# Therapeutic efficacy of molecular-targeted drugs for enthesitis in patients with PsA: a network meta-analysis

**Authors:** Daisuke Nakatsubo, Takayoshi Morita, Atsushi Kumanogoh

PMC · DOI: 10.1093/rap/rkaf077 · Rheumatology Advances in Practice · 2025-07-07

## TL;DR

This study compares the effectiveness of different molecular-targeted drugs for treating enthesitis in patients with psoriatic arthritis, finding that upadacitinib and certolizumab perform better than others.

## Contribution

The study provides a network meta-analysis comparing the efficacy of various molecular-targeted drugs for enthesitis in PsA patients.

## Key findings

- Upadacitinib significantly improved enthesitis resolution rates and reduced Leeds enthesitis index scores compared to adalimumab.
- Certolizumab also reduced Leeds enthesitis index scores, showing better efficacy than some other drugs.
- Efficacy varied among molecular-targeted therapies, even within the same drug classes.

## Abstract

Enthesitis plays a key role in the pathogenesis of PsA. This study aimed to evaluate the efficacy of molecular-targeted therapies for enthesitis in patients with PsA.

In this network meta-analysis (PROSPERO registration number: CRD42024590257), studies published up to April 2025 were searched in PubMed, Web of Science, Scopus and ClinicalTrials.gov. Only randomized controlled trials assessing molecular-targeted therapies for enthesitis in PsA were included. The primary outcomes were enthesitis resolution rates and Leeds enthesitis index score reductions at 12 and 24 weeks. A random-effects model was employed to calculate risk differences (RDs) or standardized mean differences (SMDs) with 95% confidence intervals (CIs), analysing both drug classes and individual agents.

Out of 5762 screened studies, 28 randomized controlled trials were included, encompassing 10 383 patients with PsA presenting with enthesitis. Therapies included TNF–alpha inhibitors, Janus kinase inhibitors, IL-17/IL-17 receptor inhibitors, IL-23 inhibitors and a cytotoxic T lymphocyte–associated antigen-4 immunoglobulin. At 24 weeks, upadacitinib significantly improved the enthesitis resolution rate [RD: 11.24 (95% CI: 4.26 to 18.23)] and reduced the Leeds enthesitis index scores [SMD: −0.72 (95% CI: −1.36 to −0.09)] compared with adalimumab; meanwhile, other Janus kinase inhibitors did not. Certolizumab also reduced the Leeds enthesitis index scores [SMD: −0.92 (95% CI: −1.72 to −0.13)].

This network meta-analysis identified the more therapeutic efficacy of upadacitinib and certolizumab for enthesitis in patients with PsA than those of other molecular-targeted drugs. Notably, efficacy varied among molecular-targeted therapies, even within drug classes, underscoring the need for tailored therapeutic strategies.

## Linked entities

- **Proteins:** TNF (tumor necrosis factor), IL17A (interleukin 17A), IL37 (interleukin 37)
- **Chemicals:** upadacitinib (PubChem CID 58557659)
- **Diseases:** enthesitis (MONDO:0024419)

## Full-text entities

- **Genes:** TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, IL23A (interleukin 23 subunit alpha) [NCBI Gene 51561] {aka IL-23, IL-23A, IL23P19, P19, SGRF}, IL17A (interleukin 17A) [NCBI Gene 3605] {aka CTLA-8, CTLA8, IL-17, IL-17A, IL17, ILA17}
- **Diseases:** Enthesitis (MESH:D001171)
- **Chemicals:** adalimumab (MESH:D000068879), Certolizumab (MESH:D000068582), upadacitinib (MESH:C000613732)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

72 references — full list in the complete paper: https://tomesphere.com/paper/PMC12270261/full.md

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Source: https://tomesphere.com/paper/PMC12270261