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5 年无药物缓解指导治疗早期关节炎患者的临床和放射学结果:IMPROVED 研究。

Clinical and radiological outcomes of 5-year drug-free remission-steered treatment in patients with early arthritis: IMPROVED study.

机构信息

Department of Rheumatology, Leiden University Medical Center, Leiden, Netherlands.

Department of Rheumatology, Haga Hospital, Hague, Netherlands.

出版信息

Ann Rheum Dis. 2018 Jan;77(1):111-118. doi: 10.1136/annrheumdis-2017-211375. Epub 2017 Sep 28.

Abstract

OBJECTIVES

To determine the 5-year outcomes of early remission induction therapy followed by targeted treatment aimed at drug-free remission (DFR) in patients with early arthritis.

METHODS

In 12 hospitals, 610 patients with early (<2 years) rheumatoid arthritis (RA) or undifferentiated arthritis (UA) started on methotrexate (MTX) 25 mg/week and prednisone (60 mg/day tapered to 7.5 mg/day). Patients in early remission (Disease Activity Score <1.6 after 4 months) were randomised (single blind) to arm 1, adding hydroxychloroquine 400 mg/day and sulfasalazine 2000 mg/day, or arm 2, switching to MTX plus adalimumab 40 mg/2 weeks. Treatment adjustments over time aimed at DFR. Outcomes were remission percentages, functional ability, toxicity and radiological damage progression after 5 years.

RESULTS

After 4 months, 387 patients were in early remission, 83 were randomised to arm 1 and 78 to arm 2. After 5 years, 295/610 (48%) patients were in remission, 26% in sustained DFR (SDFR) (≥1 year) (220/387 (57%) remission and 135/387 (35%) SDFR in the early remission group, 50% remission, 11% SDFR in the randomisation arms without differences between the arms). More patients with UA (37% vs 23% RA, p=0.001) and more anticitrullinated protein antibody (ACPA)-negative patients (37% vs 18% ACPA-positive, p<0.001) achieved SDFR.Overall, mean Health Assessment Questionnaire was 0.6 (0.5), and median (IQR) damage progression was 0.5 (0-2.7) Sharp/van der Heijde points, with only five patients showing progression >25 points in 5 years.

CONCLUSIONS

Five years of DFR-steered treatment in patients with early RA resulted in almost normal functional ability without clinically relevant joint damage across treatment groups. Patients who achieved early remission had the best clinical outcomes. There were no differences between the randomisation arms. SDFR is a realistic treatment goal.

摘要

目的

确定早期缓解诱导治疗后,针对无药物缓解(DFR)的靶向治疗在早期关节炎患者中的 5 年结果。

方法

在 12 家医院中,610 名患有早期(<2 年)类风湿关节炎(RA)或未分化关节炎(UA)的患者开始接受甲氨蝶呤(MTX)25mg/周和泼尼松(60mg/天,逐渐减至 7.5mg/天)治疗。4 个月后疾病活动评分(DAS)<1.6 的患者进入早期缓解期,随机(单盲)分为 1 组,加用羟氯喹 400mg/天和柳氮磺胺吡啶 2000mg/天,或 2 组,换用 MTX 加阿达木单抗 40mg/2 周。随着时间的推移,调整治疗以达到 DFR。5 年后的缓解率、功能能力、毒性和放射学损害进展是主要观察终点。

结果

4 个月后,387 名患者进入早期缓解期,83 名患者被随机分配到 1 组,78 名患者被随机分配到 2 组。5 年后,610 名患者中有 295 名(48%)处于缓解期,26%持续达到 DFR(SDFR)(≥1 年)(387 名缓解期患者中有 220 名[57%]达到缓解期,83 名缓解期患者中有 135 名[35%]达到 SDFR),随机分组组之间的缓解率和 SDFR 无差异(无差异)。UA 患者(37%比 RA 患者 23%,p=0.001)和 ACPA 阴性患者(37%比 ACPA 阳性患者 18%,p<0.001)更多达到 SDFR。总体而言,健康评估问卷平均得分为 0.6(0.5),中位数(IQR)损伤进展为 0.5(0-2.7)Sharp/van der Heijde 点,只有 5 名患者在 5 年内出现>25 点的进展。

结论

早期 RA 患者 5 年的 DFR 导向治疗可达到接近正常的功能能力,且各治疗组的关节损伤无临床意义。达到早期缓解的患者有最好的临床结果。随机分组组之间无差异。SDFR 是一个现实的治疗目标。

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