Secukinumab Drug Survival in Psoriasis and Psoriatic Arthritis Patients: A 24-Month Real-Life Study.


Journal

Dermatology (Basel, Switzerland)
ISSN: 1421-9832
Titre abrégé: Dermatology
Pays: Switzerland
ID NLM: 9203244

Informations de publication

Date de publication:
2022
Historique:
received: 20 04 2021
accepted: 12 01 2022
pubmed: 10 3 2022
medline: 8 9 2022
entrez: 9 3 2022
Statut: ppublish

Résumé

Secukinumab effectiveness has been demonstrated in both psoriasis (PsO) and psoriatic arthritis (PsA). However, it is unknown whether patients with arthritis may carry a risk factor for withdrawal. To identify predictors of secukinumab survival, including the presence of arthritis, in PsO and PsA. Consecutive PsO and PsA patients initiating secukinumab were enrolled and followed up every 6 months, up to 24 months or discontinuation. Medical history, disease activity indices and body mass index (BMI) were collected. Kaplan-Meier curves and log-rank test were used to analyze differences in drug survival according to sex, BMI, biological therapy line in the whole population (psoriatic disease), and separately for PsO/PsA. A multivariable Cox regression model was built to assess whether presence of arthritis (main independent variable) may influence drug survival by having time to secukinumab discontinuation as outcome. Results were expressed as hazard ratio and 95% confidence interval. Sixty-two PsO and 90 PsA patients were enrolled. Retention rate at 12 and 24 months, respectively, was 85% and 61% for PsO and 68% and 57% for PsA. In the whole population, naïve patients had a higher chance of drug survival (log-rank = 4.06; p = 0.04); in PsA, obese patients had a significantly higher chance to discontinue secukinumab (log-rank = 5.25; p = 0.021). The multivariable Cox regression showed that arthritis was independently associated with a higher risk of secukinumab discontinuation (hazard ratio 2.43; 95% confidence interval 1.06-5.55, p = 0.035) after adjusting for age, sex, gender, BMI, therapy line and PsO severity at baseline. Our data confirmed a very good response to secukinumab in both PsO and PsA patients. However, presence of arthritis might affect drug survival.

Sections du résumé

BACKGROUND BACKGROUND
Secukinumab effectiveness has been demonstrated in both psoriasis (PsO) and psoriatic arthritis (PsA). However, it is unknown whether patients with arthritis may carry a risk factor for withdrawal.
OBJECTIVE OBJECTIVE
To identify predictors of secukinumab survival, including the presence of arthritis, in PsO and PsA.
METHODS METHODS
Consecutive PsO and PsA patients initiating secukinumab were enrolled and followed up every 6 months, up to 24 months or discontinuation. Medical history, disease activity indices and body mass index (BMI) were collected. Kaplan-Meier curves and log-rank test were used to analyze differences in drug survival according to sex, BMI, biological therapy line in the whole population (psoriatic disease), and separately for PsO/PsA. A multivariable Cox regression model was built to assess whether presence of arthritis (main independent variable) may influence drug survival by having time to secukinumab discontinuation as outcome. Results were expressed as hazard ratio and 95% confidence interval.
RESULTS RESULTS
Sixty-two PsO and 90 PsA patients were enrolled. Retention rate at 12 and 24 months, respectively, was 85% and 61% for PsO and 68% and 57% for PsA. In the whole population, naïve patients had a higher chance of drug survival (log-rank = 4.06; p = 0.04); in PsA, obese patients had a significantly higher chance to discontinue secukinumab (log-rank = 5.25; p = 0.021). The multivariable Cox regression showed that arthritis was independently associated with a higher risk of secukinumab discontinuation (hazard ratio 2.43; 95% confidence interval 1.06-5.55, p = 0.035) after adjusting for age, sex, gender, BMI, therapy line and PsO severity at baseline.
CONCLUSIONS CONCLUSIONS
Our data confirmed a very good response to secukinumab in both PsO and PsA patients. However, presence of arthritis might affect drug survival.

Identifiants

pubmed: 35263743
pii: 000522008
doi: 10.1159/000522008
doi:

Substances chimiques

Antibodies, Monoclonal, Humanized 0
secukinumab DLG4EML025

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

897-903

Informations de copyright

© 2022 S. Karger AG, Basel.

Auteurs

Augusta Ortolan (A)

Rheumatology Unit, Department of Medicine DIMED, Padova University Hospital, Padova, Italy.

Mariagrazia Lorenzin (M)

Rheumatology Unit, Department of Medicine DIMED, Padova University Hospital, Padova, Italy.

Giovanni Leo (G)

Rheumatology Unit, Department of Medicine DIMED, Padova University Hospital, Padova, Italy.
Dermatology Clinic, Padova University Hospital, Padova, Italy.

Francesca Pampaloni (F)

Dermatology Clinic, Padova University Hospital, Padova, Italy.

Francesco Messina (F)

Dermatology Clinic, Padova University Hospital, Padova, Italy.

Andrea Doria (A)

Rheumatology Unit, Department of Medicine DIMED, Padova University Hospital, Padova, Italy.

Stefano Piaserico (S)

Dermatology Clinic, Padova University Hospital, Padova, Italy.

Roberta Ramonda (R)

Rheumatology Unit, Department of Medicine DIMED, Padova University Hospital, Padova, Italy.

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Classifications MeSH