TRIPLEX: Establishment of an ex Vivo Tumor Collection of Triple-negative Breast Cancers in Order to Validate the Interest of Innovative Therapies and the Search for Predictive Biomarkers of Response to Treatment

Sponsor
Centre Francois Baclesse (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05404321
Collaborator
(none)
163
1
50
3.3

Study Details

Study Description

Brief Summary

Initially described in 2009 on LGR5 positive stem cells from intestine, organoids correspond to a 3D cell culture that preserves the organization and part of the initial function of the organ from which the cells were derived. They use the proliferation and differentiation properties of stem cells cultured in a three-dimensional matrix.

These principles have been adapted to many human organs, including the breast. These culture conditions have thus allowed the establishment of cancer organoid lines that have the advantages of rapid amplification, a high rate of establishment success and unlimited proliferation potential. They are transfectable and cryopreservable. They are very close morphologically and genetically to the tumor from which they derive. Very recently, the in vivo response of orthotopic xenograft models of breast cancer organoids has been correlated to the in vitro response of these same organoids. In addition, the in vitro response of various of these models to PARP inhibitors was linked to the presence of the BRCA1/2 mutant signature, highlighting the potential of these models to predict patient response to these treatments.

Furthermore, one study demonstrated the value of using organoids derived from metastatic gastrointestinal tumors to predict patient response to cancer treatments (100% sensitivity, 93% specificity, 88% positive predictive value, and 100% negative predictive value.

Condition or Disease Intervention/Treatment Phase
  • Other: Establishment of ex vivo breast cancer organoid models

Study Design

Study Type:
Observational
Anticipated Enrollment :
163 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Establishment of an ex Vivo Tumor Collection of Triple-negative Breast Cancers in Order to Validate the Interest of Innovative Therapies and the Search for Predictive Biomarkers of Response to Treatment
Anticipated Study Start Date :
Oct 1, 2022
Anticipated Primary Completion Date :
Jun 1, 2026
Anticipated Study Completion Date :
Dec 1, 2026

Arms and Interventions

Arm Intervention/Treatment
Patient with early stage triple negative breast cancer

Other: Establishment of ex vivo breast cancer organoid models
This study includes 2 steps: The constitution of a collection of tumor and blood samples and the analysis of the ex vivo response of the tumor samples to the treatments for the development of functional tests and the research of predictive biomarkers of this response

Outcome Measures

Primary Outcome Measures

  1. Rate of establishment of exploitable organoids tumor [4 years]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Patient over 18 years of age

  • Patient with early stage (I-III) triple negative breast cancer who needs to have clips placed before neoadjuvant chemotherapy

  • Patient affiliated to a social security system

  • Proficiency in French language,

  • Patient having signed the consent to participate in the study.

Exclusion Criteria:
  • Pregnant women

  • Persons deprived of liberty or under guardianship (including curatorship)

  • History of any other clinically active malignancy in the last 5 years prior to inclusion

Contacts and Locations

Locations

Site City State Country Postal Code
1 Centre François Baclesse Caen France 14076

Sponsors and Collaborators

  • Centre Francois Baclesse

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Centre Francois Baclesse
ClinicalTrials.gov Identifier:
NCT05404321
Other Study ID Numbers:
  • 2021-A02676-35
First Posted:
Jun 3, 2022
Last Update Posted:
Aug 10, 2022
Last Verified:
May 1, 2022
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 10, 2022