TY - JOUR
T1 - Significance of measurement of serum trough level and anti-drug antibody of adalimumab as personalised pharmacokinetics in patients with Crohn's disease
T2 - a subanalysis of the DIAMOND trial
AU - DIAMOND study group
AU - Nakase, H.
AU - Motoya, S.
AU - Matsumoto, T.
AU - Watanabe, K.
AU - Hisamatsu, Tadakazu
AU - Yoshimura, N.
AU - Ishida, T.
AU - Kato, S.
AU - Nakagawa, T.
AU - Esaki, M.
AU - Nagahori, M.
AU - Matsui, T.
AU - Naito, Y.
AU - Kanai, T.
AU - Suzuki, Y.
AU - Nojima, M.
AU - Watanabe, M.
AU - Hibi, T.
AU - Andoh, Akira
AU - Ashida, Toshifumi
AU - Endo, Katsuya
AU - Endo, Yutaka
AU - Esaki, Motohiro
AU - Fujita, Hiroshi
AU - Fujiya, Mikihiro
AU - Haruma, Ken
AU - Hiraoka, Sakiko
AU - Hirata, Ichiro
AU - Honda, Yutaka
AU - Iijima, Hideki
AU - Iizuka, Bunei
AU - Ikeya, Kentaro
AU - Inoue, Takuya
AU - Inoue, Shuji
AU - Ishiguro, Yo
AU - Ishihara, Shunji
AU - Ito, Hiroaki
AU - Iwakiri, Ryuichi
AU - Kagaya, Takashi
AU - Kashida, Hiroshi
AU - Kato, Shingo
AU - Kato, Jun
AU - Katsurada, Takehiko
AU - Kinjyo, Fukunori
AU - Kobayashi, Kiyonori
AU - Kodama, Mayumi
AU - Kunisaki, Reiko
AU - Kurahara, Koichi
AU - Kurokami, Takafumi
AU - Kyouwon, Lee
N1 - Funding Information:
Declaration of personal interests: The authors have the following financial conflicts of interest regarding this manuscript. HN: Eisai Corporation (EC), Abbvie GK(AGK), Mitsubishi Tanabe Pharma (MTP), Astellas Pharma (AsP), Takeda Pharmaceutical Corporation (TPO), Kyorin Pharmaceutical Corporation(KPC). SM: EC, AGK, MTP, Jannsen Pharma. TM: EC, AGK, MTP. KW: EC, AGK, MTP. TH: EC, AGK, MTP, Ajinomoto Pharma (AP). NY: EC, AGK, MTP. SK: AGK. ME: EC, AGK, MTP. MN: EC, AGK, MTP. ToM: EC, AGK, MTP. YNa: AsP, Otsuka Pharmaceutical Corporation (OPC), TPO, EC, MTP. TK: EC, AGK, MTP. YS: EC, AGK, MTP, Zeria Pharmaceutical Corporation (ZPO). MW: EC, AGK, MTP, KPC, Diichi Sankyo Corporation, Ono Pharmaceutical Corporation, Gene Care Research Institute, AsP, Asahi Kasei Kuraray Corporation, Chugai Pharmaceutical Corporation, TPO, AP, OPC, Kyowa Hakko Kirin Corporation, JIMRO Corporation, ZPO, UCB Japan Corporation, Dainippon Sumitomo Pharma, Toray Industries, Bristol-Meyers KK. TH: EC, AGK, MTP.
Publisher Copyright:
© 2017 The Authors. Alimentary Pharmacology & Therapeutics published by John Wiley & Sons Ltd.
PY - 2017/11
Y1 - 2017/11
N2 - Background: Significance of monitoring adalimumab trough levels and anti-adalimumab antibodies (AAA) for disease outcome in Crohn's disease (CD) patients remained unclear. Aim: To evaluate the association of adalimumab trough levels and AAA at week 26 with clinical remission at week 52, the effect of azathiopurine on AAA and factors influencing trough levels in CD patients in the DIAMOND trial. Methods: We performed this study using adalimumab trough levels, AAA at week 26 and 6-thioguanine nucleotide (TGN) in red blood cells at week 12. A multiple regression model and receiver operating analysis was performed to identify factors influencing adalimumab trough levels and AAA, and adalimumab thresholds for predicting disease activity. Results: There was a significant difference of adalimumab trough level at week 26 between patients with disease remission and without at week 52 (7.7 ± 3.3 μg/mL vs 5.4 ± 4.3 μg/mL: P <.001). Adalimumab trough level of 5.0 μg/mL yielded optimal sensitivity and specificity for remission prediction (80.2% and 55.6%, respectively). AAA development at week 26 significantly affected remission at week 52 (P =.021), which was strongly associated with adalimumab trough levels. Female gender and increasing body weight were independently associated with low adalimumab trough levels, and female gender was associated with AAA development. A cut-off 6TGN level of >222.5 p mol/8 ×108 RBCs yielded sensitivity (100%) and specificity (60.6%) for AAA negativity. Conclusion: Adalimumab trough levels and AAA occurrence were significantly associated with clinical remission. Higher 6TGN affected AAA negativity. The combination therapy is beneficial in some relevant aspects for CD patients. (UMIN Registration No. 000005146).
AB - Background: Significance of monitoring adalimumab trough levels and anti-adalimumab antibodies (AAA) for disease outcome in Crohn's disease (CD) patients remained unclear. Aim: To evaluate the association of adalimumab trough levels and AAA at week 26 with clinical remission at week 52, the effect of azathiopurine on AAA and factors influencing trough levels in CD patients in the DIAMOND trial. Methods: We performed this study using adalimumab trough levels, AAA at week 26 and 6-thioguanine nucleotide (TGN) in red blood cells at week 12. A multiple regression model and receiver operating analysis was performed to identify factors influencing adalimumab trough levels and AAA, and adalimumab thresholds for predicting disease activity. Results: There was a significant difference of adalimumab trough level at week 26 between patients with disease remission and without at week 52 (7.7 ± 3.3 μg/mL vs 5.4 ± 4.3 μg/mL: P <.001). Adalimumab trough level of 5.0 μg/mL yielded optimal sensitivity and specificity for remission prediction (80.2% and 55.6%, respectively). AAA development at week 26 significantly affected remission at week 52 (P =.021), which was strongly associated with adalimumab trough levels. Female gender and increasing body weight were independently associated with low adalimumab trough levels, and female gender was associated with AAA development. A cut-off 6TGN level of >222.5 p mol/8 ×108 RBCs yielded sensitivity (100%) and specificity (60.6%) for AAA negativity. Conclusion: Adalimumab trough levels and AAA occurrence were significantly associated with clinical remission. Higher 6TGN affected AAA negativity. The combination therapy is beneficial in some relevant aspects for CD patients. (UMIN Registration No. 000005146).
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U2 - 10.1111/apt.14318
DO - 10.1111/apt.14318
M3 - Article
C2 - 28884856
AN - SCOPUS:85029001889
SN - 0269-2813
VL - 46
SP - 873
EP - 882
JO - Alimentary Pharmacology and Therapeutics
JF - Alimentary Pharmacology and Therapeutics
IS - 9
ER -