Recent advances in the haploidentical transplant (haplo-HSCT) platforms, particularly the development of in vivo and ex vivo T cell depletion, and the application of post-transplantation cyclophosphamide (PTCy) have drastically improved outcomes [3335]. Such strategies have resulted in equivalent if not superior outcomes, with OS and EFS values up to 94% of those using matched related and unrelated donors [36, 37].

From: Chapter 12, CURATIVE THERAPIES FOR α-THALASSAEMIA

Cover of Guidelines for the Management of α-Thalassaemia
Guidelines for the Management of α-Thalassaemia [Internet].
Amid A, Lal A, Coates TD, et al., editors.
Nicosia (Cyprus): Thalassaemia International Federation; 2023.
© Thalassaemia International Federation.

NCBI Bookshelf. A service of the National Library of Medicine, National Institutes of Health.