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Autoimmune Haemolysis in Patients with B-CLL Treated with Chlorodeoxyadenosine (CDA)
29
Citations
19
References
1998
Year
ImmunohematologyImmunologyBlood CellPathologyAutoimmune HaemolysisImmunotherapyBone Marrow FailureHematologyCertain Cll PatientsCell TransplantationHealth SciencesAutoimmune DiseaseAutoimmunityImmunologic DiseaseCda TherapyB-chronic Lymphocytic LeukaemiaMalignant Blood DisorderImmunosuppressionAdult T-cell Leukemia-lymphomaMedicine
We have treated 19 B-chronic lymphocytic leukaemia (B-CLL) patients with CDA (Leustat, Janssen-Cilag). Four patients developed severe autoimmune haemolytic anaemia, and 2 of these had severe reticulocytopenia due to red cell aplasia/hypoplasia. Two patients died as a complication of the haemolysis one during the primary episode, with a clinical course suggestive of transfusion associated graft-versus-host disease (taGVHD), and one following a relapse of haemolysis. The onset of haemolysis occurs within 4 cycles of CDA therapy and is temporally related to the T-lymphocyte nadir induced by CDA. The presence of a positive DAT prior to therapy in 3 of 4 patients developing haemolysis suggests that the CDA induced T-lymphocytopenia may exacerbate the tendency of certain CLL patients to autoimmune haemolysis.
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