THE BENEFIT OF ATG IN IMMUNOSUPPRESSIVE THERAPY OF CHILDREN WITH MODERATE APLASTIC ANEMIA

Background. Previous studies specifically focused on the immunosuppressive therapy (IST) of children with moderate aplastic anemia (MAA) are rare. The aim of this study was to evaluate the advantage of using antithymocyte globulin (ATG) in the IST and its outcome of children with MAA. Methods. Forty...

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Published inPediatric hematology and oncology Vol. 26; no. 5; pp. 313 - 320
Main Authors Jiang, Shayi, Wang, Yaoping, Shi, Wei, Shao, Yuexia, Qiao, Xiaohong, Lin, Jieliang, Kuang, Hanqin, Xie, Xiaotian
Format Journal Article
LanguageEnglish
Published England Informa UK Ltd 01.01.2009
Taylor & Francis
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Abstract Background. Previous studies specifically focused on the immunosuppressive therapy (IST) of children with moderate aplastic anemia (MAA) are rare. The aim of this study was to evaluate the advantage of using antithymocyte globulin (ATG) in the IST and its outcome of children with MAA. Methods. Forty-two children diagnosed with moderate aplastic anemia from 1993 to 2006 were retrospectively reviewed. Eighteen patients treated with ATG, cyclosporin A (CSA), and androgen are defined as the ATG group, the other 24 patients treated with CSA and androgen are defined as the non-ATG group. Survival and hematological response of the two groups were studied. Results. Response rate and transfusion-independent survival of the ATG group were both significantly higher than those of the non-ATG group (83.33 vs. 41.7%, p =. 006; and 83.33 vs. 50%, p =. 043, respectively). Compared with non-ATG group, fewer patients in ATG group progress to severe aplastic anemia (p =. 03). Conclusion. Immunosuppressive therapy including ATG benefits children with moderate aplastic anemia.
AbstractList Background. Previous studies specifically focused on the immunosuppressive therapy (IST) of children with moderate aplastic anemia (MAA) are rare. The aim of this study was to evaluate the advantage of using antithymocyte globulin (ATG) in the IST and its outcome of children with MAA. Methods. Forty-two children diagnosed with moderate aplastic anemia from 1993 to 2006 were retrospectively reviewed. Eighteen patients treated with ATG, cyclosporin A (CSA), and androgen are defined as the ATG group, the other 24 patients treated with CSA and androgen are defined as the non-ATG group. Survival and hematological response of the two groups were studied. Results. Response rate and transfusion-independent survival of the ATG group were both significantly higher than those of the non-ATG group (83.33 vs. 41.7%, p =. 006; and 83.33 vs. 50%, p =. 043, respectively). Compared with non-ATG group, fewer patients in ATG group progress to severe aplastic anemia (p =. 03). Conclusion. Immunosuppressive therapy including ATG benefits children with moderate aplastic anemia.
BACKGROUNDPrevious studies specifically focused on the immunosuppressive therapy (IST) of children with moderate aplastic anemia (MAA) are rare. The aim of this study was to evaluate the advantage of using antithymocyte globulin (ATG) in the IST and its outcome of children with MAA.METHODSForty-two children diagnosed with moderate aplastic anemia from 1993 to 2006 were retrospectively reviewed. Eighteen patients treated with ATG, cyclosporin A (CSA), and androgen are defined as the ATG group, the other 24 patients treated with CSA and androgen are defined as the non-ATG group. Survival and hematological response of the two groups were studied.RESULTSResponse rate and transfusion-independent survival of the ATG group were both significantly higher than those of the non-ATG group (83.33 vs. 41.7%, p = .006; and 83.33 vs. 50%, p = .043, respectively). Compared with non-ATG group, fewer patients in ATG group progress to severe aplastic anemia (p = .03).CONCLUSIONImmunosuppressive therapy including ATG benefits children with moderate aplastic anemia.
Previous studies specifically focused on the immunosuppressive therapy (IST) of children with moderate aplastic anemia (MAA) are rare. The aim of this study was to evaluate the advantage of using antithymocyte globulin (ATG) in the IST and its outcome of children with MAA. Forty-two children diagnosed with moderate aplastic anemia from 1993 to 2006 were retrospectively reviewed. Eighteen patients treated with ATG, cyclosporin A (CSA), and androgen are defined as the ATG group, the other 24 patients treated with CSA and androgen are defined as the non-ATG group. Survival and hematological response of the two groups were studied. Response rate and transfusion-independent survival of the ATG group were both significantly higher than those of the non-ATG group (83.33 vs. 41.7%, p = .006; and 83.33 vs. 50%, p = .043, respectively). Compared with non-ATG group, fewer patients in ATG group progress to severe aplastic anemia (p = .03). Immunosuppressive therapy including ATG benefits children with moderate aplastic anemia.
Author Wang, Yaoping
Qiao, Xiaohong
Kuang, Hanqin
Shi, Wei
Shao, Yuexia
Xie, Xiaotian
Jiang, Shayi
Lin, Jieliang
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Snippet Background. Previous studies specifically focused on the immunosuppressive therapy (IST) of children with moderate aplastic anemia (MAA) are rare. The aim of...
Previous studies specifically focused on the immunosuppressive therapy (IST) of children with moderate aplastic anemia (MAA) are rare. The aim of this study...
BACKGROUNDPrevious studies specifically focused on the immunosuppressive therapy (IST) of children with moderate aplastic anemia (MAA) are rare. The aim of...
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SubjectTerms Adolescent
Androgens - therapeutic use
Anemia, Aplastic - immunology
Anemia, Aplastic - mortality
Anemia, Aplastic - therapy
Antilymphocyte Serum - therapeutic use
antithymocyte globulin
aplastic anemia
Child
Child, Preschool
Cyclosporine - therapeutic use
Female
Humans
Immunosuppression - methods
Immunosuppressive Agents - therapeutic use
Male
Methylprednisolone - therapeutic use
pediatric
Retrospective Studies
treatment
Treatment Outcome
Title THE BENEFIT OF ATG IN IMMUNOSUPPRESSIVE THERAPY OF CHILDREN WITH MODERATE APLASTIC ANEMIA
URI https://www.tandfonline.com/doi/abs/10.1080/08880010902771549
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Volume 26
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