Journal of Dermatological Treatment (May 2022)

Efficacy and safety of proactive treatment with twice-weekly topical Cal/BD foam in patients with plaque psoriasis undergoing HPA-axis testing: a PSO-LONG subgroup analysis

  • Kim Papp,
  • Zygmunt Adamski,
  • Lyn Guenther,
  • Monika Liljedahl,
  • Agnieszka Miasik-Pogodzinska,
  • Anna Szponar-Bojda,
  • Charles Lynde,
  • Terri Nutt,
  • Marie Holst Mørch,
  • Stephen Tyring,
  • William Werschler,
  • Adam Reich,
  • Neil Sadick,
  • Irina Turchin,
  • Jean-Philippe Lacour

DOI
https://doi.org/10.1080/09546634.2021.1959501
Journal volume & issue
Vol. 33, no. 4
pp. 2297 – 2304

Abstract

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Objective In PSO-LONG, long-term proactive management (PAM) of psoriasis with fixed-dose combination calcipotriol 50 µg/g and betamethasone dipropionate 0.5 mg/g (Cal/BD) aerosol foam was superior to conventional reactive management. This post-hoc analysis investigated long-term PAM with Cal/BD foam in PSO-LONG patients who could be more susceptible to corticosteroid-induced hypothalamic-pituitary-adrenal (HPA) axis suppression. Methods Efficacy and safety of PAM with Cal/BD foam (twice-weekly) versus reactive management (twice-weekly vehicle foam), with once-daily rescue Cal/BD foam for four weeks following relapse, was assessed in the HPA subgroup (n = 66); patients had moderate-to-severe psoriasis (physician global assessment score ≥3; 10–30% body surface area affected). Primary endpoint was time to first relapse. Results PAM with Cal/BD foam was associated with longer median time to first relapse (111 versus 31 days), reduced risk of first relapse (hazard ratio: 0.49; p = .029), greater proportion of days in remission (17%; p = .001) and reduced rate of relapse (60% reduction; p < .001) than reactive management. Adverse events occurred in 37.5% (PAM) and 47.1% (reactive management) of patients, with no new safety signals. No clinically significant HPA-axis suppression was observed. Conclusion Efficacy of PAM with Cal/BD foam is maintained in patients with moderate-to-severe psoriasis, with no new safety signals.

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