P535 Effects of the Janus Kinase 1 (JAK1)-selective inhibitor filgotinib on circulating cytokines and whole-blood genes/pathways of patients with moderately to severely active Crohn’s disease (CD)

Abstract

Abstract Background A Phase 2 study of the JAK1-selective inhibitor filgotinib (FIL) dosed at 200 mg once daily for 10 weeks in moderately to severely active CD (FITZROY, ClinicalTrial.gov #NCT02048618) demonstrated significantly higher clinical remission rates compared with placebo,1 and early decrease in systemic and mucosal inflammation biomarkers that was more pronounced in endoscopic responders.2 We investigated baseline (BL) correlation of whole-blood transcriptome pathway activities with clinical disease indexes and circulating cytokines. The effect of FIL on changes in disease-related pathways in responders and nonresponders was also explored. Methods PAXgene blood samples were collected from 104 CD patients at BL and Week 10 (W10). RNA was sequenced (Illumina HiSeq 2500) after globin depletion (ThermoFisher GlobinClear). Differential gene expression analysis was performed using the limma R package,3 and Hallmark pathway4 activity scores were calculated using a single-sample Gene Set Enrichment Analysis (ssGSEA).5 All correlations were performed using the Spearman method. Results At BL, pathways with activity scores positively correlated with Simple Endoscopic Score for Crohn’s Disease (SES-CD) were immune (IL6/JAK/STAT3, inflammatory response), metabolic, and reactive oxygen species (ROS). These were also positively correlated with systemic inflammation (CRP, SAA, IL6, and OSM) and epithelial turnover (IL22, C4M2, and C3M) markers. Ten weeks of FIL treatment led to significant decreases in these pathways in endoscopic responders (50% reduction in SES-CD) (Figure), whereas there were no significant changes by placebo treatment. While interferon (IFN) response pathway scores showed a weak correlation (rho < 0.2) with SES-CD at BL, they are significantly reduced by FIL treatment, particularly in FIL responders. Conclusion In whole blood, inflammation, metabolic, and ROS pathways are reduced by FIL in endoscopic responders at W10, while a reduction in IFN response pathways was observed in all patients regardless of endoscopic response. References