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Ileal Crohn's Disease and Post-operative Outcome: Prospective Cohort Study of the REMIND Group (POP-REMIND)

Primary Purpose

Crohn Disease

Status
Recruiting
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
bio-banking collection
Sponsored by
Saint-Louis Hospital, Paris, France
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Crohn Disease focused on measuring ileo-caecal resection; post-operative recurrence

Eligibility Criteria

18 Years - 100 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Informed consent obtained before any study-related activities
  • A diagnosis of CD, based on clinical, radiologic, endoscopic, or histological evidence.
  • Men and women ≥18 years of age
  • Required surgical intervention consisting in an ileocecal resection

Exclusion Criteria:

  • Previous history of dysplasia or cancer in the ileum or colon
  • Unwillingness or inability to follow the procedures outlined in the protocol
  • Pregnant women

Sites / Locations

  • SART Tilman HospitalRecruiting
  • Amiens HospitalRecruiting
  • Haut-levêque Hospital
  • Clermont-Ferrand HospitalRecruiting
  • Beaujon HospitalRecruiting
  • Henri Mondor Hospital
  • Kremlin-Bicêtre HospitalRecruiting
  • Lille HospitalRecruiting
  • Hôpital Nord, CHU MarseilleRecruiting
  • Montpellier HospitalRecruiting
  • Brabois HospitalRecruiting
  • Nantes HospitalRecruiting
  • Archet 2 HospitalRecruiting
  • Saint Louis HospitalRecruiting
  • Saint Antoine HospitalRecruiting
  • South Lyon HospitalRecruiting
  • Strasbourg Hospital

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Crohn's disease patients

Arm Description

Patients aged 18 or more, for whom Crohn's disease diagnosis is confirmed and ileum or ileocecal Crohn's disease require surgical resection. in addition to usual practice, a bio-banking (blood samples, biopsies and surgical specimens) is collected.

Outcomes

Primary Outcome Measures

Ileal Crohn's disease classification
Ileal Crohn's disease classification will be performed using data integration (taking into account clinical data, immunological, genetic, microbiota, transcriptome data). A molecular classification will be possible due to this data integration analysis
Postoperative recurrence study
Rates of endoscopic recurrence as defined by a Rutgeerts score ≥ 1 in patients will be evaluated at the endoscopic exam
Study of Treatments efficacy to prevent recurrence
During a clinical visit, scheduled as usual practice 6 months after surgery, clinical data will be collected : treatment modification or optimization, recurrence occurrence. If treament modification or optimization is needed (clinical symptoms or endoscopic recurrence), or complication occurs (abcess, occlusive syndrom, new surgery), patient will be considered as suffering a long-term relapse
Identification of biomarkers which could predict postoperative recurrence and response to treatments
Identification of biomarkers taking into account clinical data, immunological, genetic, microbiota, transcriptome data

Secondary Outcome Measures

Full Information

First Posted
March 1, 2018
Last Updated
April 11, 2023
Sponsor
Saint-Louis Hospital, Paris, France
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1. Study Identification

Unique Protocol Identification Number
NCT03458195
Brief Title
Ileal Crohn's Disease and Post-operative Outcome: Prospective Cohort Study of the REMIND Group
Acronym
POP-REMIND
Official Title
Ileal Crohn's Disease and Post-operative Outcome: Prospective Cohort Study of the REMIND Group
Study Type
Interventional

2. Study Status

Record Verification Date
April 2023
Overall Recruitment Status
Recruiting
Study Start Date
December 10, 2009 (Actual)
Primary Completion Date
December 2025 (Anticipated)
Study Completion Date
December 2026 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Saint-Louis Hospital, Paris, France

