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Predictive Value of Innovative Prognostic Markers (Gut Microbiota, Sarcopenia, Metabolic Syndrome and Obesity) on Surgical and Oncologic Results in the Management of Sporadic Colorectal Adenocarcinoma.

Predictive Value of Innovative Prognostic Markers (Gut Microbiota, Sarcopenia, Metabolic Syndrome and Obesity) on Surgical and Oncologic Results in the Management of Sporadic Colorectal Adenocarcinoma.

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03843905
Acronym
METABIOTE
Enrollment
300
Registered
2019-02-18
Start date
2018-11-15
Completion date
2021-11-15
Last updated
2019-02-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Colorectal Neoplasms, Metabolic Syndrome, Microbiota, Prognosis, Sarcopenia

Keywords

Gut microbiota, Colorectal cancer, Sarcopenia, Metabolic syndrome, Prognostic factors, Pathogenic E.coli

Brief summary

Colorectal cancer (CRC), second leading cause of cancer worldwide, is associated with a poor prognosis, especially in patients with advanced disease. Therefore, there is still a need to develop new prognostic tools to replace or supplement those routinely used, with the aim to optimize treatment strategies. Studies on gut microbiota composition provide new strategies to identify powerful biomarkers. Indeed, beyond its beneficial functions for the host, increasing evidences suggest that gut microbiota is a key factor involved in CRC carcinogenesis. Many clinical studies have described an imbalance in the gut microbiota (dysbiosis) in CRC patients, with the emergence of pathogenic bacterial species, Recent studies reported that pks-positive E. coli, a pathogenic bacterial producing toxin encoded by the pks genomic island, is more frequently detected in CRC patients, suggesting a possible role in tumor development. Therefore, this suggests the potential use of microbial signatures associated with CRC for prognostic assessment. Furthermore, influence of body composition profile (BMI, sarcopenia, metabolic syndrome) also appears to be a new relevant prognostic tool regarding surgical and oncological outcomes following CRC surgery. The aim of this translational research project is to study the impact of these new prognostic tools on surgical and oncologic results in a prospective cohort of patients who underwent CRC surgery at the Digestive Surgery Department of the University Hospital of Clermont-Ferrand (France). This could allow to optimize treatment strategies and provide new ways to identify news promising biomarkers associations in order to better define high risk patients. Investigators aim to identify specific microbial signatures associated with some metabolic profiles in order to improve surgical morbidity and/or response to cancer therapies.

Detailed description

The METABIOTE study will be systematically proposed to patients selected for sporadic CRC surgery during the first preoperative outpatient visit. The attending surgeon will double-check all inclusion and exclusion criteria. An oral and written information will be given to patients, presenting the study. Then, the following data will be collected propectively: * Socio-demographic and medical data (personal and familial medical history, current treatments, comorbidities, allergies, Body Mass Index (BMI), ASA score…) * Blood tests results, including nutritional, hepatic assessment and exploration of a lipidic abnormality. * Body composition profile: Metabolic syndrome screening, BMI, waist circumference, sarcopenia (skeletal muscle index calculation on CT scan). * Thoraco-abdomino-pelvic CT scan: sarcopenia, hepatic and splenic density, thanks to a dedicated software (Slice-O-Matic). Following surgery will be collected : * Pathological data (TNM stage, MSI, RAS and BRAF status…) * Surgical results (30-day postoperative medical and surgical morbidity and 90-day postoperative mortality) * Oncologic results (Overall survival, Disease free survival…) * Metabolic profile evolution: sarcopenia (SMI), BMI and waist circumference after 3, 6, 12 and 36 months, postoperatively. Intraoperatively, samples of peritumoral mucosa and tumor specimen and rectal stools will be frozen (-80°) and moved to the research unit for microbiota analysis. Interest bacteria will be grown on selective gelosis and pathogenic E coli will be identified using PCR as well as other specific bacteria involved in CRC. Moreover, global microbiota modifications will be observed using high-throughput sequencing of the bacterial 16S rRNA gene. These data will be associated with body composition profile, clinical data, surgical and oncologic results, and pathological data thanks to a multivariate analysis. The patients will be monitored according to the Digestive Oncology french recommendations (TNCD).

Interventions

OTHERno intervention

The aim of this translational research project is to study the impact of these new prognostic tools on surgical and oncologic results in a prospective cohort of patients who underwent CRC surgery at the Digestive Surgery Department of the University Hospital of Clermont-Ferrand (France)

Sponsors

M2iSH laboratory
CollaboratorOTHER
Benoit Chassaing
CollaboratorUNKNOWN
University Hospital, Clermont-Ferrand
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* \- Male or female, age \> to 18 years. * Histologically proven colonic or high rectal adenocarcinoma * Absence of metastasis (CT scan) in exams performed preoperatively * No history of other tumors * Patients for whom the social and psychological status, the general condition are able to be monitored and/or compliant with the requirements of the study * Signed and dated informed consent document

Exclusion criteria

* \- \< 18 years, patient in legal incapacity (person deprived of liberty or under guardianship). * Antibiotic administration within the 2 months before surgery * Long-term probiotic oral intake * Inflammatory bowel disease (Crohn's disease, ulcerative colitis) * Preoperative bowel preparation (oral or rectal) inclued antibiotic and/or antiseptic preparation. * Metastatic disease * Genetic CRC : familial adenomatous polyposis, hereditary non polyposis colorectal cancers (HNPCC). * Patient requiring preoperative radio-chemotherapy or chemotherapy alone * Medical history of cancer

Design outcomes

Primary

MeasureTime frameDescription
Overall survival (OS)at 5 yearsdefined by the time between surgery and last follow-up. The 5 years overall survival will be recorded.

Secondary

MeasureTime frameDescription
Disease free survival (DFS)at 1, 3 and 5 yearstime between surgery and first identified recurrence. The1-3- and 5 years disease-free survivals will be recorded
post-operative morbidityat 30 daysincidence of postoperative complications (medical and surgical) according to the Clavien-Dindo classification occurring during the hospital stay and up-to 30-day after surgery will be recorded from the audit database
length of hospital stayat 3 monthslength of hospital stay includes length of stay in Intensive Care unit and Conventional Hospital Unit.
Overall survival related to CRCat 1, 3 and 5 yearstime between surgery and last follow-up. The1-3- and 5 years overall survivals will be recorded
evolution of sarcopeniaat 3,6, 12 and 36 monthsevolution of skeletal muscle index (SMI) identified from pretreatment and oncology follow-up computed tomography scans
evolution Body Mass Index (BMI)at 3,6,12 and 36 monthsevolution Body Mass Index (BMI) defined during postoperative oncologic follow up clinical consultations (weight measurement)
Microbiota compositionduring surgerycomposition of the microbiota according to the sampling site (stools, Peritumoral mucosa and tumor)
postoperative mortalityat 90 dayspostoperative death until 90 days after surgery

Countries

France

Contacts

Primary ContactLise LACLAUTRE
drci@chu-clermontferrand.fr0473754963

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 19, 2026