EichorEICHOR
Study identifier: NCT07106632 Synced from ClinicalTrials.gov · August 02, 2026
● Recruiting

Optimising Adjuvant Chemotherapy Prescription in Young Patients With Hormone-dependent Breast Cancer Using Genomic Tests

Condition: Early Breast Cancer · Premenopausal Breast Cancer · HR+/HER2- Breast Cancer  ·  Sponsor: UNICANCER

PhasePhase 3
Planned participants3380
Who can joinFemale, 35 Years to 45 Years
Healthy volunteersNo

About this study

Rationale: Around 70 to 80% of breast cancers are so-called "hormone-dependent" (HR+)/HER2-. For more than 50 years, studies have shown that chemotherapy and optimised hormonal treatments (hormone therapy), including a drug associated with ovarian suppression (OFS), improve survival in patients with these cancers, which are characterised by a high risk of relapse. However, younger patients suffer more side effects than older women, particularly from chemotherapy. This can affect their quality of life and reduce their ability to work. For post-menopausal women, genetic tests exist to assess whether chemotherapy is really necessary in addition to hormonal treatment. However, for high-risk premenopausal patients, chemotherapy is still systematically recommended, as no study has proved that it can be safely avoided. Clinical trials based on risk stratification using genetic tests have not been conclusive, but the majority of premenopausal women included had not received optimal hormone treatment. It is possible that the beneficial effect of chemotherapy is partly due to the artificial menopause it induces. Some experts believe that, for patients with a high clinical risk but a low genetic risk, an optimised hormonal treatment (drug + OFS) could suffice, without the need for chemotherapy. Objectives: Main objective: The aim of the study is to determine whether the use of a genetic test (Prosigna®) to decide whether or not to administer chemotherapy produces results as good as …

This description comes directly from the study's public registry record.

Talk to the study team

Aure Vanhecke  ·  +33662962532  ·  a-vanhecke@unicancer.fr

Vanhecke

Always discuss trial participation with your own doctor first.

Locations (105)

Institut Jules BordetBrussels, BelgiumNot Yet Recruiting
Cliniques Universitaires Saint-LucBrussels, BelgiumNot Yet Recruiting
Grand Hôpital de CharleroiCharleroi, BelgiumNot Yet Recruiting
CHU Helora Hôpital de La Louvière - Site JolimontHaine-Saint-Paul, BelgiumNot Yet Recruiting
CHU UCL Namur - Site Sainte ElisabethNamur, BelgiumNot Yet Recruiting
Clinique Saint PierreOttignies, BelgiumNot Yet Recruiting
CHR VerviersVerviers, BelgiumNot Yet Recruiting
Centre Hospitalier d'AuxerreAuxerre, FranceRecruiting
Sainte Catherine - Institut du Cancer Avignon-ProvenceAvignon, FranceRecruiting
Centre Hospitalier de la Côte BasqueBayonne, FranceNot Yet Recruiting
Centre Hospitalier Simone Veil de BeauvaisBeauvais, FranceRecruiting
Hôpital de BloisBlois, FranceNot Yet Recruiting

+ 93 more locations — full list on the registry record.

Follow this study

Save your interest here for when the public record changes — results posted, or the study's status changes. Email alerts for this study aren't switched on yet.

We keep this only about this public record, and never email you without alerts being switched on. Want it removed at any time? Email hello@eichor.com. Never medical advice. By subscribing you agree to our Terms of Use and Privacy Policy.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →