| Literature DB >> 25164427 |
Seth E Karol1, Elaine Coustan-Smith, Xueyuan Cao, Sheila A Shurtleff, Susana C Raimondi, John K Choi, Raul C Ribeiro, Gary V Dahl, William Paul Bowman, Jeffrey W Taub, Barbara Degar, Wing Leung, James R Downing, Ching-Hon Pui, Jeffrey E Rubnitz, Dario Campana, Hiroto Inaba.
Abstract
Minimal residual disease (MRD) is a strong prognostic factor in children and adolescents with acute myeloid leukaemia (AML) but nearly one-quarter of patients who achieve MRD-negative status still relapse. The adverse prognostic factors among MRD-negative patients remain unknown. We analysed the AML02 study cohort to identify demographic and genetic prognostic factors. Among the presenting features, certain 11q23 abnormalities, such as t(6;11) and t(10;11), acute megakaryoblastic leukaemia without the t(1;22), and age ≥10 years were associated with inferior outcome in patients who had MRD-negative status after either remission induction I or II. By contrast, those with rearrangement of CBF genes had superior outcome. Our study identifies patient populations for whom close post-remission MRD monitoring to detect and treat emerging relapse and adjustment in treatment intensity might be indicated.Entities:
Keywords: acute myeloid leukaemia; minimal residual disease; paediatric; prognostic factor
Mesh:
Substances:
Year: 2014 PMID: 25164427 PMCID: PMC4262553 DOI: 10.1111/bjh.13107
Source DB: PubMed Journal: Br J Haematol ISSN: 0007-1048 Impact factor: 6.998