| Literature DB >> 31471325 |
Chunfu Li1,2, Vikram Mathews3, Soyoung Kim4, Biju George3, Kyle Hebert5, Hua Jiang6, Changgang Li7, Yiping Zhu8, Daniel A Keesler5, Jaap Jan Boelens9, Christopher C Dvorak10, Rajni Agarwal11, Jeffery J Auletta12, Rakesh K Goyal13, Rabi Hanna14, Kimberly Kasow15, Shalini Shenoy16, Angela R Smith17, Mark C Walters18, Mary Eapen5.
Abstract
We studied 1110 patients with β-thalassemia major aged ≤25 years who received transplants with grafts from HLA-matched related (n = 677; 61%), HLA-mismatched related (n = 78; 7%), HLA-matched unrelated (n = 252; 23%), and HLA-mismatched unrelated (n = 103; 9%) donors between 2000 and 2016. Ninety percent of transplants were performed in the last decade. Eight-five percent of patients received ≥20 transfusions and 88% were inadequately chelated. All patients received myeloablative-conditioning regimen. Overall and event-free survival were highest for patients aged ≤6 years and after HLA-matched related and HLA-matched unrelated donor transplantation. The 5-year probabilities of overall survival for patients aged ≤6 years, 7 to 15 years, and 16 to 25 years, adjusted for donor type and conditioning regimen were 90%, 84%, and 63%, respectively (P < .001). The corresponding probabilities for event-free survival were 86%, 80%, and 63% (P < .001). Overall and event-free survival did not differ between HLA-matched related and HLA-matched unrelated donor transplantation (89% vs 87% and 86% vs 82%, respectively). Corresponding probabilities after mismatched related and mismatched unrelated donor transplantation were 73% vs 83% and 70% vs 78%. In conclusion, if transplantation is considered as a treatment option it should be offered early (age ≤6 years). An HLA-matched unrelated donor is a suitable alternative if an HLA-matched relative is not available.Entities:
Year: 2019 PMID: 31471325 PMCID: PMC6737407 DOI: 10.1182/bloodadvances.2019000291
Source DB: PubMed Journal: Blood Adv ISSN: 2473-9529