TY - JOUR
T1 - Alemtuzumab is safe and effective as immunosuppressive treatment for aplastic anaemia and single-lineage marrow failure
T2 - a pilot study and a survey from the EBMT WPSAA
AU - Risitano, Antonio Maria
AU - Selleri, Carmine
AU - Serio, Bianca
AU - Torelli, Giovanni Fernando
AU - Kulagin, Alexander
AU - Maury, Sebastien
AU - Halter, Joerg
AU - Gupta, Vikas
AU - Bacigalupo, Andrea
AU - Socie, Gerard
AU - Tichelli, Andre
AU - Schrezenmeier, Hubert
AU - Marsh, Judith
AU - Passweg, Jakob
AU - Rotoli, Bruno
AU - European Grp Blood Marrow
PY - 2010/3
Y1 - 2010/3
N2 - 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.
AB - 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.
KW - alemtuzumab
KW - aplastic anaemia
KW - pure red cell aplasia
KW - pure white cell aplasia
KW - bone marrow failure
KW - RED-CELL APLASIA
KW - ANTITHYMOCYTE GLOBULIN
KW - REMISSION
KW - CYCLOSPORINE
KW - CAMPATH-1H
KW - THERAPY
KW - LEUKEMIA
U2 - 10.1111/j.1365-2141.2009.08027.x
DO - 10.1111/j.1365-2141.2009.08027.x
M3 - Article
SN - 0007-1048
VL - 148
SP - 791
EP - 796
JO - British Journal of Haematology
JF - British Journal of Haematology
IS - 5
ER -