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 - Huinink, Sebastiaan ten Bokkel
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 - Romkens, 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, Jurrien 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.
PY - 2022/10
Y1 - 2022/10
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 The use of the model may support clinical decision-making to optimize patient selection in whom anti-TNF can be withdrawn.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 - anti-TNF therapy
KW - cessation
KW - Crohn's disease
KW - prediction
KW - BREAST-CANCER RISK
KW - INFLAMMATORY-BOWEL-DISEASE
KW - ANTITUMOR NECROSIS FACTOR
KW - FACTOR-ALPHA THERAPY
KW - WITHDRAWAL
KW - REMISSION
KW - SAFETY
KW - METAANALYSIS
KW - MAINTENANCE
KW - EFFICACY
U2 - 10.1097/MEG.0000000000002403
DO - 10.1097/MEG.0000000000002403
M3 - Article
SN - 0954-691X
VL - 34
SP - 983
EP - 992
JO - European journal of gastroenterology & hepatology
JF - European journal of gastroenterology & hepatology
IS - 10
ER -