Factors predicting the therapeutic response to infliximab during maintenance therapy in Japanese patients with Crohn's disease
- PMID: 30286108
- PMCID: PMC6171861
- DOI: 10.1371/journal.pone.0204632
Factors predicting the therapeutic response to infliximab during maintenance therapy in Japanese patients with Crohn's disease
Abstract
Since anti-tumor necrosis factor (TNF)-α agents (TNF-α inhibitors) induce both clinical response and remission in patients with moderate to severe inflammatory bowel disease (IBD), the use of anti-TNF therapies has fundamentally changed the approach to treatment for patients with IBD. Infliximab (IFX) is a TNF-α inhibitor approved for the induction and remission of Crohn's disease (CD). However, even among patients who initially demonstrate a clinical response to IFX therapy, secondary loss of response occurs, although the reason remains unknown. We therefore investigated predictive factors associated with the response to IFX in long-term maintenance treatment in Japanese CD patients. Eight types of single-nucleotide polymorphisms (SNPs) were investigated using the real-time PCR method, and patient characteristics were collected from the electronic medical records. The Crohn's Disease Activity Index criteria were used as the response to IFX therapy. The observation period was 1 year after IFX had been administered for more than 1 year. Associations between the IFX response and patient characteristics were evaluated using the multivariate logistic regression model. We studied 121 unrelated adult Japanese with CD treated for more than 1 year with IFX as outpatients at Keio University Hospital from November 1, 2014 to November 30, 2015. Among them, 71 were classified as in remisson. In multivariate analysis, patients with the TNF-α 857C>T C/C genotype, shorter disease duration, without double dosing, and combination treatment with an immunomodulator had higher remisson rates than those with the C/T or T/T genotype, longer disease duration, with double dosing, and no combination treatment with an immunomodulator. The response to IFX in Japanese CD patients may therefore be predicted by these 4 characteristics in actual clinical practice.
Conflict of interest statement
None: Shunsuke Hamada, Mikiko Shimizu, Shinta Mizuno, Hirotaka Kiyohara, Mari Arai, Shinya Sugimoto, Yasushi Iwao, Mayumi Mochizuki, Masayuki Hashiguchi. Katsuyoshi Matsuoka: Consulting; EA Pharma Co., Ltd., Research grants; Eisai Co., Ltd., Abbvie, Speaking fees; Mitsubishi-Tanabe Pharma, AbbVie GK, Kyorin Pharmaceutical Co., Ltd., Pfizer Japan Inc., ZERIA Pharmaceutical Co., Ltd., Astellas Pharma Inc., Mochida Pharmaceutical Co., Ltd., EA Pharma Co., Ltd., Takeda Pharmaceutical Co., Ltd., JIMRO Co., Ltd., Janssen Pharmaceutical K.K., Kyowa Hakko Kirin Pharmaceutical Co., Ltd. Kosaku Nanki: Research grant; Miyarisan pharmaceutical Co. Ltd. Haruhiko Ogata: Consulting: AbbVie GK, Mochida Pharmaceutical Co., Ltd., Takeda Pharmaceutical Co., Ltd., Research grants: Pfizer Japan Inc., ZERIA Pharmaceutical Co., Ltd., Astellas Pharma Inc., AstraZeneca K.K., Otsuka Pharmaceutical Co., Ltd., Eisai Co., Ltd., Mitsubishi Tanabe Pharma, Kyorin Pharmaceutical Co., Ltd., JIMRO Co., Ltd., Mochida Pharmaceutical Co., Ltd., Ajinomoto Pharmaceutical Co., Ltd., Takeda Pharmaceutical Co., Ltd., EA Pharma Co., Ltd. Tadakazu Hisamatsu: Research grants; Mitsubishi Tanabe Pharma, EA pharma Co., Ltd., AbbVie GK, JIMRO Co., Ltd., Asahi Kasei Kuraray Medical Co., Ltd., Zeria Pharmaceutical Co., Ltd., Daiichi-Sankyo, Kyorin Pharmaceutical Co., Ltd., Nippon Kayaku Co., Ltd., Astellas Pharma Inc., Takeda Pharmaceutical Co., Ltd., Pfizer Japan Inc., Mochida Pharmaceutical Co., Ltd., Consulting; EA pharma Co., Ltd., AbbVie GK, Celgene K.K., Janssen Pharmaceutical K.K., Pfizer Inc., Nichi-Iko Pharmaceutical Co., Ltd. Pfizer Inc., Lecture fee: Mitsubishi Tanabe Pharma Corporation, AbbVie GK, EA pharma Co. Ltd., Kyorin Pharmaceutical Co. Ltd., JIMRO Co. Ltd. Makoto Naganuma: Consulting; EA Pharma Co., Ltd., Research grants: EA Pharma Co., Ltd., Zeria Pharmaceutical Co., Ltd., Speaking fees; Mitsubishi Tanabe Pharma Co. Ltd., Kyorin Pharmaceutical Co. Ltd., JIMRO Co., Ltd., Astellas Pharma Inc., Mochida Pharmaceutical Co., Ltd. Takanori Kanai: Board membership; EA Pharma Co., Ltd, Takeda Pharmaceutical Co., Ltd., Research grants; Eisai Co., Ltd., Biofermin Pharmaceutical Co., Ltd., JIMRO Co., Ltd., Nippon Kayaku Co., Ltd., Otsuka Pharmaceutical Co., Ltd., Kyowa Hakko Kirin Co., Ltd., Asahi Kasei Medical Co., Ltd., Mitsubishi Tanabe Pharma, AbbVie GK, Kyorin Pharmaceutical Co., Ltd., Pfizer Japan Inc., ZERIA Pharmaceutical Co., Ltd., Miyarisan Pharmaceutical Co., Ltd., Astellas Pharma Inc., Mochida Pharmaceutical Co., Ltd., EA Pharma Co., Ltd., Takeda Pharmaceutical Co., Ltd., Speaking fees; Mitsubishi Tanabe Pharma, AbbVie GK, Kyorin Pharmaceutical Co., Ltd., Pfizer Japan Inc., ZERIA Pharmaceutical Co., Ltd., Miyarisan Pharmaceutical Co., Ltd., Astellas Pharma Inc., Mochida Pharmaceutical Co., Ltd., EA Pharma Co., Ltd., Takeda Pharmaceutical Co. Ltd. This does not alter our adherence to PLOS ONE policies on sharing data and materials.
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