Systematic literature review and network meta-analysis of therapies for psoriatic arthritis on patient-reported outcomes

被引:0
|
作者
Nash, Peter [1 ]
Dutz, Jan P. [2 ]
Peterson, Steve [3 ]
Patel, Barkha P. [4 ]
Eaton, Kiefer [4 ]
Shawi, May [5 ]
Zazzetti, Federico [6 ]
Wei, James Cheng-Chung [7 ,8 ,9 ]
机构
[1] Griffith Univ, Sch Med, Brisbane, Qld, Australia
[2] Univ British Columbia, Dept Dermatol & Skin Sci, Vancouver, BC, Canada
[3] Janssen Global Serv LLC, Immunol Global Commercial Strategy Org, Horsham, PA USA
[4] EVERSANA, Burlington, ON, Canada
[5] Janssen Global Serv LLC, Immunol Med Affairs, Horsham, PA USA
[6] Janssen Latin Amer LLC, Immunol Med Affairs, Buenos Aires, Argentina
[7] Chung Shan Med Univ Hosp, Dept Allergy Immunol & Rheumatol, Taichung, Taiwan
[8] Chung Shan Med Univ, Inst Med, Taichung, Taiwan
[9] China Med Univ, Grad Inst Integrated Med, Taichung, Taiwan
来源
BMJ OPEN | 2023年 / 13卷 / 11期
关键词
Adult dermatology; Psoriasis; RHEUMATOLOGY; DOUBLE-BLIND; CONTROLLED-TRIAL; PHASE-III; NAIVE PATIENTS; MONOCLONAL-ANTIBODY; INADEQUATE RESPONSE; BIOLOGIC-NAIVE; PLACEBO; EFFICACY; SAFETY;
D O I
10.1136/bmjopen-2022-062306
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
ObjectivesHead-to-head clinical trials are common in psoriasis, but scarce in psoriatic arthritis (PsA), making treatment comparisons between therapeutic classes difficult. This study describes the relative effectiveness of targeted synthetic (ts) and biologic (b) disease-modifying antirheumatic drugs (DMARDs) on patient-reported outcomes (PROs) through network meta-analysis (NMA).DesignA systematic literature review (SLR) was conducted in January 2020. Bayesian NMAs were conducted to compare treatments on Health Assessment Questionnaire Disability Index (HAQ-DI) and 36-item Short Form (SF-36) Health Survey including Mental Component Summary (MCS) and Physical Component Summary (PCS) scores.Data sourcesOvid MEDLINE (including Epub Ahead of Print, In-Process & Other Non-Indexed Citations and Daily),Embase and Cochrane Central Register of Controlled Trials.Eligibility criteriaPhase III randomised controlled trials (RCTs) evaluating patients with PsA receiving tsDMARDS, bDMARDs or placebo were included in the SLR; there was no restriction on outcomes.Data extraction and synthesisTwo independent researchers reviewed all citations. Data for studies meeting all inclusion criteria were extracted into a standardised Excel-based form by one reviewer and validated by a second reviewer. A third reviewer was consulted to resolve any discrepancies, as necessary. Risk of bias was assessed using the The National Institute for Health and Care Excellence clinical effectiveness quality assessment checklist.ResultsIn total, 26 RCTs were included. For HAQ-DI, SF-36 PCS and SF-36 MCS scores, intravenous tumour necrosis factor (TNF) alpha inhibitors generally ranked higher than most other classes of therapies available to treat patients with PsA. For almost all outcomes, several interleukin (IL)-23, IL-17A, subcutaneous TNF and IL-12/23 agents offered comparable improvement, while cytotoxic T-lymphocyte-associated antigen 4, phosphodiesterase-4 and Janus kinase inhibitors often had the lowest efficacy.ConclusionsWhile intravenous TNFs may provide some improvements in PROs relative to several other tsDMARDs and bDMARDs for the treatment of patients with PsA, differences between classes of therapies across outcomes were small.
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页数:9
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