Precision medicine treatment in acute myeloid leukemia using prospective genomic profiling: feasibility and preliminary efficacy of the Beat AML Master Trial. Academic Article uri icon

Overview

abstract

  • Acute myeloid leukemia (AML) is the most common diagnosed leukemia. In older adults, AML confers an adverse outcome1,2. AML originates from a dominant mutation, then acquires collaborative transformative mutations leading to myeloid transformation and clinical/biological heterogeneity. Currently, AML treatment is initiated rapidly, precluding the ability to consider the mutational profile of a patient's leukemia for treatment decisions. Untreated patients with AML ≥ 60 years were prospectively enrolled on the ongoing Beat AML trial (ClinicalTrials.gov NCT03013998 ), which aims to provide cytogenetic and mutational data within 7 days (d) from sample receipt and before treatment selection, followed by treatment assignment to a sub-study based on the dominant clone. A total of 487 patients with suspected AML were enrolled; 395 were eligible. Median age was 72 years (range 60-92 years; 38% ≥75 years); 374 patients (94.7%) had genetic and cytogenetic analysis completed within 7 d and were centrally assigned to a Beat AML sub-study; 224 (56.7%) were enrolled on a Beat AML sub-study. The remaining 171 patients elected standard of care (SOC) (103), investigational therapy (28) or palliative care (40); 9 died before treatment assignment. Demographic, laboratory and molecular characteristics were not significantly different between patients on the Beat AML sub-studies and those receiving SOC (induction with cytarabine + daunorubicin (7 + 3 or equivalent) or hypomethylation agent). Thirty-day mortality was less frequent and overall survival was significantly longer for patients enrolled on the Beat AML sub-studies versus those who elected SOC. A precision medicine therapy strategy in AML is feasible within 7 d, allowing patients and physicians to rapidly incorporate genomic data into treatment decisions without increasing early death or adversely impacting overall survival.

authors

  • Burd, Amy
  • Levine, Ross L.
  • Ruppert, Amy S
  • Mims, Alice S
  • Borate, Uma
  • Stein, Eytan M
  • Patel, Prapti
  • Baer, Maria R
  • Stock, Wendy
  • Deininger, Michael
  • Blum, William
  • Schiller, Gary
  • Olin, Rebecca
  • Litzow, Mark
  • Foran, James
  • Lin, Tara L
  • Ball, Brian
  • Boyiadzis, Michael
  • Traer, Elie
  • Odenike, Olatoyosi
  • Arellano, Martha
  • Walker, Alison
  • Duong, Vu H
  • Kovacsovics, Tibor
  • Collins, Robert
  • Shoben, Abigail B
  • Heerema, Nyla A
  • Foster, Matthew C
  • Vergilio, Jo-Anne
  • Brennan, Tim
  • Vietz, Christine
  • Severson, Eric
  • Miller, Molly
  • Rosenberg, Leonard
  • Marcus, Sonja
  • Yocum, Ashley
  • Chen, Timothy
  • Stefanos, Mona
  • Druker, Brian
  • Byrd, John C

publication date

  • October 26, 2020

Research

keywords

  • Biomarkers, Tumor
  • Genomics
  • Leukemia, Myeloid, Acute

Identity

PubMed Central ID

  • PMC8530434

Scopus Document Identifier

  • 85093850716

Digital Object Identifier (DOI)

  • 10.1038/s41591-020-1089-8

PubMed ID

  • 33106665

Additional Document Info

volume

  • 26

issue

  • 12