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Tytuł pozycji:

A cohort study of guselkumab in the treatment of psoriasis refractory to previous biologic therapies: effectiveness, safety and adherence.

Tytuł:
A cohort study of guselkumab in the treatment of psoriasis refractory to previous biologic therapies: effectiveness, safety and adherence.
Autorzy:
Medina-Catalán D; Pharmacy Department, Hospital de la Santa Creu i Sant Pau, Carrer de Sant Quintí, 89, 08041, Barcelona, Spain.
Riera P; Pharmacy Department, Hospital de la Santa Creu i Sant Pau, Carrer de Sant Quintí, 89, 08041, Barcelona, Spain.; U705, ISCIII Center for Biomedical Research on Rare Diseases (CIBERER), Barcelona, Spain.
Pagès-Puigdemont N; Pharmacy Department, Hospital de la Santa Creu i Sant Pau, Carrer de Sant Quintí, 89, 08041, Barcelona, Spain. .
Masip M; Pharmacy Department, Hospital de la Santa Creu i Sant Pau, Carrer de Sant Quintí, 89, 08041, Barcelona, Spain.
López-Ferrer A; Dermatology Department, Hospital de la Santa Creu i Sant Pau, Autonomous University of Barcelona, Barcelona, Spain.
Vilarrasa E; Dermatology Department, Hospital de la Santa Creu i Sant Pau, Autonomous University of Barcelona, Barcelona, Spain.
Puig L; Dermatology Department, Hospital de la Santa Creu i Sant Pau, Autonomous University of Barcelona, Barcelona, Spain.
Źródło:
International journal of clinical pharmacy [Int J Clin Pharm] 2022 Jun; Vol. 44 (3), pp. 725-730. Date of Electronic Publication: 2022 Apr 05.
Typ publikacji:
Journal Article
Język:
English
Imprint Name(s):
Original Publication: Dordrecht : Springer
MeSH Terms:
Antibodies, Monoclonal*/adverse effects
Psoriasis*/diagnosis
Psoriasis*/drug therapy
Antibodies, Monoclonal, Humanized ; Biological Therapy ; Cohort Studies ; Humans ; Retrospective Studies ; Severity of Illness Index ; Treatment Outcome
References:
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Reich K, Armstrong AW, Foley P, et al. 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. J Am Acad Dermatol. 2017;76(3):418–31. (PMID: 10.1016/j.jaad.2016.11.042)
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Contributed Indexing:
Keywords: Biologic; effectiveness; guselkumab; psoriasis; real-life; refractory
Substance Nomenclature:
0 (Antibodies, Monoclonal)
0 (Antibodies, Monoclonal, Humanized)
089658A12D (guselkumab)
Entry Date(s):
Date Created: 20220405 Date Completed: 20220617 Latest Revision: 20220617
Update Code:
20240105
DOI:
10.1007/s11096-022-01400-z
PMID:
35380392
Czasopismo naukowe
Background Guselkumab is indicated for moderate-to-severe plaque psoriasis. Data from real-life clinical practice regarding its use are scarce, especially concerning patients who relapse after previous biologic therapies. Aim This study aimed to evaluate the effectiveness, safety, and adherence to guselkumab in psoriasis refractory to biologic therapies. Method This real-life, retrospective study included patients who initiated guselkumab between February 2019 and October 2020. The main objective was to assess effectiveness, expressed as the psoriasis area and severity index (PASI) ≤5, ≤2 and 0, at the first follow-up medical visit. As secondary effectiveness outcomes, we assessed the body surface area (BSA) and dermatology life quality index (DLQI). We also evaluated adverse events and adherence (using the medication possession ratio [MPR]). Results The study included 35 patients who had previously received a median of two biologic drugs. The median basal PASI score (IQR) was 11 (7.3-15.9), decreasing to 0 (0-1.4) at first follow-up medical visit. At this point, 32 patients (94.1%) reached PASI ≤5, 28 (82.4%) PASI ≤2 and 19 (55.9%) PASI 0. We also found statistically significant improvements in PASI, BSA and DLQI at first follow-up (p<0.001). Three patients developed adverse events. Most patients (N=29, 85.3%) had an MPR ≥90%. The MPR was not associated with PASI score at first follow-up. Conclusion Our study supports evidence that guselkumab is an effective and safe drug in psoriasis refractory to biologic therapies. Adherence to treatment is not related to effectiveness, suggesting that, in some cases, the interval between doses could be increased.
(© 2022. The Author(s), under exclusive licence to Springer Nature Switzerland AG.)

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