Real-World Safety and Efficacy of Biosimilar CT-P13 in Patients with Immune-Mediated Inflammatory Diseases: Integrated Analysis of Three Japanese Prospective Observational Studies
Tsutomu Takeuchi,
Kiyohiro Nishikawa (),
Fumika Yamada,
Akimichi Morita,
Mamitaro Ohtsuki,
Yasuo Suzuki,
Mamoru Watanabe,
Hisashi Yamanaka and
Toshifumi Hibi
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Tsutomu Takeuchi: Keio University School of Medicine
Kiyohiro Nishikawa: Nippon Kayaku Co., Ltd.
Fumika Yamada: Nippon Kayaku Co., Ltd.
Akimichi Morita: Nagoya City University Graduate School of Medical Sciences
Mamitaro Ohtsuki: Jichi Medical University
Yasuo Suzuki: Ginza Central Clinic
Mamoru Watanabe: Tokyo Medical and Dental University
Hisashi Yamanaka: Sanno Medical Center
Toshifumi Hibi: Kitasato University Kitasato Institute Hospital
Drug Safety, 2023, vol. 46, issue 10, No 6, 1005 pages
Abstract:
Abstract Introduction Biosimilar CT-P13 was approved with limited data from clinical trials compared to the originator infliximab in biologic-naïve patients with rheumatoid arthritis. Three prospective post-marketing surveillance studies have been conducted in Japanese biologic-naïve patients and switched patients from biologics including the originator infliximab. Objective We performed an integrated analysis of final data from three post-marketing studies to provide long-term safety and efficacy data of CT-P13 in a real-world clinical setting. Methods A total of 1816 patients consisting of 987 patients with rheumatoid arthritis, 342 patients with Crohn’s disease, 322 patients with ulcerative colitis, and 165 patients with psoriasis were evaluated for safety. Efficacy was assessed in 1150 patients whose disease parameter values were serially collected. Results Adverse drug reactions were reported in 24.2% of all patients. The incidence of adverse drug reactions differed by the prior treatment status with biologics: 30.5% in patients naïve to biologics, 17.0% in patients switched from the originator infliximab, and 33.5% in patients switched from other biologics. Infusion reactions were the most frequent adverse drug reactions (8.2%), and its incidence was significantly higher in patients with ulcerative colitis and an allergy history in a multivariable Cox regression analysis. Infection was the second most frequent (6.1%), but tuberculosis only occurred in four patients (0.2%). The incidence of infection was low in patients with Crohn’s disease and psoriasis, and significant risk factors were an allergy history, comorbidities, and concomitant steroid use. Interstitial lung disease occurred in 16 patients (0.9%), including 11 patients with rheumatoid arthritis. With CT-P13 therapy, disease activity parameters decreased similarly in all four diseases, although long-term drug discontinuation rates because of inefficacy varied by disease. In naïve patients, the disease activity parameters decreased rapidly and the proportion of patients in remission increased. Patients switched from infliximab maintained lowered parameter levels with infliximab pretreatment. Decreases were also observed in patients switched from other biologics, but discontinuations were most often because of insufficient efficacy. Conclusions The integrated analysis of a large number of patients detected no new safety signals with long-term CT-P13 treatment. Efficacy in rheumatoid arthritis, psoriasis, Crohn’s disease, and ulcerative colitis cases was confirmed in biologic-naïve patients and switched patients from the originator infliximab or other biologics.
Date: 2023
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DOI: 10.1007/s40264-023-01340-1
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