GVHD prophylaxis with sirolimus-tacrolimus may overcome the deleterious effect on survival of HLA mismatch after reduced-intensity conditioning allo-SCT.
Rocio ParodyL Lopez-CorralO L GodinoI G CadenasA P MartinezL VazquezR MartinoC MartinezC SolanoP BarbaD ValcarcelT Caballero-VelazquezF J Marquez-MalaverJ SierraD CaballeroJ A Perez-SimónPublished in: Bone marrow transplantation (2014)
Large studies, mostly based on series of patients receiving CSA/tacrolimus (TKR) plus MTX as immunoprophylaxis, have demonstrated a deleterious effect on survival of the presence of a single mismatch out of eight loci after allogeneic hematopoietic SCT (alloHSCT). We retrospectively analyzed a series of 159 adult patients who received sirolimus(SRL)/TKR prophylaxis after alloHSCT. We compared overall outcomes according to HLA compatibility in A, B, C and DRB1 loci at the allele level: 7/8 (n=20) vs 8/8 (n=139). Donor type was unrelated in 95% vs 70% among 7/8 vs 8/8 pairs, respectively (P=0.01). No significant differences were observed in 3-year OS (68 vs 62%), 3-year EFS (53 vs 49%) and 1-year non-relapse mortality (9 vs 13%). Cumulative incidence of grades II-IV acute GVHD (aGVHD) was significantly higher in 7/8 alloHSCT (68% vs 42%, P<0.001) but no significant differences were found for III-IV aGVHD (4.5% vs 11%), overall (35% vs 53%) and extensive (20% vs 35%) chronic GHVD in 7/8 vs 8/8 subgroups, respectively. In summary, the present study indicates favorable outcomes after alloHSCT using the combination of SRL/TKR combination as GVHD prophylaxis with OS in the range of 55-70%, and non-significant differences in overall outcomes, irrespective of the presence of any mismatches at obligatory loci.
Keyphrases
- respiratory failure
- genome wide
- allogeneic hematopoietic stem cell transplantation
- genome wide association study
- bone marrow
- free survival
- risk factors
- stem cell transplantation
- metabolic syndrome
- cardiovascular events
- high intensity
- acute myeloid leukemia
- acute lymphoblastic leukemia
- low dose
- intensive care unit
- coronary artery disease
- cord blood
- acute respiratory distress syndrome
- high dose
- liver failure
- childhood cancer