Ocak Tuğba, Yağız Burcu, Coşkun Belkıs Nihan, Akkuzu Gamze, Bayındır Akbaş Ayşe Nur, Kudaş Özlem, İnanç Elif, Yoğurtçu Özge, Başıbüyük Fatma, Zontul Sezgin, Albayrak Fatih, Akar Zeynel Abidin, Sunkak Saliha, Ermurat Selime, Tezcan Dilek, Küçük Adem, Yolbaş Servet, Sarı İsmail, Yiğit Murat, Akar Servet, Kısacık Bünyamin, Bes Cemal, Dalkılıç Ediz, Pehlivan Yavuz
Department of Rheumatology, Bursa City Hospital, 16250 Bursa, Turkey.
Division of Rheumatology, Department of Internal Medicine, Faculty of Medicine, Uludağ University, 16059 Bursa, Turkey.
J Clin Med. 2025 Jul 22;14(15):5181. doi: 10.3390/jcm14155181.
: Secukinumab is a fully human monoclonal antibody that targets interleukin (IL)-17A and is used to treat axial spondyloarthritis (axSpA) and psoriatic arthritis (PsA). Treating axSpA and PsA can be challenging in patients with comorbidities. In this multicenter retrospective study, we aimed to evaluate the efficacy and safety of secukinumab treatment in patients with axSpA and PsA who had a history of tuberculosis, multiple sclerosis (MS), or congestive heart failure (CHF). : The study included 44 patients with a diagnosis of axSpA and PsA and a history of tuberculosis, MS, or CHF who received secukinumab treatment at 13 centers in our country. Erythrocyte sedimentation rate, C-reactive protein (CRP), Bath Ankylosing Spondylitis Disease Activity Index, Ankylosing Spondylitis Disease Activity Score CRP, visual analog scale, and Disease Activity Score-28 CRP markers at months 0, 3, and 12 of secukinumab treatment were analyzed. Alongside this, tuberculosis, MS, and CHF were evaluated at follow-up using clinical assessments and imaging methods such as chest radiographs, brain magnetic resonance, and echocardiography. : A statistically significant improvement in inflammatory markers and disease activity scores was observed in patients treated with secukinumab. There was no reactivation in patients with a history of tuberculosis. In most MS patients, the disease was stable, while clinical and radiological improvement was observed in one patient. No worsening of CHF stage was observed in patients with a history of CHF. : With regular clinical monitoring, secukinumab may be an effective and safe treatment option for axSpA and PsA patients with a history of tuberculosis, MS, or CHF.
司库奇尤单抗是一种靶向白细胞介素(IL)-17A的全人单克隆抗体,用于治疗中轴型脊柱关节炎(axSpA)和银屑病关节炎(PsA)。对于患有合并症的患者,治疗axSpA和PsA可能具有挑战性。在这项多中心回顾性研究中,我们旨在评估司库奇尤单抗治疗有结核病、多发性硬化症(MS)或充血性心力衰竭(CHF)病史的axSpA和PsA患者的疗效和安全性。
该研究纳入了44例诊断为axSpA和PsA且有结核病、MS或CHF病史的患者,这些患者在我国13个中心接受了司库奇尤单抗治疗。分析了司库奇尤单抗治疗0、3和12个月时的红细胞沉降率、C反应蛋白(CRP)、巴斯强直性脊柱炎疾病活动指数、强直性脊柱炎疾病活动评分CRP、视觉模拟量表和疾病活动评分-28 CRP标志物。与此同时,在随访期间使用胸部X光、脑磁共振和超声心动图等临床评估和成像方法对结核病、MS和CHF进行了评估。
接受司库奇尤单抗治疗的患者炎症标志物和疾病活动评分有统计学意义的改善。有结核病病史的患者未出现复发。在大多数MS患者中,疾病稳定,而在一名患者中观察到临床和影像学改善。有CHF病史的患者未观察到CHF阶段恶化。
通过定期临床监测,司库奇尤单抗可能是有结核病、MS或CHF病史的axSpA和PsA患者的一种有效且安全的治疗选择。