4.6 Article

Choice of conditioning regimens for bone marrow transplantation in severe aplastic anemia

期刊

BLOOD ADVANCES
卷 3, 期 20, 页码 3123-3131

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AMER SOC HEMATOLOGY
DOI: 10.1182/bloodadvances.2019000722

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资金

  1. National Institutes of Health, National Cancer Institute [U24-CA76518]
  2. National Institutes of Health, National Heart, Lung, and Blood Institute [U24-CA76518]
  3. National Institutes of Health, National Institute of Allergy and Infectious Diseases [U24-CA76518]
  4. Health Services Research Administration, Department of Health and Human Services [HHSH 250201200016C]

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Allogeneic bone marrow transplantation (BMT) is curative therapy for the treatment of patients with severe aplastic anemia (SAA). However, several conditioning regimens can be used for BMT. We evaluated transplant conditioning regimens for BMT in SAA after HLA-matched sibling and unrelated donor BMT. For recipients of HLA-matched sibling donor transplantation (n 5 955), fludarabine (Flu)/cyclophosphamide (Cy)/antithymocyte globulin (ATG) or Cy/ATG led to the best survival. The 5-year probabilities of survival with Flu/Cy/ATG, Cy/ATG, Cy +/- Flu, and busulfan/Cy were 91%, 91%, 80%, and 84%, respectively (P = .001). For recipients of 8/8 and 7/8 HLA allele-matched unrelated donor transplantation (n = 409), there were no differences in survival between regimens. The 5-year probabilities of survival with Cy/ATG/total body irradiation 200 cGy, Flu/Cy/ATG/total body irradiation 200 cGy, Flu/Cy/ATG, and Cy/ATG were 77%, 80%, 75%, and 72%, respectively (P = .61). Rabbit-derived ATG compared with equine-derived ATG was associated with a lower risk of grade II to IV acute graft-versus-host disease (GVHD) (hazard ratio [HR], 0.39; P <.001) but not chronic GVHD. Independent of conditioning regimen, survival was lower in patients aged.30 years after HLA-matched sibling (HR, 2.74; P < .001) or unrelated donor (HR, 1.98; P = .001) transplantation. These data support Flu/Cy/ATG and Cy/ATG as optimal regimens for HLA-matched sibling BMT. Although survival after an unrelated donor BMT did not differ between regimens, use of rabbit-derived ATG may be preferred because of lower risks of acute GVHD.

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