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Preferable outcome of Janus kinase inhibitors for a group of difficult-to-treat rheumatoid arthritis patients: from the FIRST Registry.Janus 激酶抑制剂对一组难治性类风湿关节炎患者的理想疗效:来自 FIRST 登记研究。
Arthritis Res Ther. 2022 Mar 1;24(1):61. doi: 10.1186/s13075-022-02744-7.
2
Phase III trials of JAK1 selective inhibitors in rheumatoid arthritis.JAK1 选择性抑制剂治疗类风湿关节炎的 III 期临床试验。
Rheumatology (Oxford). 2021 May 5;60(Suppl 2):ii17-ii23. doi: 10.1093/rheumatology/keaa823.
3
Upadacitinib improves patient-reported outcomes in patients with rheumatoid arthritis and inadequate response to conventional synthetic disease-modifying antirheumatic drugs: results from SELECT-NEXT.乌帕替尼改善了对常规合成疾病修饰抗风湿药物反应不足的类风湿关节炎患者的患者报告结局:SELECT-NEXT 研究结果。
Arthritis Res Ther. 2019 Dec 9;21(1):272. doi: 10.1186/s13075-019-2037-1.
4
Effects of upadacitinib on patient-reported outcomes: results from SELECT-BEYOND, a phase 3 randomized trial in patients with rheumatoid arthritis and inadequate responses to biologic disease-modifying antirheumatic drugs.Upadacitinib 对患者报告结局的影响:SELECT-BEYOND 研究的结果,这是一项在生物制剂治疗应答不足的类风湿关节炎患者中进行的 3 期随机试验。
Arthritis Res Ther. 2019 Dec 2;21(1):263. doi: 10.1186/s13075-019-2059-8.
5
Upadacitinib Versus Placebo or Adalimumab in Patients With Rheumatoid Arthritis and an Inadequate Response to Methotrexate: Results of a Phase III, Double-Blind, Randomized Controlled Trial.乌帕替尼治疗甲氨蝶呤应答不足的类风湿关节炎患者的 III 期、双盲、随机对照研究结果。
Arthritis Rheumatol. 2019 Nov;71(11):1788-1800. doi: 10.1002/art.41032. Epub 2019 Aug 28.
6
Upadacitinib as monotherapy in patients with active rheumatoid arthritis and inadequate response to methotrexate (SELECT-MONOTHERAPY): a randomised, placebo-controlled, double-blind phase 3 study.乌帕替尼单药治疗对甲氨蝶呤应答不足的活动性类风湿关节炎患者(SELECT-MONOTHERAPY):一项随机、安慰剂对照、双盲 3 期研究。
Lancet. 2019 Jun 8;393(10188):2303-2311. doi: 10.1016/S0140-6736(19)30419-2. Epub 2019 May 23.
7
Safety and efficacy of upadacitinib in patients with active rheumatoid arthritis refractory to biologic disease-modifying anti-rheumatic drugs (SELECT-BEYOND): a double-blind, randomised controlled phase 3 trial.乌帕替尼治疗生物制剂难治的活动性类风湿关节炎患者的安全性和疗效(SELECT-BEYOND):一项双盲、随机对照 3 期临床试验。
Lancet. 2018 Jun 23;391(10139):2513-2524. doi: 10.1016/S0140-6736(18)31116-4. Epub 2018 Jun 18.
8
JAK inhibition as a therapeutic strategy for immune and inflammatory diseases.JAK 抑制作为治疗免疫和炎症性疾病的策略。
Nat Rev Drug Discov. 2017 Dec;16(12):843-862. doi: 10.1038/nrd.2017.201. Epub 2017 Nov 6.
9
Novel therapies for immune-mediated inflammatory diseases: What can we learn from their use in rheumatoid arthritis, spondyloarthritis, systemic lupus erythematosus, psoriasis, Crohn's disease and ulcerative colitis?免疫介导的炎症性疾病的新型治疗方法:从类风湿关节炎、脊柱关节炎、系统性红斑狼疮、银屑病、克罗恩病和溃疡性结肠炎的应用中我们可以学到什么?
Ann Rheum Dis. 2018 Feb;77(2):175-187. doi: 10.1136/annrheumdis-2017-211555. Epub 2017 Aug 1.
10
EULAR recommendations for the management of rheumatoid arthritis with synthetic and biological disease-modifying antirheumatic drugs: 2016 update.EULAR 推荐的类风湿关节炎治疗策略:2016 年更新版
Ann Rheum Dis. 2017 Jun;76(6):960-977. doi: 10.1136/annrheumdis-2016-210715. Epub 2017 Mar 6.

