The ACR20 and defining a threshold for response in rheumatic diseases: too much of a good thing

被引:40
作者
Felson, David T. [1 ]
LaValley, Michael P. [2 ]
机构
[1] Boston Univ, Sch Med, Clin Epidemiol Res & Training Unit, Boston, MA 02118 USA
[2] Boston Univ, Sch Publ Hlth, Dept Biostat, Boston, MA 02118 USA
关键词
COLLEGE-OF-RHEUMATOLOGY; CLINICAL-TRIALS; ARTHRITIS; IMPROVEMENT; METHOTREXATE; CRITERIA; DRUGS;
D O I
10.1186/ar4428
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
In the past 20 years great progress has been made in the development of multidimensional outcome measures (such as the Disease Activity Score and ACR20) to evaluate treatments in rheumatoid arthritis, a process disseminated throughout rheumatic diseases. These outcome measures have standardized the assessment of outcomes in trials, making it possible to evaluate and compare the efficacy of treatments. The methodologic advances have included the selection of pre-existing outcome measures that detected change in a sensitive fashion (in rheumatoid arthritis, this was the Core Set Measures). These measures were then combined into a single multidimensional outcome measure and such outcome measures have been widely adopted in trials and endorsed by the American College of Rheumatology (ACR) and the European League Against Rheumatism (EULAR) and regulatory agencies. The secular improvement in treatment for patients with rheumatoid arthritis has been facilitated in part by these major methodologic advancements. The one element of this effort that has not optimized measurement of outcomes nor made it easier to detect the effect of treatments is the dichotomization of continuous measures of response, creating responders and non-responder definitions (for example, ACR20 responders; EULAR good responders). Dichotomizing response sacrifices statistical power and eliminates variability in response. Future methodologic work will need to focus on improving multidimensional outcome measurement without arbitrarily characterizing some patients as responders while labeling others as non-responders.
引用
收藏
页数:5
相关论文
共 16 条
[1]
Statistics notes - The cost of dichotomising continuous variables [J].
Altman, DG ;
Royston, P .
BRITISH MEDICAL JOURNAL, 2006, 332 (7549) :1080-1080
[2]
Comparison of rheumatoid arthritis clinical trial outcome measures - A simulation study [J].
Anderson, JJ ;
Bolognese, JA ;
Felson, DT .
ARTHRITIS AND RHEUMATISM, 2003, 48 (11) :3031-3038
[3]
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
[4]
BOERS M, 1994, J RHEUMATOL, V21, P86
[5]
THE AMERICAN-COLLEGE-OF-RHEUMATOLOGY PRELIMINARY CORE SET OF DISEASE-ACTIVITY MEASURES FOR RHEUMATOID-ARTHRITIS CLINICAL-TRIALS [J].
FELSON, DT ;
ANDERSON, JJ ;
BOERS, M ;
BOMBARDIER, C ;
CHERNOFF, M ;
FRIED, B ;
FURST, D ;
GOLDSMITH, C ;
KIESZAK, S ;
LIGHTFOOT, R ;
PAULUS, H ;
TUGWELL, P ;
WEINBLATT, M ;
WIDMARK, R ;
WILLIAMS, HJ ;
WOLFE, F .
ARTHRITIS AND RHEUMATISM, 1993, 36 (06) :729-740
[6]
USE OF SHORT-TERM EFFICACY TOXICITY TRADEOFFS TO SELECT 2ND-LINE DRUGS IN RHEUMATOID-ARTHRITIS - A METAANALYSIS OF PUBLISHED CLINICAL-TRIALS [J].
FELSON, DT ;
ANDERSON, JJ ;
MEENAN, RF .
ARTHRITIS AND RHEUMATISM, 1992, 35 (10) :1117-1125
[7]
AMERICAN-COLLEGE-OF-RHEUMATOLOGY PRELIMINARY DEFINITION OF IMPROVEMENT IN RHEUMATOID-ARTHRITIS [J].
FELSON, DT ;
ANDERSON, JJ ;
BOERS, M ;
BOMBARDIER, C ;
FURST, D ;
GOLDSMITH, C ;
KATZ, LM ;
LIGHTFOOT, R ;
PAULUS, H ;
STRAND, V ;
TUGWELL, P ;
WEINBLATT, M ;
WILLIAMS, HJ ;
WOLFE, F ;
KIESZAK, S .
ARTHRITIS AND RHEUMATISM, 1995, 38 (06) :727-735
[8]
Minimal clinically important improvement/difference (MCII/MCID) and patient acceptable symptom state (PASS): what do these concepts mean? [J].
Kvien, Tore K. ;
Heiberg, Turid ;
Hagen, Kare B. .
ANNALS OF THE RHEUMATIC DISEASES, 2007, 66 :40-41
[9]
Comparison of Certolizumab Pegol with Other Anticytokine Agents for Treatment of Rheumatoid Arthritis: A Multiple-treatment Bayesian Metaanalysis [J].
Launois, Robert ;
Avouac, Bernard ;
Berenbaum, Francis ;
Blin, Olivier ;
Bru, Isabelle ;
Fautrel, Bruno ;
Joubert, Jean-Michel ;
Sibilia, Jean ;
Combe, Bernard .
JOURNAL OF RHEUMATOLOGY, 2011, 38 (05) :835-845
[10]
Current evidence for the management of rheumatoid arthritis with biological disease-modifying antirheumatic drugs: a systematic literature review informing the EULAR recommendations for the management of RA [J].
Nam, J. L. ;
Winthrop, K. L. ;
van Vollenhoven, R. F. ;
Pavelka, K. ;
Valesini, G. ;
Hensor, E. M. A. ;
Worthy, G. ;
Landewe, R. ;
Smolen, J. S. ;
Emery, P. ;
Buch, M. H. .
ANNALS OF THE RHEUMATIC DISEASES, 2010, 69 (06) :976-986