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

AI Article Synopsis

  • This study aims to compare the effectiveness of targeted synthetic and biologic DMARDs in treating psoriatic arthritis (PsA) through a network meta-analysis, addressing the lack of head-to-head clinical trials in this area.
  • A systematic literature review included 26 Phase III randomized controlled trials assessing patient-reported outcomes like HAQ-DI and SF-36 scores, with thorough data extraction and bias assessment procedures.
  • Results showed that intravenous TNF alpha inhibitors generally performed better for HAQ-DI and SF-36 scores, while various interleukin agents provided comparable improvements across outcomes.

Article Abstract

Objectives: Head-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).

Design: A 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 Sources: Ovid MEDLINE (including Epub Ahead of Print, In-Process & Other Non-Indexed Citations and Daily),Embase and Cochrane Central Register of Controlled Trials.

Eligibility Criteria: Phase 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 Synthesis: Two 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.

Results: In 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.

Conclusions: While 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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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10632897PMC
http://dx.doi.org/10.1136/bmjopen-2022-062306DOI Listing

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