Background: Clinical trials have demonstrated the efficacy of guselkumab in psoriasis, however, limited data are available from real-life studies evaluating the long-term effectiveness and drug survival (DS) of guselkumab. Objective: This multicenter study assessed the 5-year efficacy, DS, and predictors of treatment response in a large cohort of patients with psoriasis. Methods: In this retrospective, longitudinal study, we analyzed data from 1024 patients with moderate-to-severe psoriasis treated with guselkumab between 2019 and 2024. PASI scores were evaluated at baseline, 6 months, and 1-5 years. DS (ie, duration of continuous treatment with guselkumab without discontinuation) was assessed using Kaplan-Meier analysis, and logistic regression analysis was used to identify predictors of PASI response. Results: Mean PASI decreased from 14.3 +/- 8.8 at baseline to 1.3 +/- 2.4 at 6 months, with sustained improvement from 12-60 months (PASI values ranging from 1.0 +/- 2.2 to 1.3 +/- 3.5). Bioexperienced (ie having previous biological treatment) patients and obese individuals had lower PASI response. Subgroup analyses revealed significantly lower PASI response rates in obese patients, those previously treated with biologics, and those switched from anti-IL-17 agents (p<0.05). Multivariate logistic regression analysis revealed that previous biologic exposure and obesity remained significant negative predictors of achieving PASI 75, PASI 90, and PASI 100 across different time points. Cardiovascular disease emerged as a negative predictor for PASI 90 at 3 months (OR 0.64, 95% CI: 0.42-0.97, p=0.035). The probability of remaining on treatment at 12, 24, 36, 48, and 60 months were 95.85%, 91.73%, 89.74%, 87.08%, and 85.76% respectively. Female sex, >= 3 prior biologics, longer disease duration, and previous anti-IL-17 therapy increased the risk of treatment discontinuation. No significant differences in drug discontinuation were noted between patients with or without comorbidities. Conclusion: This real-world study demonstrates the sustained long-term efficacy and DS of guselkumab in patients with psoriasis. Prior biologic exposure, obesity, and patient history are important factors to consider when initiating treatment for long-term management.

Long-term real-world effectiveness and drug survival of guselkumab in patients with psoriasis. A 5-year retrospective study / Mortato, Edoardo; Talamonti, Marina; Marcelli, Lorenzo; Megna, Matteo; Raimondo, Annunziata; Caldarola, Giacomo; Bernardini, Nicoletta; Balato, Anna; Campanati, Anna; Esposito, Maria; Bonifati, Claudio; Lora, Viviana; Potestio, Luca; Lembo, Serena; Loconsole, Francesco; De Luca, Eleonora; Skroza, Nevena; Buononato, Dario; Bianchelli, Tommaso; Fargnoli, Maria Concetta; Tommasino, Nello; Foti, Caterina; De Simone, Clara; Bianchi, Luca; Galluzzo, Marco. - In: PSORIASIS. - ISSN 2230-326X. - Volume 15:(2025), pp. 455-469. [10.2147/ptt.s533005]

Long-term real-world effectiveness and drug survival of guselkumab in patients with psoriasis. A 5-year retrospective study

Bernardini, Nicoletta;Skroza, Nevena;
2025

Abstract

Background: Clinical trials have demonstrated the efficacy of guselkumab in psoriasis, however, limited data are available from real-life studies evaluating the long-term effectiveness and drug survival (DS) of guselkumab. Objective: This multicenter study assessed the 5-year efficacy, DS, and predictors of treatment response in a large cohort of patients with psoriasis. Methods: In this retrospective, longitudinal study, we analyzed data from 1024 patients with moderate-to-severe psoriasis treated with guselkumab between 2019 and 2024. PASI scores were evaluated at baseline, 6 months, and 1-5 years. DS (ie, duration of continuous treatment with guselkumab without discontinuation) was assessed using Kaplan-Meier analysis, and logistic regression analysis was used to identify predictors of PASI response. Results: Mean PASI decreased from 14.3 +/- 8.8 at baseline to 1.3 +/- 2.4 at 6 months, with sustained improvement from 12-60 months (PASI values ranging from 1.0 +/- 2.2 to 1.3 +/- 3.5). Bioexperienced (ie having previous biological treatment) patients and obese individuals had lower PASI response. Subgroup analyses revealed significantly lower PASI response rates in obese patients, those previously treated with biologics, and those switched from anti-IL-17 agents (p<0.05). Multivariate logistic regression analysis revealed that previous biologic exposure and obesity remained significant negative predictors of achieving PASI 75, PASI 90, and PASI 100 across different time points. Cardiovascular disease emerged as a negative predictor for PASI 90 at 3 months (OR 0.64, 95% CI: 0.42-0.97, p=0.035). The probability of remaining on treatment at 12, 24, 36, 48, and 60 months were 95.85%, 91.73%, 89.74%, 87.08%, and 85.76% respectively. Female sex, >= 3 prior biologics, longer disease duration, and previous anti-IL-17 therapy increased the risk of treatment discontinuation. No significant differences in drug discontinuation were noted between patients with or without comorbidities. Conclusion: This real-world study demonstrates the sustained long-term efficacy and DS of guselkumab in patients with psoriasis. Prior biologic exposure, obesity, and patient history are important factors to consider when initiating treatment for long-term management.
2025
guselkumab; effectiveness; long-term; drug survival; psoriasis; comorbidities
01 Pubblicazione su rivista::01a Articolo in rivista
Long-term real-world effectiveness and drug survival of guselkumab in patients with psoriasis. A 5-year retrospective study / Mortato, Edoardo; Talamonti, Marina; Marcelli, Lorenzo; Megna, Matteo; Raimondo, Annunziata; Caldarola, Giacomo; Bernardini, Nicoletta; Balato, Anna; Campanati, Anna; Esposito, Maria; Bonifati, Claudio; Lora, Viviana; Potestio, Luca; Lembo, Serena; Loconsole, Francesco; De Luca, Eleonora; Skroza, Nevena; Buononato, Dario; Bianchelli, Tommaso; Fargnoli, Maria Concetta; Tommasino, Nello; Foti, Caterina; De Simone, Clara; Bianchi, Luca; Galluzzo, Marco. - In: PSORIASIS. - ISSN 2230-326X. - Volume 15:(2025), pp. 455-469. [10.2147/ptt.s533005]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/1753124
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