Implications for sequencing of biologic therapy and choice of second anti‐TNF in patients with inflammatory bowel disease: results from the IMmunogenicity to Second Anti‐TNF therapy ( IMSAT ) therapeutic drug monitoring study
Year: 2022
Type: article
Study design: Observational Study
Abstract: BACKGROUND: Anti-drug antibodies are associated with treatment failure to anti-TNF agents in patients with inflammatory bowel disease (IBD). AIM: To assess whether immunogenicity to a patient's first anti-TNF agent would be associated with immunogenicity to the second, irrespective of drug sequence METHODS: We conducted a UK-wide, multicentre, retrospective cohort study to report rates of immunogenicity and treatment failure of second anti-TNF therapies in 1058 patients with IBD who underwent therapeutic drug monitoring for both infliximab and adalimumab. The primary outcome was immunogenicity to the second anti-TNF agent, defined at any timepoint as an anti-TNF antibody concentration ≥9 AU/ml for infliximab and ≥6 AU/ml for adalimumab. RESULTS: In patients treated with infliximab and then adalimumab, those who developed antibodies to infliximab were more likely to develop antibodies to adalimumab, than patients who did not develop antibodies to infliximab (OR 1.99, 95%CI 1.27-3.20, p = 0.002). Similarly, in patients treated with adalimumab and then infliximab, immunogenicity to adalimumab was associated with subsequent immunogenicity to infliximab (OR 2.63, 95%CI 1.46-4.80, p < 0.001). For each 10-fold increase in anti-infliximab and anti-adalimumab antibody concentration, the odds of subsequently developing antibodies to adalimumab and infliximab increased by 1.73 (95% CI 1.38-2.17, p < 0.001) and 1.99 (95%CI 1.34-2.99, p < 0.001), respectively. Patients who developed immunogenicity with undetectable drug levels to infliximab were more likely to develop immunogenicity with undetectable drug levels to adalimumab (OR 2.37, 95% CI 1.39-4.19, p < 0.001). Commencing an immunomodulator at the time of switching to the second anti-TNF was associated with improved drug persistence in patients with immunogenic, but not pharmacodynamic failure. CONCLUSION: Irrespective of drug sequence, immunogenicity to the first anti-TNF agent was associated with immunogenicity to the second, which was mitigated by the introduction of an immunomodulator in patients with immunogenic, but not pharmacodynamic treatment failure.
DOI: 10.1111/apt.17170
Authors: Neil Chanchlani, Simeng Lin, Marcus K. Auth, Chai Leng Lee, Helena Robbins, Shi Looi, Senthil V. Murugesan, Tom Riley, Cathryn Preston, Sophie Stephenson, Wendy Cardozo, Sunil A. Sonwalkar, Mohammed Allah‐Ditta, Lynne Mansfield, Dharmaraj Durai, Mark Baker, Ian London, Emily London, Sanjay Gupta, Alex Di Mambro, Aisling Murphy, Edward Gaynor, Kelsey D. J. Jones, Andrew Claridge, Shaji Sebastian, Sankaranarayanan Ramachandran, Christian P. Selinger, Simon P. Borg‐Bartolo, Paul Knight, Michael B. Sprakes, Julie Burton, Patricia Kane, Stephanie Lupton, Aimee Fletcher, Daniel R. Gaya, Roghan Colbert, John Paul Seenan, Jonathan MacDonald, Lucy Lynch, Iain McLachlan, Stephanie Shields, Richard Hansen, Lisa Gervais, Mwansa Jere, Muhammad Akhtar, Karen Black, Paul Henderson, Richard K. Russell, Charlie W. Lees, Lauranne A. A. P. Derikx, Melanie Lockett, Frederica Betteridge, Aminda De Silva, Arif Hussenbux, John Beckly, Oliver Bendall, James W. Hart, Amanda Thomas, Ben Hamilton, Claire Gordon, Desmond Chee, Timothy J. McDonald, Rachel Nice, Marian Parkinson, Helen Gardner‐Thorpe, Jeff R. Butterworth, Asima Javed, Sarah Al‐Shakhshir, Rekha Yadagiri, Sebrene Maher, Richard C. G. Pollok, Tze Ng, Priscilla Appiahene, Fiona Donovan, James Lok, Rajiv Chandy, Reema Jagdish, Daniyal Baig, Zahid Mahmood, Liane Marsh, Allison Moss, Amin Abdulgader, Angus Kitchin, Gareth J. Walker, Becky George, Yuen‐Hui Lim, James Gulliver, Stuart Bloom, Holly Theaker, Sean Carlson, J. R. Fraser Cummings, Robert Livingstone, Amanda Beale, Josiah O. Carter, Andrew Bell, Archibald Coulter, Jonathon Snook, Helen Stone, Nicholas A. Kennedy, James R. Goodhand, Tariq Ahmad, IMSAT study investigators
Institutions: Royal Devon University Healthcare NHS Foundation Trust, Alder Hey Children's NHS Foundation Trust, Alder Hey Children's Hospital, St Peter's Hospital, Ashford and St Peter's Hospitals NHS Foundation Trust, Blackpool Teaching Hospitals NHS Foundation Trust, Bradford Teaching Hospitals NHS Foundation Trust, Huddersfield Royal Infirmary, Cardiff and Vale University Health Board, Countess of Chester Hospital NHS Foundation Trust, Croydon Health Services NHS Trust, Gloucestershire Hospitals NHS Foundation Trust, Great Ormond Street Hospital, Great Western Hospital, Great Western Hospitals NHS Foundation Trust, Leeds Teaching Hospitals NHS Trust, Manchester University NHS Foundation Trust, Mid Yorkshire Hospitals NHS Trust, NHS Greater Glasgow and Clyde, Glasgow Royal Infirmary, Queen Elizabeth University Hospital, Royal Hospital for Children, NHS Lanarkshire, NHS Lothian, Royal Hospital for Sick Children, Western General Hospital, North Bristol NHS Trust, Royal Berkshire NHS Foundation Trust, Royal Cornwall Hospital Trust, Royal Cornwall Hospital, Shrewsbury and Telford Hospital NHS Trust, St George’s University Hospitals NHS Foundation Trust, Mersey and West Lancashire Teaching Hospitals NHS Trust, Stockport NHS Foundation Trust, Taunton & Somerset NHS Foundation Trust, Somerset NHS Foundation Trust, Torbay and South Devon NHS Foundation Trust, University College London Hospitals NHS Foundation Trust, University Hospital Southampton NHS Foundation Trust, University Hospitals Bristol and Weston NHS Foundation Trust, Poole Hospital, University Hospitals Dorset NHS Foundation Trust
Language: English
Topic: Inflammatory Bowel Disease
Subfield: Gastroenterology
Field: Medicine
Domain: Health Sciences
Open Access status: hybrid
Estimated APC paid: $4,900
OpenAlex ID: W4293536498