Prognostic factors for neutrophil engraftment after haploidentical cell transplantation with PT-Cy in patients with acute myeloid leukemia in complete remission, on behalf of the ALWP-EBMT

The use of haplo-HCT with posttransplant cyclophosphamide (PT-Cy) is a new standard in the treatment of hematological diseases. A paucity of data exists on risk factors for engraftment failure in haplo-HCT with PT-Cy. We analyzed 1939 adults with acute myeloid leukemia (AML) who received a first hap...

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Veröffentlicht in:Bone marrow transplantation (Basingstoke) 2021-08, Vol.56 (8), p.1842-1849
Hauptverfasser: Ruggeri, Annalisa, Labopin, Myriam, Angelucci, Emanuele, Blaise, Didier, Ciceri, Fabio, Koc, Yener, Chiusolo, Patrizia, Diez-Martin, Jose Luiz, Gülbas, Zafer, Castagna, Luca, Bruno, Benedetto, Arat, Mutlu, Martino, Massimo, Nagler, Arnon, Mohty, Mohamad
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Sprache:eng
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Zusammenfassung:The use of haplo-HCT with posttransplant cyclophosphamide (PT-Cy) is a new standard in the treatment of hematological diseases. A paucity of data exists on risk factors for engraftment failure in haplo-HCT with PT-Cy. We analyzed 1939 adults with acute myeloid leukemia (AML) who received a first haplo-HCT from 2010 to 2019. Status at haplo-HCT was first complete remission (CR1) in 72.5% of patients, secondary AML was reported in 9.9%. Median follow-up was 24.4 months and median age at haplo-HCT was 51 years. Stem cell source was bone marrow (BM) in 42% and peripheral blood stem cell (PBSC) in 58%, and 64% of patients received a myeloablative conditioning (MAC) regimen. Cumulative incidence of primary graft failure (GF) was 6%; GF was reported in 110 patients and 54 died before day +30 with no sign of cell recovery. Overall, 33 patients underwent a second HCT in a median time of 45 days and 13 were alive at last follow-up, the 2-year overall survival (OS) after second HCT being 32.4%. In multivariate analysis, factors independently associated with the risk of nonengraftment were: secondary AML (HR 1.30, p  = 0.003), use of RIC (HR 1.22, p  
ISSN:0268-3369
1476-5365
DOI:10.1038/s41409-021-01248-3