Journal of Dermatological Treatment (Apr 2022)

Unmet needs in patients with moderate-to-severe plaque psoriasis treated with methotrexate in real world practice: FirST study

  • Raquel Rivera,
  • E. Vilarrasa,
  • M. Ribera,
  • E. Roe,
  • T. Kueder-Pajares,
  • A. I. Zayas,
  • L. Martínez-Molina,
  • J. Mataix Díaz,
  • I. M. Rodríguez-Nevado,
  • T. Usero-Bárcena,
  • D. de la Mano,
  • C. García-Donoso,
  • A. Olveira,
  • G. Guinea,
  • V. Martín-Vázquez,
  • M. Ferran

DOI
https://doi.org/10.1080/09546634.2020.1801977
Journal volume & issue
Vol. 33, no. 3
pp. 1329 – 1338

Abstract

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Background Methotrexate (MTX) is frequently used in the treatment of moderate-to-severe psoriasis, however, there is limited data on health-related quality-of-life (HRQoL), psoriasis clinical outcomes and hepatic fibrosis in MTX-treated patients in routine clinical practice. Objectives To investigate the impact of moderate-to-severe psoriasis in MTX-treated patients in Spain regarding to HRQoL, psoriasis clinical data and risk of hepatic fibrosis. Methods Observational, non-interventional, cross-sectional, retrospective, multicentre study, performed in Spain in moderate-to-severe plaque psoriasis patients treated with MTX > 16 weeks prior to inclusion. Results Despite ongoing treatment, 17.1% of 457 evaluable patients reported moderate-to-extreme impact on HRQoL (DLQI > 5); 21.4% BSA > 5 and 35.2% moderate-to-severe pruritus (VAS ≥ 4). Persistent severe psoriasis (PASI ≥ 10 and/or DLQI ≥ 10) was observed in 10.7%. Hepatic steatosis was identified in 64.1% of patients (HSI ≥ 36) and 37.2% of the patients were at-risk of advanced fibrosis which was associated to the MTX treatment duration. Conclusions The study identified unmet needs in moderate-to-severe plaque psoriasis patients treated with MTX, revealing a significant proportion of sub-optimally controlled patients in terms of HRQoL and different domains of the disease. This study also found patients at-risk of advanced fibrosis, with evidence suggesting a correlation between longer exposures to MTX and higher risk of advanced fibrosis.

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