Alemtuzumab is safe and effective as immunosuppressive treatment for aplastic anaemia and single-lineage marrow failure: a pilot study and a survey from the EBMT WPSAA

Antonio Maria Risitano*, Carmine Selleri, Bianca Serio, Giovanni Fernando Torelli, Alexander Kulagin, Sebastien Maury, Joerg Halter, Vikas Gupta, Andrea Bacigalupo, Gerard Socie, Andre Tichelli, Hubert Schrezenmeier, Judith Marsh, Jakob Passweg, Bruno Rotoli, European Grp Blood Marrow

*Corresponding author for this work

    Research output: Contribution to journalArticlepeer-review

    63 Citations (Scopus)

    Abstract

    An alemtuzumab-based experimental immunosuppressive treatment (IST) regimen was investigated in 35 patients with severe aplastic anaemia (SAA), pure red cell (PRCA) or pure white cell aplasia (PWCA). Alemtuzumab total dose was 73-103 mg s.c., followed by cyclosporine. No serious toxicity due to the regimen was observed. Adverse events were clinically irrelevant; infectious events were rare. The total response rate was 58%, 84% and 100% in SAA, PRCA and PWCA, respectively, with corresponding 6 months cumulative response probabilities of 84%, 84% and 100%. Subcutaneous alemtuzumab is a feasible and sufficiently safe IST regimen for patients suffering from immune-mediated marrow failures.

    Original languageEnglish
    Pages (from-to)791-796
    Number of pages6
    JournalBritish Journal of Haematology
    Volume148
    Issue number5
    DOIs
    Publication statusPublished - Mar 2010

    Keywords

    • alemtuzumab
    • aplastic anaemia
    • pure red cell aplasia
    • pure white cell aplasia
    • bone marrow failure
    • RED-CELL APLASIA
    • ANTITHYMOCYTE GLOBULIN
    • REMISSION
    • CYCLOSPORINE
    • CAMPATH-1H
    • THERAPY
    • LEUKEMIA

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