| Literature DB >> 26022709 |
Joshua F Zeidner1, Matthew C Foster2, Amanda L Blackford3, Mark R Litzow4, Lawrence E Morris5, Stephen A Strickland6, Jeffrey E Lancet7, Prithviraj Bose8, M Yair Levy9, Raoul Tibes10, Ivana Gojo11, Christopher D Gocke3, Gary L Rosner3, Richard F Little12, John J Wright12, L Austin Doyle12, B Douglas Smith3, Judith E Karp3.
Abstract
Serial studies have demonstrated that induction therapy with FLAM [flavopiridol (alvocidib) 50 mg/m(2) days 1-3, cytarabine 667 mg/m(2)/day continuous infusion days 6-8, and mitoxantrone (FLAM) 40 mg/m(2) day 9] yields complete remission rates of nearly 70% in newly diagnosed poor-risk acute myeloid leukemia. Between May 2011-July 2013, 165 newly diagnosed acute myeloid leukemia patients (age 18-70 years) with intermediate/adverse-risk cytogenetics were randomized 2:1 to receive FLAM or 7+3 (cytarabine 100 mg/m(2)/day continuous infusion days 1-7 and daunorubicin 90 mg/m(2) days 1-3), across 10 institutions. Some patients on 7+3 with residual leukemia on day 14 received 5+2 (cytarabine 100 mg/m(2)/day continuous infusion days 1-5 and daunorubicin 45 mg/m(2) days 1-2), whereas patients on FLAM were not re-treated based on day 14 bone marrow findings. The primary objective was to compare complete remission rates between one cycle of FLAM and one cycle of 7+3. Secondary end points included safety, overall survival and event-free survival. FLAM led to higher complete remission rates than 7+3 alone (70% vs. 46%; P=0.003) without an increase in toxicity, and this improvement persisted after 7+3+/-5+2 (70% vs. 57%; P=0.08). There were no significant differences in overall survival and event-free survival in both arms but post-induction strategies were not standardized. These results substantiate the efficacy of FLAM induction in newly diagnosed AML. A phase III study is currently in development. This study is registered with clinicaltrials.gov identifier: 01349972. Copyright© Ferrata Storti Foundation.Entities:
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Year: 2015 PMID: 26022709 PMCID: PMC4800702 DOI: 10.3324/haematol.2015.125849
Source DB: PubMed Journal: Haematologica ISSN: 0390-6078 Impact factor: 9.941