P337 Switching from originator infliximab to CT-P13: single-centre experience from the UK
A. P. Bhandare*1, B. Crooks1, G. B. Nigam1, J. K. Limdi1,2
1Pennine Acute Hospitals Trust, Gastroenterology, Manchester, UK, 2University of Manchester, Institute of Inflammation and Repair, Manchester, UK
The infliximab biosimilar (CT-P13) received market authorisation for inflammatory bowel disease in late 2016 with the aim of reducing cost and increasing access to therapy. The prospect of ‘switching’ patients from originator to CT-P13 has concerned clinicians. #8232;We present an experience of ‘switching’ from originator infliximab (IFX-O) to CT-P13 and present efficacy, safety, and immunogenicity data from our cohort.
We performed a retrospective review of patients switched from IFX-O to CT-P13. Disease demographics, clinical course and outcomes were analysed from electronic case records at a median of 8 months and at last follow-up at 13 months.
Ninety-six patients (35 females) were ‘switched’ from IFX-O to CT-P13. Of these 44 had Ulcerative colitis (UC) and 52 had Crohn’s disease (CD) with a mean age at diagnosis of 34.7 years (median = 33, IQR = 24.5). Montreal phenotype for UC was E1 = 1, E2 = 16, E3 = 27 and for CD (L1 = 10, L2 = 12 , L3 = 29, L4 = 1) and (B1 = 27, #8232;B2 = 14 , B3 = 11), 9 patients had perianal disease. Mean duration of IFX-O treatment was 49. 8 months (median = 44, IQR = 52) and on CT-P13 11.5 months (median 13). At switch, 76 patients had a normal CRP (UC = 33, CD = 43), and in 15 patients it was elevated (UC = 10, CD = 5). At 8 months, 80 patients remained in biochemical remission (UC = 35, CD = 45 ) and in 14 patients (UC = 8, CD = 6 ) CRP increased. Seventy-two patients (UC = 34, CD = 38 ) were in clinical remission (pMayo < 2 and HBI < 5). Of 51 patients (UC = 21, CD = 30) undergoing endoscopic assessment, 31 achieved mucosal healing (UC = 13, CD = 18). At 13 months, 69 patients remained on CT-P13. Twenty-seven discontinued the drug due to immunogenicity (
Biosimilar IFX (CT-P13) was well tolerated. Clinical efficacy and loss of response rates with CT-P13 appears to be similar to IFX-O. This holds promise for a wider adoption of ‘switching’ to fulfil the purported aims of wider access to treatment at a lower cost.