Annals of Oncology Advance Access published online on October 22, 2009
Annals of Oncology, doi:10.1093/annonc/mdp411
Incidence of brain metastases in renal cell carcinoma treated with sorafenib
1 Department of Medical Oncology, Institut Gustave Roussy, Villejuif, France
2 Department of Oncology, Central Clinical Hospital of Military Medical Academy, Warsaw, Poland
* Correspondence to: Dr B. Escudier, Immunotherapy Unit, Department of Medical Oncology, Institut Gustave Roussy, 39 rue C. Desmoulins, Villejuif, France. Tel: +33-142115410; Fax: +33-142115211; E-mail: escudier{at}igr.fr
Background: This retrospective study evaluated the incidence of brain metastases in a subgroup of patients with metastatic renal cell carcinoma (RCC) who were randomly assigned to receive sorafenib, an oral multikinase inhibitor (400 mg b.i.d.), versus placebo in the phase III Treatment Approaches in Renal Cancer Global Evaluation Trial (TARGET).
Patients and methods: Patients enrolled in TARGET at two centres (Institut Gustave Roussy, Villejuif, France, n = 85; Central Clinical Hospital of Military Medical Academy, Warsaw, Poland, n = 54) made up the current subgroup, who were retrospectively evaluated for the incidence of brain metastases during follow-up. The association between treatment (sorafenib versus placebo) and occurrence of brain metastases was evaluated by univariate analysis.
Results: The overall incidence of brain metastases in patients receiving sorafenib was 3% (2 of 70 patients) compared with 12% (8 of 69 patients) in patients receiving placebo (P < 0.05). The incidence of brain metastases was also significantly lower in the sorafenib group after 1 (P = 0.0447) and 2 years (P = 0.005) of treatment compared with the placebo group.
Conclusions: In this subpopulation, sorafenib may reduce the occurrence of brain metastases. Antiangiogenic therapy, such as sorafenib, could be an effective preventive therapy for brain metastases in advanced RCC.
antiangiogenic agents, brain metastases, renal cell carcinoma, sorafenib
Received for publication April 28, 2009. Revision received July 15, 2009. Accepted for publication July 16, 2009.