Composite end points to assess delay of disability progression by MS treatments

被引:23
作者
Zhang, J. [1 ]
Waubant, E. [2 ]
Cutter, G. [3 ]
Wolinsky, J. S. [4 ]
Leppert, D. [5 ,6 ]
机构
[1] Genentech Inc, Dept Biostat, San Francisco, CA 94080 USA
[2] UCSF Multiple Sclerosis Ctr, Dept Neurosci, San Francisco, CA USA
[3] Univ Alabama Birmingham, Dept Biostat, Birmingham, AL 35294 USA
[4] Univ Texas Hlth Sci Ctr Houston, Dept Neurol, Houston, TX 77030 USA
[5] F Hoffmann La Roche Ltd, Pharmaceut Div PDN, Basel, Switzerland
[6] Univ Basel Hosp, Dept Neurol, Basel, Switzerland
关键词
Multiple sclerosis; EDSS; T25WT; 9HPT; rituximab; disability progression; composite end point; PPMS; SCLEROSIS FUNCTIONAL COMPOSITE; MULTIPLE-SCLEROSIS; CLINICAL-TRIALS; OUTCOME MEASURE; EDSS;
D O I
10.1177/1352458514527180
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: The Expanded Disability Status Scale (EDSS) has low sensitivity and reliability for detecting sustained disability progression (SDP) in multiple sclerosis (MS) trials. Objective: This study evaluated composite disability end points as alternatives to EDSS alone. Methods: SDP rates were determined using 96-week data from the Olympus trial (rituximab in patients with primary progressive MS). SDP was analyzed using composite disability end points: SDP in EDSS, timed 25-foot walk test (T25FWT), or 9-hole peg test (9HPT) (composite A); SDP in T25FWT or 9HPT (composite B); SDP in EDSS and (T25FWT or 9HPT) (composite C); and SDP in any two (EDSS, T25FWT, and 9HPT) (composite D). Results: Overall agreements between EDSS and other disability measures in defining SDP were 66%-73%. Composite A showed similar treatment effect estimate versus EDSS alone with much higher SDP rates. Composite B, C, and D all showed larger treatment effect estimate with different or similar SDP rates versus EDSS alone. Using composite A (24-week confirmation only), B, C, or D could reduce sample sizes needed for MS trials. Conclusion: Composite end points including multiple accepted disability measures could be superior to EDSS alone in analyzing disability progression and should be considered in future MS trials.
引用
收藏
页码:1494 / 1501
页数:8
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