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Monocyte subpopulation recovery as predictors of hematopoietic cell transplantation outcomes.

07:00 EST 6th January 2019 | BioPortfolio

Summary of "Monocyte subpopulation recovery as predictors of hematopoietic cell transplantation outcomes."

Monocyte recovery following hematopoietic cell transplantation (HCT) has been correlated with overall survival (OS). However, monocytes are heterogeneous and consist of classical (CD14CD16), intermediate (CD14CD16) and non-classical (CD14CD16) subpopulations, with unique functional properties. We hypothesized that monocyte subpopulation reconstitution would vary based on allogeneic stem cell source and would be associated with outcomes. We studied monocyte subpopulation recovery at days 28, 60, 100, 180 and 365 post-HCT among 202 patients with hematologic malignancy. Significant differences in absolute monocyte count (AMC) and monocyte subpopulation counts at days 60 and 100 were identified based on stem cell source (all p<0.01), with more robust recovery in umbilical cord blood (UCB) recipients. Using two-fold cross validation, optimal cutpoints were calculated for day 28 AMC and monocyte subpopulations based on OS. These were used to calculate hazard ratios for OS, disease free survival (DFS), relapse, transplant related mortality (TRM), acute and chronic GVHD. OS and DFS were superior when AMC and classical monocyte recovery were above optimal cutpoints (all p<0.03). Relapse was reduced for those with AMC (p<0.01) and classical (p=0.05) monocyte counts above optimal cutpoints. TRM was also reduced when classical (p=0.02) monocyte count exceeded optimal cutpoint. Intermediate and non-classical monocyte recovery were not associated with outcomes. In summary, hematopoietic cell source is associated with monocyte subpopulation recovery, with the early robust recovery in UCB recipients. Recovery of AMC and classical monocytes were prognostic for survival, relapse and TRM. These indicators may identify patients at increased risk for post-HCT failure and guide therapeutic interventions.

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This article was published in the following journal.

Name: Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation
ISSN: 1523-6536
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