Department of Internal Medicine and Therapeutics, Università di Pavia, Pavia, Italy.
Division of Rheumatology, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.
Intern Emerg Med. 2023 Sep;18(6):1733-1740. doi: 10.1007/s11739-023-03350-4. Epub 2023 Jul 27.
Pain remains one of the most difficult-to-treat domains in patients with rheumatoid arthritis (RA). In clinical trials, the Janus kinase inhibitors (JAKis) have demonstrated good efficacy in pain relief. Aim of our study was to evaluate the real-life effectiveness of JAKis in improving pain in patients with RA in different states of baseline disease activity. A monocentric prospective cohort of 181 RA patients starting treatment with JAKis was studied. Pain was evaluated on a 0-100 mm visual analogue scale (VAS). Clinically meaningful improvements over 24 weeks were defined as follows: proportion of patients achieving ≥ 30%, ≥ 50%, and ≥ 70% pain relief, and remaining pain ≤ 20 or ≤ 10 mm. Results were analysed after stratification for baseline inflammatory activity; patients with swollen joints and C-reactive protein ≤ 1 at treatment start were considered pauci-inflammatory. Proportion of patients who achieved ≥ 30%, ≥ 50% and ≥ 70% pain improvement at 24 weeks was 61.4%, 49.3% and 32.9%. Furthermore, 40.6% and 28.5% of the patients achieved thresholds of remaining pain equivalent to mild pain or no/limited pain. Pain improvements were more evident in patients naive to previous biologics, although nearly 30% of multiple failures achieved VAS ≤ 20 mm. No significant differences were observed in relation to monotherapy. Pauci-inflammatory patients at treatment start achieved good outcomes, with 40.4% experiencing ≥ 70% pain improvement, and 35.7% VAS ≤ 10 mm. JAKis show efficacy in pain relief in real life. The improvement of painful symptoms also in those patients with limited objective inflammation may open new perspectives on the management of difficult-to-treat RA.
疼痛仍然是类风湿关节炎(RA)患者最难治疗的领域之一。在临床试验中,Janus 激酶抑制剂(JAKi)已被证明在缓解疼痛方面具有良好的疗效。我们的研究目的是评估 JAKi 在改善不同基线疾病活动度 RA 患者疼痛方面的真实疗效。对 181 例开始接受 JAKi 治疗的 RA 患者进行了单中心前瞻性队列研究。疼痛采用 0-100mm 视觉模拟评分(VAS)进行评估。24 周内临床意义上的改善定义为:达到≥30%、≥50%和≥70%疼痛缓解的患者比例,以及残留疼痛≤20 或≤10mm 的患者比例。根据基线炎症活动度进行分层后分析结果;治疗开始时肿胀关节和 C 反应蛋白≤1 的患者被认为是少关节炎。24 周时达到≥30%、≥50%和≥70%疼痛改善的患者比例分别为 61.4%、49.3%和 32.9%。此外,40.6%和 28.5%的患者达到相当于轻度疼痛或无/有限疼痛的残留疼痛阈值。在未接受过先前生物制剂治疗的患者中,疼痛改善更为明显,尽管近 30%的多次失败患者达到了 VAS≤20mm。与单药治疗相比,没有观察到显著差异。治疗开始时少关节炎的患者取得了良好的疗效,40.4%的患者疼痛改善≥70%,35.7%的患者 VAS≤10mm。JAKi 在缓解疼痛方面具有真实疗效。在那些客观炎症有限的患者中,疼痛症状的改善也可能为治疗难治性 RA 开辟新的视角。