Rapid Donor Identification Improves Survival in High-Risk First-Remission Patients with Acute Myeloid Leukemia

  • John M. Pagel
  • , Megan Othus
  • , Guillermo Garcia-Manero
  • , Min Fang
  • , Jerald P. Radich
  • , David A. Rizzieri
  • , Guido Marcucci
  • , Stephen A. Strickland
  • , Mark R. Litzow
  • , M. Lynn Savoie
  • , Stephen R. Spellman
  • , Dennis L. Confer
  • , Jeffrey W. Chell
  • , Maria Brown
  • , Bruno C. Medeiros
  • , Mikkael A. Sekeres
  • , Tara L. Lin
  • , Geoffrey L. Uy
  • , Bayard L. Powell
  • , Ruthee Lu Bayer
  • Richard A. Larson, Richard M. Stone, David Claxton, James Essell, Selina M. Luger, Sanjay R. Mohan, Anna Moseley, Harry P. Erba, Frederick R. Appelbaum

Research output: Contribution to journalArticlepeer-review

19 Scopus citations

Abstract

PURPOSE Patients with acute myeloid leukemia with high-risk cytogenetics in first complete remission (CR1) achieve better outcomes if they undergo allogeneic hematopoietic cell transplantation (HCT) compared with consolidation chemotherapy alone. However, only approximately 40% of such patients typically proceed to HCT. METHODS We used a prospective organized approach to rapidly identify donors to improve the allogeneic HCT rate in adults with high-risk acute myeloid leukemia in CR1. Newly diagnosed patients had cytogenetics obtained at enrollment, and those with high-risk cytogenetics underwent expedited HLA typing and were encouraged to be referred for consultation with a transplantation team with the goal of conducting an allogeneic HCT in CR1. RESULTS Of 738 eligible patients (median age, 49 years; range, 18-60 years of age), 159 (22%) had high-risk cytogenetics and 107 of these patients (67%) achieved CR1. Seventy (65%) of the high-risk patients underwent transplantation in CR1 (P, .001 compared with the historical rate of 40%). Median time to HCT from CR1 was 77 days (range, 20-356 days). In landmark analysis, overall survival (OS) among patients who underwent transplantation was significantly better compared with that of patients who did not undergo transplantation (2-year OS, 48% v 35%, respectively [P = .031]). Median relapse-free survival after transplantation in the high-risk cohort who underwent transplantation in CR1 (n = 70) was 11.5 months (range, 4-47 months), and median OS after transplantation was 14 months (range, 4-44 months). CONCLUSION Early cytogenetic testing with an organized effort to identify a suitable allogeneic HCT donor led to a CR1 transplantation rate of 65% in the high-risk group, which, in turn, led to an improvement in OS when compared with the OS of patients who did not undergo transplantation.

Original languageEnglish
Pages (from-to)E464-E475
JournalJCO Oncology Practice
Volume16
Issue number6
DOIs
StatePublished - Jun 1 2020

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