Blood Advances (Apr 2018)

Hypomethylating agents in relapsed and refractory AML: outcomes and their predictors in a large international patient cohort

  • Maximilian Stahl,
  • Michelle DeVeaux,
  • Pau Montesinos,
  • Raphael Itzykson,
  • Ellen K. Ritchie,
  • Mikkael A. Sekeres,
  • John D. Barnard,
  • Nikolai A. Podoltsev,
  • Andrew M. Brunner,
  • Rami S. Komrokji,
  • Vijaya R. Bhatt,
  • Aref Al-Kali,
  • Thomas Cluzeau,
  • Valeria Santini,
  • Amir T. Fathi,
  • Gail J. Roboz,
  • Pierre Fenaux,
  • Mark R. Litzow,
  • Sarah Perreault,
  • Tae Kon Kim,
  • Thomas Prebet,
  • Norbert Vey,
  • Vivek Verma,
  • Ulrich Germing,
  • Juan Miguel Bergua,
  • Josefina Serrano,
  • Steven D. Gore,
  • Amer M. Zeidan

Journal volume & issue
Vol. 2, no. 8
pp. 923 – 932

Abstract

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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.