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        Allogeneic hematopoietic stem cell transplantation in 24 patients with β-thalassemia major

        2011-08-15 00:54:32LiuRongrong劉容容DepyHematol1stHospGuangxiMedUnivNanning530021ChinOrganTransplant201132144147
        外科研究與新技術 2011年4期

        Liu Rongrong(劉容容,Depy Hematol,1st Hosp,Guangxi Med Univ,Nanning 530021)…∥Chin J Organ Transplant.-2011,32(3).-144 ~147

        Allogeneic hematopoietic stem cell transplantation in 24 patients with β-thalassemia major

        Liu Rongrong(劉容容,Depy Hematol,1st Hosp,Guangxi Med Univ,Nanning 530021)…∥Chin J Organ Transplant.-2011,32(3).-144 ~147

        ObjectiveTo investigate the effect of allgeneic hematopoietic stem cell transplantation(allo-HSCT)for β - thalassemia major.MethodsTwenty - four β -thalassemia major patients with median age of 4 years(range:2-15 years),18 boys and 6 girls,received allo-HSCT.They were classified into classⅡ -Ⅲ according to Pesaro thalassemia classification.Twentythree transplantations were from sibling donor and 1 was from mother,either HLA -identical(n=23)or HLA -mismatched(5/6)(n=1).Fifteen patients received bone marrow transplantation(BMT)plus peripheral blood stem cell transplantation(PBSCT),and 9 were subjected to umbilical cord blood transplantation(UCBT).The conditioning regimen consisted of busalphan,cyclophosphamide,fludarabine,plus hydroxyurea before transplantation.Graft-versus-h(huán)ost disease(GVHD)prophylaxis included CsA,methotrexate,antilymphpcute globulin,and mycophenolate mofetil.The median follow-up period was 13 months(range:3 -69).ResultsOf 24 patients,there were 21 cases(87.5%)of disease-free survival,1(4.2%)transplantation - related death,and 2 cases(8.3%)of rejection.Three-year overall survival and disease-free survival rate was 91.7%and 87.5%,respectively.The cumulative incidence of gradeⅡ-Ⅳacute GVHD and chronic GVHD was 16.7 and 20.3%,particularly cumulative extensive chronic GVHD was 5.0%.ConclusionThe sibling donor BMT plus PBSCT is an effective and safe way to treat β - thalassemia major.Cord blood is an important source of hematopoietic stem cells for HSCT.The protocol GVHD prophylaxis of CsA,MTX,ATG with a low-dose and short course of MMF can effectively reduce the incidence of severe acute GVHD,improve the outcome of thalassemia transplantation.12 refs,1 fig,1 tab.

        (Authors)

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