An open-label study to evaluate biomarkers and safety in systemic sclerosis patients treated with paquinimod

Language
en
Document Type
Article
Issue Date
2021-11-19
Issue Year
2021
Authors
Hesselstrand, Roger
Distler, Jörg H. W.
Riemekasten, Gabriela
Wuttge, Dirk M.
Törngren, Marie
Nyhlén,, Helén C.
Andersson, Fredrik
Eriksson, Helena
Sparre, Birgitta
Tuvesson, Helén
Editor
Abstract

Objectives

To evaluate the changes in disease-related biomarkers and safety of paquinimod, an oral immunomodulatory compound, in patients with systemic sclerosis (SSc). Methods

In this open-label, single-arm, multicenter study, SSc patients with a rapidly progressive disease received paquinimod for 8 weeks. Blood and skin biopsies were collected at baseline, during treatment, and at follow-up for the analyses of type I interferon (IFN) activity, chemokine (C-C motif) ligand 2 (CCL2), and the number of myofibroblasts. The safety of paquinimod was evaluated throughout the study. Results

Nine SSc patients were enrolled and completed the study treatment with paquinimod at 3 mg/day for 8 weeks. After the treatment, a reduction of type I IFN activity in the plasma from one patient with elevated baseline IFN activity was recorded. A trend towards reduced IFN activity in the skin after treatment was also observed in patients. The serum level of CCL2 was reduced in 7 of 9 patients after paquinimod treatment. There was a median reduction of 10% of the number of myofibroblasts in skin biopsies at week 8 compared to baseline. No change in modified Rodnan skin score and quality of life was detected in the study. Reported adverse events (AEs) were mild to moderate and expected with the most common being arthralgia (n = 3) and headache (n = 3), and C-reactive protein (CRP) increase. Conclusions

Analysis of biomarkers before and after treatment suggest reduced type I IFN activity and reduced number of myofibroblasts in lesional skin. Paquinimod was overall well tolerated with mild to moderate and expected AEs.

Journal Title
Arthritis Research & Therapy
Volume
23
Citation
Arthritis Research & Therapy 23 (2021): 204. <https://arthritis-research.biomedcentral.com/articles/10.1186/s13075-021-02573-0>
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