| Literature DB >> 30393825 |
Melissa A Reimers1, Maryann M Shango2, Stephanie Daignault-Newton3, Rachel Dedinsky4, Danielle Karsies5, Shawna Kraft6, Liam Riddle7, Jeremy A Felton6, Bo Wen6, Christina Gersch8, James M Rae9, Bruce G Redman10, Ajjai S Alva10.
Abstract
Background Pazopanib is approved for metastatic renal cell carcinoma (RCC). We assessed the safety and efficacy of pazopanib with a low fat meal (LFM): <400 cal and < 20% fat or 10 g per meal. Methods A single arm study of pazopanib with a LFM in 16 adult patients with metastatic RCC with a clear cell component, RECIST 1.1 measurable disease, ECOG PS ≤ 2, and ≤ 3 prior therapies. Pazopanib at 400 mg daily given with LFM for 12 weeks. Incremental dose increases up to 800 mg, or irreversible decreases to 200 mg, allowed every 2 weeks. Primary study endpoint was safety; adverse events (AE) measured per CTCAE version 4.0. Secondary endpoints of RECIST 1.1 response with assessment as 12 weeks; pharmacokinetic (PK) analysis at nine time points, and CYP3A4 polymorphism evaluation. Results Pazopanib with a LFM was well tolerated; 13 of 16 subjects completed all 12 weeks. Three patients withdrew due to adverse events (AEs), with five occurrences of grade 3 AEs. Conclusions Pazopanib with a LFM has acceptable safety and comparable efficacy to fasting administration. Total median pazopanib dose per subject for the study duration was 63.5% of maximum possible conventional dose. A larger study is warranted. Clinical Trial Registration Number: NCT02729194.Entities:
Keywords: Advanced disease; Fat meal; Pazopanib; Renal cell carcinoma; Tyrosine kinase inhibitor therapy
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Year: 2018 PMID: 30393825 DOI: 10.1007/s10637-018-0692-8
Source DB: PubMed Journal: Invest New Drugs ISSN: 0167-6997 Impact factor: 3.850