Diagnosis and Management of Rheumatoid Arthritis A Review

被引:2024
作者
Aletaha, Daniel [1 ]
Smolen, Josef S. [1 ]
机构
[1] Med Univ Vienna, Div Rheumatol, Dept Med 3, Spitalgasse 23, A-1090 Vienna, Austria
来源
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION | 2018年 / 320卷 / 13期
关键词
MODIFYING ANTIRHEUMATIC DRUGS; HEAD-TO-HEAD; DOUBLE-BLIND; DISEASE-ACTIVITY; EULAR RECOMMENDATIONS; JOINT DAMAGE; RHEUMATOLOGY/EUROPEAN LEAGUE; CLASSIFICATION CRITERIA; PHYSICAL-DISABILITY; RECEPTOR INHIBITION;
D O I
10.1001/jama.2018.13103
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
IMPORTANCE Rheumatoid arthritis (RA) occurs in about 5 per 1000 people and can lead to severe joint damage and disability. Significant progress has been made over the past 2 decades regarding understanding of disease pathophysiology, optimal outcome measures, and effective treatment strategies, including the recognition of the importance of diagnosing and treating RA early. OBSERVATIONS Early diagnosis and treatment of RA can avert or substantially slow progression of joint damage in up to 90% of patients, thereby preventing irreversible disability. The development of novel instruments to measure disease activity and identify the presence or absence of remission have facilitated new treatment strategies to arrest RA before joints are damaged irreversibly. Outcomes have been improved by recognizing the benefits of early diagnosis and early therapy with disease-modifying antirheumatic drugs (DMARDs). The treatment target is remission or a state of at least low disease activity, which should be attained within 6 months. Methotrexate is first-line therapy and should be prescribed at an optimal dose of 25mg weekly and in combination with glucocorticoids; 40% to 50% of patients reach remission or at least low disease activity with this regimen. If this treatment fails, sequential application of targeted therapies, such as biologic agents (eg, tumor necrosis factor [TNF] inhibitors) or Janus kinase inhibitors in combination with methotrexate, have allowed up to 75% of these patients to reach the treatment target over time. New therapies have been developed in response to new pathogenetic findings. The costs of some therapies are considerable, but these costs are decreasing with the advent of biosimilar drugs (drugs essentially identical to the original biologic drugs but usually available at lower cost). CONCLUSIONS AND RELEVANCE Scientific advances have improved therapies that prevent progression of irreversible joint damage in up to 90% of patients with RA. Early treatment with methotrexate plus glucocorticoids and subsequently with other DMARDs, such as inhibitors of TNF, IL-6, or Janus kinases, improves outcomes and prevents RA-related disability. A treat-to-target strategy aimed at reducing disease activity by at least 50% within 3 months and achieving remission or low disease activity within 6 months, with sequential drug treatment if needed, can prevent RA-related disability.
引用
收藏
页码:1360 / 1372
页数:13
相关论文
共 110 条
[11]
Tumor necrosis factorinhibiting therapy preferentially targets bone destruction but not synovial inflammation in a tumor necrosis factordriven model of rheumatoid arthritis [J].
Binder, Nikolaus B. ;
Puchner, Antonia ;
Niederreiter, Birgit ;
Hayer, Silvia ;
Leiss, Harald ;
Blueml, Stephan ;
Kreindl, Roman ;
Smolen, Josef S. ;
Redlich, Kurt .
ARTHRITIS AND RHEUMATISM, 2013, 65 (03) :608-617
[12]
Phosphatase and tensin homolog (PTEN) in antigen-presenting cells controls Th17-mediated autoimmune arthritis [J].
Blueml, Stephan ;
Sahin, Emine ;
Saferding, Victoria ;
Goncalves-Alves, Eliana ;
Hainzl, Eva ;
Niederreiter, Birgit ;
Hladik, Anastasia ;
Lohmeyer, Tobias ;
Brunner, Julia S. ;
Bonelli, Michael ;
Koenders, Marije I. ;
van den Berg, Wim B. ;
Superti-Furga, Giulio ;
Smolen, Josef S. ;
Schabbauer, Gernot ;
Redlich, Kurt .
ARTHRITIS RESEARCH & THERAPY, 2015, 17
[13]
Incidence and Mortality of Interstitial Lung Disease in Rheumatoid Arthritis [J].
Bongartz, Tim ;
Nannini, Carlotta ;
Medina-Velasquez, Yimy F. ;
Achenbach, Sara J. ;
Crowson, Cynthia S. ;
Ryu, Jay H. ;
Vassallo, Robert ;
Gabriel, Sherine E. ;
Matteson, Eric L. .
