Tanaka Yoshiya, Taylor Peter C, Elboudwarej Emon, Hertz Angie, Shao Xiaorong, Malkov Vladislav A, Matsushima Hironori, Emoto Kahaku, Downie Bryan, Takeuchi Tsutomu
The First Department of Internal Medicine, School of Medicine, University of Occupational and Environmental Health, Japan, 1-1, Iseigaoka, Kitakyushu, 807-8555, Japan.
Botnar Research Centre, Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford, Windmill Road, Headington, Oxford, OX3 7LD, UK.
Rheumatol Ther. 2023 Oct;10(5):1335-1348. doi: 10.1007/s40744-023-00583-9. Epub 2023 Jul 25.
Our aim was to evaluate protein biomarker changes related to the administration of filgotinib, a Janus kinase (JAK) 1 preferential inhibitor, in patients with moderately to severely active rheumatoid arthritis (RA) with inadequate response to methotrexate.
Plasma and serum samples were collected from patients enrolled in FINCH 1 (NCT02889796), a Phase 3 trial. Patients with stable backgrounds of methotrexate were randomly assigned once-daily oral filgotinib 200 or 100 mg, subcutaneous adalimumab 40 mg every 2 weeks (W), or placebo. Up to 35 biomarkers were analyzed at baseline, W4, and W12 with enzyme-linked immunosorbent assays and chemiluminescence and electrochemiluminescence assays.
At baseline, four distinct biomarker clusters were identified. The strongest intragroup correlations were in bone-cartilage resorption/inflammation and JAK/signal transducer and activator of transcription (STAT) signaling activity. At baseline, significant positive correlations were identified for cytokines with patient-reported pain and with patient measures of fatigue. Filgotinib reduced levels of cytokines associated with inflammation and cell migration as early as W4 and through W12. Compared to adalimumab, filgotinib induced significant reductions in bone-related turnover biomarkers, N-telopeptide of type 1 collagen and C-telopeptide 1, as well as biomarkers associated with baseline disease activity. No baseline predictors of therapeutic response to filgotinib were identified.
Filgotinib reduced peripheral protein biomarkers associated with JAK/STAT signaling, inflammatory signaling, immune cell migration, and bone resorption as soon as W4 in FINCH 1. Effects were dose-dependent and consistent with the clinical efficacy of filgotinib observed in FINCH 1. The changes in peripheral biomarkers associated with filgotinib treatment in methotrexate-experienced patients are consistent with changes observed in both methotrexate-naïve and biologic disease-modifying antirheumatic drug-experienced RA populations. These data demonstrate dose-dependent effects of preferential JAK1 inhibition by filgotinib on peripheral blood protein biomarkers in methotrexate-experienced patients with RA.
ClinicalTrials.gov, NCT02889796.
我们的目的是评估在对甲氨蝶呤反应不足的中度至重度活动性类风湿关节炎(RA)患者中,与给予托法替布(一种Janus激酶(JAK)1选择性抑制剂)相关的蛋白质生物标志物变化。
从一项3期试验FINCH 1(NCT02889796)的入组患者中采集血浆和血清样本。甲氨蝶呤背景稳定的患者被随机分配,每日口服200或100 mg托法替布,每2周皮下注射40 mg阿达木单抗,或服用安慰剂。在基线、第4周和第12周,使用酶联免疫吸附测定、化学发光和电化学发光测定法分析多达35种生物标志物。
在基线时,识别出四个不同的生物标志物簇。最强的组内相关性存在于骨-软骨吸收/炎症以及JAK/信号转导子和转录激活子(STAT)信号活性中。在基线时,细胞因子与患者报告的疼痛以及患者的疲劳指标之间存在显著正相关。托法替布早在第4周并持续至第12周降低了与炎症和细胞迁移相关的细胞因子水平。与阿达木单抗相比,托法替布显著降低了与骨相关的周转生物标志物、I型胶原N-端肽和C-端肽1,以及与基线疾病活动相关的生物标志物。未识别出托法替布治疗反应的基线预测指标。
在FINCH 1中,托法替布早在第4周就降低了与JAK/STAT信号、炎症信号、免疫细胞迁移和骨吸收相关的外周蛋白质生物标志物。效果呈剂量依赖性,且与在FINCH 1中观察到的托法替布临床疗效一致。在有甲氨蝶呤治疗经验的患者中,与托法替布治疗相关的外周生物标志物变化与在未使用过甲氨蝶呤和有生物改善病情抗风湿药治疗经验的RA人群中观察到的变化一致。这些数据证明了托法替布对JAK1的选择性抑制在有甲氨蝶呤治疗经验的RA患者外周血蛋白质生物标志物上的剂量依赖性作用。
ClinicalTrials.gov,NCT02889796。