首页> 外文期刊>Modern rheumatology >Effectiveness and safety of adalimumab in Japanese patients with rheumatoid arthritis: retrospective analyses of data collected during the first year of adalimumab treatment in routine clinical practice (HARMONY study).
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Effectiveness and safety of adalimumab in Japanese patients with rheumatoid arthritis: retrospective analyses of data collected during the first year of adalimumab treatment in routine clinical practice (HARMONY study).

机译:阿达木单抗在日本类风湿性关节炎患者中的有效性和安全性:对阿达木单抗治疗第一年在常规临床实践中收集的数据进行回顾性分析(HARMONY研究)。

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摘要

We retrospectively investigated the ability of adalimumab (ADA) to reduce disease activity, improve physical function, and retard the progression of structural damage in 167 patients with rheumatoid arthritis. Clinical and functional outcomes were compared between patients with or without prior biologic treatment and those with or without concomitant methotrexate (MTX) treatment. At week 52, 38.3% achieved clinical remission: 42.4 and 28.6% of patients achieved remission in those without and with previous biologics, respectively, while 42.7 and 12.5% of patients achieved remission in those with and without concomitant MTX, respectively. ADA treatment significantly reduced the rate of radiographic progression from 27.1 ± 46.0 (median 13.6; 25th-75th percentiles 8.3 to 28.9) at baseline to 0.8 ± 5.0 (median 0.0; 25th-75th percentiles -0.9 to 2.0) at week 52 (P < 0.0001). Radiographic progression was absent in 59.8% of patients. Sixty adverse events (34.21/100 patient-years) were reported, 16 of which were serious (9.12/100 patient-years). ADA therapy is highly effective for reducing disease activity, improving physical function, and limiting radiographic progression. It is generally safe and well tolerated by Japanese RA patients in routine clinical practice.
机译:我们回顾性研究了167例类风湿关节炎患者中阿达木单抗(ADA)降低疾病活性,改善身体机能和延缓结构性损伤进展的能力。比较接受或不接受生物治疗的患者与接受或不接受甲氨蝶呤(MTX)治疗的患者的临床和功能结局。在第52周时,有38.3%的患者达到了临床缓解:在有或没有既往使用生物制剂的患者中,分别达到了缓解的42.4和28.6%,而有或没有MTX的患者中分别有42.7和12.5%的患者实现了缓解。 ADA治疗显着降低了X线摄片进展的速度,从基线时的27.1±46.0(中值13.6; 25-75%百分率8.3降至28.9)降至第52周的0.8±5.0(中值0.0; 25-75%百分率-0.9至2.0)(P < 0.0001)。 59.8%的患者无影像学进展。报告了60次不良事件(34.21 / 100患者-年),其中16个严重事件(9.12 / 100患者-年)。 ADA治疗对于减少疾病活动,改善身体机能和限制射线照相进展非常有效。日本RA患者在常规临床实践中通常安全且耐受良好。

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