Effectiveness of early adalimumab therapy in psoriatic arthritis patients from Reuma.pt - EARLY PsA
Authors
Helena Santos; Mónica Eusébio; Joana Borges; Diana Gonçalves; Pedro Ávila-Ribeiro; Daniela Santos Faria; Carina Lopes; João Rovisco; Ana Águeda; Patrícia Nero; Paula Valente; Ana Rita Cravo; Maria José Santos;
Objective
To compare outcomes in psoriatic arthritis (PsA) patients initiating adalimumab (ADA), with short- and long-term disease duration and to evaluate the potential effect of concomitant conventional synthetic disease-modifying antirheumatic drugs (csDMARD) or glucocorticoids.
Methods
Analyses included adult PsA patients registered in the Rheumatic Diseases Portuguese Register (Reuma.pt) between June 2008–June 2016 who received ADA for ≥3 months. Psoriatic Arthritis Response Criteria (PsARC) response, tender and swollen joint count, inflammatory parameters, patient (PtGA) and physician global assessment (PhGA), Disease Activity Score-28 joints (DAS28), and Health Assessment Questionnaire Disability Index (HAQ-DI) were compared between patients with <5 years of disease (early PsA) and those with ≥5 years of disease duration (late PsA). Time to achieving PsARC response was estimated using the Kaplan-Meier method.
Results
Of 135 PsA patients treated with ADA, 126 had information on disease duration (earlyPsA, n=41). PsARC response was achieved by 72.9% of the patients (88.0% early PsA vs 62.2% late PsA; P=0.022) after 3 months and by 85.4% after 24 months (100% early PsA vs 75.9% late PsA; P=0.044). Early PsA patients achieved significantly less painful joints (2.7 vs 6.7, p=0.006), lower mean C-reactive protein (0.5 mg/dL vs 1.3 mg/dL; P=0.011), and PhGA (18.3 vs 28.1; P=0.020) at 3 months. In the long term, early PsA patients also had fewer swollen joints (0.3 vs 1.7; P=0.030) and lower PhGA (6.3 vs 21.9; P<0.001), C-reactive protein (0.4 mg/dL vs 1.0 mg/dL; P=0.026), and DAS28 (2.2 vs 3.2; P=0.030). HAQ-DI decreased in both groups reaching a mean value at 24 months of 0.4 and 0.8 (P=ns) in early and late PsA, respectively. Early PsA patients obtained PsARC response more rapidly than late PsA (3.8 and 7.4 months, respectively; P=0.008). Concomitant csDMARDs showed clinical benefit (2-year PsARC response, 88.3% vs 60.0%; P=0.044). Concomitant glucocorticoids had no effect on PsARC response over 2 years of follow-up. Persistence on ADA was similar in both groups.
Conclusion
Early PsA patients had a greater chance of improvement after ADA therapy and better functional outcome, and achieved PsARC response more rapidly than late PsA. In this cohort, comedication with csDMARDs was beneficial over 2 years.
Helena Santos
Instituto Português de Reumatologia
Mónica Eusébio
Joana Borges
Instituto Português de Reumatologia
Diana Gonçalves
Centro Hospitalar de São João
Pedro Ávila-Ribeiro
Centro Hospitalar Lisboa Norte
Daniela Santos Faria
ULSAM
Carina Lopes
Hospital de Egas Moniz-CHLO
João Rovisco
Centro Hospitalar e Universitário de Coimbra
Ana Águeda
Centro Hospitalar do Baixo Vouga
Patrícia Nero
Hospital CUF Descobertas
Paula Valente
Centro Hospitalar Entre o Douro e Vouga
Ana Rita Cravo
AbbVie
Maria José Santos
Hospital Garcia de Orta
Instituto Português de Reumatologia
Mónica Eusébio
Joana Borges
Instituto Português de Reumatologia
Diana Gonçalves
Centro Hospitalar de São João
Pedro Ávila-Ribeiro
Centro Hospitalar Lisboa Norte
Daniela Santos Faria
ULSAM
Carina Lopes
Hospital de Egas Moniz-CHLO
João Rovisco
Centro Hospitalar e Universitário de Coimbra
Ana Águeda
Centro Hospitalar do Baixo Vouga
Patrícia Nero
Hospital CUF Descobertas
Paula Valente
Centro Hospitalar Entre o Douro e Vouga
Ana Rita Cravo
AbbVie
Maria José Santos
Hospital Garcia de Orta