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Allogeneic Stem Cell Transplantation in Congenital Hemoglobinopathies Using a Tailored Busulfan-Based Conditioning Regimen: Single-Center Experience 

Published byAlberta Hutchinson Modified over 5 years ago

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Presentation on theme: "Allogeneic Stem Cell Transplantation in Congenital Hemoglobinopathies Using a Tailored Busulfan-Based Conditioning Regimen: Single-Center Experience "— Presentation transcript:

1 Allogeneic Stem Cell Transplantation in Congenital Hemoglobinopathies Using a Tailored Busulfan-Based Conditioning Regimen: Single-Center Experience  Irina Zaidman, Jacob M. Rowe, Abdalla Khalil, Myriam Ben-Arush, Ronit Elhasid  Biology of Blood and Marrow Transplantation  Volume 22, Issue 6, Pages (June 2016) DOI: /j.bbmt Copyright © 2016 The American Society for Blood and Marrow Transplantation Terms and Conditions

2 Figure 1 Survival function. (A) Rate of 5-year overall survival for thalassemia patients after first transplantation was 90.5% ± 5.3%. (B) Rate of 5-year event-free survival (thalassemia-free survival) was 81.7% ± 6.8%. (C) Overall survival of patients receiving stem cells from related donors (MSDs and MFDs) compared with unrelated donors, 96.6% ± 3.4% versus 53.3% ± 24.8%, respectively (P = .005). Biology of Blood and Marrow Transplantation  , DOI: ( /j.bbmt ) Copyright © 2016 The American Society for Blood and Marrow Transplantation Terms and Conditions

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