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Crohn's disease (CD), a chronic inflammatory process in intestinal segments leads to tissue damage. More than two thirds of CD patients need intestinal resection. Symptomatic clinical recurrence occurs in 60% by 10 years. The principal factors affecting postoperative recurrence are active smoking, penetrating disease, perianal lesions history, prior intestinal resection, small bowel resection extent, and prophylaxis treatment absence. Ileocolonoscopy within one year of surgery can predict clinical recurrence risk. Different therapies are proposed after surgery, to prevent post-operative recurrence : Thiopurines, 6-mercaptopurine (positive for clinical and endoscopic postoperative recurrence prevention), Anti-tumour necrosis factor therapy (anti-TNF), the most effective therapy. Intestinal microbiota acts as a central factor in the CD pathogenesis, and fecal stream role is clearly shown. Various changes in luminal flora with a possible link to local inflammation was also demonstrated. Bacteria associated with postoperative recurrence could be more pathogenic as adherent invasive E coli (AIEC), which could be a pathogen in CD through several mechanisms including increased mucosal colonization, adherence, replication and induction of TNF secretion. Alternatively, postoperative CD recurrence could be linked to a protective commensal species lack, such as Faecalibacterium prausnitzii. Microscopic inflammation occurs as early as 8 days after anastomosis in the neoterminal ileum mucosa. IL6, IL10 and TGFb levels, measured in neoterminal ileum early after surgery are associated with different rates of postoperative recurrence. It suggests cytokines implication in postoperative recurrence. T cells are major players in the intestinal immune response. The presence at time of surgery and persistence of disease inducing T cell clonal expansions could play an important role in post-operative recurrence. The main objective is to define a classification of ileal Crohn's Disease based on data integration on a large cohort of patients.
Detailed Description
Crohn's Disease is a major health issue with a complex etiology and despite available medical treatment, patients endure poor quality of life. The disease 's characterization on a molecular level will allow for a better management of patients treatment. To do so, the strategy is to integrate precise prospective clinical records with extensive biological data in a large cohort of patients. All the clinical centers, participating to the study, include patients, with a tight collaboration between Gastroenterology and Surgery departments. Demographics and clinical parameters are collected in an eCRF. Inclusion of patients is performed, before a scheduled ileocecal resection or ileal resection, and after eligibility criteria checking, and consent form signature. During surgery, several samples are collected : blood samples, mucosal biopsies, and surgical specimens. As usual practice, post-operative treatment will be prescribed at investigator's discretion, with help of a pre-established algorithm. Then, an endoscopic exam is scheduled, at least 6 months after surgery, or at least 6 months after intestine continuity restoration, in case of temporary stoma. Several samples are also collected during this exam (blood, ileal and colon biopsies). At the same time as these 2 visits, clinical data regarding medical history, CD history, surgical history, treatments history, post-operative treatment if prescribed, treatments history between surgery and colonoscopy 6 months later, endoscopic score. Clinical data are also collected 18 months after surgery during a scheduled visit organized as usual practice, for long-term study : Clinical relapse, surgical recurrence, change in the therapy, hospitalizations and complications A patient has achieved the study after the endoscopic exam. Several studies will be performed along the cohort setting-up: Transcriptomic analyses of mucosal tissues: Identification of a molecular signature predictive of post-operative recurrence Molecular classification of ileal Crohn's Disease Study of the mucosa-associated microbiota Study of association of AIEC Study of anti-TNF efficacy in post-operative recurrence prevention Study of new biologics in the treatment of post-operative recurrence All the biologic samples are stored on sites at -80°C, or at room temperature depending on the samples : Samples collected in Formol tubes, are sent immediatly, at room temperature, to the central pathology department in Beaujon Hospital, Paris. All the other samples, stored at -80°C, are sent to a central department, the Bio-Bank of Pasteur Hospital, Nice (every 3 months). Samples analyses are performed by dedicated research centers: DNA, and RNA extraction for transcriptome analysis, Micobiota analysis, Lipids analysis, AIEC analysis : Histological analyzes: Analyzis of the structure and inflammatory status of intestinal tissue of patients of the cohort, particularly at the ileal limit of the surgical specimens. Molecular Biology: Whole genome expression analyses are performed using microarray and followed by Gene Ontology and clustering analyses. Microbiology: Adherent Invasive E.Coli (AIEC): The search for AIEC bacteria is carried out by culturing and investigating the characteristics of adhesion, invasion in Int-407 cells, and survival within THP-1 macrophages. Microbiota: Bacterial composition of the ileal mucosa associated microbiota is analyzed at time of surgery using 16S (MiSeq, Illumina) sequencing. The obtained sequences are analyzed using the Qiime pipeline to assess composition, alpha and beta diversity. Immunology: Phenotype of mucosal and peripheral immune cells: Immune cells are extracted from blood and fresh mucosal tissues. The phenotype of these cells is analyzed by cytometry. T cell repertoire: T cell receptor analysis on DNA extracted from biopsies is performed by next generation sequencing (Adaptive Biotechnology Inc., Seattle, Washington, USA). It is hypothesized that the persistence of these clonal expansions could be linked to the presence of specific microbial antigens. Data Integration: The aim is to predict post-operative recurrence at M6. Integration of all datasets will explore the ability to predict post-operative recurrence. This will also allow to establish a molecular classification of CD, similar to what is already available in the oncology field. It will also be tried to find regulatory genes of the intestinal mucosa ("hubs"), using causal models (Bayesian networks) and co-expression networks (WCGNA). These findings could help drive potential innovative therapy for the treatment of CD. The comparative analysis of the mucosa-associated transcriptome and microbiome will be performed. This could allow to elucidate the relations between bacteria and the intestinal mucosa, and to uncover pathways implicated in the bacteria-mucosa dialog. The correlations between certain groups of bacteria and the activation of a number of genes will be looked at. And genes known to play a role in the interaction between the microbiome and the mucosa will be specifically studied (MUC, DEF, REG, NOD2, …). Lastly, once the patient genotypes will be available, an analysis of the genome together with the transcriptome and the relationship between genotype, transcriptome, and microbiome will be performed. This analysis should help to robustly identify major pathways involved in intestinal inflammation, study the role played by genetics, and the impact on the gut microbiome. And finally to correlate these results with carefully curated clinical data: relapse/remission, post-operative recurrence, efficacy of post-operative therapies (anti TNF agents, ustekinumab).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Crohn Disease
Keywords
ileo-caecal resection; post-operative recurrence

