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Predictive value of serum amyloid a levels for requirement of concomitant methotrexate in tocilizumab initiation: A post hoc analysis of the SURPRISE study.

Authors :
Kato M
Kaneko Y
Tanaka Y
Inoo M
Kobayashi-Haraoka H
Amano K
Miyata M
Murakawa Y
Yasuoka H
Hirata S
Nagasawa H
Tanaka E
Miyasaka N
Yamanaka H
Yamamoto K
Yokota I
Atsumi T
Takeuchi T
Source :
Modern rheumatology [Mod Rheumatol] 2020 May; Vol. 30 (3), pp. 442-449. Date of Electronic Publication: 2019 Jun 07.
Publication Year :
2020

Abstract

Objectives: To identify predictive factors for remission by tocilizumab monotherapy in rheumatoid arthritis (RA) patients. Methods: This is a post hoc analysis of the SURPRISE study, a 2-year randomized, controlled study comparing the efficacy of tocilizumab with (ADD-ON) and without methotrexate (SWITCH). The primary endpoint was DAS28-ESR remission (<2.6) at week 24. The change in modified total Sharp score from baseline to week 52 (ΔmTSS/year) was also assessed as an endpoint. The effect of clinical parameters at baseline on remission was estimated by logistic regression analysis. Results: In SWITCH ( n  = 96), CRP, SAA, RF, and DAS28 at baseline showed predictive value for DAS28 remission in unadjusted analysis. Adjusted analysis confirmed SAA and DAS28 as predictive factors, with SAA having the highest value (ROC-AUC = 0.731). Furthermore, structural remission (ΔmTSS/year ≤ 0.5) rate was significantly higher in patients with SAA of < 50.0 μg/mL than other patients. In contrast, in ADD-ON ( n  = 98), only DAS28 showed predictive value for DAS28 remission. In patients with SAA < 50.0 μg/mL, both DAS28 remission and structural remission rate were comparable between SWITCH and ADD-ON. Conclusion: RA patients with low SAA levels at baseline may benefit similarly from tocilizumab with and without methotrexate. Trial registration number: NCT01120366.

Details

Language :
English
ISSN :
1439-7609
Volume :
30
Issue :
3
Database :
MEDLINE
Journal :
Modern rheumatology
Publication Type :
Academic Journal
Accession number :
31106666
Full Text :
https://doi.org/10.1080/14397595.2019.1621026