Treatment modifying factors of biologics for psoriatic arthritis: a systematic review and Bayesian meta-regression

被引:0
作者
Druyts, E. [1 ]
Palmer, J. B. [2 ]
Balijepalli, C. [1 ]
Chan, K. [1 ]
Fazeli, M. S. [1 ]
Herrera, V. [2 ]
Jansen, J. P. [1 ]
Park, J. J. H. [1 ]
Kanters, S. [1 ]
Reimold, A. [3 ,4 ]
机构
[1] Precis Hlth Econ, 1505 West 2nd Ave,Suite 300, Vancouver, BC V6H 3Y4, Canada
[2] Novartis Pharmaceut, E Hanover, NJ USA
[3] Dallas VA Med Ctr, Rheumatol Sect, Dallas, TX USA
[4] Univ Texas Southwestern Med Ctr Dallas, Dept Internal Med, Div Rheumat Dis, Dallas, TX USA
关键词
psoriatic arthritis; disease-modifying anti-rheumatic drugs; biologics; systematic review; meta-regression analysis; PATIENT-REPORTED OUTCOMES; DOUBLE-BLIND; MONOCLONAL-ANTIBODY; CERTOLIZUMAB PEGOL; CLINICAL-RESPONSE; PHASE-III; EFFICACY; SAFETY; DISEASE; MULTICENTER;
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective. The aim of this study was to explore factors that modify treatment effects of non-conventional biologics versus placebo in patients with psoriatic arthritis. Methods. A systematic literature review and meta-regression was conducted. The biologics included etanercept, infliximab, adalimumab, golimumab, certolizumab, ustekinumab, tocilizumab, anakinra, abatacept, rituximab, and secukinumab. Outcomes included American College of Rheumatology (ACR) 20 and 50, Psoriasis Area Severity Index (PASI) 75, and 36-Item Short Form Health Survey (SF-36) Physical and Mental Component Summaries (PCS and MCS). Results. Twelve RCTs were eligible for meta-regression. Treatment effects for ACR-20 at 12 weeks were higher in trials with longer disease durations (OR=2.94), and lower in trials enrolling older patients (OR=0.48), and those recently published (OR=0.49). Treatment effects for ACR-50 at 12 weeks were higher in trials with more males (OR=2.27), but lower in trials with high prior anti-TNF use (OR=0.28) and recently published trials (OR=0.37). For PASI-75, trials with more male patients (24 weeks: OR=2.56), and with higher swollen and tender joint counts (12 weeks: OR=8.33; 24 weeks: OR=14.44) showed higher treatment effects, and trials with high prior antiTNF use had lower effects (OR=0.41). Treatment effects for SF-36 PCS at 24 weeks were higher in trials with longer psoriasis disease durations (OR=2.95) and PsA disease durations (OR=4.76), and those published earlier (OR=4.19). Conclusion. Our analyses show that differences in baseline characteristics may explain some of the differences in response to biologics versus placebo across different trials. Accounting for these factors in future studies will likely be important.
引用
收藏
页码:681 / 688
页数:8
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