FLT3 ligand plasma levels have no impact on outcomes after allotransplant in acute leukemia

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Peterlin, Pierre | Gaschet, Joëlle | Guillaume, Thierry | Garnier, Alice | Eveillard, Marion | Le Bourgeois, Amandine | Chérel, Michel | Debord, Camille | Le Bris, Yannick | Theisen, Olivier | Mahé, Béatrice | Dubruille, Viviane | Godon, Catherine | Robillard, Nelly | Wuilleme, Soraya | Touzeau, Cyrille | Gastinne, Thomas | Blin, Nicolas | Lok, Anne | Bonnet, Antoine | Le Gouill, Steven | Moreau, Philippe | Béné, Marie-C | Chevallier, Patrice

Edité par CCSD ; Elsevier -

International audience. Objective: This study was designed to assess the impact on outcomes of early soluble Fms-like tyrosine kinase 3 ligand concentrations (sFLc) in patients receiving an allogeneic hematopoietic stem cell transplantation (allo-HSCT) for acute lymphoblastic leukemia (ALL) and acute myeloid leukemia (AML). Methods: This was a prospective monocentric study including all allo-HSCT patients included in the previous FLAM/FLAL study (Peterlin et al., 2019). Blood samples collected before the start of conditioning then post-transplant were frozen, stored and tested by ELISA. The parameters considered were hematopoietic recoveries, Leukemia Free Survival and Overall Survival, acute and chronic GVHD, grade 3 or 4 acute and/or extensive chronic GVHD-free and relapse-free survival (GRFS). Results: Forty-one patients were included, a total of 179 samples were assayed for sFLc. There was no impact of sFLc levels (< =median vs > median) on acute and chronic GVHD incidences, LFS, OS nor GRFS. Conclusion: At variance with induction results for AML (Peterlin et al., 2019) endogenous sFLc do not appear to be a prognostic marker at the time of or after allo-HSCT. Even though the results are negatives, this is, to the best of our knowledge, the only prospective series specifically addressing the question of sFLc impact after allo-HSCT in acute leukemias.

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