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Sustained remission with methotrexate monotherapy after 22-week induction treatment with TNF-alpha inhibitor and methotrexate in early psoriatic arthritis: an open-label extension of a randomized placebo-controlled trial

机译:22周诱导治疗后的甲氨蝶呤单药治疗持续缓解TNF-α抑制剂和甲氨蝶呤在初期的银屑病关节炎:随机安慰剂对照试验的开放标签延伸

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摘要

Abstract Background If TNF inhibitors are initiated in the early stages of psoriatic arthritis, this could potentially modulate disease and therefore allow us to discontinue the TNF inhibitor after achieving remission. Objective To investigate whether remission induced by tumour necrosis factor alpha inhibitor (TNFi) and methotrexate in patients with early psoriatic arthritis is sustained after withdrawal of TNFi. Methods Open-label extension of a recently published double-blind, randomized placebo-controlled trial. Patients with psoriatic arthritis fulfilling the CASPAR criteria and with active disease at baseline (swollen and tender joint count ≥ 3) were randomized to either golimumab and methotrexate or matched placebo and methotrexate. Patients in Disease Activity Score (DAS) remission at week 22 continued in the open-label extension on methotrexate monotherapy. The primary end point was the percentage of patients in DAS-CRP remission (DAS < 1.6) at week 50. Results Eight patients from the original placebo group and 18 patients from the original TNFi group continued in the extension phase. At week 50, 6 out of 8 (75%) patients from the original MTX (methotrexate) group versus 10 out of 18 (56%) patients from the original MTX+TNFi group were in DAS-CRP remission (p = 0.347). Considering the total study population, 6 out of 24 (25%) of the original MTX group versus 10 out of 26 (38.5%) of the original MTX+TNFi group were in DAS remission at week 50 (p = 0.308). Conclusions Remission achieved by initial combination treatment with TNFi and methotrexate in early psoriatic arthritis is maintained on methotrexate monotherapy in approximately half of the patients. Trial registration Registered at Clinicaltrials.gov with number NCT01871649 on June 7, 2013.
机译:摘要背景如果在银屑病关节炎的早期阶段启动TNF抑制剂,这可能会调节疾病,因此允许我们在实现缓解后停止TNF抑制剂。目的探讨肿瘤坏死因子α抑制剂(TNFI)和甲氨蝶呤在早期银屑病关节炎患者中是否患有缓解后的缓解率在TNFI撤离后持续。方法开放标签延伸最近发表的双盲,随机安慰剂对照试验。患有基石性关节炎的患者,满足基线的基础标准和活性疾病(肿胀和柔软的关节计数≥3)被随机化为Golimumab和甲氨蝶呤或匹配的安慰剂和甲氨蝶呤。第22周疾病活动评分(DAS)缓解患者在甲氨蝶呤单一疗法的开放标签延伸期间继续进行。第50周的DAS-CRP缓解(DAS <1.6)患者的百分比是患者的百分比。结果,原始安慰剂组和18名来自原版TNFI组患者的患者继续在延伸阶段。在第50周,来自原始MTX(甲氨蝶呤)组的8名(75%)患者中的6例,来自原始MTX + TNFI组的18例(56%)患者中的10名(56%)是DAS-CRP缓解(P = 0.347)。考虑到24个(25%)原始MTX组的总研究人群,26个(38.5%)原始MTX + TNFI组的10个(28.5%)在第50周的DAS缓解中(P = 0.308)。结论初始组合治疗与早期银屑病关节炎的初始组合治疗可缓解在大约一半的患者中甲氨蝶呤单药治疗。试用注册在Clinicaltrials.gov注册,2013年6月7日与NCT01871649号码NCT01871649。

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