TY - JOUR
T1 - Leucine-Rich Alpha-2 Glycoprotein May Be Predictive of the Adalimumab Trough Level and Antidrug Antibody Development for Patients with Inflammatory Bowel Disease
T2 - A Sub-Analysis of the PLANET Study
AU - Yanai, Shunichi
AU - Shinzaki, Shinichiro
AU - Matsuoka, Katsuyoshi
AU - Mizuno, Shinta
AU - Iijima, Hideki
AU - Naka, Tetsuji
AU - Kanai, Takanori
AU - Matsumoto, Takayuki
N1 - Funding Information:
This work was supported by Eisai Co., Ltd. Eisai Co., Ltd was involved in the study design but not in data acquisition or analysis.
Publisher Copyright:
© 2021 The Author(s) Published by S. Karger AG, Basel.
PY - 2021/11/1
Y1 - 2021/11/1
N2 - Introduction: The aim of this study was to examine whether biomarkers are predictive of the adalimumab (ADA) trough level and antidrug antibody development in patients with Crohn's disease (CD) and ulcerative colitis (UC). Methods: Using data obtained in a prospective, multicenter, observational study (PLANET), we assessed serial changes in a novel biomarker-leucine-rich alpha-2 glycoprotein (LRG)-during ADA treatment for patients with active CD and UC. We measured serum LRG, C-reactive protein (CRP), and fecal calprotectin (fCAL) at weeks 0, 12, 24, and 52. The ADA trough level and anti-ADA antibody (AAA) were also measured at weeks 12 and 52. Correlations between the ADA trough level, AAA, and biomarkers were examined. Results: In all, 34 patients with CD and 47 patients with UC were enrolled. The ADA trough level at week 12 or at the time of ADA withdrawal was 8.5 ± 3.9 in the AAA-negative group (n = 70) and 2.9 ± 2.7 μg/mL in the AAA-positive group (n = 8) (p < 0.0001). The ADA trough level at week 12 or at the time of ADA withdrawal was associated with pretreatment LRG (p = 0.0437 and r =-0.23). Conclusion: LRG, rather than CRP or fCAL, may be a marker for predicting the trough level of ADA for patients with CD and UC treated with ADA.
AB - Introduction: The aim of this study was to examine whether biomarkers are predictive of the adalimumab (ADA) trough level and antidrug antibody development in patients with Crohn's disease (CD) and ulcerative colitis (UC). Methods: Using data obtained in a prospective, multicenter, observational study (PLANET), we assessed serial changes in a novel biomarker-leucine-rich alpha-2 glycoprotein (LRG)-during ADA treatment for patients with active CD and UC. We measured serum LRG, C-reactive protein (CRP), and fecal calprotectin (fCAL) at weeks 0, 12, 24, and 52. The ADA trough level and anti-ADA antibody (AAA) were also measured at weeks 12 and 52. Correlations between the ADA trough level, AAA, and biomarkers were examined. Results: In all, 34 patients with CD and 47 patients with UC were enrolled. The ADA trough level at week 12 or at the time of ADA withdrawal was 8.5 ± 3.9 in the AAA-negative group (n = 70) and 2.9 ± 2.7 μg/mL in the AAA-positive group (n = 8) (p < 0.0001). The ADA trough level at week 12 or at the time of ADA withdrawal was associated with pretreatment LRG (p = 0.0437 and r =-0.23). Conclusion: LRG, rather than CRP or fCAL, may be a marker for predicting the trough level of ADA for patients with CD and UC treated with ADA.
KW - Adalimumab
KW - Antidrug antibodies
KW - Crohn's disease
KW - Leucine-rich alpha-2 glycoprotein
KW - Ulcerative colitis
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U2 - 10.1159/000517339
DO - 10.1159/000517339
M3 - Article
C2 - 34350873
AN - SCOPUS:85111692220
SN - 0012-2823
VL - 102
SP - 929
EP - 937
JO - Digestion
JF - Digestion
IS - 6
ER -