Long-term effectiveness and drug survival of golimumab in patients affected by psoriatic arthritis with cutaneous involvement.


Journal

Clinical rheumatology
ISSN: 1434-9949
Titre abrégé: Clin Rheumatol
Pays: Germany
ID NLM: 8211469

Informations de publication

Date de publication:
Jan 2022
Historique:
received: 22 05 2021
accepted: 28 07 2021
revised: 19 07 2021
pubmed: 20 8 2021
medline: 6 1 2022
entrez: 19 8 2021
Statut: ppublish

Résumé

To determine the effectiveness of golimumab (GLM) in improving joint, periarticular structures and cutaneous manifestations in patients with moderate to severe psoriatic arthritis (PsA) with cutaneous psoriasis in different real-life clinical settings and 48-month drug survival. Clinical and laboratory records were collected from PsA patients treated with GLM at baseline (T0) and after 6, 12, 24, 36, and 48 months of treatment. Comparisons were performed using a paired t-test or Wilcoxon test. Drug survival rates were analyzed using Kaplan-Meier estimates. p value < 0.05 was considered statistically significant. Data from 105 patients were collected. PsO occurred in 80% of patients and enthesitis in 78%, peripheral and axial arthritis in 63.8% and 35.3%, respectively, while erosions in 36.2%. The main comorbidities were cardiovascular diseases (31.4%) and metabolic syndrome (MetS) (19%). A statistically significant improvement in articular and cutaneous psoriasis was registered at T48 of GLM-therapy in clinical (DAPSA p < 0.0001; PASI p < 0.01; BASDAI p < 0.0001) and laboratory (CRP < 0.05) indexes. Gender (p = 0.652), BMI (p = 0.655), smoking habit (p = 0.466), and line of treatment (p = 0.208) did not affect treatment efficacy nor persistence. At T48, 42% of patients discontinued GLM: the most frequent reason was an insufficient response or loss of efficacy (28.6%). A 48-month GLM high drug persistence of PsA patients was observed in real-life, in patients presenting high disease activity, elevated prevalence of comorbidities, and more than one line of treatment at baseline. Patients' characteristics as gender, smoke, BMI, different lines of treatment, and concomitant methotrexate treatment affected treatment persistence, making GLM effective and safe in moderate-severe PsA in a long-term real-life setting. Key Points • Golimumab was effective in psoriatic arthritis, including both musculoskeletal and cutaneous manifestations. • Golimumab effectiveness and drug survival were not affected by comorbidities and patient-related characteristics. • The 4-year drug survival curves confirm the efficacy and safety of golimumab in psoriatic arthritis patients in a real-life setting.

Identifiants

pubmed: 34410550
doi: 10.1007/s10067-021-05874-6
pii: 10.1007/s10067-021-05874-6
pmc: PMC8724144
doi:

Substances chimiques

Antibodies, Monoclonal 0
Antirheumatic Agents 0
golimumab 91X1KLU43E

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

75-84

Informations de copyright

© 2021. The Author(s).

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Auteurs

Maria Sole Chimenti (MS)

Rheumatology, Allergology and Clinical Immunology, Department of Medicina Dei Sistemi, University of Rome Tor Vergata, Via Montpellier 1, Rome, Italy. maria.sole.chimenti@uniroma2.it.

Paola Conigliaro (P)

Rheumatology, Allergology and Clinical Immunology, Department of Medicina Dei Sistemi, University of Rome Tor Vergata, Via Montpellier 1, Rome, Italy.

Francesco Caso (F)

Rheumatology Unit, Department of Clinical Medicine and Surgery, University Federico II, Naples, Italy.

Luisa Costa (L)

Rheumatology Unit, Department of Clinical Medicine and Surgery, University Federico II, Naples, Italy.

Augusta Ortolan (A)

Rheumatology Unit, Department of Medicine DIMED, University of Padova, Via Giustiniani 2, Padua, Italy.

Paola Triggianese (P)

Rheumatology, Allergology and Clinical Immunology, Department of Medicina Dei Sistemi, University of Rome Tor Vergata, Via Montpellier 1, Rome, Italy.

Marco Tasso (M)

Rheumatology Unit, Department of Clinical Medicine and Surgery, University Federico II, Naples, Italy.

Giulia Lavinia Fonti (GL)

Rheumatology, Allergology and Clinical Immunology, Department of Medicina Dei Sistemi, University of Rome Tor Vergata, Via Montpellier 1, Rome, Italy.

Maria Grazia Lorenzin (MG)

Rheumatology Unit, Department of Medicine DIMED, University of Padova, Via Giustiniani 2, Padua, Italy.

Roberto Perricone (R)

Rheumatology, Allergology and Clinical Immunology, Department of Medicina Dei Sistemi, University of Rome Tor Vergata, Via Montpellier 1, Rome, Italy.

Roberta Ramonda (R)

Rheumatology Unit, Department of Medicine DIMED, University of Padova, Via Giustiniani 2, Padua, Italy.

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