TY - JOUR
T1 - Long-term safety and effectiveness of adalimumab in Japanese patients with Crohn’s disease
T2 - 3-year results from a real-world study
AU - Hisamatsu, Tadakazu
AU - Suzuki, Yasuo
AU - Kobayashi, Mariko
AU - Hagiwara, Takashi
AU - Kawaberi, Takeshi
AU - Ogata, Haruhiko
AU - Matsui, Toshiyuki
AU - Watanabe, Mamoru
AU - Hibi, Toshifumi
N1 - Funding Information:
The standard operation procedure manual for data management and transformation was developed by A2 Healthcare Corporation (Tokyo, Japan) and approved by the Postmarket-ing Surveillance group at AbbVie GK (Tokyo, Japan). This support was funded by the sponsors (AbbVie GK and Eisai Co., Ltd.). AbbVie GK participated in the study design; data collection; analysis and interpretation of data; and writing, reviewing, and approval of the publication. Medical writing support was provided by Avinash Thakur (Mumbai, India) and Nicola West (London, UK) of Cactus Life Sciences (a part of Cactus Communications) and funded by the sponsors. The authors would like to thank Kazuo Morita and Kaori Hozumi, employees of AbbVie, for assistance.
Publisher Copyright:
© 2021. All Rights Reserved.
PY - 2021
Y1 - 2021
N2 - Background/Aims: Crohn’s disease is a chronic disorder; therefore, it is essential to investigate long-term safety and efficacy of treatments. This study assessed the safety and effectiveness of adalimumab for up to 3 years in Japanese patients with Crohn’s disease in real-world settings. Methods: This was a multicenter, single-cohort, observational study of patients with Crohn’s disease. Safety assessments included incidence of adverse drug reactions. Effectiveness assessments included clinical remission, mucosal healing, and Work Productivity and Activity Impairment (WPAI). Results: The safety and effectiveness analysis populations comprised 389 and 310 patients, respectively. Mean (standard deviation) exposure to adalimumab in the safety analysis population was 793.4 (402.8) days, with a 58.1% retention rate. A total of 105 patients (27.0%) and 43 patients (11.1%) experienced adverse drug reactions and serious adverse drug reactions, respectively, with no patient reporting tuberculosis or hepatitis B. Infections and serious infections were reported in 37 patients (9.5%) and 17 patients (4.4%), respectively. Malignancy was reported as an adverse drug reaction in 2 patients (0.5%). Remission rate increased from 37.8% (98/259) at baseline to 73.9% (167/226) at week 4 and remained >70% over 3 years. Proportion of patients without mucosal ulcerations increased from 2.7% (2/73) at baseline to 42.3% (11/26) between years >2 to ≤3. WPAI improvement started at 4 weeks, with the overall work impairment score improving from 42.7 (n=102) at baseline to 26.9 (n = 84) at 4 weeks. Conclusions: Results from this study confirm the long-term safety and effectiveness of adalimumab treatment in Japanese patients with Crohn’s disease in the real-world setting.
AB - Background/Aims: Crohn’s disease is a chronic disorder; therefore, it is essential to investigate long-term safety and efficacy of treatments. This study assessed the safety and effectiveness of adalimumab for up to 3 years in Japanese patients with Crohn’s disease in real-world settings. Methods: This was a multicenter, single-cohort, observational study of patients with Crohn’s disease. Safety assessments included incidence of adverse drug reactions. Effectiveness assessments included clinical remission, mucosal healing, and Work Productivity and Activity Impairment (WPAI). Results: The safety and effectiveness analysis populations comprised 389 and 310 patients, respectively. Mean (standard deviation) exposure to adalimumab in the safety analysis population was 793.4 (402.8) days, with a 58.1% retention rate. A total of 105 patients (27.0%) and 43 patients (11.1%) experienced adverse drug reactions and serious adverse drug reactions, respectively, with no patient reporting tuberculosis or hepatitis B. Infections and serious infections were reported in 37 patients (9.5%) and 17 patients (4.4%), respectively. Malignancy was reported as an adverse drug reaction in 2 patients (0.5%). Remission rate increased from 37.8% (98/259) at baseline to 73.9% (167/226) at week 4 and remained >70% over 3 years. Proportion of patients without mucosal ulcerations increased from 2.7% (2/73) at baseline to 42.3% (11/26) between years >2 to ≤3. WPAI improvement started at 4 weeks, with the overall work impairment score improving from 42.7 (n=102) at baseline to 26.9 (n = 84) at 4 weeks. Conclusions: Results from this study confirm the long-term safety and effectiveness of adalimumab treatment in Japanese patients with Crohn’s disease in the real-world setting.
KW - Adalimumab
KW - Crohn disease
KW - Inflammatory bowel diseases
KW - Japanese
KW - Postmarketing surveillance
UR - http://www.scopus.com/inward/record.url?scp=85115207597&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85115207597&partnerID=8YFLogxK
U2 - 10.5217/ir.2020.00025
DO - 10.5217/ir.2020.00025
M3 - Article
AN - SCOPUS:85115207597
SN - 1598-9100
VL - 19
SP - 408
EP - 418
JO - Intestinal Research
JF - Intestinal Research
IS - 4
ER -