...
首页> 外文期刊>Medicine. >Effectiveness of Adalimumab in Non-radiographic Axial Spondyloarthritis Evaluation of Clinical and Magnetic Resonance Imaging Outcomes in a Monocentric Cohort
【24h】

Effectiveness of Adalimumab in Non-radiographic Axial Spondyloarthritis Evaluation of Clinical and Magnetic Resonance Imaging Outcomes in a Monocentric Cohort

机译:阿达木单抗在非放射性轴索性脊柱关节炎的临床评价和磁共振成像结果在单中心队列中的有效性。

获取原文
获取原文并翻译 | 示例

摘要

The primary aim of the study was to evaluate the long-term effectiveness of adalimumab (ADA) in a cohort of non-radiographic axial spondyloarthritis (nr-axSpA), and the secondary aims were to identify predictive factors of response and evaluate radiological progression.We evaluated 37 patients (male/female: 12/25; mean age 4914; mean disease duration: 6.35.8) with active nr-axSpA (Assessment of SpondyloArthritis International Society criteria), despite the treatment with 1 nonsteroidal anti-inflammatory drug for at least 3 months, initiating the treatment with ADA 40mg every other week. Patients were treated for 24 months, and evaluated at baseline, 6, 12, and 24 months. Outcome measures included Ankylosing Spondylitis Disease Activity Score, Bath Ankylosing Spondylitis Disease Activity Index (BASDAI), and Bath Ankylosing Spondylitis Functional Index. Radiograph of the spine and sacroiliac joints and magnetic resonance of the sacroiliac joints were performed at baseline and according to the standard of assessment for the disease.The proportion of patients that achieved a BASDAI50 response at 6, 12 and 24 months was 51.3%, 70.3%, and 76.8%, respectively. Treatment was well tolerated with no unexpected adverse events and/or serious adverse events. All patients remained on treatment for 2 years, with a good compliance. We did not identify any predictive factor of response to therapy. Moreover, modified Stoke Ankylosing Spondylitis Spine Score and Spondyloarthritis Research Consortium of Canada scores showed a trend of improvement during the study period.ADA was effective on clinical and radiological outcomes at 2-year follow-up; thus, early treatment with ADA may prevent radiographic damage and be associated with low disease activity or remission. Moreover, data from this cohort study have confirmed safety and tolerability profile of ADA in nr-axSpA in the long term.
机译:这项研究的主要目的是评估阿达木单抗(ADA)在非放射线轴性脊椎关节炎(nr-axSpA)队列中的长期有效性,其次要目的是确定反应的预测因素并评估放射学进展。尽管使用1种非甾体类抗炎药治疗了活跃的nr-axSpA(脊柱关节炎国际社会标准评估)的患者,我们仍评估了37例患者(男性/女性:12/25;平均年龄:4914;平均病程:6.35.8)。至少3个月,每隔一周开始用ADA 40mg开始治疗。对患者进行了24个月的治疗,并在基线,6、12和24个月进行了评估。结果指标包括强直性脊柱炎疾病活动评分,巴斯强直性脊柱炎疾病活动指数(BASDAI)和巴斯强直性脊柱炎功能指数。在基线并根据疾病评估标准对脊柱和sa关节进行X线照相,并对joint关节进行磁共振检查。在6、12和24个月时达到BASDAI50反应的患者比例为51.3%,70.3 %和76.8%。治疗耐受性良好,没有意外的不良事件和/或严重的不良事件。所有患者均保持治疗2年,依从性良好。我们没有发现任何对治疗反应的预测因素。此外,改良的斯托克强直性脊柱炎脊柱评分和加拿大脊柱关节炎研究协会评分在研究期间呈改善趋势。ADA在2年的随访中对临床和放射学结局有效;因此,采用ADA进行早期治疗可以预防放射线照相损伤,并降低疾病活动性或缓解率。此外,该队列研究的数据已长期确认了ADA在nr-axSpA中的安全性和耐受性。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

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