7. Study Design

Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
Patients aged 18 or more, for whom Crohn's disease diagnosis is confirmed and ileum or ileocecal Crohn's disease require surgical resection. in addition to usual practice, a bio-banking (blood samples, biopsies and surgical specimens) is collected.
Masking
None (Open Label)
Allocation
N/A
Enrollment
575 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Crohn's disease patients
Arm Type
Experimental
Arm Description
Patients aged 18 or more, for whom Crohn's disease diagnosis is confirmed and ileum or ileocecal Crohn's disease require surgical resection. in addition to usual practice, a bio-banking (blood samples, biopsies and surgical specimens) is collected.
Intervention Type
Other
Intervention Name(s)
bio-banking collection
Intervention Description
blood samples, biopsies, and surgical specimen collected in addition to usual practice
Primary Outcome Measure Information:
Title
Ileal Crohn's disease classification
Description
Ileal Crohn's disease classification will be performed using data integration (taking into account clinical data, immunological, genetic, microbiota, transcriptome data). A molecular classification will be possible due to this data integration analysis
Time Frame
surgery time, Time 0
Title
Postoperative recurrence study
Description
Rates of endoscopic recurrence as defined by a Rutgeerts score ≥ 1 in patients will be evaluated at the endoscopic exam
Time Frame
6 months after surgery
Title
Study of Treatments efficacy to prevent recurrence
Description
During a clinical visit, scheduled as usual practice 6 months after surgery, clinical data will be collected : treatment modification or optimization, recurrence occurrence. If treament modification or optimization is needed (clinical symptoms or endoscopic recurrence), or complication occurs (abcess, occlusive syndrom, new surgery), patient will be considered as suffering a long-term relapse
Time Frame
6 months after surgery time
Title
Identification of biomarkers which could predict postoperative recurrence and response to treatments
Description
Identification of biomarkers taking into account clinical data, immunological, genetic, microbiota, transcriptome data
Time Frame
surgery time, Time 0