ARTHRITIS AND RHEUMATISM, 2010, 62 (06) :1583-1591
[14]
The PREMIER study - A multicenter, randomized, double-blind clinical trial of combination therapy with adalimumab plus methotrexate versus methotrexate alone or adalimumab alone in patients with early, aggressive rheumatoid arthritis who had not had previous methotrexate treatment [J].
Breedveld, FC ;
Weisman, MH ;
Kavanaugh, AF ;
Cohen, SB ;
Pavelka, K ;
van Vollenhoven, R ;
Sharp, J ;
Perez, JL ;
Spencer-Green, GT .
ARTHRITIS AND RHEUMATISM, 2006, 54 (01) :26-37
[15]
Safety and efficacy of upadacitinib in patients with rheumatoid arthritis and inadequate response to conventional synthetic disease-modifying anti-rheumatic drugs (SELECT-NEXT): a randomised, double-blind, placebo-controlled phase 3 trial [J].
Burmester, Gerd R. ;
Kremer, Joel M. ;
Van den Bosch, Filip ;
Kivitz, Alan ;
Bessette, Louis ;
Li, Yihan ;
Zhou, Yijie ;
Othman, Ahmed A. ;
Pangan, Aileen L. ;
Camp, Heidi S. .
LANCET, 2018, 391 (10139) :2503-2512
[16]
Mavrilimumab, a Fully Human Granulocyte-Macrophage Colony-Stimulating Factor Receptor α Monoclonal Antibody Long-Term Safety and Efficacy in Patients With Rheumatoid Arthritis [J].
Burmester, Gerd R. ;
McInnes, Iain B. ;
Kremer, Joel M. ;
Miranda, Pedro ;
Vencovsky, Jiri ;
Godwood, Alex ;
Albulescu, Marius ;
Michaels, M. Alex ;
Guo, Xiang ;
Close, David ;
Weinblatt, Michael .
ARTHRITIS & RHEUMATOLOGY, 2018, 70 (05) :679-689
[17]
Efficacy and safety of sarilumab monotherapy versus adalimumab monotherapy for the treatment of patients with active rheumatoid arthritis (MONARCH): a randomised, double-blind, parallel-group phase III trial [J].
Burmester, Gerd R. ;
Lin, Yong ;
Patel, Rahul ;
van Adelsberg, Janet ;
Mangan, Erin K. ;
Graham, Neil M. H. ;
van Hoogstraten, Hubert ;
Bauer, Deborah ;
Ignacio Vargas, Juan ;
Lee, Eun Bong .
ANNALS OF THE RHEUMATIC DISEASES, 2017, 76 (05) :840-847
[18]
Tocilizumab in early progressive rheumatoid arthritis: FUNCTION, a randomised controlled trial [J].
Burmester, Gerd R. ;
Rigby, William F. ;
van Vollenhoven, Ronald F. ;
Kay, Jonathan ;
Rubbert-Roth, Andrea ;
Kelman, Ariella ;
Dimonaco, Sophie ;
Mitchell, Nina .
ANNALS OF THE RHEUMATIC DISEASES, 2016, 75 (06) :1081-1091
[19]
Tofacitinib (CP-690,550) in combination with methotrexate in patients with active rheumatoid arthritis with an inadequate response to tumour necrosis factor inhibitors: a randomised phase 3 trial [J].
Burmester, Gerd R. ;
Blanco, Ricardo ;
Charles-Schoeman, Christina ;
Wollenhaupt, Juergen ;
Zerbini, Cristiano ;
Benda, Birgitta ;
Gruben, David ;
Wallenstein, Gene ;
Krishnaswami, Sriram ;
Zwillich, Samuel H. ;
Koncz, Tamas ;
Soma, Koshika ;
Bradley, John ;
Mebus, Charles .
LANCET, 2013, 381 (9865) :451-460
[20]
Efficacy of glucocorticoids, conventional and targeted synthetic disease-modifying antirheumatic drugs: a systematic literature review informing the 2016 update of The EULAR recommendations for the management of rheumatoid arthritis [J].
Chatzidionysiou, Katerina ;
Emamikia, Sharzad ;
Nam, Jackie ;
Ramiro, Sofia ;
Smolen, Josef ;
van der Heijde, Desiree ;
Dougados, Maxime ;
Bijlsma, Johannes ;
Burmester, Gerd ;
Scholte, Marieke ;
van Vollenhoven, Ronald ;
Landewe, Robert .
ANNALS OF THE RHEUMATIC DISEASES, 2017, 76 (06) :1102-1107