Are CK+/CD45+ Double-Positive Circulating Cells of Tumor-origin? Characterization in METAstatic Breast Cancer

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

A prospective, single-centre, proof-of-concept pilot study in patients with metastatic breast cancers (MBC) (whatever the immunohistochemical subtype) treated at the IUCT-O. Eligible patients will be selected and informed of this study during a medical consultation for cancer that has metastasised, has relapsed or is progressing metastatically, by medical oncologists at the Oncopole Claudius Regaud (OCR). Then, with the patient's agreement and before the start of anti-tumour treatment, a blood sample will be taken to detect DP-circulating cells. A breast cancer tumour sample (non-bone metastasis or, failing that, primary tumour) must be available (FFPE archived tumour block). Each patient will participate in the study for one day. 60 patients will be included in this interventional study.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Patients with metastatic breast cancer eligible for 1st, 2nd or 3rd line treatment at stage IV, regardless of immunohistochemical subtype (triple-negative, RH+/HER2-negative or HER2-positive).

• Patient with metastatic disease or metastatic relapse or progression who has not yet started 1st line treatment for metastatic disease or line 2 or line 3.

• Tumour sample available (archived tumour block): non-bone metastasis preferred if available or, failing this, primary breast tumour.

• Age ≥ 18 years and WHO ≤ 2.

• Patient affiliated to a French Social Security scheme.

• Patient having signed his/her informed consent prior to inclusion in the study and prior to any specific procedure for the study.

Locations
Other Locations
France
IUCT-O
RECRUITING
Toulouse
Contact Information
Primary
Florence DALENC
dalenc.florence@iuct-oncopole.fr
05 31 15 51 04
Backup
Vincent NICOLAI
nicolai.vincent@iuct-oncopole.fr
05 31 15 51 22
Time Frame
Start Date: 2024-06-25
Estimated Completion Date: 2025-10
Participants
Target number of participants: 60
Treatments
Other: Patients with MBC
Related Therapeutic Areas
Sponsors
Collaborators: Fondation Toulouse Cancer Santé
Leads: Institut Claudius Regaud

This content was sourced from clinicaltrials.gov