| Literature DB >> 36258924 |
Arnon Nagler1, Myriam Labopin2,3, Ryszard Swoboda4, Pietro Pioltelli5, Mutlu Arat6, Ibrahim Yakoub-Agha7, Alexander Kulagin8, Anna Maria Raiola9, Hakan Ozdogu10, Antonio Risitano11, Zubeyde Nur Ozkurt12, Jaime Sanz13, Eolia Brissot14, Peric Zina15, Sebastian Giebel4, Fabio Ciceri16, Mohamad Mohty17.
Abstract
The results of haploidentical stem cell transplantation (haploHCT) for patients with acute lymphoblastic leukemia (ALL) transplanted in active disease remain largely unknown. We retrospectively analyzed adult patients with R/R ALL who underwent haploHCT or matched sibling donor (MSD-HCT) as a first transplantation between 2012 and 2020. The analysis comprised 274 patients, 94 had a haploHCT, and 180 had an MSD-HCT. The median follow-up was 32 months. The median age was 33 (range 18-76) and 37 (18-76) years in the haplo- and MSD-HCT groups, respectively. Post-transplant cyclophosphamide (PTCy) was used in 88% of haploHCT and in 4% of the MSD-HCT group. Graft-versus-host disease grade III-IV was higher in haploHCT than in the MSD-HCT group (18% versus 9%; P = 0.042). The 2-year chronic (c) graft-versus-host disease rates were 17% versus 33% (hazard ratio [HR] = 0.56; P = 0.14), respectively. By multivariate analysis, relapse incidence, and leukemia-free survival were not significatively different between the transplant groups, while nonrelapse mortality (NRM) was significantly higher (25% versus 18% at 2 years; HR = 2.03; P = 0.042) and overall survival (OS) lower (22% versus 38% at 2 years; HR = 1.72; P = 0.009) in the haploHCT group compared with the MSD-HCT group. We conclude that the 2-year OS of R/R ALL patients undergoing MSD transplants is significantly better than in haploHCT with a higher NRM in the latter.Entities:
Year: 2022 PMID: 36258924 PMCID: PMC9575736 DOI: 10.1097/HS9.0000000000000790
Source DB: PubMed Journal: Hemasphere ISSN: 2572-9241