The conventional treatment in warm-antibody dependent autoimmune haemolytic anaemia (AIHA) is high-dose glucocorticoid, but in more than half of the patients, haemolytic activity will recur after end of treatment or during the gradual reduction in dose of the drug. As a result, many patients will finally be splenectomized or be treated with long-term glucocorticoids or other immunosuppressive drugs as azathioprine or cyclophosphamide. Recent studies have shown however, that some patients will respond to treatment with the chimeric anti-CD 20 antibody Rituximab and is some cases, the response is permanent. In most of the studies, Rituximab has been used in refractory disease or at least as second line treatment. In this study, patients with AIHA are randomized to receive either high-dose prednisolone with gradual reduction in dose over 2-3 months alone or in combination with Rituximab 375 mg/m2 once a week for 4 weeks. The efficacy of Rituximab will be evaluated by a comparison of the patients in the two treatment arms. The primary treatment goal is a reduction in the number of patients who obtain long-term complete or partial remission. The secondary treatment goal is a reduction in patients who will be splenectomised or receive other immunosuppressive drugs. Finally a comparison of side effects of the treatments will take place.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
65
Prednisolone: 1,5 mg/kg for two weeks with gradually reduced dosis over two months. Mabthera: 375 mg/m2 once a week for four weeks
Prednisolone: 1,5 mg/kg for two weeks and then gradually reduced dosis over two months
Aalborg Hospital
Aalborg, Denmark
Rigshospitalet - Copenhagen University Hospital
Copenhagen, Denmark
Esbjerg Sygehus
Esbjerg, Denmark
Haderslev Sygehus
Haderslev, Denmark
Department of Haematology, Herlev Hospital
Herlev, Denmark
Holstebro Sygehus
Holstebro, Denmark
Naestved Sygehus
Næstved, Denmark
Odense University Hospital
Odense, Denmark
Roskilde Hospital
Roskilde, Denmark
Vejle Hospital
Vejle, Denmark
...and 1 more locations
Number of patients in each group in complete or partial remission
Time frame: End of treatment and follow-up for 12 months
Side effects
Time frame: End of treatment plus follow-up for 12 months
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