Abstract
Background:We evaluated week-on/week-off axitinib dosing plus chemotherapy in patients with gastrointestinal tumours, including tumour thymidine uptake by fluorine-18 3′-deoxy-3′-fluorothymidine positron emission tomography (18 FLT-PET).Methods:During a lead-in period, patients received twice daily (b.i.d.) axitinib 7 mg (n=3) or 10 mg (n=18) for 7 days followed by a 7-day dosing interruption; serial 18 FLT-PET scans were performed before day 1 and on days 7, 10, and 14. Axitinib plus FOLFIRI or FOLFOX was then administered in 2-week cycles; axitinib was interrupted on day 10 of each cycle for 7 days.Results:The maximum tolerated dose of axitinib was 10 mg b.i.d., in a week-on/week-off schedule, combined with FOLFIRI or FOLFOX. Common all-causality grade 3 adverse events were neutropenia (38%), hypertension (33%), and fatigue (29%). Of 21 patients, 2 (10%) had a partial response and 12 (57%) had stable disease. Following 7 days of continuous axitinib dosing, tumour 18 FLT uptake decreased -49% from baseline and recovered to -28% and -17% from baseline, respectively, after 3 and 7 days of axitinib interruption.Conclusion:Axitinib administered in a week-on/week-off schedule combined with FOLFIRI or FOLFOX is supported by 18 FLT-PET data and was well tolerated in patients with gastrointestinal tumours. © 2014 Cancer Research UK.
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CITATION STYLE
Hoh, C. K., Burris, H. A., Bendell, J. C., Tarazi, J., Rosbrook, B., Kim, S., … Reid, T. R. (2014). Intermittent dosing of axitinib combined with chemotherapy is supported by 18 FLT-PET in gastrointestinal tumours. British Journal of Cancer, 110(4), 875–881. https://doi.org/10.1038/bjc.2013.806
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