| Literature DB >> 28003274 |
Yasmin Abaza1, Hagop Kantarjian1, Guillermo Garcia-Manero1, Elihu Estey2, Gautam Borthakur1, Elias Jabbour1, Stefan Faderl3, Susan O'Brien4, William Wierda1, Sherry Pierce1, Mark Brandt1, Deborah McCue5, Rajyalakshmi Luthra6, Keyur Patel6, Steven Kornblau1, Tapan Kadia1, Naval Daver1, Courtney DiNardo1, Nitin Jain1, Srdan Verstovsek1, Alessandra Ferrajoli1, Michael Andreeff1, Marina Konopleva1, Zeev Estrov1, Maria Foudray1, David McCue1, Jorge Cortes1, Farhad Ravandi1.
Abstract
The combination of all-trans-retinoic acid (ATRA) plus arsenic trioxide (ATO) has been shown to be superior to ATRA plus chemotherapy in the treatment of standard-risk patients with newly diagnosed acute promyelocytic leukemia (APL). A recent study demonstrated the efficacy of this regimen with added gemtuzumab ozogamicin (GO) in high-risk patients. We examined the long-term outcome of patients with newly diagnosed APL treated at our institution on 3 consecutive prospective clinical trials, using the combination of ATRA and ATO, with or without GO. For induction, all patients received ATRA (45 mg/m2 daily) and ATO (0.15 mg/kg daily) with a dose of GO (9 mg/m2 on day 1) added to high-risk patients (white blood cell count, >10 × 109/L), as well as low-risk patients who experienced leukocytosis during induction. Once in complete remission, patients received 4 cycles of ATRA plus ATO consolidation. One hundred eighty-seven patients, including 54 with high-risk and 133 with low-risk disease, have been treated. The complete remission rate was 96% (52 of 54 in high-risk and 127 of 133 in low-risk patients). Induction mortality was 4%, with only 7 relapses. Among low-risk patients, 60 patients (45%) required either GO or idarubicin for leukocytosis. Median duration of follow-up was 47.6 months. The 5-year event-free, disease-free, and overall survival rates are 85%, 96%, and 88%, respectively. Late hematological relapses beyond 1 year occurred in 3 patients. Fourteen deaths occurred beyond 1 year; 12 were related to other causes. This study confirms the durability of responses with this regimen.Entities:
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Year: 2016 PMID: 28003274 PMCID: PMC5413297 DOI: 10.1182/blood-2016-09-736686
Source DB: PubMed Journal: Blood ISSN: 0006-4971 Impact factor: 22.113