Real World Experience of Disease Activity in Patients With Rheumatoid Arthritis and Response to Treatment With Varios Biologic DMARDs

被引:7
|
作者
Boyadzhieva, Vladimira [1 ]
Stoilov, Nikolay [1 ]
Ivanova, Mariana [1 ]
Petrova, Guenka [2 ]
Stoilov, Rumen [1 ]
机构
[1] Med Univ Sofia, Univ Hosp St Ivan Rilski, Fac Med, Sofia, Bulgaria
[2] Med Univ Sofia, Fac Pharm, Sofia, Bulgaria
来源
FRONTIERS IN PHARMACOLOGY | 2018年 / 9卷
关键词
rheumatoid arthritis; disease activity; biological therapy; DAS28-CRP; CDAI; MODIFYING ANTIRHEUMATIC DRUGS; AMERICAN-COLLEGE; CLINICAL-PRACTICE; RHEUMATOLOGY/EUROPEAN LEAGUE; IMPROVEMENT CRITERIA; FAILED TREATMENT; ACTIVITY INDEX; ETANERCEPT; INFLIXIMAB; EFFICACY;
D O I
10.3389/fphar.2018.01303
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The current study investigate the disease activity and effectiveness of treatment in patients with RA on biological disease modifying antirheumatic drugs (bDMARDs) in combination with a conventional synthetic DMARD (csDMARD) and determine whether or not the benefits of different therapies were sustained over a follow up period of 1 year. 124 patients were selected with a mean age 55.26 +/- 13, 18SD years, meeting the 1987 ACR and /or ACR/ EULAR (2010) classification criteria for Rheumatoid arthritis (RA). Patients were arranged according to treatment regimens: Tocilizumab (TCL) - 30 patients, Certolizumab (CZP) - 16, Golimumab (GOL) - 22, Etanercept (FIN) 20, Adalimumab (ADA) 20, Rituximab (RTX) - 16. Disease activities was the primary concern. Independent joint assessor evaluated 28 joints on baseline, 6th and 12th month's thereafter. C-reactive protein (CRP) was used to measure the inflammatory process. DAS28-CRP, clinical disease activity index (CDAI) and simplified disease activity index (SDAI) were calculated. On baseline all of the patients' groups had severe disease activity (mean DAS28-CRP > 5.2, mean CDAI > 22, mean SDAI > 26. It was noted that, during the 6th month follow-up period all of the treatment groups significantly decreased DAS28-CRP, CDAI, SDAI and reach moderate disease activity. After 6th and 12th months of treatment all of the groups on bDMARDs had significantly lower disease activity. The GOL group reach remission only according to DAS28-CRP: 2.49 +/- 0.76, and low disease activity as measured by CDAI: 6.78 +/- 4.51 and SDAI 7.80 +/- 5.67. The other 5 groups after 12 months reach the level of low disease activity according to the three activity parameters: DAS28-CRP (TCL 3.07 +/- 0.73, CZP 3.06 +/- 0.65, ETN 2.85 +/- 0.55, ADA 3.15 +/- 0.82, RTX 2.90 +/- 0.70), CDAI (TCL 9.80 +/- 4.91, CZP - 9.33 +/- 4.22, ETN 7.97 +/- 3.80, ADA 10.00 +/- 5.25, RTX 7.48 +/- 2.99) and SDAI (TCL 10.45 +/- 5.14, CZP 9.94 +/- 4.43, ETN 9.03 +/- 4.25, ADA 10.50 +/- 5.61, RTX 8.08 +/- 3.24). The therapy with different bDMARDs added to a csDMARD led to very similar results - a minimal disease activity and a state of remission in the GOL treatment group only as per DAS28-CRP.
引用
收藏
页数:8
相关论文
共 50 条
  • [31] RISK OF VENOUS THROMBOEMBOLISM IN RHEUMATOID ARTHRITIS PATIENTS TREATED WITH BIOLOGIC AND NON-BIOLOGIC DMARDS
    Maro, J. C.
    Menzin, T.
    Hornbuckle, K.
    Giles, J. T.
    Kavanaugh, A.
    Doerner, T.
    Martin, D.
    Huang, T.
    Salinas, C. A.
