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阿达木单抗治疗免疫介导性疾病。

Adalimumab in the treatment of immune-mediated diseases.

机构信息

Rheumatology Unit, Interdisciplinary Department of Medicine, Medical School, University of Bari, Bari, Italy.

G. Pini Orthopedic Institute, Milano, Italy.

出版信息

Int J Immunopathol Pharmacol. 2014 Jan-Mar;27(1 Suppl):33-48. doi: 10.1177/03946320140270S103.

Abstract

Tumour necrosis factor (TNF) plays an important role in the pathogenesis of immune-mediated inflammatory diseases (IMIDs). TNF inhibition results in down-regulation of abnormal and progressive inflammatory processes, resulting in rapid and sustained clinical remission, improved quality of life and prevention of target organ damage. Adalimumab is the first fully human monoclonal antibody directed against TNF. In this article, we review the role and cost effectiveness of adalimumab in the treatment of IMIDs in adults and children. The efficacy and tolerability of adalimumab has been demonstrated in patients with a wide range of inflammatory conditions, leading to regulatory approval in rheumatoid arthritis (RA), psoriatic arthritis (PsA), plaque psoriasis, inflammatory bowel diseases (Crohn's disease, ulcerative colitis, paediatric Crohn's disease, and intestinal Behçet's disease), ankylosing spondylitis (AS), axial spondyloarthritis (SpA) and juvenile idiopathic arthritis. The major tolerability issues with adalimumab are class effects, such as injection site reactions and increased risk of infection and lymphoma. As with all anti-TNF agents, adalimumab is immunogenic, although less than infliximab, and some patients receiving long-term adalimumab will develop anti-drug antibodies, causing a loss of response. Comparisons of its clinical utility and cost effectiveness have shown it to be a valid treatment choice in a wide range of patients. Recent data from Italian economic studies show the cost effectiveness of adalimumab to be below the threshold value for health care interventions for most indications. In addition, analysis of indirect costs shows that adalimumab significantly reduces social costs associated with RA, PsA, AS, Crohn's disease and psoriasis. The fact that adalimumab has the widest range of approved indications, many often presenting together in the same patient due to the common pathogenesis, may further improve the utility of adalimumab. Current clinical evidence shows adalimumab to be a valuable resource in the management of IMIDs. Further research, designed to identify patients who may benefit most from this drug, will better highlight the role and cost-effectiveness of this versatile TNF inhibitor.

摘要

肿瘤坏死因子(TNF)在免疫介导的炎症性疾病(IMIDs)的发病机制中起着重要作用。TNF 抑制导致异常和进行性炎症过程的下调,从而迅速和持续的临床缓解,改善生活质量和预防靶器官损伤。阿达木单抗是第一个针对 TNF 的完全人源单克隆抗体。本文综述了阿达木单抗在成人和儿童 IMIDs 治疗中的作用和成本效益。阿达木单抗在广泛的炎症性疾病患者中的疗效和耐受性已得到证实,导致其在类风湿关节炎(RA)、银屑病关节炎(PsA)、斑块状银屑病、炎症性肠病(克罗恩病、溃疡性结肠炎、儿童克罗恩病和肠贝切特病)、强直性脊柱炎(AS)、中轴型脊柱关节炎(SpA)和幼年特发性关节炎中的监管批准。阿达木单抗的主要耐受性问题是类效应,如注射部位反应和感染和淋巴瘤风险增加。与所有抗 TNF 药物一样,阿达木单抗是免疫原性的,尽管不如英夫利昔单抗,一些接受长期阿达木单抗治疗的患者会产生抗药物抗体,导致反应丧失。对其临床应用和成本效益的比较表明,它在广泛的患者中是一种有效的治疗选择。来自意大利经济研究的最新数据表明,阿达木单抗在大多数适应症下的成本效益低于卫生保健干预的阈值。此外,间接成本分析表明,阿达木单抗可显著降低与 RA、PsA、AS、克罗恩病和银屑病相关的社会成本。阿达木单抗具有最广泛的批准适应症,由于共同的发病机制,许多适应症通常同时出现在同一患者中,这可能进一步提高阿达木单抗的应用价值。目前的临床证据表明,阿达木单抗在 IMIDs 的治疗中是一种有价值的资源。旨在确定最可能从这种药物中受益的患者的进一步研究将更好地突出这种多功能 TNF 抑制剂的作用和成本效益。

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