Abstract
The majority of patients with psoriasis vulgaris (chronic plaque psoriasis) can be treated successfully with short-term topical therapies. However, long-term management of psoriasis with topicals is challenging and tends to take a reactive approach to disease relapse, rather than a proactive approach aimed at maintaining disease remission. Patients are often dissatisfied with the delay in treatment response and inconvenience of applying topical treatments, and therefore frequently discontinue treatment leading to poor outcomes. Relapse is common, particularly with reactive management, as underlying residual disease can remain following initial skin clearance; some patients find that their disease at relapse may be worse than their initial symptoms. This can have a detrimental effect on patient quality of life (QoL) and increase the risk of psoriasis-associated depression. A long-term proactive management approach, with maintenance treatment following initial treatment success, could help sustain disease remission and improve clinical and QoL outcomes for patients. Treatment with fixed-dose calcipotriol 50 µg/g betamethasone dipropionate 0.5 mg/g cutaneous foam (Cal/BD foam) is effective in the short term, providing a fast onset of action and improvements in disease at 4 weeks. Results from the Phase III PSO-LONG study demonstrated that long-term proactive management was superior to reactive management in prolonging time to first relapse, reducing number of relapses and increasing days in remission in adults with psoriasis vulgaris. Furthermore, Cal/BD foam was well tolerated in PSO-LONG. No new safety concerns were identified over 52 weeks; the safety profile was consistent with that described previously. Given this, Cal/BD foam should be considered when prescribing topicals for the long-term proactive management for patients with psoriasis.
| Original language | English |
|---|---|
| Journal | Journal of the European Academy of Dermatology and Venereology |
| Volume | 35 Suppl 1 |
| Issue number | S1 |
| Pages (from-to) | 35-41 |
| Number of pages | 7 |
| ISSN | 0926-9959 |
| DOIs | |
| Publication status | Published - 02.2021 |
Funding
Development of this manuscript was funded by LEO Pharma. ML is an employee of Mount Sinai and receives research funds from: AbbVie, Amgen, Arcutis, Boehringer Ingelheim, Dermavant, Eli Lilly, Incyte, Janssen Research & Development LLC, Ortho Dermatologics, Pfizer and UCB Inc. and is a consultant for Aditum Bio, Allergan, Almirall, Arcutis Inc., Avotres Therapeutics, BirchBioMed Inc., BMD Skincare, Boehringer Ingelheim, Bristol Myers Squibb, Cara Therapeutics, Castle Biosciences, Corrona, Dermavant Sciences, Evelo, Facilitate International Dermatologic Education, Foundation for Research and Education in Dermatology, Inozyme Pharma, Kyowa Kirin, LEO Pharma, Meiji Seika Pharma, Menlo, Mitsubishi, Neuroderm, Pfizer, Promius/Dr. Reddy’s Laboratories, Serono, Theravance and Verrica. DT has been a consultant and advisor and/or received speaking fees and/or grants and/or served as an investigator in clinical trials for the following companies: AbbVie Inc., Almirall, Amgen, Asana, Biogen, Boehringer Ingelheim, Bristol Myers Squibb, Celgene, Dermira, DS‐Biopharma, Eli Lilly and Company, Galapagos NV, Galderma, Janssen‐Cilag Ltd., Kymab, LEO Pharma, MorphoSys AG, Novartis, Pfizer, Regeneron Pharmaceuticals, Roche, Sandoz, Sanofi, Samsung and UCB. RBW receives research grants from AbbVie Inc., Almirall, Amgen, Celgene, Janssen Pharmaceuticals, Eli Lilly and Company, LEO Pharma, Novartis, Pfizer and UCB, and is a consultant for AbbVie Inc., Almirall, Amgen, Bristol Myers Squibb, Boehringer Ingelheim, Celgene, Janssen Pharmaceuticals, LEO Pharma, Eli Lilly and Company, Novartis, Pfizer, Sanofi and UCB.
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Research Areas and Centers
- Academic Focus: Center for Infection and Inflammation Research (ZIEL)
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