Using short-term evidence to predict six-month outcomes in clinical trials of signs and symptoms in rheumatoid arthritis

被引:3
作者
Nixon, Richard M. [1 ]
Bansback, Nick [2 ]
Stevens, John W. [3 ]
Brennan, Alan [4 ]
Madan, Jason [4 ]
机构
[1] Univ Forvie Site, MRC Biostat Unit, Inst Publ Hlth, Cambridge CB2 2SR, England
[2] St Pauls Hosp, Ctr Hlth Evaluat & Outcome Sci, Vancouver, BC V6Z 1Y6, Canada
[3] Univ Sheffield, Ctr Bayesian Stat Hlth Econ, Sheffield, S Yorkshire, England
[4] Univ Sheffield, Sheffield Sch Hlth & Related Res, Sheffield, S Yorkshire, England
关键词
rheumatoid arthritis; systematic review; ACR; prediction; INTERLEUKIN-1 RECEPTOR ANTAGONIST; ANTITUMOR NECROSIS FACTOR; RECEIVING CONCOMITANT METHOTREXATE; PLACEBO-CONTROLLED TRIAL; SURROGATE END-POINTS; MONOCLONAL-ANTIBODY; DOUBLE-BLIND; ETANERCEPT; THERAPY; COMBINATION;
D O I
10.1002/pst.351
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
A model is presented to generate a distribution for the probability of an ACR response at six months for a new treatment for rheumatoid arthritis given evidence from a one- or three-month clinical trial. The model is based on published evidence from 11 randomized controlled trials on existing treatments. A hierarchical logistic regression model is used to find the relationship between the proportion of patients achieving ACR20 and ACR50 at one and three months and the proportion at six months. The model is assessed by Bayesian predictive P-values that demonstrate that the model fits the data well. The model can be used to predict the number of patients with an ACR response for proposed six-month clinical trials given data from clinical trials of one or three months duration. Copyright (C) 2008 John Wiley & Sons, Ltd.
引用
收藏
页码:150 / 162
页数:13
相关论文
共 29 条
[1]   A comparison of etanercept and methotrexate in patients with early rheumatoid arthritis [J].
Bathon, JM ;
Martin, RW ;
Fleischmann, RM ;
Tesser, JR ;
Schiff, MH ;
Keystone, EC ;
Genovese, MC ;
Wasko, MC ;
Moreland, LW ;
Weaver, AL ;
Markenson, J ;
Finck, BK .
NEW ENGLAND JOURNAL OF MEDICINE, 2000, 343 (22) :1586-1593
[2]  
Bresnihan B, 1998, ARTHRITIS RHEUM, V41, P2196, DOI 10.1002/1529-0131(199812)41:12<2196::AID-ART15>3.3.CO
[3]  
2-U
[4]  
Buyse M, 2000, Biostatistics, V1, P49, DOI 10.1093/biostatistics/1.1.49
[5]   Treatment of rheumatoid arthritis with anakinra, a recombinant human interleukin-1 receptor antagonist, in combination with methotrexate - Results of a twenty-four-week, multicenter, randomized, double-blind, placebo-controlled trial [J].
Cohen, S ;
Hurd, E ;
Cush, J ;
Schiff, M ;
Weinblatt, ME ;
Moreland, LW ;
Kremer, J ;
Bear, MB ;
Rich, WJ ;
McCabe, D .
ARTHRITIS AND RHEUMATISM, 2002, 46 (03) :614-624
[6]   A multicentre, double blind, randomised, placebo controlled trial of anakinra (Kineret), a recombinant interleukin 1 receptor antagonist, in patients with rheumatoid arthritis treated with background methotrexate [J].
Cohen, SB ;
Moreland, LW ;
Cush, JJ ;
Greenwald, MW ;
Block, S ;
Shergy, WJ ;
Hanrahan, PS ;
Khraishi, MM ;
Patel, A ;
Sun, G ;
Bear, MB .
ANNALS OF THE RHEUMATIC DISEASES, 2004, 63 (09) :1062-1068
[7]  
European Medicines Agency, 2003, POINTS CONS CLIN INV
[8]  
*FDA CDER CBER CDR, 1999, GUID IND CLIN DEV PR
[9]   STATISTICAL VALIDATION OF INTERMEDIATE END-POINTS FOR CHRONIC DISEASES [J].
FREEDMAN, LS ;
GRAUBARD, BI ;
SCHATZKIN, A .
STATISTICS IN MEDICINE, 1992, 11 (02) :167-178
[10]  
Gail M H, 2000, Biostatistics, V1, P231, DOI 10.1093/biostatistics/1.3.231