Haploidentical transplantation in primary refractory/relapsed secondary vs de novo AML: from the ALWP/EBMT
Jazyk angličtina Země Spojené státy americké Médium print
Typ dokumentu časopisecké články
PubMed
38598754
PubMed Central
PMC11372397
DOI
10.1182/bloodadvances.2024012798
PII: 515690
Knihovny.cz E-zdroje
- MeSH
- akutní myeloidní leukemie * terapie mortalita MeSH
- dítě MeSH
- dospělí MeSH
- haploidentická transplantace * MeSH
- lidé středního věku MeSH
- lidé MeSH
- mladiství MeSH
- mladý dospělý MeSH
- nemoc štěpu proti hostiteli etiologie MeSH
- recidiva MeSH
- senioři MeSH
- transplantace hematopoetických kmenových buněk * metody škodlivé účinky MeSH
- výsledek terapie MeSH
- Check Tag
- dítě MeSH
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mladiství MeSH
- mladý dospělý MeSH
- mužské pohlaví MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
We compared the outcomes of haploidentical stem cell transplantation (haplo-HSCT) with posttransplant cyclophosphamide (PTCy) in 719 patients with primary refractory (PR) or first relapse (Rel) secondary acute myeloid leukemia (sAML; n = 129) vs those with de novo AML (n = 590), who received HSCT between 2010 and 2022. A higher percentage of patients with sAML vs de novo AML had PR disease (73.6% vs 58.6%; P = .002). In 81.4% of patients with sAML , the antecedent hematological disorder was myelodysplastic syndrome. Engraftment was 83.5% vs 88.4% in sAML and de novo AML, respectively (P = .13). In multivariate analysis, haplo-HSCT outcomes did not differ significantly between the groups: nonrelapse mortality hazard ratio (HR), 1.38 (95% confidence interval [CI], 0.96-1.98; P = .083), relapse incidence HR, 0.68 (95% CI, 0.4.7.-1.00; P = .051). The HRs for leukemia-free survival, overall survival, and graft-versus-host disease (GVHD)-free, and GVHD and relapse-free survival were 0.99 (95% CI, 0.76-1.28; P = .94), 0.99 (95% CI, 0.77-1.29; P = .97), and 0.99 (95% CI, 0.77-1.27; P = .94), respectively. We conclude that outcomes of haplo-HSCT with PTCy are not different for PR/Rel sAML in comparison with PR/Rel de novo AML, a finding of major clinical importance.
Azienda Ospedaliero Universitaria di Udine Udine Italy
CHU Bordeaux Hopital Haut Leveque Pessac France
Department of Hematology Sorbonne University Saint Antoine Hospital INSERM UMR 938 Paris France
Division of Haematology Sheba Medical Center Tel Hashomer Israel
Institute of Hematology and Blood Transfusion Prague Czech Republic
IRCCS Ospedale Policlinico San Martino Genoa Italy
Klinikum Grosshadern Munich Germany
Ospedale San Raffaele Haematology and Bone Marrow Transplantation Milan Italy
Programme de Transplantation and Therapie Cellulaire Marseille France
University Hospital Erlangen Erlangen Germany
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