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Drugs. 2014 Jun;74(9):999-1016. doi: 10.1007/s40265-014-0239-z.
Certolizumab pegol (Cimzia(®)) is a polyethylene glycolylated antigen-binding fragment of a recombinant human monoclonal antibody that binds to and selectively neutralizes tumour necrosis factor (TNF) α. In the EU, subcutaneous certolizumab pegol is indicated for the treatment of adults with severe active axial spondyloarthritis (axSpA), comprising ankylosing spondylitis (AS) and non-radiographic axSpA (nr-axSpA), and for adults with active psoriatic arthritis (PsA). In the USA it is indicated for the treatment of adults with active AS or active PsA. This article reviews the efficacy and tolerability of certolizumab pegol in these patients and briefly summarizes its pharmacology. In two ongoing, well-designed studies, data at 12 and 24 weeks showed that treatment with certolizumab pegol (200 mg every 2 weeks or 400 mg every 4 weeks) was effective in improving the clinical signs and symptoms of disease, health-related quality of life and productivity in patients with axSpA (the RAPID-axSpA study) or PsA (the RAPID-PsA study), with the improvements maintained during longer-term (48 weeks) treatment. Within the axSpA population, clinical benefits with certolizumab pegol were seen both in patients with AS and in those with nr-axSpA. In addition, 12 weeks' treatment with certolizumab pegol reduced inflammation in the sacroiliac joints and spine in patients with axSpA and 24 weeks' treatment with the agent slowed radiographic disease progression in patients with PsA. Certolizumab pegol was generally well tolerated in these studies, with a tolerability profile consistent with that seen in previous clinical trials in other indications. Although additional long-term and comparative data are needed to position certolizumab pegol with respect to other TNFα antagonists, current evidence indicates that certolizumab pegol is an effective option for the treatment of axSpA (including AS and nr-axSpA) and PsA.
培塞利珠单抗(Cimzia(®))是一种聚乙二醇化的人源单克隆抗体抗原结合片段,可结合并选择性中和肿瘤坏死因子(TNF)α。在欧盟,皮下注射培塞利珠单抗适用于治疗成年重度活动性中轴型脊柱关节炎(axSpA),包括强直性脊柱炎(AS)和非放射学中轴型脊柱关节炎(nr-axSpA),以及成年活动性银屑病关节炎(PsA)患者。在美国,它适用于治疗成年活动性 AS 或活动性 PsA 患者。本文综述了培塞利珠单抗在这些患者中的疗效和耐受性,并简要总结了其药理学特性。在两项正在进行的、设计良好的研究中,12 周和 24 周的数据显示,培塞利珠单抗(每 2 周 200mg 或每 4 周 400mg)治疗可有效改善 axSpA(RAPID-axSpA 研究)或 PsA(RAPID-PsA 研究)患者的疾病临床体征和症状、健康相关生活质量和生产力,并且在更长时间(48 周)治疗期间保持改善。在 axSpA 人群中,培塞利珠单抗在 AS 患者和 nr-axSpA 患者中均观察到临床获益。此外,培塞利珠单抗治疗 12 周可减轻 axSpA 患者的骶髂关节和脊柱炎症,治疗 24 周可减缓 PsA 患者的放射学疾病进展。在这些研究中,培塞利珠单抗总体耐受性良好,其耐受性特征与其他适应证的先前临床试验一致。尽管需要更多的长期和对照数据来确定培塞利珠单抗与其他 TNFα 拮抗剂的定位,但现有证据表明,培塞利珠单抗是治疗 axSpA(包括 AS 和 nr-axSpA)和 PsA 的有效选择。