Tytuł pozycji:
Risk factors for transplant outcomes in children and adolescents with non-malignant diseases following allogeneic hematopoietic stem cell transplantation
- Tytuł:
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Risk factors for transplant outcomes in children and adolescents with non-malignant diseases following allogeneic hematopoietic stem cell transplantation
- Autorzy:
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Dębski, Robert
Pieczonka, Anna
Sadurska, Elżbieta
Wachowiak, Jacek
Styczyński, Jan
Drabko, Katarzyna
Zaucha-Prażmo, Agnieszka
Lejman, Monika
Goździk, Jolanta
Zawitkowska, Joanna
Kowalczyk, Jerzy R.
- Data publikacji:
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2019
- Słowa kluczowe:
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child
risk factors
adolescent
hematopoietic stem cell transplantation
- Język:
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angielski
- ISBN, ISSN:
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14259524
- Prawa:
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Udzielam licencji. Uznanie autorstwa - Użycie niekomercyjne - Bez utworów zależnych 4.0 Międzynarodowa
http://creativecommons.org/licenses/by-nc-nd/4.0/legalcode.pl
- Dostawca treści:
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Repozytorium Uniwersytetu Jagiellońskiego
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BACKGROUND: The objective of this study was the analysis of transplant outcomes and survival in children treated with allogeneic hematopoietic cell transplantation (alloHCT) for non-malignant disorders, with a focus on risk factor analysis of transplant-related mortality (TRM).
MATERIAL AND METHODS: The treatment outcome was analyzed retrospectively in 10 consecutive years in 4 pediatric transplant centers in Poland. To compare the outcomes, patient data were analyzed according to the diagnosis, age at transplant, donor type, stem cell source, conditioning regimens, transplanted CD34+ cells dose, and pediatric TRM score.
RESULTS: From 183 analyzed patients, 27 (14.8%) died, all of them due to transplant-related complications. TRM occurred more frequently in matched unrelated donor (MUD) transplant recipients vs. matched sibling donor (MSD) transplant recipients (p=0.02); in peripheral blood (PB) recipients vs. bone marrow (BM) recipients (p=0.004); and in patients receiving >5×10⁶/kg CD34+ cells (p<0.0001). OS differed significantly according to underlying disease comparing to other diagnoses. Lower survival was found in patients transplanted from MUD (p=0.02). OS was higher in patients receiving BM (p=0.001) and in those receiving ≤5×10⁶/kg CD34+ cells (p<0.001). Multivariate analysis showed lower probability of TRM in BM recipients (p=0.04). The probability of TRM was higher in SCID patients (p=0.02) and in patients receiving >5×10⁶/kg CD34+ cells (p=0.0001).
CONCLUSIONS: Underlying disease, stem cell source, and CD34+ dose higher than 5×10⁶/kg were the most important risk factors for TRM, and they all affected OS.