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In patients with aplastic anemia (AA), allogeneic stem cell transplantation (ASCT) is the treatment of choice for younger patients with HLA-matched siblings. In patients older than 40 years, transplant-related mortality approaches 50% and survival does not differ between patients who receive ASCT and those who receive immunosuppressive therapy [1]. In this age group, immunosuppressive therapy has been advocated as upfront therapy, with ASCT offered only for failed immunosuppressive therapy or relapse [2].
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Koh et al. (2006) studied this question.
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