| Literature DB >> 29685952 |
Maximilian Stahl1, Michelle DeVeaux2, Pau Montesinos3, Raphael Itzykson4, Ellen K Ritchie5, Mikkael A Sekeres6, John D Barnard6, Nikolai A Podoltsev1, Andrew M Brunner7, Rami S Komrokji8, Vijaya R Bhatt9, Aref Al-Kali10, Thomas Cluzeau11, Valeria Santini12, Amir T Fathi7, Gail J Roboz5, Pierre Fenaux4, Mark R Litzow10, Sarah Perreault13, Tae Kon Kim1, Thomas Prebet1, Norbert Vey14, Vivek Verma9, Ulrich Germing15, Juan Miguel Bergua16, Josefina Serrano17, Steven D Gore1, Amer M Zeidan1.
Abstract
Although hypomethylating agents (HMAs) are frequently used in the frontline treatment of older acute myeloid leukemia (AML) patients, little is known about their effectiveness in relapsed or primary treatment-refractory (RR)-AML. Using an international multicenter retrospective database, we studied the effectiveness of HMAs in RR-AML and evaluated for predictors of response and overall survival (OS). A total of 655 patients from 12 centers received azacitidine (57%) or decitabine (43%), including 290 refractory (44%) and 365 relapsed (56%) patients. Median age at diagnosis was 65 years. Best response to HMAs was complete remission (CR; 11%) or CR with incomplete count recovery (CRi; 5.3%). Additionally, 8.5% experienced hematologic improvement. Median OS was 6.7 months (95% confidence interval, 6.1-7.3). As expected, OS differed significantly by best response, with patients achieving CR and CRi having a median OS of 25.3 and 14.6 months, respectively. In multivariate analysis, the presence of ≤5% circulating blasts and a 10-day schedule of decitabine were associated with improved response rates, whereas the presence of >5% circulating blasts and >20% bone marrow blasts were associated with decreased OS. A significant subset of RR-AML patients (16%) achieved CR/CRi with HMAs and experienced a median OS of 21 months. Outside of a clinical trial, HMAs represent a reasonable therapeutic option for some patients with RR-AML.Entities:
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Year: 2018 PMID: 29685952 PMCID: PMC5916007 DOI: 10.1182/bloodadvances.2018016121
Source DB: PubMed Journal: Blood Adv ISSN: 2473-9529