Cure8 news brief
Cure8 news brief
Early prediction of who will not respond to infliximab could help clinicians avoid prolonged ineffective treatment, enabling earlier reassessment and changes in therapy as part of treat-to-target care.
Adults with Crohn's disease starting infliximab, clinicians managing biologic induction, researchers studying treatment response prediction and biomarker-based models.
This is a two-center, retrospective real-world cohort study of adults with Crohn’s disease starting infliximab as their first biologic (derivation cohort and an external validation cohort).
The investigators combined clinical non-response, objective inflammatory evidence (CRP, fecal calprotectin, endoscopy, imaging), and treatment-failure events to define PNR at ~Week 14, and they developed a parsimonious risk model using baseline and Week 2 indicators.
The model aims chiefly to identify patients at lower risk of PNR to support earlier, risk-informed clinical reassessment rather than to dictate immediate treatment changes.
The analysis used consecutively treated patients from two university hospitals, prespecified model selection and internal bootstrap validation in the derivation center, and independent external validation in the second center.
Because the work is retrospective, some data types (endoscopy, fecal biomarkers, drug levels) were variably available in routine practice, which the authors note as a limitation.
This is a retrospective real-world study with variable availability of endoscopy, fecal biomarkers, and therapeutic drug monitoring; findings are promising for risk stratification but require prospective validation before changing practice.
Review the original publication for the complete reporting, methods, and context.
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