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The Use of Etiocholanolone and Antithymus Globulin to Treat Aplastic Anemia: An Uncontrolled Comparative Study

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Abstract

In the past 25 years a variety of therapies have been introduced for the treatment of aplastic anemia. The most encouraging results have been the complete hematological recovery associated with bone marrow transplantation from sibling donors to patients less than 25 years of age.1 In older patients the results with bone marrow transplantation have been less desirable because of the complications of graft-versus-host (GVH) disease and infection. In this older age group, immune suppression therapy with glucocorticoids or antithymus globulin (ATG) has been used with variable enthusiasm in the past decade. From the Cooperative Group report in Europe, ATG or methylprednisolone therapy appears to have had similar response rates, and the side effects from these immune suppressive drugs have been tolerable.2,3 The recovery rate of aplastic anemia with different preparations of ATG has varied.4 However, in the United States the sustained clinical responses have ranged about 40%, but most clinical series have used one ATG preparation (Atgam, UpJohn).5

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© 1990 Springer-Verlag Inc.

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Gardner, F.H., Juneja, H.S. (1990). The Use of Etiocholanolone and Antithymus Globulin to Treat Aplastic Anemia: An Uncontrolled Comparative Study. In: Shahidi, N.T. (eds) Aplastic Anemia and Other Bone Marrow Failure Syndromes. Springer, New York, NY. https://doi.org/10.1007/978-1-4612-3254-4_13

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  • DOI: https://doi.org/10.1007/978-1-4612-3254-4_13

  • Publisher Name: Springer, New York, NY

  • Print ISBN: 978-1-4612-7935-8

  • Online ISBN: 978-1-4612-3254-4

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