TY - JOUR
T1 - Anti-TNF treatment response in rheumatoid arthritis patients with moderate disease activity
T2 - A prospective observational multicentre study (MODERATE)
AU - Ceccarelli, Fulvia
AU - Massafra, Umberto
AU - Perricone, Carlo
AU - Idolazzi, Luca
AU - Giacomelli, Roberto
AU - Tirri, Rosella
AU - Russo, Romualdo
AU - Pistone, Giovanni
AU - Ruscitti, Piero
AU - Parisi, Simone
AU - Sainaghi, Pier Paolo
AU - Cacciapaglia, Fabio
AU - Zullo, Alessandro
AU - Marino, Valentina
AU - Migliore, Alberto
AU - Valesini, Guido
N1 - Publisher Copyright:
© Clinical and Experimental Rheumatology 2017.
PY - 2017
Y1 - 2017
N2 - Objective Rheumatoid arthritis (RA) patients with moderate disease activity show progression of joint damage and have impaired quality of life, physical function, work and daily activities. Little is known about management of patients with moderate RA. The aim of the study was to assess the 1-year response to anti-TNF in biologic-naïve RA patients with moderate (3.2 < DAS28 ≤5.1) disease activity despite DMARD treatment, in the Italian clinical practice. Methods The MODERATE study is a multicentre prospective, cohort non-interventional study, conducted in 19 Italian rheumatology sites. Patients with moderate RA, diagnosed according to the 2010 American College of Rheumatology (ACR)/EULAR criteria, were enrolled if they also were aged ≥18 years, had disease onset after 16 years old, moderate disease at baseline (DAS28 score > 3.2 and ≤5.1), and were naïve to anti-TNF treatment. Results Among 157 RA patients, 93 (59%) underwent etanercept, 43 (22%) adalimumab, 26 (17%) certolizumab, 10 golimumab and 2 infliximab; 80% of patients were still in treatment after 12-month observation. One-year clinical remission was achieved by 27 RA patients (21%), reduction of DAS28 score greater than 1.2 was observed in 75 (58%) patients. Moderate and good response according to EULAR criteria was observed in 59 (46%) and 45 (35%) patients, respectively. Conclusion Results confirm the efficacy of anti-TNF alpha also in moderate RA patients, who may achieve a substantial decrease of disease activity, and improve their quality of life. The low rate of patients achieving remission may suggest that therapeutic strategies should be more timely and aggressive.
AB - Objective Rheumatoid arthritis (RA) patients with moderate disease activity show progression of joint damage and have impaired quality of life, physical function, work and daily activities. Little is known about management of patients with moderate RA. The aim of the study was to assess the 1-year response to anti-TNF in biologic-naïve RA patients with moderate (3.2 < DAS28 ≤5.1) disease activity despite DMARD treatment, in the Italian clinical practice. Methods The MODERATE study is a multicentre prospective, cohort non-interventional study, conducted in 19 Italian rheumatology sites. Patients with moderate RA, diagnosed according to the 2010 American College of Rheumatology (ACR)/EULAR criteria, were enrolled if they also were aged ≥18 years, had disease onset after 16 years old, moderate disease at baseline (DAS28 score > 3.2 and ≤5.1), and were naïve to anti-TNF treatment. Results Among 157 RA patients, 93 (59%) underwent etanercept, 43 (22%) adalimumab, 26 (17%) certolizumab, 10 golimumab and 2 infliximab; 80% of patients were still in treatment after 12-month observation. One-year clinical remission was achieved by 27 RA patients (21%), reduction of DAS28 score greater than 1.2 was observed in 75 (58%) patients. Moderate and good response according to EULAR criteria was observed in 59 (46%) and 45 (35%) patients, respectively. Conclusion Results confirm the efficacy of anti-TNF alpha also in moderate RA patients, who may achieve a substantial decrease of disease activity, and improve their quality of life. The low rate of patients achieving remission may suggest that therapeutic strategies should be more timely and aggressive.
KW - Anti-TNF-alpha
KW - DAS28
KW - Moderate rheumatoid arthritis
KW - Observational study
KW - Treatment persistence
UR - http://www.scopus.com/inward/record.url?scp=85013168147&partnerID=8YFLogxK
M3 - Article
SN - 0392-856X
VL - 35
SP - 24
EP - 32
JO - Clinical and Experimental Rheumatology
JF - Clinical and Experimental Rheumatology
IS - 1
ER -