A study of Japanese patients with ulcerative colitis who were naïve to anti–tumor necrosis factor treatment found that patients preferred adalimumab to infliximab, but the researchers also reported no differences in the efficacy of the 2 treatments.
A study of Japanese patients with ulcerative colitis (UC) who were naïve to anti—tumor necrosis factor (TNF) treatment found that patients preferred adalimumab to infliximab, but the researchers also reported no differences in the efficacy of the 2 treatments. The study was conducted by Tsutomu Mizoshita, MD, PhD, and colleagues, and was published in Medicine (Baltimore) in August 2017.
During regular outpatient visits or during hospital stays, 25 patients with UC who were naïve to anti-TNF therapy were asked to evaluate, via questionnaire, whether they preferred to receive infliximab or adalimumab, and to provide reasons that contributed to their choice of therapy.
The researchers used the Mayo score and endoscopic activity index (EAI) as a measure of disease activity in the patients, before they initiated the treatment of their preference and at weeks 14 and 54. The primary difference between the 2 treatments is the mode (intravenous versus subcutaneous) and interval (every 2 months versus every 2 weeks) of administration. There is no difference in cost to the patient between infliximab and adalimumab in Japan, as healthcare is publicly funded.
Of the 25 patients who answered the questionnaire, 40% (n = 10) preferred infliximab, while 60% (n = 15) preferred adalimumab.
Patients who favored infliximab considered the following factors:
Patients who favored adalimumab considered the following factors:
There were no statistical differences in remission induction and maintenance between the infliximab and adalimumab groups with regard to response, remission, mucosal healing, steroid-free, or steroid-free remission rates at weeks 14 and 54. The efficacy of adalimumab in remission induction and maintenance was equivalent to that of infliximab in patients with UC who were naïve to anti-TNF therapy in this prospective study, but more patients preferred adalimumab.
The researchers believe their study is the first to show that there were no differences between infliximab and adalimumab with regard to response, remission, mucosal healing, steroid-free, and steroid-free remission rates in Japanese patients with UC who were naïve to anti-TNF therapy. It is also the first head-to-head comparison trial of the efficacy of remission induction and maintenance between infliximab and adalimumab in this population. The investigators suggest that further studies be conducted in larger populations to clarify which anti-TNF therapy is preferred by patients with UC.
Subcutaneous Infliximab CT-P13 Superior to Placebo as Maintenance Therapy for IBD
November 16th 2024In 2 randomized controlled trials of maintenance therapy for inflammatory bowel disease (IBD), the subcutaneous formulation of the infliximab biosimilar CT-P13 demonstrated superiority to placebo in patients with Crohn disease and ulcerative colitis.
Biosimilars Gastroenterology Roundup for May 2024—Podcast Edition
June 2nd 2024On this episode of Not So Different, we review the biggest gastroenterology biosimilar stories from May 2024, covering new data from conferences and journals on infliximab and adalimumab products that demonstrate positive clinical results and confirm the safety of these biosimilars, as well as the feasibility of switching to them.
Skyrizi Overtakes Humira: “Product Hopping” Leaves Biosimilar Market in Limbo
November 7th 2024For the first time, Skyrizi (risankizumab-rzaa) has replaced Humira (reference adalimumab) as AbbVie’s sales driver, largely due to companies encouraging “product hopping” to avoid competition, creating concerns for the sustainability of the burgeoning adalimumab biosimilar market.
Insights from Festival of Biologics: Dracey Poore Discusses Cardinal Health’s 2024 Biosimilar Report
May 19th 2024The discussion highlights key emerging trends from the Festival of Biologics conference and the annual Cardinal Health Biosimilars Report, including the importance of sustainability in the health care landscape and the challenges and successes in biosimilar adoption and affordability.
Eye on Pharma: Henlius, Organon Updates; Meitheal Portfolio Expansion; Celltrion Zymfentra Data
November 5th 2024Henlius and Organon’s pertuzumab biosimilar met phase 3 goals; Meitheal expanded its US biosimilars; Celltrion’s subcutaneous infliximab (Zymfentra) showed monotherapy could be as effective as combination therapy for inflammatory bowel disease.