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Obesity is associated with residual leukemia following induction therapy for childhood B-precursor acute lymphoblastic leukemia

Obesity is associated with poorer event-free survival (EFS) in pediatric acute lymphoblastic leukemia (ALL). Persistent minimal residual disease (MRD) in the bone marrow as measured by multidimensional flow cytometry (MDF) is a key early prognostic indicator and is strongly associated with EFS. We t...

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Bibliographic Details
Published in:Blood 2014-12, Vol.124 (26), p.3932-3938
Main Authors: Orgel, Etan, Tucci, Jonathan, Alhushki, Waseem, Malvar, Jemily, Sposto, Richard, Fu, Cecilia H., Freyer, David R., Abdel-Azim, Hisham, Mittelman, Steven D.
Format: Article
Language:English
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Summary:Obesity is associated with poorer event-free survival (EFS) in pediatric acute lymphoblastic leukemia (ALL). Persistent minimal residual disease (MRD) in the bone marrow as measured by multidimensional flow cytometry (MDF) is a key early prognostic indicator and is strongly associated with EFS. We therefore hypothesized that obesity during induction would be associated with positive end-of-induction MRD (≥0.01%). We analyzed MDF of end-induction bone marrow samples from a historical cohort of 198 children newly diagnosed with B-precursor ALL (BP-ALL) and treated with Children’s Oncology Group induction regimens. We assessed the influence of body mass index on risk for positive end-induction MRD in the bone marrow. In our cohort of BP-ALL, 30 children (15.2%) were overweight and 41 (20.7%) were obese at diagnosis. Independent of established predictors of treatment response, obesity during induction was associated with significantly greater risk for persistent MRD (odds ratio, 2.57; 95% confidence interval, 1.19 to 5.54; P = .016). Obesity and overweight were associated with poorer EFS irrespective of end-induction MRD (P = .012). Obese children with newly diagnosed BP-ALL are at increased risk for positive end-induction MRD and poorer EFS. •Obesity is associated with increased risk for persistent minimal residual disease after induction therapy for pediatric BP-ALL.
ISSN:0006-4971
1528-0020
DOI:10.1182/blood-2014-08-595389