Breast Cancer Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- People who are 18 years of age or older
- People who have been diagnosed with invasive breast cancer, confirmed through a biopsy or surgical sample
- People whose breast cancer can be treated with surgery
- People whose breast cancer is hormone receptor-positive (at least estrogen receptor-positive) and HER2-negative
- People who have already had an Oncotype DX (ODX) test performed on their tumour (a genetic test used to guide treatment decisions)
Who may not be able to join:
- People whose tumour cannot be surgically removed, or who are considered too unwell to safely undergo surgery
- People who have two breast cancers at the same time with different biological characteristics (for example, one hormone receptor-positive/HER2-negative tumour alongside a triple-negative or HER2-positive tumour)
- People who are currently receiving chemotherapy or hormone therapy before surgery (neoadjuvant therapy)
- People whose cancer has spread to more than 4 lymph nodes
- People whose breast cancer has already spread to other parts of the body at the time of diagnosis
- People who have been diagnosed with another cancer in the past 10 years (skin cancers other than melanoma are generally excepted — confirm with trial site)
- People who previously participated in the RxPONDER study in France
- People who have formally declined to participate in the study by submitting a refusal letter to the investigator
- People who do not have the legal capacity to consent to participation in a study
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Elsa CURTIT, Centre Hospitalier Universitaire de Besancon
Phone: +33381219086
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
to evaluate the clinical outcomes represented by iDFS in French early breast cancer patients with Oncotype DX (ODX) Breast Recurrence Score® (RS) results-guided therapy
Can't join this trial?
Data last synced from ClinicalTrials.gov: 26 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.