TY - JOUR
T1 - Validation and update of a prediction model for risk of relapse after cessation of anti-TNF treatment in Crohn's disease
AU - ten Bokkel Huinink, Sebastiaan
AU - de Jong, Djuna C.
AU - Nieboer, Daan
AU - Thomassen, Doranne
AU - Steyerberg, Ewout W.
AU - Dijkgraaf, Marcel G. W.
AU - Bodelier, Alexander G. L.
AU - West, Rachel L.
AU - Römkens, Tessa E. H.
AU - Hoentjen, Frank
AU - Mallant, Rosalie C.
AU - van Tuyl, Bas A. C.
AU - Mares, Wout G. N.
AU - Wolfhagen, Frank H. J.
AU - Dijkstra, Gerard
AU - Reijnders, Jurriën G. P.
AU - de Boer, Nanne K.
AU - Tan, Adriaan C. I. T. L.
AU - van Boeckel, Petra G. A.
AU - Tack, Greetje J.
AU - van Asseldonk, Dirk P.
AU - D'Haens, Geert R. A. M.
AU - van der Woude, C. Janneke
AU - Duijvestein, Marjolijn
AU - de Vries, Annemarie C.
N1 - Funding Information: R.W. has participated in advisory boards or as a speaker or consultant for AbbVie, and Janssen, Takeda and Galapagos. T.R. has participated in advisory board and/or received financial compensation from the following company: Takeda. F.H. has served on advisory boards or as speaker for Abbvie, Janssen-Cilag, MSD, Takeda, Celltrion, Teva, Sandoz and Dr Falk. Funding (Grants/Honoraria): Dr Falk, Janssen-Cilag, Abbvie, Takeda.Consulting Fees: Celgene. N.B. has served as a speaker for AbbVie and MSD and has served as consultant and principal investigator for TEVA Pharma BV and Takeda. Received a (unrestricted) research grant from Dr. Falk, TEVA Pharma BV, MLDS and Takeda, all outside the submitted work. D.A. advisor for galapagos, Takeda, Ferring. Received educational grants from Janssen, DrFalk and Ferring. G.R.D. has served as advisor for Abbvie, Ablynx, Alimentiv, Amgen, AM Pharma, Biogen, Bristol Meiers Squibb, Boerhinger Ingelheim, Celgene/Receptos, Celltrion, Cosmo, Covidien/Medtronics, Ferring, DrFALK Pharma, Eli Lilly, Engene, Galapagos, Genentech/Roche, Gilead, Glaxo Smith Kline, Immunic, Johnson and Johnson, Lamepro, Lument, Mitsubishi Pharma, Merck Sharp Dome, Mundipharma, Nextbiotics, Novonordisk, Otsuka, Pfizer, Polpharm, Prometheus laboratories/Nestle, Procise diagnostics, Protagonist, Salix, Samsung Bioepis, Sandoz, Setpoint, Shire, Takeda, Tigenix, Tillotts, Topivert, Versant and Vifor; received speaker fees from Abbvie, Biogen, Ferring, Johnson and Johnson, Merck Sharp Dome, Mundipharma, Norgine, Pfizer, Samsung Bioepis, Shire, Takeda, Tillotts and Vifor. C.W.received grant support from Falk Benelux and Pfizer; received speaker fees from AbbVie, Takeda, Ferring, Dr. Falk Pharma, Hospira, Pfizer; and served as a consultant for AbbVie, MSD, Takeda, Celgene, Mundipharma and Janssen. M.D.has served as advisor for Echo pharma and Robarts Clinical Trials, reports nonfinancial support from Dr. Falk Pharma, and received speaker fees from Janssen, Merck & Co., Pfizer, Takeda and Tillotts Pharma. A.V.Advisory board Jansen, Takeda and Abbvie. For the remaining authors, there are no conflicts of interest. Funding Information: This work was supported by ZonMW GoedGebruik-Geneesmiddelen (project number: 848101009). Publisher Copyright: © 2022 The Author(s).
PY - 2022/10/1
Y1 - 2022/10/1
N2 - BACKGROUND: Anti-tumor necrosis factor (TNF) therapy is effective for the treatment of Crohn's disease. Cessation may be considered in patients with a low risk of relapse. We aimed to externally validate and update our previously developed prediction model to estimate the risk of relapse after cessation of anti-TNF therapy. METHODS: We performed a retrospective cohort study in 17 Dutch hospitals. Crohn's disease patients in clinical, biochemical or endoscopic remission were included after anti-TNF cessation. Primary outcome was a relapse necessitating treatment. Discrimination and calibration of the previously developed model were assessed. After external validation, the model was updated. The performance of the updated prediction model was assessed in internal-external validation and by using decision curve analysis. RESULTS: 486 patients were included with a median follow-up of 1.7 years. Relapse rates were 35 and 54% after 1 and 2 years. At external validation, the discriminative ability of the prediction model was equal to that found at the development of the model [c-statistic 0.58 (95% confidence interval (CI) 0.54-0.62)], though the model was not well-calibrated on our cohort [calibration slope: 0.52 (0.28-0.76)]. After an update, a c-statistic of 0.60 (0.58-0.63) and calibration slope of 0.89 (0.69-1.09) were reported in internal-external validation. CONCLUSION: Our previously developed and updated prediction model for the risk of relapse after cessation of anti-TNF in Crohn's disease shows reasonable performance. The use of the model may support clinical decision-making to optimize patient selection in whom anti-TNF can be withdrawn. Clinical validation is ongoing in a prospective randomized trial.
AB - BACKGROUND: Anti-tumor necrosis factor (TNF) therapy is effective for the treatment of Crohn's disease. Cessation may be considered in patients with a low risk of relapse. We aimed to externally validate and update our previously developed prediction model to estimate the risk of relapse after cessation of anti-TNF therapy. METHODS: We performed a retrospective cohort study in 17 Dutch hospitals. Crohn's disease patients in clinical, biochemical or endoscopic remission were included after anti-TNF cessation. Primary outcome was a relapse necessitating treatment. Discrimination and calibration of the previously developed model were assessed. After external validation, the model was updated. The performance of the updated prediction model was assessed in internal-external validation and by using decision curve analysis. RESULTS: 486 patients were included with a median follow-up of 1.7 years. Relapse rates were 35 and 54% after 1 and 2 years. At external validation, the discriminative ability of the prediction model was equal to that found at the development of the model [c-statistic 0.58 (95% confidence interval (CI) 0.54-0.62)], though the model was not well-calibrated on our cohort [calibration slope: 0.52 (0.28-0.76)]. After an update, a c-statistic of 0.60 (0.58-0.63) and calibration slope of 0.89 (0.69-1.09) were reported in internal-external validation. CONCLUSION: Our previously developed and updated prediction model for the risk of relapse after cessation of anti-TNF in Crohn's disease shows reasonable performance. The use of the model may support clinical decision-making to optimize patient selection in whom anti-TNF can be withdrawn. Clinical validation is ongoing in a prospective randomized trial.
KW - Crohn's disease
KW - anti-TNF therapy
KW - cessation
KW - prediction
UR - http://www.scopus.com/inward/record.url?scp=85137182601&partnerID=8YFLogxK
U2 - https://doi.org/10.1097/MEG.0000000000002403
DO - https://doi.org/10.1097/MEG.0000000000002403
M3 - Article
C2 - 36062493
SN - 0954-691X
VL - 34
SP - 983
EP - 992
JO - European Journal of Gastroenterology & Hepatology
JF - European Journal of Gastroenterology & Hepatology
IS - 10
ER -