TY - JOUR
T1 - Clinical and Pharmacokinetic Factors Associated With Adalimumab-Induced Mucosal Healing in Patients With Crohn's Disease
AU - DIAMOND study group
AU - Watanabe, Kenji
AU - Matsumoto, Takayuki
AU - Hisamatsu, Tadakazu
AU - Nakase, Hiroshi
AU - Motoya, Satoshi
AU - Yoshimura, Naoki
AU - Ishida, Tetsuya
AU - Kato, Shingo
AU - Nakagawa, Tomoo
AU - Esaki, Motohiro
AU - Nagahori, Masakazu
AU - Matsui, Toshiyuki
AU - Naito, Yuji
AU - Kanai, Takanori
AU - Suzuki, Yasuo
AU - Nojima, Masanori
AU - Watanabe, Mamoru
AU - Hibi, Toshifumi
AU - Andoh, Akira
AU - Ashida, Toshifumi
AU - Endo, Katsuya
AU - Endo, Yutaka
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, Syuji
AU - Ishiguro, Yo
AU - Ishihara, Shyunji
AU - Ito, Hiroaki
AU - Iwakiri, Ryuichi
AU - Kagaya, Takashi
AU - Kashida, Hiroshi
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
AU - Matsuda, Koichiro
AU - Matsueda, Kazuhiro
N1 - Funding Information:
Funding This work was supported in part by Health and Labour Sciences Research Grants for research on intractable diseases from the Ministry of Health, Labour and Welfare of Japan.
Publisher Copyright:
© 2018 AGA Institute
PY - 2018/4/1
Y1 - 2018/4/1
N2 - Background & Aims: We previously reported results from a prospective randomized controlled trial comparing the efficacy of adalimumab monotherapy versus combination with azathioprine for patients with Crohn's disease (CD) who were naive to biologics and thiopurines. We performed a subanalysis of data from this study to evaluate factors associated with endoscopic response and mucosal healing in study participants. Methods: We compared simple endoscopic scores for CD between patients with moderate to severe active CD randomly assigned groups that received adalimumab monotherapy (n = 85) or adalimumab in combination with azathioprine (n = 91), from June 2011 to June 2014 in Japan. We evaluated associations of simple endoscopic scores for CD with clinical factors and trough levels of adalimumab. Ultimately, 135 patients at Week 26 and 139 patients at Week 52 from 44 referral sites were analyzed for the present investigation. Results: The odds for endoscopic response were significantly higher in the combination group than in the monotherapy group at Week 26 (odds ratio [OR], 2.12; 95% confidence interval [CI], 1.04–4.32) but not at Week 52 (OR, 1.50; 95% CI, 0.77–2.94). The odds of mucosal healing did not differ significantly between groups at Weeks 26 or 52. Simple endoscopic scores for CD at Week 0 was significantly associated with mucosal healing at Week 26 (OR, 0.80; 95% CI, 0.72–0.90) and at Week 52 (OR, 0.91; 95% CI, 0.84–0.99). Higher adalimumab trough level at Week 26 associated with mucosal healing at Week 52 (OR, 1.34; 95% CI, 1.14–1.58; P for trend =.001) and was significantly higher in patients with endoscopic response than in patients without endoscopic response at Weeks 26 and 52 (P <.001). Conclusions: In a post hoc analysis of data from a randomized controlled trial of patients with moderate to severe CD, we found that adalimumab in combination with azathioprine increased trough levels of adalimumab. Higher trough levels of adalimumab associated with endoscopic response and mucosal healing at Weeks 26 and 52. UMIN registration No: 000005146.
AB - Background & Aims: We previously reported results from a prospective randomized controlled trial comparing the efficacy of adalimumab monotherapy versus combination with azathioprine for patients with Crohn's disease (CD) who were naive to biologics and thiopurines. We performed a subanalysis of data from this study to evaluate factors associated with endoscopic response and mucosal healing in study participants. Methods: We compared simple endoscopic scores for CD between patients with moderate to severe active CD randomly assigned groups that received adalimumab monotherapy (n = 85) or adalimumab in combination with azathioprine (n = 91), from June 2011 to June 2014 in Japan. We evaluated associations of simple endoscopic scores for CD with clinical factors and trough levels of adalimumab. Ultimately, 135 patients at Week 26 and 139 patients at Week 52 from 44 referral sites were analyzed for the present investigation. Results: The odds for endoscopic response were significantly higher in the combination group than in the monotherapy group at Week 26 (odds ratio [OR], 2.12; 95% confidence interval [CI], 1.04–4.32) but not at Week 52 (OR, 1.50; 95% CI, 0.77–2.94). The odds of mucosal healing did not differ significantly between groups at Weeks 26 or 52. Simple endoscopic scores for CD at Week 0 was significantly associated with mucosal healing at Week 26 (OR, 0.80; 95% CI, 0.72–0.90) and at Week 52 (OR, 0.91; 95% CI, 0.84–0.99). Higher adalimumab trough level at Week 26 associated with mucosal healing at Week 52 (OR, 1.34; 95% CI, 1.14–1.58; P for trend =.001) and was significantly higher in patients with endoscopic response than in patients without endoscopic response at Weeks 26 and 52 (P <.001). Conclusions: In a post hoc analysis of data from a randomized controlled trial of patients with moderate to severe CD, we found that adalimumab in combination with azathioprine increased trough levels of adalimumab. Higher trough levels of adalimumab associated with endoscopic response and mucosal healing at Weeks 26 and 52. UMIN registration No: 000005146.
KW - Crohn's Disease Activity Index
KW - DIAMOND Trial
KW - Ileocolonoscopy
KW - Narrowing
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U2 - 10.1016/j.cgh.2017.10.036
DO - 10.1016/j.cgh.2017.10.036
M3 - Article
C2 - 29104132
AN - SCOPUS:85043997414
SN - 1542-3565
VL - 16
SP - 542-549.e1
JO - Clinical Gastroenterology and Hepatology
JF - Clinical Gastroenterology and Hepatology
IS - 4
ER -