Controlled trial of cyclophosphamide in rheumatoid arthritis.

A S Townes, J M Sowa, L E Shulman
Author Information

Abstract

Twenty-four patients with severe progressive rheumatoid arthritis were randomly assigned to cyclophosphamide or placebo in a double-blind crossover trial. Eleven patients who completed 9 months on cyclophosphamide (average dose: 1.8 mg/kg/day) demonstrated significant decrease in painful joints, swollen joints, and morning stiffness and increase in grip strength when compared to 11 patients on placebo. After crossover, significant improvement was observed in patients switched to cyclophosphamide, and deterioration within 2 months was observed in most patients changed from drug to placebo. Serum immunoglobulins and rheumatoid factor titers decreased with cyclophosphamide but antibody response to Vi antigen was unaffected. Primary delayed immune response to 2,4-dinitrochlorobenzene was markedly depressed. Adverse effects were troublesome--hemorrhagic cystitis affected 4 patients and amenorrhea occurred in 3. Despite striking beneficial effect, cyclophosphamide should be prescribed cautiously and only in severe resistant cases of rheumatoid arthritis.

MeSH Term

Adult
Aged
Amenorrhea
Antigen-Antibody Reactions
Arthritis, Rheumatoid
Blood Sedimentation
Clinical Trials as Topic
Cyclophosphamide
Cystitis
Drug Administration Schedule
Drug Evaluation
Female
Finger Joint
Hematuria
Humans
Immunity, Cellular
Immunoglobulins
Male
Middle Aged
Movement
Radiography
Remission, Spontaneous
Rheumatoid Factor
Wrist Joint

Chemicals

Immunoglobulins
Cyclophosphamide
Rheumatoid Factor

Word Cloud

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