Author:
Colombo Delia,Frassi Micol,Pagano Mariano Giusy,Fusaro Enrico,Lomater Claudia,Del Medico Patrizia,Iannone Florenzo,Foti Rosario,Limonta Massimiliano,Marchesoni Antonio,Raffeiner Bernd,Viapiana Ombretta,Grassi Walter,Grembiale Rosa Daniela,Guggino Giuliana,Mazzone Antonino,Tirri Enrico,Perricone Roberto,Sarzi Puttini Pier Carlo,De Vita Salvatore,Conti Fabrizio,Ori Alessandra,Simoni Lucia,Fiocchi Martina,Orsenigo Roberto,Zagni Emanuela,Frassi Micol,Caminiti Maurizio,Fusaro Enrico,Lomater Claudia,Del Medico Patrizia,Iannone Florenzo,Foti Rosario,Limonta Massimiliano,Marchesoni Antonio,Raffeiner Bernd,Viapiana Ombretta,Grassi Walter,Grembiale Rosa Daniela,Guggino Giuliana,Mazzone Antonino,Tirri Enrico,Perricone Roberto,Puttini Pier Carlo Sarzi,De Vita Salvatore,Conti Fabrizio,
Abstract
Abstract
Background
Biologics have demonstrated efficacy in PsA in randomized clinical trials. More evidence is needed on their effectiveness under real clinical practice conditions. The aim of the present work is to provide real-world evidence of the effectiveness of biologics for PsA in the daily clinical practice.
Methods
CHRONOS was a multicenter, non-interventional, cohort study conducted in 20 Italian hospital rheumatology clinics.
Results
399 patients were eligible (56.9% females, mean (SD) age: 52.4 (11.6) years). The mean (SD) duration of PsA and psoriasis was 7.2 (6.9) and 15.3 (12.2) years, respectively. The mean (SD) duration of the biologic treatment under analysis was 18.6 (6.5) months. The most frequently prescribed biologic was secukinumab (40.4%), followed by adalimumab (17.8%) and etanercept (16.5%). The proportion of overall responders according to EULAR DAS28 criteria was 71.8% (95% CI: 66.7–76.8%) out of 308 patients at 6 months and 68.0% (95% CI: 62.7–73.3%) out of 297 patients at 1 year. Overall, ACR20/50/70 responses at 6 months were 41.2% (80/194), 29.4% (57/194), 17.1% (34/199) and at 1-year were 34.9% (66/189), 26.7% (51/191), 18.4% (36/196), respectively. Secondary outcome measures improved rapidly already at 6 months: mean (SD) PASI, available for 87 patients, decreased from 3.2 (5.1) to 0.6 (1.3), the proportion of patients with dactylitis from 23.6% (35/148) to 3.5% (5/142) and those with enthesitis from 33.3% (49/147) to 9.0% (12/133).
Conclusions
The CHRONOS study provides real-world evidence of the effectiveness of biologics in PsA in the Italian rheumatological practice, confirming the efficacy reported in RCTs across various outcome measures.
Funder
Novartis Farma S.p.A. Origgio (VA), Italy
Publisher
Springer Science and Business Media LLC