- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02893761
Bergonie Institute Breast Cancer Database
September 22, 2025 updated by: Institut Bergonié
A database of breast cancer patients was established at Institute Bergonié since the 90s , to assess patients' survival, assess practice, search for prognostic factors.
Study Overview
Status
Recruiting
Conditions
Study Type
Observational
Enrollment (Estimated)
30000
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Gaetan Mac Grogan, MD
- Phone Number: + 33 5 56 33 33 33
- Email: g.macgrogan@bordeaux.unicancer.fr
Study Contact Backup
- Name: Simone Mathoulin-Pélissier, MD PhD
Study Locations
-
-
-
Bordeaux, France
- Recruiting
- Institut Bergonié, Comprehensive Cancer Center
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
Patient with breast cancer treated at Bergonie Institute
Description
Inclusion Criteria:
- Breast cancer
- Aged 18 years and over
- First treatment at Bergonie Institute
Exclusion Criteria:
-
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Distant metastasis-free survival at 5 years
Time Frame: 5 years
|
5 years
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Distant disease-free survival
Time Frame: 10 years
|
D-DFS, distant disease-free survival, as defined following DATECAN guidelines (Gourgou et al.
Annals Oncol 2015).
D-DFS is defined as the time to death or appearance/occurrence of metastases/distant recurrence, whichever occurs first
|
10 years
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Gaetan Mac Grogan, MD, Institut Bergonie
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Lhenaff M, Tunon de Lara C, Fournier M, Charitansky H, Brouste V, Mathoulin-Pelissier S, Pinsolles V, Rousvoal A, Bussieres E, Chassaigne F, Croce S, Ben Rejeb H, MacGrogan G. A single-center study on total mastectomy versus skin-sparing mastectomy in case of pure ductal carcinoma in situ of the breast. Eur J Surg Oncol. 2019 Jun;45(6):950-955. doi: 10.1016/j.ejso.2019.01.014. Epub 2019 Jan 17.
- de Mascarel I, MacGrogan G, Debled M, Sierankowski G, Brouste V, Mathoulin-Pelissier S, Mauriac L. D2-40 in breast cancer: should we detect more vascular emboli? Mod Pathol. 2009 Feb;22(2):216-22. doi: 10.1038/modpathol.2008.151. Epub 2008 Sep 26.
- de Mascarel I, Debled M, Brouste V, Mauriac L, Sierankowski G, Velasco V, Croce S, Chibon F, Boudeau J, Debant A, MacGrogan G. Comprehensive prognostic analysis in breast cancer integrating clinical, tumoral, micro-environmental and immunohistochemical criteria. Springerplus. 2015 Sep 21;4:528. doi: 10.1186/s40064-015-1297-8. eCollection 2015.
- Ragage F, Debled M, MacGrogan G, Brouste V, Desrousseaux M, Soubeyran I, de Lara CT, Mauriac L, de Mascarel I. Is it useful to detect lymphovascular invasion in lymph node-positive patients with primary operable breast cancer? Cancer. 2010 Jul 1;116(13):3093-101. doi: 10.1002/cncr.25137.
- Morgat C, MacGrogan G, Brouste V, Velasco V, Sevenet N, Bonnefoi H, Fernandez P, Debled M, Hindie E. Expression of Gastrin-Releasing Peptide Receptor in Breast Cancer and Its Association with Pathologic, Biologic, and Clinical Parameters: A Study of 1,432 Primary Tumors. J Nucl Med. 2017 Sep;58(9):1401-1407. doi: 10.2967/jnumed.116.188011. Epub 2017 Mar 9.
- Mazroui Y, Mauguen A, Mathoulin-Pelissier S, MacGrogan G, Brouste V, Rondeau V. Time-varying coefficients in a multivariate frailty model: Application to breast cancer recurrences of several types and death. Lifetime Data Anal. 2016 Apr;22(2):191-215. doi: 10.1007/s10985-015-9327-y. Epub 2015 May 6.
- Debled M, Auxepaules G, de Lara CT, Garbay D, Brouste V, Bussieres E, Mauriac L, MacGrogan G. Neoadjuvant endocrine treatment in breast cancer: analysis of daily practice in large cancer center to facilitate decision making. Am J Surg. 2014 Nov;208(5):756-763. doi: 10.1016/j.amjsurg.2013.12.032. Epub 2014 Apr 3.
- Jones N, Gros A, Velasco V, Dapremont V, Brouste V, Gastaldello B, Debled M, Tunon de Lara C, Bonnet F, Barouk-Simonet E, Bubien V, Venat L, MacGrogan G, Longy M, Sevenet N. PTEN alterations in sporadic and BRCA1-associated triple negative breast carcinomas. Cancer Genet. 2022 Jun;264-265:8-15. doi: 10.1016/j.cancergen.2022.02.008. Epub 2022 Feb 25.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
January 1, 1990
Primary Completion (Estimated)
December 1, 2030
Study Completion (Estimated)
December 1, 2050
Study Registration Dates
First Submitted
August 18, 2016
First Submitted That Met QC Criteria
September 2, 2016
First Posted (Estimated)
September 8, 2016
Study Record Updates
Last Update Posted (Estimated)
September 23, 2025
Last Update Submitted That Met QC Criteria
September 22, 2025
Last Verified
September 1, 2025
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- IB BASE SEIN
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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