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Clinical Trials/NCT05038358
NCT05038358
Recruiting
Not Applicable

Tumor Immune Microenvironment Involvement in Colorectal Cancer Chemoresistance Mechanisms: a Patient-derived Tumoroids Prospective Collection From Systemic Treatment Naive Tumors

University Hospital, Grenoble1 site in 1 country60 target enrollmentDecember 12, 2022

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Primary Tumor
Sponsor
University Hospital, Grenoble
Enrollment
60
Locations
1
Primary Endpoint
Percentage of viable organoids for 60 days of culture maintenance.
Status
Recruiting
Last Updated
last year

Overview

Brief Summary

Colorectal cancer is the third most common cancer worldwide and its progression-free survival is still low, around 10 months. Thirthy to 50% of patients do not respond to chemotherapy upon initiation of treatment, suggesting that early development of chemoresistance mechanisms remains a major challenge. In order to better characterize these mechanisms, the aim is to develop a model of tumoroids derived from patients with a colorectal tumors prior to any systemic anti cancer treatment. This project will both allow us to study the role of the immunological microenvironment in chemoresistance and identify new predictive markers of tumor response. It will then serve to develop innovative personalized medicine strategies by targeting the newly identified mechanisms. This study should in fine help to improve the cancer patient's care.

Registry
clinicaltrials.gov
Start Date
December 12, 2022
End Date
December 31, 2030
Last Updated
last year
Study Type
Observational
Sex
All

Investigators

Sponsor
University Hospital, Grenoble
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Male and female over 18 years old.
  • Managed at the CHUGA for a colorectal adenocarcinoma
  • With an indication for immediate surgical resection as part of the care.
  • Patient naive from neo-adjuvant chemotherapy
  • Patient did not object to the CRC-ORGA-2 study

Exclusion Criteria

  • Patients protected by law (pregnant or breastfeeding women, minors, patients under guardianship or trusteeship, persons deprived of their liberty or hospitalized under duress).
  • Patients with positive HIV, HBV, HCV serology.

Outcomes

Primary Outcomes

Percentage of viable organoids for 60 days of culture maintenance.

Time Frame: 60 days of culture maintenance.

Study Sites (1)

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