在真实临床实践中,接受乌帕替尼治疗的类风湿关节炎患者的治疗目标是否可实现?

Are the Goals of Therapy Achievable in Patients with Rheumatoid Arthritis Receiving Upadacitinib in Real Clinical Practice?

机构信息

Nasonova Research Institute of Rheumatology, Moscow, Russia.

Mechnikov Northwestern State Medical University, Ministry of Health of the Russian Federation, St. Petersburg, Russia.

出版信息

Dokl Biochem Biophys. 2023 Aug;511(1):180-186. doi: 10.1134/S1607672923700308. Epub 2023 Oct 13.

DOI:10.1134/S1607672923700308
PMID:37833604
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10739522/
Abstract

The aim of the study was to evaluate the effectiveness of UPA in RA patients in real clinical practice after 3 and 6 months of therapy. The study included 63 RA patients with high activity of the disease. Activity was assessed according to the DAS28(ESR), DAS28(CRP), SDAI, CDAI; functional ability to HAQ; quality of life to the EQ-5D; disease activity according to the patient's RAPID-3 index; the level of depression and anxiety to the HADS scale. The effectiveness of therapy was evaluated after 3 (n = 45) and 6 (n = 31) months of UPA therapy. Remission or low activity of the disease by 3 months of therapy was achieved by most patients: remission of 69.8% of patients, low activity of the disease-16.3% of patients. Moderate or high activity persisted in 13.9% of patients. By the 6th month of UPA therapy, the number of remissions reached 90%, low activity 3.3%, moderate activity persisted in 6.7% of patients, high activity of the disease was not in any patient. 20% improvement in function was achieved in 71.8% of patients by the 3rd month of therapy and in 77.8% by the 6th month of treatment; the difference in average HAQ values by the 3rd month of therapy was 0.38 points, by the 6th month-0.58 points. After 3 months of follow-up, 31.1% of patients continued taking GC, by 6 months-24.2%. The dose of GC was reduced from an average of 7.23 to 5.6 mg/s. The percentage of patients requiring NSAIDs decreased from 95.2 to 35.6% and 33.3%, respectively. DMARDs continued to be received by 75.6% of patients by 3 months and 69.7% by 6 months of follow-up. Achieving remission or low activity of the disease in patients with RA receiving UPA in real clinical practice is possible in most patients. A rapid decrease in inflammatory activity is accompanied by a significant improvement in the functional state and quality of life of patients. UPA therapy reduces the need for the use of NSAIDs and reduces the dose of GC in a third of patients.

摘要

本研究旨在评估 UPA 在真实临床实践中治疗 RA 患者 3 和 6 个月后的疗效。该研究纳入了 63 例疾病活动度较高的 RA 患者。根据 DAS28(ESR)、DAS28(CRP)、SDAI、CDAI 评估疾病活动度;用 HAQ 评估患者的功能能力;用 EQ-5D 评估生活质量;根据患者的 RAPID-3 指数评估疾病活动度;用 HADS 量表评估抑郁和焦虑程度。在接受 UPA 治疗 3(n = 45)和 6(n = 31)个月后评估治疗效果。大多数患者在 3 个月的治疗后达到疾病缓解或低活动度:缓解率为 69.8%,疾病低活动度率为 16.3%。13.9%的患者仍处于中度或高度活动度。在 UPA 治疗 6 个月时,缓解率达到 90%,疾病低活动度率为 3.3%,中度活动度持续率为 6.7%,没有患者处于高度活动度。在治疗第 3 个月,71.8%的患者实现了功能 20%的改善,在治疗第 6 个月,这一比例达到了 77.8%;治疗第 3 个月平均 HAQ 值降低了 0.38 分,第 6 个月降低了 0.58 分。在 3 个月的随访后,有 31.1%的患者继续服用 GC,到 6 个月时则有 24.2%的患者继续服用。GC 的剂量从平均 7.23mg 降至 5.6mg/s。需要 NSAIDs 的患者比例从 95.2%降至 35.6%和 33.3%,分别。在第 3 个月和第 6 个月的随访中,分别有 75.6%和 69.7%的患者继续接受 DMARDs 治疗。在接受 UPA 治疗的 RA 患者中,大多数患者可实现缓解或低疾病活动度。炎症活动度的快速下降伴随着患者功能状态和生活质量的显著改善。UPA 治疗减少了 NSAIDs 的使用需求,并使三分之一的患者 GC 剂量降低。