TY - JOUR
T1 - Early Prognostic Factors Associated with the Efficacy of Infliximab Treatment for Patients with Rheumatoid Arthritis with Inadequate Response to Methotrexate
AU - Hayashi, Satoko
AU - Suzuki, Katsuya
AU - Yoshimoto, Keiko
AU - Takeshita, Masaru
AU - Kurasawa, Takahiko
AU - Yamaoka, Kunihiro
AU - Takeuchi, Tsutomu
N1 - Funding Information:
This study was funded by Eisai Co., Ltd. and by internal research grants from Keio University. The authors thank the patients and staff involved in this study. The authors also thank Dr. Guy Harris (DMC Corp.) for editing of the manuscript. Support for this assistance was funded by Eisai Co., Ltd. All named authors meet the International Committee of Medical Journal Editors (ICMJE) criteria for authorship for this manuscript, take responsibility for the integrity of the work as a whole, and have given final approval for the version to be published.
Funding Information:
This study was funded by Eisai Co., Ltd. and by internal research grants from Keio University. The authors thank the patients and staff involved in this study. The authors also thank Dr. Guy Harris (DMC Corp.) for editing of the manuscript. Support for this assistance was funded by Eisai Co., Ltd. All named authors meet the International Committee of Medical Journal Editors (ICMJE) criteria for authorship for this manuscript, take responsibility for the integrity of the work as a whole, and have given final approval for the version to be published. KS has received research grants from Eisai Co., Ltd. and Bristol-Myers Squibb. TT has received grants from Astellas Pharma; Bristol-Myers K.K.; Chugai Pharmaceutical Co., Ltd.; Daiichi Sankyo Co., Ltd.; Eisai Co., Ltd.; Mitsubishi Tanabe Pharma Co.; Pfizer Japan Inc.; Santen Pharmaceutical Co., Ltd.; Takeda Pharmaceutical Co., Ltd.; Teijin Pharma Ltd.; AbbVie G.K.; Asahikasei Pharma Corp.; Taisho Toyama Pharmaceutical Co., Ltd.; and SymBio Pharmaceuticals Ltd.; speaking fees from AbbVie G.K., Bristol-Myers K.K.; Chugai Pharmaceutical Co,. Ltd.; Eisai Co., Ltd.; Janssen Pharmaceutical K.K.; Mitsubishi Tanabe Pharma Co.; Pfizer Japan Inc.; Takeda Pharmaceutical Co., Ltd.; Astellas Pharma; Diaichi Sankyo Co., Ltd.; Celtrion; and Nipponkayaku Co., Ltd.; and consultant fees from Astra Zeneca K.K., Eli Lilly Japan K.K., Novartis Pharma K.K., Mitsubishi Tanabe Pharma Co.; Asahi Kasei Medical K.K.; AbbVie G.K.; Daiichi Sankyo Co., Ltd.; Bristol–Myers K.K.; and Nipponkayaku Co., Ltd. Observational and investigational study protocols were approved by the ethics committee of Keio University School of Medicine, Tokyo, Japan, and followed the Declaration of Helsinki and Good Clinical Practice guidelines. Written informed consent was obtained from all patients before investigation. This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/ ), which permits any noncommercial use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
Publisher Copyright:
© 2015, The Author(s).
PY - 2016/6
Y1 - 2016/6
N2 - Introduction: Early prognostic factors for the clinical response in patients with rheumatoid arthritis (RA) after 1 year of treatment with infliximab (IFX) as part of routine clinical practice were investigated. Methods: Thirty-five patients with RA with an inadequate response to methotrexate were enrolled and administered IFX (3–9 mg/kg, every 4–8 weeks). Serum trough levels of IFX and levels of 9 cytokines were measured at baseline and at 3, 6 months, and 1 year. Associations between these parameters and clinical indicators were statistically analyzed. Results: Serum trough levels of IFX and serum levels of interleukin (IL)-6 in the early phase of IFX treatment were investigated. Patients with low serum IL-6 achieved a higher clinical response as evaluated by the European League Against Rheumatism response criteria. Notably, the serum levels of IL-6 and IL-10 at baseline exhibited a significant positive correlation with disease activity at 1 year. Low serum levels of IL-6 and IL-10 at baseline were associated with low Disease Activity Score 28 erythrocyte sedimentation rate (DAS28-ESR). Cut-off values of IL-6 (5.45 pg/mL) and IL-10 and (1.68 pg/mL) enabled discrimination of DAS28-ESR remission from non-remission with high sensitivity and moderate specificity. Conclusion: Following the initiation of IFX treatment, early disease activity and remission were associated with serum levels of IL-6. Serum levels of IL-6 and IL-10 at baseline predict the efficacy after 1 year of treatment with IFX. Patients with high serum levels of IL-6 and IL-10 at baseline before IFX treatment might require more intensive therapy to achieve higher rates of clinical remission at 1 year. Funding: Eisai Co., Ltd.
AB - Introduction: Early prognostic factors for the clinical response in patients with rheumatoid arthritis (RA) after 1 year of treatment with infliximab (IFX) as part of routine clinical practice were investigated. Methods: Thirty-five patients with RA with an inadequate response to methotrexate were enrolled and administered IFX (3–9 mg/kg, every 4–8 weeks). Serum trough levels of IFX and levels of 9 cytokines were measured at baseline and at 3, 6 months, and 1 year. Associations between these parameters and clinical indicators were statistically analyzed. Results: Serum trough levels of IFX and serum levels of interleukin (IL)-6 in the early phase of IFX treatment were investigated. Patients with low serum IL-6 achieved a higher clinical response as evaluated by the European League Against Rheumatism response criteria. Notably, the serum levels of IL-6 and IL-10 at baseline exhibited a significant positive correlation with disease activity at 1 year. Low serum levels of IL-6 and IL-10 at baseline were associated with low Disease Activity Score 28 erythrocyte sedimentation rate (DAS28-ESR). Cut-off values of IL-6 (5.45 pg/mL) and IL-10 and (1.68 pg/mL) enabled discrimination of DAS28-ESR remission from non-remission with high sensitivity and moderate specificity. Conclusion: Following the initiation of IFX treatment, early disease activity and remission were associated with serum levels of IL-6. Serum levels of IL-6 and IL-10 at baseline predict the efficacy after 1 year of treatment with IFX. Patients with high serum levels of IL-6 and IL-10 at baseline before IFX treatment might require more intensive therapy to achieve higher rates of clinical remission at 1 year. Funding: Eisai Co., Ltd.
KW - Clinical efficacy
KW - Infliximab
KW - Interleukin-6
KW - Prognostic serum marker
KW - Rheumatoid arthritis
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U2 - 10.1007/s40744-015-0022-y
DO - 10.1007/s40744-015-0022-y
M3 - Article
AN - SCOPUS:84992208916
SN - 2198-6576
VL - 3
SP - 155
EP - 166
JO - Rheumatology and Therapy
JF - Rheumatology and Therapy
IS - 1
ER -