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
100 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Informed consent obtained before any study-related activities A diagnosis of CD, based on clinical, radiologic, endoscopic, or histological evidence. Men and women ≥18 years of age Required surgical intervention consisting in an ileocecal resection Exclusion Criteria: Previous history of dysplasia or cancer in the ileum or colon Unwillingness or inability to follow the procedures outlined in the protocol Pregnant women
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Matthieu ALLEZ, Pr
Phone
+33(1) 42 49 95 75
Email
Matthieu.allez@aphp.fr
First Name & Middle Initial & Last Name or Official Title & Degree
Philippe SEKSIK, Pr
Phone
+33(1) 49 28 31 62
Email
Philippe.seksik@aphp.fr
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Matthieu ALLEZ, Pr
Organizational Affiliation
Remind
Official's Role
Principal Investigator
Facility Information:
Facility Name
SART Tilman Hospital
City
Liège
Country
Belgium
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Edouard Louis
Facility Name
Amiens Hospital
City
Amiens
ZIP/Postal Code
80054
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Mathurin Fumery, Dr
Facility Name
Haut-levêque Hospital
City
Bordeaux
ZIP/Postal Code
33
Country
France
Individual Site Status
Active, not recruiting
Facility Name
Clermont-Ferrand Hospital
City
Clermont-Ferrand
ZIP/Postal Code
63003
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Anthony Buisson, Dr
Facility Name
Beaujon Hospital
City
Clichy
ZIP/Postal Code
92110
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Xavier Treton, Dr
Facility Name
Henri Mondor Hospital
City
Créteil
Country
France
Individual Site Status
Active, not recruiting
Facility Name
Kremlin-Bicêtre Hospital
City
Le Kremlin-Bicêtre
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Franck Carbonnel
Facility Name
Lille Hospital
City
Lille
ZIP/Postal Code
59037
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Maria Nachury
Facility Name
Hôpital Nord, CHU Marseille
City
Marseille
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Mélanie Serrero
Facility Name
Montpellier Hospital
City
Montpellier
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Guillaume Pineton de Chambrun
Facility Name
Brabois Hospital
City
Nancy
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Laurent PEYRIN-BIROULET
Facility Name
Nantes Hospital
City
Nantes
ZIP/Postal Code
44093
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Arnaud Boureille, Dr
Facility Name
Archet 2 Hospital
City
Nice
ZIP/Postal Code
06202
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jérome Filippi, Dr
Facility Name
Saint Louis Hospital
City
Paris
ZIP/Postal Code
75010
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Matthieu Allez, Pr
Facility Name
Saint Antoine Hospital
City
Paris
ZIP/Postal Code
75012
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Philippe Seksik, Pr
Facility Name
South Lyon Hospital
City
Pierre-Bénite
ZIP/Postal Code
69495
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Stéphane Nancey, Pr
Facility Name
Strasbourg Hospital
City
Strasbourg
Country
France
Individual Site Status
Active, not recruiting

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
31142586
Citation
Sokol H, Brot L, Stefanescu C, Auzolle C, Barnich N, Buisson A, Fumery M, Pariente B, Le Bourhis L, Treton X, Nancey S, Allez M, Seksik P; REMIND Study Group Investigators. Prominence of ileal mucosa-associated microbiota to predict postoperative endoscopic recurrence in Crohn's disease. Gut. 2020 Mar;69(3):462-472. doi: 10.1136/gutjnl-2019-318719. Epub 2019 May 29.
Results Reference
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Citation
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Results Reference
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PubMed Identifier
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Citation
Allez M, Auzolle C, Le Bourhis L, Seksik P. Editorial: predicting recurrence of Crohn's disease after surgical resection-Close to a crystal ball. Authors' reply. Aliment Pharmacol Ther. 2018 Nov;48(10):1157-1158. doi: 10.1111/apt.14998. No abstract available.
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Ileal Crohn's Disease and Post-operative Outcome: Prospective Cohort Study of the REMIND Group

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