4.2 Article

Prognostic impact of immune status and hematopoietic recovery before and after fludarabine, IV busulfan, and antithymocyte globulins (FB2 regimen) reduced-intensity conditioning regimen (RIC) allogeneic stem cell transplantation (allo-SCT)

Journal

EUROPEAN JOURNAL OF HAEMATOLOGY
Volume 90, Issue 3, Pages 177-186

Publisher

WILEY
DOI: 10.1111/ejh.12049

Keywords

reduced-intensity conditioning; allo-stem cells transplantations; FB2; antithymocyte globulin; immune reconstitution; hematopoietic recovery

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This retrospective analysis aimed to assess hematopoietic and immune recovery in a cohort of 53 patients [males: n=33; median age: 59yr (range: 2270)] who received a FB2 (fludarabine 120150mg/m2+IV busulfan 6.4mg/kg+antithymocyte globulin thymoglobulin 5mg/kg) reduced-intensity conditioning (RIC) allo-stem cells transplantations (SCT). With a median follow-up of 19months (range: 253), the 2-yr overall survival, disease-free survival (DFS), relapse incidence, and non-relapse mortality were 63%, 59.5%, 35%, and 6%, respectively. In univariate analysis, the factors correlated with a significantly higher 2-yr OS and DFS were a higher total circulating lymphocytes count at transplant (>730/mm3; OS: 81% vs. 43%, P=0.02; DFS: 73% vs. 45.5%, P=0.03) and a higher recovery of leukocytes (>5300/mm3) (2-yr OS: 81% vs. 44%, P=0.007; 2-yr DFS: 72% vs. 46%, P=0.08), neutrophils (>3200/mm3) (2-yr OS: 76% vs. 50%, P=0.03; 2-yr DFS: 67% vs. 52.0%, P=0.1), and monocytes (>590/mm3; 2-yr OS: 80% vs. 45%, P=0.004; 2-yr DFS: 76% vs. 42%, P=0.01) at day +30 post-transplant. In multivariate analysis, the only independent factors associated with a significantly higher OS and DFS were a better immune status at transplant (lymphocytes count >730/mm3) and a higher monocytes count (>590/mm3) at day +30 post-transplant. These results suggest that immune status and hematopoietic recovery before and after FB2 RIC allo-SCT can be significant predictors of outcome. This paves the way for future studies aiming to closely monitor the kinetics of immune recovery after RIC allo-SCT and to evaluate the impact of growth factors and other immunostimulatory cytokines in the setting of RIC allo-SCT.

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