Key result
Systemic lymphoblastoid interferon fails to reduce MRI lesions versus placebo in chronic progressive MS.
Why the study?
Does systemic lymphoblastoid interferon reduce MRI-detected lesions in patients with chronic progressive multiple sclerosis?
RCT (n=63)
Does systemic lymphoblastoid interferon reduce MRI-detected lesions in patients with chronic progressive multiple sclerosis?
Systemic lymphoblastoid interferon is not effective in decreasing MRI-detected lesion activity or load in chronic progressive multiple sclerosis.
Systemic lymphoblastoid interferon should not be used in chronic progressive multiple sclerosis; confirms no MRI lesion benefit versus placebo in this RCT.
Magnetic resonance imaging (MRI) was used to evaluate the efficacy of systemic lymphoblastoid interferon therapy in chronic progressive multiple sclerosis. The clinical outcome of this trial has been reported previously. Thirty-six patients with chronic progressive multiple sclerosis were treated with interferon daily for 6 months and 27 received placebo. Patients had MRI at the outset of the study and after 6 and 24 months. Lesion activity and changes in lesion load were determined. As the study progressed, both the interferon- and the placebo-treated group developed more active lesions. There was no difference in lesion activity between the two groups. Comparison of lesion load, however, showed a trend toward improvement after 6 months for the interferon-treated group. This difference between the two groups had disappeared by the end of the study. We conclude that lymphoblastoid interferon was not effective in decreasing active MRI-detected lesions or in decreasing MRI lesion load in patients with chronic progressive multiple sclerosis.
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Koopmans et al. (1993) conducted an RCT in Chronic progressive multiple sclerosis (n=63). Systemic lymphoblastoid interferon vs. Placebo was evaluated on Lesion activity and changes in lesion load on MRI. Systemic lymphoblastoid interferon was not effective in decreasing active MRI-detected lesions or MRI lesion load in patients with chronic progressive multiple sclerosis compared to placebo.
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