2000 breast cancer patients to help Fine-Tune treatment decisions
NCT ID NCT07389408
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study follows 2000 people with early-stage, hormone-sensitive breast cancer to see how doctors decide on treatments, especially when using a test called EndoPredict. The goal is to track long-term outcomes like cancer return and survival over 5 to 10 years. No new treatments are tested—just observation of real-world care.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 2,000 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Apr 2025
- Expected to finish
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Dec 2038
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
All subjects diagnosed with invasive breast cancer, pT1-pT3, with 0 to 3 positive axillary lymph nodes, ER-positive, HER2-negative, that have not received neo-adjuvant chemotherapy and therefore are eligible for EndoPredict® testing.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Age ≥ 18 years old. * Histological diagnosis of invasive breast cancer. * T1-T3 tumor size. * 0-3 positive axillary lymph nodes. * Documented ER-positive tumor by immunohistochemistry (≥1% or Allred Score: ≥3/8 or H-score: ≥50/ 300) * Documented HER2-negative tumor by immunohistochemistry and/or in situ hybridization * Subject with signed and dated informed consent form. Exclusion Criteria: * History of another primary malignancy within the last 5 years, except for resected non-melanoma skin cancer. * Pre-operative chemotherapy administered. * Subject without signed and dated informed consent form.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
13 sites. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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"Apollonio-Theotokos" General Clinic, Department of Surgery
RECRUITINGLarissa, Greece
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"Elena Venizelou" General Hospital, Department of Surgery
RECRUITINGAthens, Greece
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"Prolipsis" Center, Breast Unit
RECRUITINGAthens, Greece
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General Hospital of Trikala, Breast Surfery Dept.
RECRUITINGTrikala, Greece
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Henry Dunant Hospital Center, 3rd Breast Surgical Department
RECRUITINGAthens, Greece
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IASO General Clinic, 2nd Breast Clinic
RECRUITINGMarousi, Greece
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IASO Thessalias General Clinic, Breast Surgery Department
RECRUITINGLarissa, Greece
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Laiko Hospital, National and Kapodistrian University of Athens, Medical School
RECRUITINGAthens, Greece
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MITERA, 1st Breast Clinic
RECRUITINGMarousi, Greece
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Mediterraneo Hospital, Breast Clinic
RECRUITINGAthens, Greece
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Metropolitan General Hospital, 3rd Breast Clinic
RECRUITINGCholargós, Greece
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Metropolitan General Hospital, 4th Breast Clinic
RECRUITINGCholargós, Greece
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Thessaloniki Bioclinic Hospital, Breast Unit
RECRUITINGThessaloniki, Greece
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