Ulcerative Colitis
Conditions
Keywords
ulcerative colitis, patient reported outcomes, histological scoring, disability, inflammatory bowel disease
Brief summary
Background and rationale: In ulcerative colitis, treating beyond endoscopic healing has shown a reduction of relapse and hospitalization, pushing for histological remission in daily clinical practice.1 However, very little is known on how histological remission is associated with patient reported outcomes (PROMs).2,3 In recent years, several questionnaires have been developed to assess what really matters to patients: symptoms and the burden UC exerts on them.4 As PROMs are getting more and more attention during drug development programs and drug approval by international organizations, including FDA and EMA, the link between objective outcome measures (endoscopic, histological, biochemical) and PROMs should therefore be better characterized. Objectives and design: To investigate prospectively the association of patient reported outcomes (PROMs) and biochemical, endoscopic and histological outcome measures in patients with ulcerative colitis.
Detailed description
After informed consent, patients will undergo endoscopic assessment evaluating endoscopic disease activity using established scoring systems * Mayo endoscopic sub-score5 * Ulcerative Colitis Endoscopic Index of Severity \[UCEIS\]6 All endoscopic assessments will be recorded, allowing blinded scoring by independent endoscopists afterwards. Study protocol APOLLO - 2 During endoscopy, colonic biopsies will be taken according to standard of care from the most inflamed area of the colon and normal area if applicable, 0-60cm from the anal verge. All biopsies will be scored histologically using the Nancy Index.7 During the same study visit, clinical symptoms (Simple clinical colitis activity index \[SCCAI\]) and patient reported outcomes (PROMs) will be evaluated digitally using validated scoring systems8 * IBD disk * PRO-2 * Visual Analogue Scale * IBD control in case of non-remission Finally, patients will be biochemically (C-reactive protein, hemoglobin, albumin) evaluated, including measurement of drug level (infliximab, adalimumab, vedolizumab) in case of ongoing exposure to biological agents. All evaluations are part of standard-of-care. Definitions * Endoscopic remission: Mayo endoscopic sub-score 0 AND UCEIS 0 * Endoscopic response according to * Mayo score: decrease in Mayo endoscopic sub-score ≥ 1 * UCEIS: decrease in UCEIS ≥ 2 * Endoscopic improvement: Mayo endoscopic sub-score 1 * Histological remission: Nancy histological index 0 * Absence of active/acute histological inflammation: Nancy histological index 0-1 * Histological response: Nancy histological index \> 1 * PRO2 remission: stool frequency ≤ 1 (absolute stool frequency ≤ 3 OR 1-2 stools more than usual) AND rectal bleeding score of 0 (average of 3 days prior to endoscopy) * IBD disk remission per item: * Abdominal pain * Regulating defecation * Interpersonal interactions * Education and work * Sleep * Energy * Emotions * Body Image * Sexual function * Joint pain
Interventions
DIAGNOSTIC_TESTendoscopic biopsies
patients with planned endoscopy for ulcerative colitis have endosocpic data recorded aswell as biopsy sampling and blood tests
Sponsors
Imelda GI Clinical Research Center
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
16 Years to No maximum
Healthy volunteers
No
Inclusion criteria
All patients with ulcerative colitis (≥ 16 years) undergoing planned endoscopic assessment as part of standard of care between 01.07.2020 and 30.06.2021. Evidence of a personally signed and dated informed consent document (ICF) indicating that the subject has been informed of all aspects of the study.
Exclusion criteria
Subjects with a diagnosis of indeterminate colitis, ischemic colitis, radiation colitis, diverticular disease associated with colitis, microscopic colitis or Crohn's disease. Subjects with clinical findings suggestive of CD (e.g. fistulae, granulomas on biopsy) are also excluded. Similar data collection within 8 weeks prior to endoscopic assessment
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| correlation between histological disease activity and disability | 1 day | histological activity is based on the Nancy score, disability is based on the IBD disk |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| correlation between histological disease activity and patient reported outcomes | 1 day | histological activity is based on the Nancy score, PRO is based on the SCCAI |
| correlation between histological disease activity and endoscopic disease activity | 1 day | histological activity is based on the Nancy score, endoscopic disease activityis based on the Mayo endoscopic subscore |
| correlation between histological disease activity and biomarkers | 1 day | histological activity is based on the Nancy score, biomarkers (CRP, hemoglobine, albumin) |
Other
| Measure | Time frame | Description |
|---|---|---|
| correlation between histological disease activity and patient reported outcomes | 1 day | histological activity is based on the Nancy score, disability is based on the IBD control in case of non remission |
Countries
Belgium
Outcome results
None listed