Journal
JOURNAL OF THE NEUROLOGICAL SCIENCES
Volume 361, Issue -, Pages 158-167Publisher
ELSEVIER SCIENCE BV
DOI: 10.1016/j.jns.2015.12.043
Keywords
Multiple sclerosis; Interferon beta; Glatiramer acetate; Suboptimal response; Disability; Prediction
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Funding
- Novartis S.A
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Introduction: There is no consensus about short-term suboptimal response to first-line treatments in relapsing remitting multiple sclerosis. Methods: We searched studies with interferon beta or glatiramer acetate in which a long-term (>= 2 years (y)) outcome could be predicted using short-term (<= 1 y) suboptimal response criteria (EDSS-, imaging- and/or relapse based). We obtained pooled diagnostic accuracy parameters for the 1-y criteria used to predict disability progression between 2-5 y. Results: We selected 45 articles. Eight studies allowed calculating pooled estimates of 16 criteria. The three criteria with best accuracy were: new or enlarging 12-weighted lesions (newT2) >= 1 (pooled sensitivity: 85.5%; specificity:70.2%; positive predictive value:48.0%; negative predictive value:93.8%), newT2 >= 2 (62.4%, 83.6%, 55.0% and 87.3%, respectively) and RIO score >= 2 (55.8%, 84.4%, 47.8% and 882%). Pooled percentages of suboptimal responders were 43.3%, 27.6% and 23.7%, respectively. Pooled diagnostic odds ratios were 14.6 (95% confidence interval: 1.4-155), 9.2 (1.4-59.0) and 82 (3.5-192). Conclusions: All criteria had a limited predictive value. RIO score >= 2 at 1-y combined fair accuracy and consistency, limiting the probability of disability progression in the next years to 1 in 8 optimal responders. NewT2 >= 1 at 1-y had similar positive predictive value, but diminished the false negatives to 1 in 16 patients. More sensitive measures of treatment failure at short term are needed. (C) 2015 Elsevier B.V. All rights reserved.
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