TY - JOUR
T1 - High titers of both rheumatoid factor and anti-CCP antibodies at baseline in patients with rheumatoid arthritis are associated with increased circulating baseline TNF level, low drug levels, and reduced clinical responses
T2 - A post hoc analysis of the RISING study
AU - Takeuchi, Tsutomu
AU - Miyasaka, Nobuyuki
AU - Inui, Takashi
AU - Yano, Toshiro
AU - Yoshinari, Toru
AU - Abe, Tohru
AU - Koike, Takao
N1 - Funding Information:
TT has received grant support, consultant’s fees, and/or lecture fees from AbbVie GK, Asahi Kasei Medical, Asahi Kasei Pharma, Astellas Pharma, AstraZeneca K.K., AYUMI Pharmaceutical, Bristol-Myers K.K., Celltrion, Chugai Pharmaceutical, Daiichi Sankyo, Eisai, Eli Lilly Japan, Janssen Pharmaceutical K.K., Merck Serono, Mitsubishi Tanabe Pharma, Nippon Kayaku, Nippon Shinyaku, Novartis Pharma K.K., Pfizer Japan, Taisho Toyama Pharmaceutical, Takeda Pharmaceutical, and Teijin Pharma. TI, TYano, and TYoshinari are employees of Mitsubishi Tanabe Pharma. TK has received consultant’s fees and/or lecture fees from AbbVie GK, Astellas Pharma, Bristol-Myers K.K., Chugai Pharmaceutical, Daiichi Sankyo, Eisai, Eli Lilly Japan, Mitsubishi Tanabe Pharma, Pfizer Japan, Santen Pharmaceutical, Taisho Toyama Pharmaceutical, Teijin Pharma, and UCB Japan. NM and TA declare that they have no competing interests.
Publisher Copyright:
© 2017 The Author(s).
PY - 2017/9/2
Y1 - 2017/9/2
N2 - Background: Although both rheumatoid factor (RF) and anticyclic citrullinated peptide antibodies (anti-CCP) are useful for diagnosing rheumatoid arthritis (RA), the impact of these autoantibodies on the efficacy of tumor necrosis factor (TNF) inhibitors has been controversial. The aim of this post hoc analysis of a randomized double-blind study (the RISING study) was to investigate the influences of RF and anti-CCP on the clinical response to infliximab in patients with RA. Methods: Methotrexate-refractory patients with RA received 3 mg/kg of infliximab from weeks 0 to 6 and then 3, 6, or 10 mg/kg every 8 weeks from weeks 14 to 46. In this post hoc analysis, patients were stratified into three classes on the basis of baseline RF/anti-CCP titers: "low/low-C" (RF < 55 IU/ml, anti-CCP < 42 U/ml), "high/high-C" (RF ≥ 160 IU/ml, anti-CCP ≥ 100 U/ml), and "middle-C" (neither low/low-C nor high/high-C). Baseline plasma TNF level, serum infliximab level, and disease activity were compared between the three classes. Results: Baseline RF and anti-CCP titers showed significant correlations with baseline TNF and infliximab levels in weeks 2-14. Comparison of the three classes showed that baseline TNF level was lowest in the low/low-C group and highest in the high/high-C group (median 0.73 versus 1.15 pg/ml), that infliximab levels at week 14 were highest in the low/low-C group and lowest in the high/high-C group (median 1.0 versus 0.1 μg/ml), and that Disease Activity Score in 28 joints based on C-reactive protein at week 14 was lowest in the low/low-C group and highest in the high/high-C group (median 3.17 versus 3.82). A similar correlation was observed at week 54 in the 3 mg/kg dosing group, but not in the 6 or 10 mg/kg group. Significant decreases in both RF and anti-CCP were observed during infliximab treatment. Conclusions: RF/anti-CCP titers correlated with TNF level. This might explain the association of RF/anti-CCP with infliximab level and clinical response in patients with RA. Baseline RF/anti-CCP titers may serve as indices that aid infliximab treatment. Trial registration: ClinicalTrials.gov, NCT00691028. Retrospectively registered on 3 June 2008.
AB - Background: Although both rheumatoid factor (RF) and anticyclic citrullinated peptide antibodies (anti-CCP) are useful for diagnosing rheumatoid arthritis (RA), the impact of these autoantibodies on the efficacy of tumor necrosis factor (TNF) inhibitors has been controversial. The aim of this post hoc analysis of a randomized double-blind study (the RISING study) was to investigate the influences of RF and anti-CCP on the clinical response to infliximab in patients with RA. Methods: Methotrexate-refractory patients with RA received 3 mg/kg of infliximab from weeks 0 to 6 and then 3, 6, or 10 mg/kg every 8 weeks from weeks 14 to 46. In this post hoc analysis, patients were stratified into three classes on the basis of baseline RF/anti-CCP titers: "low/low-C" (RF < 55 IU/ml, anti-CCP < 42 U/ml), "high/high-C" (RF ≥ 160 IU/ml, anti-CCP ≥ 100 U/ml), and "middle-C" (neither low/low-C nor high/high-C). Baseline plasma TNF level, serum infliximab level, and disease activity were compared between the three classes. Results: Baseline RF and anti-CCP titers showed significant correlations with baseline TNF and infliximab levels in weeks 2-14. Comparison of the three classes showed that baseline TNF level was lowest in the low/low-C group and highest in the high/high-C group (median 0.73 versus 1.15 pg/ml), that infliximab levels at week 14 were highest in the low/low-C group and lowest in the high/high-C group (median 1.0 versus 0.1 μg/ml), and that Disease Activity Score in 28 joints based on C-reactive protein at week 14 was lowest in the low/low-C group and highest in the high/high-C group (median 3.17 versus 3.82). A similar correlation was observed at week 54 in the 3 mg/kg dosing group, but not in the 6 or 10 mg/kg group. Significant decreases in both RF and anti-CCP were observed during infliximab treatment. Conclusions: RF/anti-CCP titers correlated with TNF level. This might explain the association of RF/anti-CCP with infliximab level and clinical response in patients with RA. Baseline RF/anti-CCP titers may serve as indices that aid infliximab treatment. Trial registration: ClinicalTrials.gov, NCT00691028. Retrospectively registered on 3 June 2008.
KW - Anticyclic citrullinated peptide antibodies
KW - Clinical response
KW - Infliximab
KW - Pharmacokinetics
KW - Prediction
KW - Rheumatoid arthritis
KW - Rheumatoid factor
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U2 - 10.1186/s13075-017-1401-2
DO - 10.1186/s13075-017-1401-2
M3 - Article
C2 - 28865493
AN - SCOPUS:85028630920
SN - 1478-6354
VL - 19
JO - Arthritis Research and Therapy
JF - Arthritis Research and Therapy
IS - 1
M1 - 194
ER -