Spatially and Temporally Resolving Predictive Biomarkers of Postoperative Recurrence and Complications in Chronic Intestinal Inflammation

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-69
SponsorIRCCS Ospedale San Raffaele

About this trial

A portion of patients with Inflammatory bowel disease often require surgical intervention since they do not respond to the current therapies. Besides this risk, patients may develop post-operative disease complications, and the factors beneath are far from being understood or predicted. The investigators hypothesize that some priming factors remain in the resection margin after surgery and act as a memory of the evolution of the disease, leading to the recurrence or complications. The following proposals are made:

1. defining and validating in humanized experimental models of intestinal inflammation the spatial and temporal dynamics of the postoperative complications-priming factors 2. integrating them into a machine-learning-driven model to determine risk indices of disease recurrence in IBD patients. This risk prediction model will not change the clinical decision-making process but will only be built for research. Consequently, patients enrolled in this study will be monitored and treated as per the standard of care.

This project will reveal possible causes and build methods predictive of postoperative complications ultimately resulting in changes in clinical management in the near future.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

adult (age >18 years) patients with histologically confirmed CD or UC undergoing intestinal resection due to stricturing disease, regardless of their current or past medical treatment;

given that it is an observational study, also pregnant and breastfeeding patients could be included;

able and willing to sign the informed consent.

Disqualifiers

patients <18 years or > 70 years;

patients with unconfirmed both UC and CD diagnoses;

patients with superimposed dysplasia or cancer diagnosis and resections for which post- operative endoscopic assessment of recurrence is not feasible;

patients unable or unwilling to sign the informed consent.

Trial population

This is an observational multicenter study with additional procedures performed on patients with an established diagnosis of UC and CD. It consists of a prospective and a retrospective part. The prospective part involves surgical leftover and blood collected at the time of surgery ad hoc for the study, without other risks for the patients. For the retrospective analysis, paraffin-embedded specimens already stored in the pathology unit from at least two years before the project starting date (from 1st August 2022 to 31st August 2024), will be used. Moreover, we will select and include in this study adult (age ≥18 years) patients with histologically confirmed CD or UC who have undergone surgery as per standard of care and whose surgical tissue- and blood-derived cell-suspensions have been previously collected for the already approved project IBD Biobank and stored at -80° C. The retrospective analysis will include IBD biobank samples collected since 1st August 2022 up to August 2024.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • CD patients

    Procedure/Surgery

    The study will involve the collection of leftover surgical material after pathologist analysis, mucosal brushes, an additional volume of blood and feces of patients at the time of surgery

  • UC patients

    Procedure/Surgery

    The study will involve the collection of leftover surgical material after pathologist analysis, mucosal brushes, an additional volume of blood and feces of patients at the time of surgery

Treatment groups

35 Participants
are divided into 2 treatment groups
Group A: UC patients1 intervention
Group B: CD patients1 intervention

Trial outcomes

Primary outcomes

1

To define spatial, cellular, and molecular characteristics of IBD-derived intestinal samples

To define the spatial transcriptome of UC and CD-derived intestinal mucosa, IBD-derived tissues will be analized by spatial transcriptomics, either at molecular or at microbiota level on formalin-fixed paraffin-embedded (FFPE) tissues stored at our pathology unit.

Time frame
6 months from surgery

Secondary outcomes

1

To build the predictive model of postoperative complications based on spatially and temporally resolved IBD characteristics

Other variables to be considered are CD4+ T-cells from the processing of blood

Time frame
6-12 months from surgery
2

To determine the mechanism underlying post-operative complications by exploiting in-vivo (mouse) experimental models of intestinal inflammation.

At the time of surgery, feces will be collected from patients. The microbial component from the IBD surgical specimens will be isolated and injected into humanized animal models.

Time frame
19-24 months from surgery

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

IRCCS Ospedale San Raffaele

Lead sponsor

IRCCS Casa Sollievo della Sofferenza, San Giovanni Rotondo

Collaborator

Azienda Ospedaliera OO.RR. S. Giovanni di Dio e Ruggi D'Aragona

Collaborator

Ministero della Salute, Italy

Collaborator