Observational study on Olaparib treatment for early breast cancer in France
REBECCA Real-world Early BrEast CanCer mAnagement REBECCA. a French National Multicentric Real-world Study of Early Breast Cancer Patients
This study is looking at how well patients with early HER2-negative breast cancer in France stick to their Olaparib treatment and what their outcomes are.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 126 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | AstraZeneca Industry-sponsored |
| Locations | 58 sites (Clermont-Ferrand, Auvergne-Rh ne-Alpes and 57 other locations) |
| Trial ID | NCT06856343 on ClinicalTrials.gov |
What this trial studies
This observational study aims to evaluate the completion rates of adjuvant Olaparib treatment among patients with HER2-negative early breast cancer in France. It involves a multicenter prospective cohort of patients who are about to start treatment at their physician's discretion. The study will collect data on patient outcomes and treatment adherence to better understand the real-world effectiveness of Olaparib in this population.
Who should consider this trial
Good fit: Ideal candidates are adults aged 18 and older diagnosed with HER2-negative early breast cancer who are about to begin adjuvant Olaparib treatment.
Not a fit: Patients who do not consent to participate or are enrolled in the Early Access Program may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could provide insights into the effectiveness and adherence to Olaparib treatment, potentially improving management strategies for early breast cancer patients.
How similar studies have performed: While this study focuses on a specific treatment in a real-world setting, similar observational studies have shown success in evaluating treatment adherence and outcomes in cancer care.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Male or female aged ≥ 18 years * Patient diagnosed with HER2-negative eBC * Patient about to be initiated with adjuvant Olaparib at their physician's discretion * Patient has been informed and does not object to participation in the study. Exclusion Criteria: * Patient not consenting to participate. * Patients included in the Early Access Program
Where this trial is running
Clermont-Ferrand, Auvergne-Rh ne-Alpes and 57 other locations
- Research Site — Clermont-Ferrand, Auvergne-Rh ne-Alpes, France (Recruiting)
- Research Site — Gleizé, Auvergne-Rh ne-Alpes, France (Recruiting)
- Research Site — Grenoble, Auvergne-Rh ne-Alpes, France (Not_yet_recruiting)
- Research Site — Lyon, Auvergne-Rh ne-Alpes, France (Recruiting)
- Research Site — Metz-Tessy, Auvergne-Rh ne-Alpes, France (Recruiting)
- Research Site — Saint-Etienne, Auvergne-Rh ne-Alpes, France (Not_yet_recruiting)
- Research Site — Saint-Priest-en-Jarez, Auvergne-Rh ne-Alpes, France (Not_yet_recruiting)
- Research Site — Thonon-les-Bains, Auvergne-Rh ne-Alpes, France (Recruiting)
- Research Site — Valence, Auvergne-Rh ne-Alpes, France (Recruiting)
- Research Site — Valence, Auvergne-Rh ne-Alpes, France (Not_yet_recruiting)
- Research Site — Dijon, Bourgogne-Franche-Comt, France (Not_yet_recruiting)
- Research Site — Plérin, Brittany Region, France (Recruiting)
- Research Site — Rennes, Brittany Region, France (Not_yet_recruiting)
- Research Site — Saint-Brieuc, Brittany Region, France (Not_yet_recruiting)
- Research Site — Saint-Grégoire, Brittany Region, France (Recruiting)
- Research Site — Chambray-lès-Tours, Centre-Val de Loire, France (Recruiting)
- Research Site — Saint-Doulchard, Centre-Val de Loire, France (Recruiting)
- Research Site — Bezannes, Grand Est, France (Recruiting)
- Research Site — Haguenau, Grand Est, France (Not_yet_recruiting)
- Research Site — Nancy, Grand Est, France (Recruiting)
- Research Site — Beauvais, Hauts-de-France, France (Recruiting)
- Research Site — Beuvry, Hauts-de-France, France (Recruiting)
- Research Site — Compiègne, Hauts-de-France, France (Not_yet_recruiting)
- Research Site — Creil, Hauts-de-France, France (Not_yet_recruiting)
- Research Site — Dechy, Hauts-de-France, France (Recruiting)
- Research Site — Lille, Hauts-de-France, France (Not_yet_recruiting)
- Research Site — Lille, Hauts-de-France, France (Not_yet_recruiting)
- Research Site — Saint-Martin-Boulogne, Hauts-de-France, France (Not_yet_recruiting)
- Research Site — Salouël, Hauts-de-France, France (Recruiting)
- Research Site — Saint-Pierre-des-Corps, La R Union, France (Not_yet_recruiting)
- Research Site — FORT de France Cedex, Martinique, France (Not_yet_recruiting)
- Research Site — Agen, New Aquitaine, France (Not_yet_recruiting)
- Research Site — Libourne, New Aquitaine, France (Not_yet_recruiting)
- Research Site — Limoges, New Aquitaine, France (Not_yet_recruiting)
- Research Site — Périgueux, New Aquitaine, France (Recruiting)
- Research Site — Poitiers, New Aquitaine, France (Recruiting)
- Research Site — Caen, Normandy, France (Recruiting)
- Research Site — Rouen, Normandy, France (Recruiting)
- Research Site — Béziers, Occitanie, France (Not_yet_recruiting)
- Research Site — Montpellier, Occitanie, France (Recruiting)
- Research Site — Montpellier, Occitanie, France (Recruiting)
- Research Site — Nîmes, Occitanie, France (Recruiting)
- Research Site — Perpignan, Occitanie, France (Recruiting)
- Research Site — Toulouse, Occitanie, France (Recruiting)
- Research Site — Nantes, Pays de la Loire Region, France (Not_yet_recruiting)
- Research Site — Avignon, Provence-Alpes-C Te d'Azur, France (Not_yet_recruiting)
- Research Site — Fréjus, Provence-Alpes-C Te d'Azur, France (Not_yet_recruiting)
- Research Site — Marseille, Provence-Alpes-C Te d'Azur, France (Not_yet_recruiting)
- Research Site — Nice, Provence-Alpes-C Te d'Azur, France (Not_yet_recruiting)
- Research Site — Argenteuil, Île-de-France Region, France (Not_yet_recruiting)
+8 more sites — see ClinicalTrials.gov for the full list.
Study contacts
- Study coordinator: AstraZeneca Clinical Study Information Center
- Email: information.center@astrazeneca.com
- Phone: 1-877-240-9479
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.