Fludarabine, Busulfan, Thiotepa, and Melphalan: A Novel Low‐Toxicity Myeloablative Conditioning Regimen for Haploidentical HSCT in Children and Adolescents Aged ≥7 Years With Transfusion‐Dependent β‐Thalassemia
Prospective trial demonstrates improved transplant outcomes in children with transfusion-dependent thalassemia, suggesting enhanced safety and efficacy.
Key Points
This research evaluates a new low-toxicity myeloablative conditioning regimen for haploidentical HSCT in children with transfusion-dependent thalassemia.