Clinical trial Recruiting at 1 site Interventional Ages 18 and up Women only

Evaluating Circulating Tumor Cells in Breast Cancer Follow-up

Official title: Evaluation of Circulating Tumor Cells (CTC) Relevance in Breast Cancer Follow-up Using the ScreenCell Device

Run by ScreenCell · NCT06807502 · Data updated 2026-11-12

This study is testing a new way to track cancer cells in the blood of breast cancer patients to see how their condition changes during treatment.

More Breast Cancer Metastatic trials

Quick facts

Study typeInterventional
Ages18 Years and up
SexWomen only
Enrollment93 (estimated)
SponsorScreenCell
Industry-sponsored
Locations1 site (Neuilly-sur-Seine)
StatusRecruiting
StartedFebruary 24, 2025
Main results expectedSeptember 30, 2026
Study endsNovember 30, 2026
Registry record updatedApril 24, 2026
Trial IDNCT06807502 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates include adults aged 18 and older with either metastatic breast cancer or non-metastatic invasive breast cancer who have not yet received treatment.

Probably not a fit

Patients with other types of cancer or those who are pregnant or breastfeeding may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study focuses on the use of liquid biopsy to detect and quantify circulating tumor cells (CTCs) in patients with breast cancer. Utilizing ScreenCell technology, it aims to monitor the evolution of CTCs during the follow-up phase of breast cancer treatment. By identifying and characterizing these cells, the study seeks to provide insights into the stage and molecular characteristics of the cancer. Participants include those with metastatic and non-metastatic breast cancer, as well as healthy volunteers for comparison.

Why it matters

Potential benefit: If successful, this study could enhance the monitoring and management of breast cancer by providing noninvasive insights into tumor progression.

How similar studies have gone: Other studies utilizing liquid biopsy techniques have shown promise in cancer monitoring, suggesting potential success for this approach.

Who can join: the full rules

Show full inclusion / exclusion criteria
INCLUSION CRITERIA

For all participants :

* Female with age greater than or equal to 18 years

For participants with metastatic breast cancer:

\- Patient observed with metastatic breast cancer from the outset or metastatic fall from previously treated breast cancer with change of therapeutic line at the time of inclusion.

For participants with non-metastatic invasive breast cancer:

\- Patient observed with non-metastatic infiltrative breast cancer who had not received any treatment at the time of inclusion (naïve to any treatment)

For healthy volunteers:

* Participant free of any cancer at the time of inclusion, confirmed using a mammogram whose results must be satisfactory, done at the latest two years before inclusion
* Participant with no history of cancer

EXCLUSION CRITERIA

For all participants:

* Male
* Age less than 18 years old
* Refusal to participate or withdrawal of consent
* Pregnant and/or breastfeeding women
* Discovery of a cancerous pathology (other than breast cancer for patients) during participant follow-up.

For healthy volunteers:

* History of cancer
* Detection of CTC (positive profile) during screening

Where it's running

  • CMC Ambroise Paré Hartmann
    Neuilly-sur-Seine, France
    Recruiting

Study contacts

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.