Long-term drug survival and predictor analysis of the whole psoriatic patient population on biological therapy in Hungary

J Dermatolog Treat. 2017 Nov;28(7):635-641. doi: 10.1080/09546634.2017.1329504. Epub 2017 Aug 9.

Abstract

Persistence is an important component of therapeutic success, which depends on a variety of factors. Persistence measured under optimal conditions during clinical trials does not necessarily coincide with persistence observed in the real-world settings. The aim of the present study was to compare persistence rate of TNF-alpha inhibitors and interleukin 12/23 inhibitor in all psoriasis patients in Hungary, as well as to analyze the predictors of persistence. Data collected from 1263 patients over a period of 46 months were subjected to a retrospective analysis. Drug survival rate has been calculated according to Kaplan-Meier analysis and Cox regression was used to study the predictors. The overall persistence rate for the four biologicals exceeded 60% after 3 years. The persistence rate of ustekinumab at 3 years was 67.83%, which was superior compared to that of the TNF-alpha inhibitors, where the mean persistence rate was shown to be 50.76% (p < .05). Male patients showed significantly higher persistence than females (HR = .76, p < .05 CI: 0.63, 0.92). Age, therapy-naïve status and use of concomitant MTX did not have significant effect on drug survival. Persistence rate of ustekinumab was significantly higher than that of TNF-alpha inhibitors, and among predictors, only male gender influenced persistence significantly.

Keywords: Biological therapy; comparison; hazard ratios; persistence; predictors; psoriasis.

MeSH terms

  • Adalimumab / therapeutic use
  • Adult
  • Aged
  • Dermatologic Agents / therapeutic use*
  • Etanercept / therapeutic use
  • Female
  • Humans
  • Hungary
  • Infliximab / therapeutic use
  • Kaplan-Meier Estimate
  • Male
  • Middle Aged
  • Proportional Hazards Models
  • Psoriasis / drug therapy*
  • Psoriasis / mortality
  • Registries
  • Retrospective Studies
  • Tumor Necrosis Factor-alpha / immunology
  • Ustekinumab / therapeutic use

Substances

  • Dermatologic Agents
  • Tumor Necrosis Factor-alpha
  • Infliximab
  • Ustekinumab
  • Adalimumab
  • Etanercept