TY - JOUR
T1 - Timing matters
T2 - recommendations for outcome assessment in real-world evidence studies of Crohn's disease
AU - Endpoints Cluster of the International Organization for the Study of Inflammatory Bowel Diseases
AU - Moreira, Paula Leão
AU - Dignass, Axel
AU - Estevinho, Maria Manuela
AU - Santiago, Mafalda
AU - Reinisch, Walter
AU - Sands, Bruce E.
AU - D'Haens, Geert
AU - Mantzaris, Gerassimos J.
AU - Danese, Silvio
AU - Peyrin-Biroulet, Laurent
AU - Dotan, Iris
AU - Jairath, Vipul
AU - Magro, Fernando
N1 - Publisher Copyright:
© The Author(s) 2026. Published by Oxford University Press on behalf of European Crohn’s and Colitis Organisation. All rights reserved. For commercial re-use, please contact [email protected] for reprints and translation rights for reprints. All other permissions can be obtained through our RightsLink service via the Permissions link on the article page on our site—for further information please
PY - 2026/3/10
Y1 - 2026/3/10
N2 - BACKGROUND: Real-world evidence (RWE) studies complement randomized trials by assessing treatment effectiveness and safety in routine clinical practice. In Crohn's disease (CD), heterogeneous disease progression makes standardized timing of outcome assessment critical, yet guidance is limited. METHODS: We conducted a two-round Delphi survey with international inflammatory bowel disease experts to identify clinically meaningful time points for 10 priority outcomes across four clinical scenarios: during and after the first year, with and without advanced therapy. RESULTS: Baseline and 12 months were identified as essential time points across all treatment contexts. Intermediate assessments at 3 and 6 months were recommended for dynamic outcomes (eg, biomarkers, clinical remission), while annual evaluations were suggested for slowly evolving outcomes (eg, colorectal cancer risk, CD-related surgeries). Timing preferences varied by treatment exposure and disease activity phase. CONCLUSIONS: We provide the first expert-endorsed temporal framework for outcome assessment in RWE studies of CD. Standardized measurement timing can enhance study comparability and methodological rigor, supporting more consistent interpretation of real-world data. Claims are limited to framework development and do not extend to direct clinical or regulatory impact.
AB - BACKGROUND: Real-world evidence (RWE) studies complement randomized trials by assessing treatment effectiveness and safety in routine clinical practice. In Crohn's disease (CD), heterogeneous disease progression makes standardized timing of outcome assessment critical, yet guidance is limited. METHODS: We conducted a two-round Delphi survey with international inflammatory bowel disease experts to identify clinically meaningful time points for 10 priority outcomes across four clinical scenarios: during and after the first year, with and without advanced therapy. RESULTS: Baseline and 12 months were identified as essential time points across all treatment contexts. Intermediate assessments at 3 and 6 months were recommended for dynamic outcomes (eg, biomarkers, clinical remission), while annual evaluations were suggested for slowly evolving outcomes (eg, colorectal cancer risk, CD-related surgeries). Timing preferences varied by treatment exposure and disease activity phase. CONCLUSIONS: We provide the first expert-endorsed temporal framework for outcome assessment in RWE studies of CD. Standardized measurement timing can enhance study comparability and methodological rigor, supporting more consistent interpretation of real-world data. Claims are limited to framework development and do not extend to direct clinical or regulatory impact.
KW - Crohn’s disease
KW - inflammatory bowel disease
KW - outcome measurement
KW - real-world evidence
KW - timing of assessment
UR - https://www.scopus.com/pages/publications/105034610466
U2 - 10.1093/ecco-jcc/jjag030
DO - 10.1093/ecco-jcc/jjag030
M3 - Article
C2 - 41891896
AN - SCOPUS:105034610466
SN - 1873-9946
VL - 20
JO - Journal of Crohn's and Colitis
JF - Journal of Crohn's and Colitis
IS - 3
ER -