| Literature DB >> 30348653 |
Alice Bertaina1, Marco Zecca2, Barbara Buldini3, Nicoletta Sacchi4, Mattia Algeri1, Francesco Saglio5, Cesare Perotti6, Anna Maria Gallina4, Valentina Bertaina1, Edoardo Lanino7, Arcangelo Prete8, Walter Barberi9, Manuela Tumino3, Claudio Favre10, Simone Cesaro11, Francesca Del Bufalo1, Mimmo Ripaldi12, Stella Boghen2,13, Gabriella Casazza14, Marco Rabusin15, Adriana Balduzzi16, Franca Fagioli5, Daria Pagliara1, Franco Locatelli1,17.
Abstract
Traditionally, hematopoietic stem cell transplantation (HSCT) from both HLA-matched related and unrelated donors (UD) has been used for treating children with acute leukemia (AL) in need of an allograft. Recently, HLA-haploidentical HSCT after αβ T-cell/B-cell depletion (αβhaplo-HSCT) was shown to be effective in single-center studies. Here, we report the first multicenter retrospective analysis of 127 matched UD (MUD), 118 mismatched UD (MMUD), and 98 αβhaplo-HSCT recipients, transplanted between 2010 and 2015, in 13 Italian centers. All these AL children were transplanted in morphological remission after a myeloablative conditioning regimen. Graft failure occurred in 2% each of UD-HSCT and αβhaplo-HSCT groups. In MUD vs MMUD-HSCT recipients, the cumulative incidence of grade II to IV and grade III to IV acute graft-versus-host disease (GVHD) was 35% vs 44% and 6% vs 18%, respectively, compared with 16% and 0% in αβhaplo-HSCT recipients (P < .001). Children treated with αβhaplo-HSCT also had a significantly lower incidence of overall and extensive chronic GVHD (P < .01). Eight (6%) MUD, 32 (28%) MMUD, and 9 (9%) αβhaplo-HSCT patients died of transplant-related complications. With a median follow-up of 3.3 years, the 5-year probability of leukemia-free survival in the 3 groups was 67%, 55%, and 62%, respectively. In the 3 groups, chronic GVHD-free/relapse-free (GRFS) probability of survival was 61%, 34%, and 58%, respectively (P < .001). When compared with patients given MMUD-HSCT, αβhaplo-HSCT recipients had a lower cumulative incidence of nonrelapse mortality and a better GRFS (P < .001). These data indicate that αβhaplo-HSCT is a suitable therapeutic option for children with AL in need of transplantation, especially when an allele-matched UD is not available.Entities:
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Year: 2018 PMID: 30348653 DOI: 10.1182/blood-2018-07-861575
Source DB: PubMed Journal: Blood ISSN: 0006-4971 Impact factor: 22.113