Reactions 1680, p63 - 2 Dec 2017 Haematological toxicities: case report In a retrospective study, a 66-year-old man developed thrombocytopenia, leucopenia and neutropenia during treatment with azacitidine [time to reactions onsets and outcomes not stated]. The man had a history of rheumatoid arthritis, resection of right thigh and antiphospholipid antibody syndrome (diagnosed at the age of 65). He was diagnosed with myelodysplastic syndrome (MDS) with neutrophilic dermatosis (ND). Following its relapse, he started receiving treatment with a single course of azacitidine 75 mg/m /day, infusions for 7 days (1 cycle of 28 days). Because of noticeable improvement in ND, he was released on day 25 of disease (day 15 of hospitalisation). His concomitant prednisolone dose was decreased, but on day 24 the ND flared up again, thus the prednisolone dose was increased and second course of azacitidine was administered, which led to quick improvement in ND, and no more flare up was observed. The grade 3 haematological toxicities included thrombocytopenia and leucopenia after the first course, as well as neutropenia in the st nd 1 and 2 courses. He continued to receive azacitidine and the therapy was completed after 12 courses. Author comment: Regarding adverse events, the patient developed grade 3 blood toxicity as defined by the Common Terminology Criteria for Adverse Events v4.0 (CTCAE), and included thrombocytopenia and leukopenia after the first course, as well as neutropenia in the 1st and 2nd courses. Kudo D, et al. Myelodysplastic syndrome with neutrophilic dermatosis successfully treated with azacitidine. Rinsho Ketsueki 58: 607-612, No. 6, 2017. Available from: URL: http://doi.org/10.11406/rinketsu.58.607 [Japanese; summarised from a translation] - Japan 803286002 0114-9954/17/1680-0001/$14.95 Adis © 2017 Springer International Publishing AG. All rights reserved Reactions 2 Dec 2017 No. 1680
Reactions Weekly – Springer Journals
Published: Dec 2, 2017
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