TY - JOUR
T1 - Supratherapeutic Infliximab Levels Do Not Predict Risk of Short-term Complications in Adults with Crohn's Disease
AU - Bhattacharya, Abhik
AU - Travis, Daniel
AU - Osterman, Mark T.
AU - Lewis, James D.
AU - Bhagya Rao, Bhavana
AU - Lee, Helen
AU - Lichtenstein, Gary R.
N1 - Funding Information:
M.T.O. serves as an advisory board consultant for AbbVie, Elan, Genentech/Roche, Janssen, Lycera, Merck, Pfizer, and UCB; receives research grant support from UCB. J.D.L. reports having received honorarium for consulting or serving on Data Monitoring Committees from Celgene, Merck, Janssen Pharmaceuticals, Bridge Biotherapeutics, Pfizer, Gilead, Arena Pharmaceuticals and Protagonist Therapeutics. He reports research support from Janssen Pharmaceuticals and Takeda. G.R.L.: Abbvie (consultant), American College of Gastroenterology (honorarium for associate editor of American Journal of Gastroenterology), CellCeutrix (consultant), Celgene (research, consultant), Clinical Advances in Gastroenterology (associate editor—honorarium), Ferring (consultant), Gastroenterology and Hepatology (Gastro-Hep Communications) (editor—honorarium), Gilead (consultant), Janssen Orthobiotech [consultant, research, funding to University of PA (IBD Fellow Education)], Eli Lily (consultant, DSMB), Luitpold/American Regent [consulting, honorarium (CME Programs)], Merck [consulting, honorarium (CME Program)], McMahon Publishing [author (honorarium)], Pfizer Pharmaceuticals [consultant, research, funding to University of PA (IBD Fellow Education)], Prometheus Laboratories Inc. (consultant), Romark (consultant, honorarium for CME), Salix Pharmaceuticals/Valeant (consultant, research), Shire Pharmaceuticals (consultant, research), SLACK Inc. (book royalty), Springer Science and Business Media (editor—honorarium), Takeda [consultant, funding to University of PA (IBD Fellow Education)], UCB (consultant, research), Up-To-Date (author—honorarium). The remaining authors declare that they have nothing to disclose.
Publisher Copyright:
© 2021 Wolters Kluwer Health, Inc. All rights reserved.
PY - 2023/1/15
Y1 - 2023/1/15
N2 - Background: It is uncertain if higher infliximab trough levels (TLs) confer a greater risk of infectious/noninfectious complications (IC/NIC). We aimed to assess the risk of IC and NIC in patients with different TLs. Methods: We retrospectively evaluated a cohort of Crohn's disease (CD) patients treated with infliximab who underwent therapeutic drug monitoring (TDM), at a tertiary inflammatory bowel disease center, between January 1, 2010, and December 1, 2019. TDM was defined as checking of infliximab trough and antibody levels within a 48-hour period before administration. Patients with a minimum of 3-month assessment pre-TDM and post-TDM were included. In the case of multiple TDMs, the highest TL was considered, and patients were distributed across 4 predefined TL groups (A: <5 µg/mL, B: 5 to 10 µg/mL, C: 10 to 15 µg/mL, and D: ≥15 µg/mL). Rates of IC and NIC during the 3-month prior and following TDM were compared across the groups. In addition, duration of exposure, in terms of months up to TDM, was collected to analyze differences in rates of IC and NIC. Results: Our study included 341 CD patients (median age: 35 y, 58% men). IC and NIC occurred in 52 (15%) and 30 (9%) patients, respectively. Rates of IC and NIC were similar across the 4 TL groups (P=0.9 and 0.7, respectively for IC and NIC). On multivariable analysis, exposure to infliximab >40 months (as determined by receiver operating characteristic curve analysis) was associated with decreased odds for IC (adjusted odds ratio=0.51, P=0.04), but not NIC (adjusted odds ratio=0.72, P=0.46). Conclusions: In this large CD cohort, there was no association between infliximab TL and risk of short-term IC or NIC. Interestingly, a shorter duration of exposure predicted higher rates of IC. This supports the safety of targeting higher infliximab TLs when necessary and greater vigilance during the early stages of treatment.
AB - Background: It is uncertain if higher infliximab trough levels (TLs) confer a greater risk of infectious/noninfectious complications (IC/NIC). We aimed to assess the risk of IC and NIC in patients with different TLs. Methods: We retrospectively evaluated a cohort of Crohn's disease (CD) patients treated with infliximab who underwent therapeutic drug monitoring (TDM), at a tertiary inflammatory bowel disease center, between January 1, 2010, and December 1, 2019. TDM was defined as checking of infliximab trough and antibody levels within a 48-hour period before administration. Patients with a minimum of 3-month assessment pre-TDM and post-TDM were included. In the case of multiple TDMs, the highest TL was considered, and patients were distributed across 4 predefined TL groups (A: <5 µg/mL, B: 5 to 10 µg/mL, C: 10 to 15 µg/mL, and D: ≥15 µg/mL). Rates of IC and NIC during the 3-month prior and following TDM were compared across the groups. In addition, duration of exposure, in terms of months up to TDM, was collected to analyze differences in rates of IC and NIC. Results: Our study included 341 CD patients (median age: 35 y, 58% men). IC and NIC occurred in 52 (15%) and 30 (9%) patients, respectively. Rates of IC and NIC were similar across the 4 TL groups (P=0.9 and 0.7, respectively for IC and NIC). On multivariable analysis, exposure to infliximab >40 months (as determined by receiver operating characteristic curve analysis) was associated with decreased odds for IC (adjusted odds ratio=0.51, P=0.04), but not NIC (adjusted odds ratio=0.72, P=0.46). Conclusions: In this large CD cohort, there was no association between infliximab TL and risk of short-term IC or NIC. Interestingly, a shorter duration of exposure predicted higher rates of IC. This supports the safety of targeting higher infliximab TLs when necessary and greater vigilance during the early stages of treatment.
KW - Crohn's disease
KW - complications
KW - infliximab
KW - therapeutic drug monitoring
UR - http://www.scopus.com/inward/record.url?scp=85126770142&partnerID=8YFLogxK
U2 - 10.1097/MCG.0000000000001637
DO - 10.1097/MCG.0000000000001637
M3 - Article
C2 - 34907922
AN - SCOPUS:85126770142
SN - 0192-0790
VL - 57
SP - 66
EP - 73
JO - Journal of Clinical Gastroenterology
JF - Journal of Clinical Gastroenterology
IS - 1
ER -