Post hoc analysis of clinical characteristics of patients with radiographic progression in a Japanese phase 3 trial of peficitinib and methotrexate treatment (RAJ4)

Author:

Tanaka Yoshiya1ORCID,Takeuchi Tsutomu2,Kato Daisuke3,Kaneko Yuichiro4,Fukuda Musashi5,Izutsu Hiroyuki6,Rokuda Mitsuhiro7ORCID,van der Heijde Désirée8

Affiliation:

1. The First Department of Internal Medicine, University of Occupational and Environmental Health , Japan, Kitakyushu, Japan

2. Division of Rheumatology, Department of Internal Medicine, Keio University School of Medicine , Tokyo, Japan

3. Corporate Strategy Department , Astellas Pharma Inc., Tokyo, Japan

4. Biostatistics Group , Japan-Asia Data Science, Development, Astellas Pharma Inc., Tokyo, Japan

5. Astellas Pharma Inc. , Tokyo, Japan

6. Japan-Asia Clinical Development 1 , Development, Astellas Pharma Inc., Tokyo, Japan

7. Medical Science, Medical Affairs Japan , Astellas Pharma Inc., Tokyo, Japan

8. Department of Rheumatology, Leiden University Medical Center , Leiden, The Netherlands

Abstract

ABSTRACT Objective To determine the efficacy of peficitinib in reducing joint damage and predictive factors affecting treatment response in Japanese patients with rheumatoid arthritis. Methods This post hoc analysis used data from a placebo-controlled, phase 3 trial (RAJ4) of peficitinib in patients with rheumatoid arthritis and inadequate response to methotrexate. Erosion and joint space narrowing (JSN) were assessed at baseline and at Week 28/early termination of treatment using the van der Heijde-modified Sharp method. A univariate logistic regression analysis of change from baseline in a modified total Sharp score identified predictive factors with significant treatment interaction; the effects of these factors on treatment response were further evaluated using a multivariate model. Results The analyses included 481 patients. For most joint groups, peficitinib demonstrated a reduced change from baseline at Week 28/early termination in erosion and JSN scores versus placebo; a numerically greater effect was observed with peficitinib 150 mg versus 100 mg. Baseline C-reactive protein (CRP) and prednisolone dose were identified as clinically significant negative predictive factors: the treatment effect decreased as CRP or prednisolone dose increased for both peficitinib doses. Conclusions Peficitinib 100 mg and 150 mg reduced joint damage versus placebo, across almost all joint groups. Higher baseline CRP and/or prednisolone dose were associated with reduced peficitinib efficacy. ClinicalTrials.gov identifier NCT02305849

Publisher

Oxford University Press (OUP)

Subject

Rheumatology

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