| Literature DB >> 23953882 |
Thomas Prebet1, Thorsten Braun2, Odile Beyne-Rauzy3, Francois Dreyfus4, Aspasia Stammatoullas5, Eric Wattel6, Shanti Ame7, Emmanuel Raffoux8, Jacques Delaunay9, Aude Charbonnier1, Lionel Adès2, Pierre Fenaux2, Norbert Vey10.
Abstract
Outcome of patients with myelodysplastic syndrome after azacitidine failure is poor. In this population, we combined cytarabine (10-20mg/m²/day 14 days) with vorinostat (400mg/day) for escalating durations (7 days, 10 days and 14 days), and starting on day 1 (concomitant arm) or on day 14 (sequential arm) following a 3+3 phase I design. 40 patients were treated. Dose limiting toxicities were all seen in sequential arm. The overall response rate was 15% with 4 responses in concomitant arm (ORR=25%). We conclude that this combination is tolerable and concomitant administration might be less toxic and have better therapeutic effect (clinicaltrials.gov NCT00776503).Entities:
Keywords: Azacitidine failure; Epigenetic; HDAC; Myelodysplasia
Mesh:
Substances:
Year: 2013 PMID: 23953882 DOI: 10.1016/j.leukres.2013.07.023
Source DB: PubMed Journal: Leuk Res ISSN: 0145-2126 Impact factor: 3.156