Evolution of Drug Survival with Biological Agents and Apremilast Between 2012 and 2018 in Patients with Psoriasis from the PsoBioTeq Cohort

Acta Derm Venereol. 2022 Mar 8:102:adv00665. doi: 10.2340/actadv.v101.566.

Abstract

Drug survival reflects treatment effectiveness and safety in real life. There is limited data on the variation of drug survival with the availability of systemic treatments with additional biological disease-modifying antirheumatic drugs (bDMARDs) or synthetic disease-modifying antirheumatic drugs (sDMARDs). The aim of this study was to determine whether the increasing number of available systemic treatments for psoriasis affects drug survival over time. Patients were selected from the PsoBioTeq cohort, a French prospective observational cohort enrolling patients with moderate to severe psoriasis. All patients initiating a first bDMARD or sDMARD were included. The primary outcome was comparison of drug survival over time. A multivariate Cox proportional hazard ratio model was computed. A total of 1,866 patients were included; 739 females (39%), median age 47 years. In the multivariate Cox model, no association was found between the calendar year of initiation and drug survival (hazard ratio) overlapping from 0.80 (0.42-1.52) to 1.17 (0.64-2.17), p = 0.633). In conclusion, drug survival in psoriasis is not affected by the year of initiation.

Publication types

  • Observational Study

MeSH terms

  • Antirheumatic Agents* / therapeutic use
  • Biological Factors / therapeutic use
  • Biological Products* / adverse effects
  • Female
  • Humans
  • Middle Aged
  • Psoriasis* / diagnosis
  • Psoriasis* / drug therapy
  • Thalidomide / adverse effects
  • Thalidomide / analogs & derivatives

Substances

  • Antirheumatic Agents
  • Biological Factors
  • Biological Products
  • Thalidomide
  • apremilast