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  Vol. 40 No. 11, October 1983 TABLE OF CONTENTS
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  2. ANALYSIS OF CLINICAL TRIAL PROTOCOLS RECENTLY USED IN MULTIPLE SCLEROSIS
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Immunosuppression and Plasmapheresis in Chronic Progressive Multiple Sclerosis

Design of a Clinical Trial

Stephen L. Hauser, MD; David M. Dawson, MD; James R. Lehrich, MD; M. Flint Beal, MD; Sherwin V. Kevy, MD; Howard L. Weiner, MD

Arch Neurol. 1983;40(11):687-690.

Since this article does not have an abstract, we have provided the first 150 words of the full text PDF and any section headings.

We recently completed a prospective randomized trial of three different immunosuppressive regimens in patients with chronic progressive multiple sclerosis (MS).1 The treatments administered were corticotropin, intravenous (IV) high-dosage cyclophosphamide, and plasma exchange. This article reviews the design of the study, focusing on the choice of therapeutic agents, selection of patients, and evaluation of response to treatment.

THE THERAPEUTIC PROBLEM

Current evidence suggests that MS is an autoimmune disease related in some way to an antecedent viral infection.1,2 At present, there is no generally accepted effective therapy. Corticotropin therapy has been shown to accelerate recovery from acute relapses,3 although neither it nor corticosteroid therapy seem to modify the long-term course of the disease.4-7

Recently, several uncontrolled studies have suggested that a short course ("pulse") of intensive immunosuppression with cyclophosphamide or other cytotoxic drugs may favorably influence the natural course of active MS. Hommes and colleagues8 . . . [Full Text PDF of this Article]


Author Affiliations

From the Multiple Sclerosis Clinical and Research Unit, Department of Medicine, Division of Neurology, Brigham & Women's Hospital (Drs Hauser, Dawson, and Weiner); the Department of Neuroscience (Drs Hauser and Weiner) and Transfusion Service (Dr Kevy), Children's Hospital Medical Center; and the Department of Neurology, Massachusetts General Hospital (Drs Lehrich and Beal), Boston.


Footnotes

Reprints not available.



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