Allogeneic hematopoietic cell transplantation compared to chemotherapy consolidation in older acute myeloid leukemia (AML) patients 60-75 years in first complete remission (CR1): an alliance (A151509), SWOG, ECOG-ACRIN, and CIBMTR study.

Author(s): Ustun C,  Le-Rademacher J,  Wang HL,  Othus M,  Sun Z,  Major B,  Zhang MJ,  Storrick E,  Lafky JM,  Chow S,  Mrózek K,  Attar EC,  Nand S,  Bloomfield CD,  Cripe LD,  Tallman MS,  Appelbaum F,  Larson RA,  Marcucci G,  Roboz GJ,  Uy GL,  Stone RM,  Jatoi A,  Shea TC,  de Lima M,  Foran JM,  Sandmaier BM,  Litzow MR,  Erba HP,  Hurria A,  Weisdorf DJ,  Artz AS

Journal: Leukemia

Date: 2019 Nov

Major Program(s) or Research Group(s): NCORP

PubMed ID: 31073153

PMC ID: PMC6842042

Abstract: The preferred post-remission therapy for older patients with acute myeloid leukemia (AML) in first complete remission (CR1) remains uncertain. In this retrospective, multicenter study, we compared the outcomes for older AML patients (age 60-77 years) receiving allogeneic hematopoietic cell transplantation (alloHCT) (n = 431) with those treated on prospective National Clinical Trials Network induction and nontransplantation chemotherapy (CT) consolidation trials (n = 211). AlloHCT patients were younger (median age: 64.2 versus 67.9 years, p < 0.001), but more frequently had high-risk AML (high WBC, secondary AML, and unfavorable cytogenetics). Overall survival (OS) was worse in alloHCT during the first 9 months after CR1 (HR = 1.52, p = 0.02), but was significantly better thereafter (HR = 0.53, p < 0.0001) relative to CT. Treatment-related mortality (TRM) following HCT was worse in the first 9 months (HR = 2.8, 95% CI: 1.5-5.2, p = 0.0009), while post-HCT relapse was significantly less frequent beyond 9 months (HR = 0.42, 95% CI: 0.29-0.61, p < 0.0001). Despite higher early TRM, alloHCT recipients had superior long-term OS [29% (24-34%) versus CT 13.8% (9-21%) at 5 years]. Although this is a retrospective analysis with potential biases, it indicates that alloHCT led to heightened early risks from TRM, yet reduced relapse and superior long-term survival relative to CT in older AML patients in CR1.