dc.contributor.author | Albert, MH | |
dc.contributor.author | Slatter, MA | |
dc.contributor.author | Gennery, ar | |
dc.contributor.author | Güngör, T | |
dc.contributor.author | Bakunina, K | |
dc.contributor.author | Markovitch, B | |
dc.contributor.author | Hazelaar, S | |
dc.contributor.author | Sirait, T | |
dc.contributor.author | Courteille, V | |
dc.contributor.author | Aiuti, A | |
dc.contributor.author | Aleinikova, OV | |
dc.contributor.author | Balashov, D | |
dc.contributor.author | Bernardo, ME | |
dc.contributor.author | Bodova, I | |
dc.contributor.author | Bruno, B | |
dc.contributor.author | Cavazzana, M | |
dc.contributor.author | Chiesa, R | |
dc.contributor.author | Fischer, A | |
dc.contributor.author | Hauck, F | |
dc.contributor.author | Ifversen, M | |
dc.contributor.author | Kałwak, K | |
dc.contributor.author | Klein, C | |
dc.contributor.author | Kulagin, A | |
dc.contributor.author | Kupesiz, A | |
dc.contributor.author | Kuskonmaz, Baris | |
dc.contributor.author | Lindemans, CA | |
dc.contributor.author | Locatelli, F | |
dc.contributor.author | Lum, SH | |
dc.contributor.author | Maschan, A | |
dc.contributor.author | Meisel, R | |
dc.contributor.author | Moshous, D | |
dc.contributor.author | Porta, F | |
dc.contributor.author | Sauer, MG | |
dc.contributor.author | Sedlacek, P | |
dc.contributor.author | Schulz, A | |
dc.contributor.author | Suarez, F | |
dc.contributor.author | Vallée, TC | |
dc.contributor.author | Winiarski, JH | |
dc.contributor.author | Zecca, M | |
dc.contributor.author | Neven, B | |
dc.contributor.author | Veys, P | |
dc.contributor.author | Lankester, AC | |
dc.date.accessioned | 2022-10-12T13:08:46Z | |
dc.date.available | 2022-10-12T13:08:46Z | |
dc.date.issued | 2022-03 | |
dc.identifier.uri | https://doi.org/10.1182/blood.2021014687 | |
dc.identifier.uri | http://hdl.handle.net/11655/26889 | |
dc.description.abstract | Allogeneic hematopoietic stem cell transplantation (HSCT) is a potentially curative
treatment for patients affected by Wiskott-Aldrich syndrome (WAS). Reported HSCT
outcomes have improved over time with respect to overall survival, but some studies
have identified older age and HSCT from alternative donors as risk factors predicting
poorer outcome. We analyzed 197 patients undergoing transplant at European Society for
Blood and Marrow Transplantation centers between 2006 and 2017 who received
conditioning as recommended by the Inborn Errors Working Party (IEWP): either busulfan
(n 5 103) or treosulfan (n 5 94) combined with fludarabine 6 thiotepa. After a median
follow-up post-HSCT of 44.9 months, 176 patients were alive, resulting in a 3-year overall
survival of 88.7% and chronic graft-versus-host disease (GVHD)-free survival (events
Q:4 include death, graft failure, and severe chronic GVHD) of 81.7%. Overall survival and
chronic GVHD-free survival were not significantly affected by conditioning regimen
(busulfan- vs treosulfan-based), donor type (matched sibling donor/matched family donor
vs matched unrelated donor/mismatched unrelated donor vs mismatched family donor), or
period of HSCT (2006-2013 vs 2014-2017). Patients aged <5 years at HSCT had a significantly better overall survival. The overall cumulative incidences of grade III to IV acute GVHD and extensive/
moderate/severe chronic GVHD were 6.6% and 2.1%, respectively. Patients receiving treosulfan-based conditioning
had a higher incidence of graft failure and mixed donor chimerism and more frequently underwent secondary
procedures (second HSCT, unconditioned stem cell boost, donor lymphocyte infusion, or splenectomy). In summary,
HSCT for WAS with conditioning regimens currently recommended by IEWP results in excellent survival and low rates
of GVHD, regardless of donor or stem cell source, but age ≥5 years remains a risk factor for overall survival | tr_TR |
dc.language.iso | en | tr_TR |
dc.rights | info:eu-repo/semantics/openAccess | tr_TR |
dc.subject | Wiskott-Aldrich syndrome, HSCT | tr_TR |
dc.title | Hematopoietic stem cell transplantation for Wiskott-Aldrich syndrome: an EBMT Inborn Errors Working Party analysis | tr_TR |
dc.type | info:eu-repo/semantics/article | tr_TR |
dc.relation.journal | Blood | tr_TR |
dc.contributor.department | Çocuk Sağlığı ve Hastalıkları | tr_TR |
dc.description.index | WoS | tr_TR |
dc.funding | Yok | tr_TR |