    ANNALS OF THE RHEUMATIC DISEASES, 2018, 77 : 932 - 932
  • [32] Comparative safety of biologic versus conventional synthetic DMARDs in rheumatoid arthritis with COPD: a real-world population study
    Hudson, Marie
    Dell'Aniello, Sophie
    Shen, Sophie
    Simon, Teresa A.
    Ernst, Pierre
    Suissa, Samy
    RHEUMATOLOGY, 2020, 59 (04) : 820 - 827
  • [33] Effectiveness of infliximab in patients with rheumatoid arthritis 'real world' experience
    Barr, SG
    Steber, W
    Kindopp-Bugo, K
    Martin, L
    JOURNAL OF RHEUMATOLOGY, 2003, 30 (08) : 1876 - 1876
  • [34] Patient-individual tapering of DMARDs in rheumatoid arthritis patients in a real-world setting
    Birkner, Benjamin
    Rech, Juergen
    Edelmann, Edmund
    Verheyen, Frank
    Schett, Georg
    Stargardt, Tom
    RHEUMATOLOGY, 2023, 62 (04) : 1476 - 1484
  • [35] Initiation of Biologic DMARDs and the Risk of Hospitalized Bacterial Infections in Patients with Rheumatoid Arthritis
    Grijalva, Carlos G.
    Chen, Lang
    Delzell, Elizabeth
    Baddley, John W.
    Beukelman, Timothy
    Griffin, Marie R.
    Herrinton, Lisa
    Liu, Liyan
    Nourjah, Parivash
    Ouellet-Hellstrom, Rita
    Patkar, Nivedita M.
    Solomon, Daniel H.
    Winthrop, Kevin L.
    Xie, Fenglong
    Saag, Kenneth G.
    Curtis, Jeffrey R.
    PHARMACOEPIDEMIOLOGY AND DRUG SAFETY, 2011, 20 : S182 - S183
  • [36] Impact of treatment with biologic DMARDs on the risk of sepsis or mortality after serious infection in patients with rheumatoid arthritis
    Richter, A.
    Listing, J.
    Schneider, M.
    Klopsch, T.
    Kapelle, A.
    Kaufmann, J.
    Zink, A.
    Strangfeld, A.
    ANNALS OF THE RHEUMATIC DISEASES, 2016, 75 (09) : 1667 - 1673
  • [37] REAL WORLD POPULATION-BASED ASSESSMENT OF COVID-19 OUTCOMES AMONG RHEUMATOID ARTHRITIS PATIENTS USING BIOLOGIC OR SYNTHETIC DMARDs
    Wegrzyn, L.
    Winthrop, K.
    Kim, S.
    Ye, Y.
    Huisingh, C.
    Krueger, W.
    Maniccia, A.
    Kilpatrick, R.
    ANNALS OF THE RHEUMATIC DISEASES, 2021, 80 : 886 - 886
  • [38] Influenza vaccination status in rheumatoid arthritis and spondyloarthritis patients receiving biologic DMARDs
    Michel, Murielle
    Vincent, Fabien B.
    Rio, Simon
    Leon, Nathalie
    Marcelli, Christian
    JOINT BONE SPINE, 2016, 83 (02) : 237 - 238
  • [39] CHANGE IN DISEASE ACTIVITY AND TREATMENT RESPONSE AFTER ABATACEPT TREATMENT FOR RHEUMATOID ARTHRITIS: REAL-WORLD EVIDENCE FROM THE UK
    Henning, S.
    Groves, L.
    Hurst, M.
    Sugrue, D.
    Gordon, J.
    Choy, E.
    ANNALS OF THE RHEUMATIC DISEASES, 2020, 79 : 1442 - 1443
  • [40] Macrophage activity assessed by soluble CD163 in early rheumatoid arthritis: association with disease activity but different response patterns to synthetic and biologic DMARDs
    Greisen, S. R.
    Moller, H. J.
    Stengaard-Pedersen, K.
    Hetland, M. L.
    Horslev-Petersen, K.
    Junker, P.
    Ostergaard, M.
    Hvid, M.
    Deleuran, B.
    CLINICAL AND EXPERIMENTAL RHEUMATOLOGY, 2015, 33 (04) : 498 - 502