sunitinib malate daily for 3 months before nephrectomy. The primary end point was safety.
Results
In an 18-month period 20 patients were enrolled. The most common toxicities were gastrointestinal symptoms and hematological effects. Grade 3 toxicity developed in 6 patients (30%). No surgical complications were attributable to sunitinib treatment. Of the 20 patients 17 (85%) experienced reduced tumor diameter (mean change −11.8%, range −27% to 11%) and cross-sectional area (mean change −27.9%, range −43% to 23%). Enhancement on contrast enhanced computerized tomography decreased in 15 patients (mean HU change −22%, range −74% to 29%). After tumor reduction 8 patients with cT1b disease underwent laparoscopic partial nephrectomy. Surgical parameters, such as blood loss, transfusion rate, operative time and complications, were similar to those in patients who underwent surgery during the study period and were not enrolled in the trial.
Conclusions
Preoperative treatment with sunitinib is safe. Sunitinib decreased the size of primary renal cell carcinoma in 17 of 20 patients. Future trials can be considered to evaluate neoadjuvant sunitinib to maximize nephron sparing and decrease the recurrence of high risk, localized renal cell carcinoma.
Key Words: kidney, carcinoma, renal cell, neoplasm metastasis, sunitinib, nephrectomy
Abbreviations and Acronyms: CrCl, creatinine clearance, CT, computerized tomography, RCC, renal cell carcinoma, RECIST, Response Evaluation Criteria in Solid Tumors
To access this article, please choose from the options below
Supplementary material for this article can be obtained at http://www.csmc.edu/rcc.
Study received institutional review board approval.
Supported by Pfizer (HLK) and National Institutes of Health R01CA133072-01.
For another article on a related topic see page 1166.
PII: S0022-5347(10)03560-3
doi:10.1016/j.juro.2010.05.041
© 2010 American Urological Association Education and Research, Inc. Published by Elsevier Inc All rights reserved.

