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      Dose Adjustment of Biologic Treatments for Moderate-to-Severe Plaque Psoriasis in the Real World: A Systematic Review

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          Abstract

          Introduction

          Dose escalation and reduction of biologic treatments are frequent in clinical practice. The aim of this systematic review is to summarise evidence on dose adjustment of biologic treatments for moderate-to-severe plaque psoriasis in the real-world.

          Methods

          A systematic review of real-world evidence on dose adjustment of biologics for plaque psoriasis was performed. Searches were conducted in BIOSIS Previews ®, Embase ®, International Pharmaceutical Abstracts, MEDLINE ®, and SciSearch ® in March 2020. Real-world studies that reported biologic dose adjustment for moderate-to-severe plaque psoriasis were included.

          Results

          The search identified 162 papers, and 20 studies with 30,912 patients were included from 2014 to 2020. More studies reported on dose escalation than dose reduction. For adalimumab, 3–54% of patients had dose reduction while 0–37% had dose escalation. For infliximab, only two studies reported a dose reduction, with rates of 22–29%, while dose escalation rates varied from 14 to 67%. Dose reduction rates of 5–49% were reported for etanercept while 0–55% of patients had doses escalated. For ustekinumab, dose escalation and reduction rates ranged from 3 to 37% and 7 to 42%, respectively. Two studies reported on dose adjustment for secukinumab; in one 52% of patients initiated on 150 mg instead of the recommended 300 mg, while another reported no dose increase.

          Conclusions

          Dose adjustment of biologics for psoriasis is common, with escalation more frequently reported than reduction. Dose escalation may have economic and safety consequences, while dose reduction may impact efficacy. These aspects are important to consider when making decisions on treatment dosing.

          Supplementary Information

          The online version contains supplementary material available at 10.1007/s13555-021-00559-z.

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          Most cited references32

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          Efficacy and safety of guselkumab, an anti-interleukin-23 monoclonal antibody, compared with adalimumab for the continuous treatment of patients with moderate to severe psoriasis: Results from the phase III, double-blinded, placebo- and active comparator-controlled VOYAGE 1 trial.

          Guselkumab, an interleukin-23 blocker, was superior to adalimumab in treating moderate to severe psoriasis in a phase II trial.
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            Secukinumab is superior to ustekinumab in clearing skin of subjects with moderate to severe plaque psoriasis: CLEAR, a randomized controlled trial.

            Secukinumab, a fully human anti-interleukin-17A monoclonal antibody, has shown superior efficacy to etanercept with similar safety in moderate to severe plaque psoriasis (FIXTURE study).
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              Efficacy and safety of guselkumab, an anti-interleukin-23 monoclonal antibody, compared with adalimumab for the treatment of patients with moderate to severe psoriasis with randomized withdrawal and retreatment: Results from the phase III, double-blind, placebo- and active comparator-controlled VOYAGE 2 trial.

              Phase II data suggested that guselkumab, an anti-interleukin-23 monoclonal antibody, was efficacious in psoriasis.
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                Author and article information

                Contributors
                gaetano.licata89@gmail.com
                Journal
                Dermatol Ther (Heidelb)
                Dermatol Ther (Heidelb)
                Dermatology and Therapy
                Springer Healthcare (Cheshire )
                2193-8210
                2190-9172
                3 June 2021
                3 June 2021
                August 2021
                : 11
                : 4
                : 1141-1156
                Affiliations
                [1 ]GRID grid.9841.4, ISNI 0000 0001 2200 8888, Università degli Studi della Campania “Luigi Vanvitelli”, ; Caserta, Italy
                [2 ]GRID grid.420009.f, ISNI 0000 0001 1010 7950, LEO Pharma A/S, ; Ballerup, Denmark
                Author information
                http://orcid.org/0000-0002-0834-1331
                Article
                559
                10.1007/s13555-021-00559-z
                8322248
                34081304
                044343d3-c2f7-4ed8-bedc-8e10b7281792
                © The Author(s) 2021

                Open Access This article is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License, which permits any non-commercial use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc/4.0/.

                History
                : 12 April 2021
                Categories
                Review
                Custom metadata
                © The Author(s) 2021

                Dermatology
                plaque psoriasis,dosing,adalimumab,etanercept,infliximab,secukinumab,ustekinumab
                Dermatology
                plaque psoriasis, dosing, adalimumab, etanercept, infliximab, secukinumab, ustekinumab

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