Abstract

ABSTRACT Background There is no effective therapy for recurrent GBM pts following progression on the vascular endothelial growth factor (VEGF)-targeting agent bevacizumab (BV), with historical series reporting progression-free survival at 6 months (PFS-6) of only 2%. Several mechanisms of tumor adaptation following anti-VEGF therapy have been proposed, including upregulation of alternative angiogenic cytokines. We therefore performed a single-arm phase 2 study to evaluate lenvatinib (L), an oral tyrosine kinase inhibitor targeting FGFR1-4, PDGFRβ, VEGFR1-3, RET, and KIT, in pts with recurrent GBM progressing on BV. Methods 32 pts with recurrent GBM (≤2 prior progressions) and progression on BV received L 24 mg once daily in 28-day cycles until PD or unacceptable toxicity. Dynamic contrast-enhanced MRI was performed before and after 1 day of L on a subset of pts (n = 16). Response was assessed using Response Assessment in Neuro-Oncology criteria. Primary endpoint was PFS-6. This cohort has completed enrollment; 1 pt is still ongoing. Results Median age was 52 y, 56% were male, and 19% had a KPS Conclusions Lenvatinib has modest activity and a similar toxicity profile when compared with other tyrosine kinase inhibitors. Further study of VEGF therapy failure mechanisms as well as biomarkers of outcome is needed. Disclosure D.A. Reardon: D. Reardon discloses reimbursement for serving as an advisory board member for Genentech/Roche and Schering/Merck in the past year. E. Pan: E. Pan has been reimbursed as an advisory board member for Genentech in the past year. He has also been on the Speakers' Bureau for Genentech, Merck, and Sigma Tau in the past year. J. Fan: J. Fan is an Eisai employee. J. Mink: J. Mink is an employee of Eisai. D.P. Barboriak: D. Barboriak discloses receiving imaging core lab support from Eisai Pharmaceuticals, ACRIN, NIBIB / RSNA QIBA Member of GE Medical Systems Neuro MRI advisory board Pulse sequence support from Siemens Healthcare. J.J. Vredenburgh: J.J. Vredenburgh received financial compensation from Genentech/Roche for Speakers Bureau participation and consultation. A. Desjardins: A. Desjardins received financial compensation from Genentech/Roche for Speakers Bureau participation. J.P. O'Brien: J. P. O'Brien is an employee of Eisai. P.Y. Wen: P. Wen discloses research support from Eisai. All other authors have declared no conflicts of interest.

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