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[Umbilical cord blood transplantation (UCBT) in thalassemia children]

[Umbilical cord blood transplantation (UCBT) in thalassemia children] Research Abstract Details 

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  • [Umbilical cord blood transplantation (UCBT) in thalassemia children] Abstract Text:

    s huangS Huang,j fangJ Fang,c chenC Chen,r baoR Bao,y wuY Wu,d zhouD Zhou,s liS Li,

    OBJECTIVE: To evaluate the efficacy of allo-UCBT in thalassemia children. METHODS: Five patients with beta-thalassemia major (genotypes were homozygote of beta41-42, beta654 and double heterozygosities of beta41-42/beta654, beta41-42/-28, beta654/-28, respectively) were treated by allo-UCBT. The median age was 3 year and ten month old (31/2 - 7 2/12). Four donor-recipient pairs were HLA-identical and one 1 locus mismatch. The patients received a median UCB nucleated cells (NC) of 5.5 x 10(7)/kg body weight [range (4.7 - 7.7) x 10(7)/kg] and CD(34)(+)CD(38)(-) cells 2.8 x 10(5)/kg [range (0.6 - 4.5) x 10(5)/kg] and CFU-GM 1.09 x 10(5)/kg [range (0.24 - 230.00) x 10(5)/kg]. The conditioning regimen consisted ofbusalphan 16 - 20 mg/kg, cyclophosphamide 180 - 200 mg/kg, horse antithymocyte globulin (ATG) 90 mg/kg or rabbit anti-lymphocyte globulin (ALG) 25 mg/kg and melphalan of 90 mg/m(2) was added to four cases. Cyclosporine A (CsA) alone was administered in 3 cases, and a combination of CsA and methotrexate in the other 2 cases. RESULTS: Four cases were engrafted, but one rejected and recurred thalassemia state at day 60 past UCBT. One case had autologous reconstitution. The reconstitutions were found in all patients with neutrophils 0.5 x 10(9)/L at day 19 (14 - 22), platelets > 20 x 10(9)/L at day 37 (21 - 63). Two cases developed grade I and II acute GVHD respectively. None developed chronic GVHD. Three patients survived disease-freely (survival with ex-thalassemia state). The median follow-up was 18 months, the probability of survival was 100%. CONCLUSION: Allo-UCBT could reconstitute hematopoiesis with low frequency and mild grade of GVHD. It is an effective treatment for thalassemia.

    [Umbilical cord blood transplantation (UCBT) in thalassemia children] Publishing Authors By Initials

    s huangS Huang,j fangJ Fang,c chenC Chen,r baoR Bao,y wuY Wu,d zhouD Zhou,s liS Li,

    For similar abstracts research abstracts see: abstracts research

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    [Umbilical cord blood transplantation (UCBT) in thalassemia children] Journal Published:

    PUBLICATION TYPE: Research Support, Non-U.S. Gov

    Journal: Zhonghua xue ye xue za zhi = Zhonghua xueyexue zaz

    VOLUME: 22

    Page Numbers: 182-5

    Journal Abbreviation: Zhonghua Xue Ye Xue Za Zhi

    ISSN: 0253-2727

    DAY: 5

    MONTH: Apr

    YEAR: 2001

    [Umbilical cord blood transplantation (UCBT) in thalassemia children] Information

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    LANGUAGE: chi

    NlmUniqueID: 8212398

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    Grant and Affiliation Information for [Umbilical cord blood transplantation (UCBT) in thalassemia children]

    AFFILIATION: Department of Pediatrics, Sun Yat-Sen Memorial Hospital, Sun Yat-Sen University of Medical Sciences, Guangzhou 510120, China.

    Country: China

    China Research PublicationChina Research Publication

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    MEDLINETA: Zhonghua Xue Ye Xue Za Zhi

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