| Literature DB >> 29526774 |
Guillermo Ortí1, Jaime Sanz2, Irene García-Cadenas3, Isabel Sánchez-Ortega4, Laura Alonso5, Maria José Jiménez6, Luisa Sisinni7, Carmen Azqueta8, Olga Salamero9, Isabel Badell7, Christelle Ferra6, Cristina Diaz de Heredia5, Rocio Parody4, Miguel Angel Sanz2, Jorge Sierra3, Jose Luis Piñana2, Sergi Querol8, David Valcárcel9.
Abstract
Relapse of acute leukemia (AL) after allogeneic hematopoietic cell transplantation (Allo-HCT) entails a dismal prognosis. In this scenario, donor lymphocyte infusions (DLIs) and second Allo-HCT are two major approaches. We compared outcomes of AL patients treated for relapse with DLI or second Allo-HCT after receiving debulking therapy. In total, 46 patients were included in the study; 30 (65%) had acute myeloid leukemia and 16 (35%) had acute lymphoblastic leukemia. The median age was 38 years (range 4-66). Twenty-seven patients received a second Allo-HCT and 19 patients received DLI. The median follow-up of the cohort was 273 days (range 9-7013). Overall survival (OS), disease-free survival (DFS), nonrelapse mortality, and cumulative incidence (CI) of relapse were calculated from DLI or second Allo-HCT date. In univariate analysis, second Allo-HCT was associated with higher OS (p = 0.021) and a trend to higher DFS (p = 0.097) and CI of relapse (p = 0.094) on univariate analysis. However, multivariate analysis showed comparable outcomes between DLI and second Allo-HCT, with the time interval to relapse before DLI or second Allo-HCT the only statistically significant factor with an impact on OS and DFS. Within the DLI cohort, T-cell-depleted Allo-HCT was associated with higher OS (p = 0.003) and DFS (p < 0.001) and lower CI of relapse (p = 0.002) than T-cell-replete Allo-HCT. Overall, in this cohort of AL patients, second Allo-HCT and DLI associated similar outcomes. As in other relapse studies, the length of remission (time to relapse) was identified as a factor with statistical impact on survival. Further studies are warranted.Entities:
Mesh:
Year: 2018 PMID: 29526774 DOI: 10.1016/j.exphem.2018.03.002
Source DB: PubMed Journal: Exp Hematol ISSN: 0301-472X Impact factor: 3.084