Predicting gadolinium enhancement status in MS patients eligible for randomized clinical trials

被引:38
作者
Barkhof, F
Held, U
Simon, JH
Daumer, M
Fazekas, F
Filippi, M
Frank, JA
Kappos, L
Li, D
Menzler, S
Miller, DH
Petkau, J
Wolinsky, J
机构
[1] Vrije Univ Amsterdam, Dept Radiol, Med Ctr, NL-1007 MB Amsterdam, Netherlands
[2] Sylvia Lawry Ctr, Munich, Germany
[3] Univ Colorado, Hlth Sci Ctr, Denver, CO 80202 USA
[4] Karl Franzens Univ Graz, A-8010 Graz, Austria
[5] Osped San Raffaele, Milan, Italy
[6] NIH, Lab Diagnost Radiol, Bethesda, MD 20892 USA
[7] Kantonsspital, CH-4031 Basel, Switzerland
[8] Univ British Columbia, Vancouver, BC V5Z 1M9, Canada
[9] Stiftung Tierzart Hsch, Hannover, Germany
[10] Inst Neurol, London WC1N 3BG, England
[11] Univ Texas, Hlth Sci Ctr, Houston, TX USA
关键词
D O I
10.1212/01.wnl.0000183149.87975.32
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Gadolinium enhancement is often used in randomized clinical trials to evaluate the efficacy of new drugs in multiple sclerosis (MS). Knowledge about predictors of enhancement status is important for the selection of patients for MRI monitored trials. Methods: Data from 17 trials were available in anonymized format through the Sylvia Lawry Centre for MS Research. In an open part containing 1,328 (non primary progressive) patients, two logistic regression analyses were explored, including demographic, clinical, and MRI predictors. The authors examined the area under the curve (AUC) and the increase in positive predictive value (PPV). The final selection of models was validated in a closed part of 848 comparable patients. Results: Age at onset, disease duration, and disease course (CIS/RR/SP) were important predictors from the multivariate models. Further, a multivariate model including T2 burden of disease was more predictive than one with only clinical predictors (AUC 0.719 vs 0.625, p < 0.001). For the model with T2 burden of disease, the PPV was 66.8%, compared to 58.5% for the model without (a priori chance 46.4%). These findings were unequivocally confirmed in the closed part of the database. Conclusion: Gadolinium status can be predicted by a set of baseline variables, certainly when T2 burden of disease is included. These findings may benefit the design and statistical power of future randomized clinical trials.
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页码:1447 / 1454
页数:8
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