Long-Term Safety With Axitinib in Previously Treated Patients With Metastatic Renal Cell Carcinoma

Axitinib is approved for second-line treatment of advanced renal cell carcinoma (RCC). Analyses using pooled data from clinical trials in 672 previously treated patients with metastatic RCC showed long-term (>= 2 years) axitinib treatment was not associated with unexpected or more severe adverse events. Common adverse events were generally reported during the first 6 months to 1 year of therapy. Background: Axitinib is an approved treatment for advanced renal cell carcinoma (RCC) after failure of 1 systemic therapy. Patients and Methods: Long-term safety with single-agent axitinib was analyzed using pooled data from clinical trials in 672 previously treated patients with metastatic RCC (mRCC) and in 1304 patients with different advanced solid tumors. In all studies, except the phase I first-in-human, dose-finding study, the starting dose of oral axitinib was 5 mg twice daily continuously. Common long-term treatment-emergent adverse events (AEs) were identified in patients who received axitinib for >= 2 years, then evaluated in all patients, and assessed using interval, cumulative, and latency analyses. Results: In all, 108 (16%) previously treated patients with mRCC received axitinib for >= 2 years. In interval analysis, most AEs occurred during the first 6 months of treatment, with rates stable or decreased over time; rates increased for proteinuria, peripheral edema, and increased blood creatinine. Common Grade >= 3 AE rates declined or plateaued over time, except for increased amylase and myocardial infarction. Results were similar in cumulative analysis in this population, and in interval and cumulative analyses in all patients with mRCC and those with advanced solid tumors. Conclusion: Declining or stable rates of most AEs support an acceptable long-term safety profile for axitinib in patients with mRCC. However, increases in the rates of some AEs warrant monitoring. This analysis is limited in that it was retrospective and included a relatively small patient population. (C) 2015 Elsevier Inc. All rights reserved.