首页> 美国卫生研究院文献>International Journal of General Medicine >Management of rheumatoid arthritis in People’s Republic of China – focus on tocilizumab and patient considerations
【2h】

Management of rheumatoid arthritis in People’s Republic of China – focus on tocilizumab and patient considerations

机译:中华人民共和国类风湿关节炎的治疗-重点关注托珠单抗和患者注意事项

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

The prevalence of rheumatoid arthritis (RA) is 0.19%–0.41% in Chinese population. RA exerts profound influence on health-related quality of life (HRQoL), which imposed huge burdens on patients physically, mentally, and economically. As a developing country, People’s Republic of China faces enormous challenges in management of RA. Conventional-synthesized disease-modifying antirheumatic drugs (csDMARDs) remain the most selective therapeutic options for RA in People’s Republic of China owing to their affordable price and fair efficacy as well as tolerability. Unfortunately, there are substantial RA patients who are poor responders to csDMARDs, even to subsequently combined therapy with tumor necrosis factor antagonist (anti-TNF). Tocilizumab (TCZ) has been approved as a subsequent-line biological agent in patients with moderate-to-severe RA worldwide including People’s Republic of China. TCZ is the first biological agent approved for the treatment of RA inhibiting interlukin-6 (IL-6) by blocking both membrane-bound and soluble IL-6 receptors. Open-label studies in real-life practice and strictly controlled clinical trials demonstrated its high efficacy and safety profile in treatment of patients with RA who have inadequate responses to csDMARDs and anti-TNF. HRQoL of RA patients was improved in various measurements. TCZ was associated with 1.2 times the risk of adverse events, such as infections, dyslipidemia, and hepatic transaminases elevation, compared with pooled placebo. A relatively long half-life allowing for monthly intravenous administration and a newly developed subcutaneous injection make TCZ more acceptable. However, data are not enough so far comparing TCZ to anti-TNF. Lack of evidence in Chinese patients and high cost of TCZ limit its prescription in People’s Republic of China being a developing country. Further clinical trials and post-marketing surveillance may offer a comprehensive assessment of patient satisfaction and acceptability, which may help us define the optimal role for TCZ in therapeutic strategy.
机译:在中国人群中,类风湿关节炎(RA)的患病率为0.19%–0.41%。 RA对与健康相关的生活质量(HRQoL)产生了深远的影响,这给患者的身心,经济造成了沉重负担。作为发展中国家,中华人民共和国在RA管理方面面临着巨大挑战。常规合成的抗疾病风湿病药物(csDMARDs)由于价格合理,功效合理且耐受性强,因此仍然是中华人民共和国RA的最选择性治疗选择。不幸的是,有大量的RA患者对csDMARDs甚至对随后与肿瘤坏死因子拮抗剂(anti-TNF)联合治疗的反应都较差。 Tocilizumab(TCZ)已被批准为包括中国在内的全球中度至重度RA患者的继发线生物制剂。 TCZ是第一种通过阻断膜结合和可溶性IL-6受体而被批准用于治疗RA抑制白介素6(IL-6)的生物制剂。在现实生活中进行的开放标签研究和严格控制的临床试验表明,它对治疗csDMARDs和抗TNF反应不足的RA患者具有很高的疗效和安全性。 RA患者的HRQoL在各种测量中得到改善。与合并的安慰剂相比,TCZ与诸如感染,血脂异常和肝转氨酶升高等不良事件发生风险的关系是其1.2倍。相对较长的半衰期允许每月静脉内给药和新开发的皮下注射方式使TCZ更易被接受。然而,到目前为止,将TCZ与抗TNF进行比较的数据还不够。中国患者缺乏证据,TCZ的高昂费用限制了它在发展中国家这个发展中国家的处方。进一步的临床试验和上市后的监视可能会提供患者满意度和可接受性的全面评估,这可能有助于我们确定TCZ在治疗策略中的最佳作用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号