Günther Florian, Fleck Martin, Löffler Selina, Hartung Wolfgang, Pongratz Georg
Department of Rheumatology and Clinical Immunology, Asklepios Clinic, Bad Abbach, Germany.
Department of Internal Medicine I, University Medical Center, Regensburg, Germany.
Rheumatol Adv Pract. 2025 Jul 15;9(3):rkaf081. doi: 10.1093/rap/rkaf081. eCollection 2025.
To assess the feasibility of the Giant Cell Arteritis Actemra (GiACTA)-based 26-week glucocorticoid (GC) taper in patients with newly diagnosed GCA.
We conducted a retrospective, single-centre study including patients with newly diagnosed active GCA treated with tocilizumab (TCZ) and GCs, GC monotherapy or GCs combined with conventional DMARDs. In all patients treated with TCZ the standard GC taper was the GiACTA-based 26-week GC taper. A subgroup of TCZ-treated patients at high risk for GC-associated adverse events was identified, in which, based on a decision between the patient and physician, a shorter 16-week prednisone taper was used. Data on relapses, steroid doses and therapy-related adverse events were collected from patients' records.
A total of 101 patients with newly diagnosed GCA were included; 47 (46.5%) patients were treated from the beginning with TCZ. Of the 47 patients, 28 (59.6%) treated with TCZ tapered off GCs completely within 26 weeks. Of these patients off GCs within 26 weeks, 25 (89.3%) were in relapse-free remission at week 52. In 15 patients treated with TCZ, GCs were tapered off completely within 16 weeks. Of these patients off GCs within 16 weeks, 14 (93.3%) were still in relapse-free remission at week 52 and no further flares occurred in this group of patients by week 104. No case of GCA-related vision loss or cerebrovascular ischaemia occurred during follow-up.
In this real-world setting, 26- and 16-week GC tapers were effective and safe in patients with newly diagnosed GCA treated with TCZ.
评估基于巨细胞动脉炎托珠单抗治疗(GiACTA)方案的26周糖皮质激素(GC)减量方案在新诊断的巨细胞动脉炎(GCA)患者中的可行性。
我们进行了一项回顾性单中心研究,纳入了新诊断的活动性GCA患者,这些患者接受了托珠单抗(TCZ)和GC治疗、GC单药治疗或GC联合传统改善病情抗风湿药(DMARDs)治疗。在所有接受TCZ治疗的患者中,标准的GC减量方案是基于GiACTA方案的26周GC减量方案。确定了一组接受TCZ治疗且发生GC相关不良事件风险较高的患者亚组,根据患者与医生的共同决策,采用了更短的16周泼尼松减量方案。从患者记录中收集了复发、类固醇剂量和治疗相关不良事件的数据。
共纳入101例新诊断的GCA患者;47例(46.5%)患者从一开始就接受TCZ治疗。在这47例接受TCZ治疗的患者中,28例(59.6%)在26周内完全停用了GC。在这些26周内停用GC的患者中,25例(89.3%)在第52周时处于无复发缓解状态。在15例接受TCZ治疗的患者中,GC在16周内完全减量。在这些16周内停用GC的患者中,14例(93.3%)在第52周时仍处于无复发缓解状态,并且在该组患者中到第104周时未再发生病情复发。随访期间未发生GCA相关的视力丧失或脑血管缺血事件。
在这一真实世界环境中,26周和16周的GC减量方案对于接受TCZ治疗的新诊断GCA患者是有效且安全的。