Acquired pure red cell aplasia: updated review of treatment |
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Authors: | Sawada Kenichi Fujishima Naohito Hirokawa Makoto |
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Affiliation: | Department of Internal Medicine III, Division of Haematology, Akita University Graduate School of Medicine;, and Oncology Centre, Akita University Graduate School of Hospital, Akita, Japan |
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Abstract: | Pure red cell aplasia (PRCA) is a syndrome characterized by a severe normocytic anaemia, reticulocytopenia, and absence of erythroblasts from an otherwise normal bone marrow. Primary PRCA, or secondary PRCA which has not responded to treatment of the underlying disease, is treated as an immunologically-mediated disease. Although vigorous immunosuppressive treatments induce and maintain remissions in a majority of patients, they carry an increased risk of serious complications. Corticosteroids were used in the treatment of PRCA and this has been considered the treatment of first choice although relapse is not uncommon. Cyclosporine A (CsA) has become established as one of the leading drugs for treatment of PRCA. However, common concerns have been the number of patients treated with CsA who achieve sustained remissions and the number that relapse. This article reviews the current status of CsA therapy and compares it to other treatments for diverse PRCAs. |
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Keywords: | pure red cell aplasia corticosteroids cyclosporine A cyclophosphamide alemtuzumab rituximab |
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