Predictive Clinical and Biological Parameters in Breast Cancer (BC-BIO)
Primary Purpose
Breast Cancer
Status
Recruiting
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
molecular alteration
Sponsored by

About this trial
This is an interventional basic science trial for Breast Cancer focused on measuring breast cancer
Eligibility Criteria
Inclusion Criteria:
- breast cancer
- age > 18
- signed informed consent
Exclusion Criteria:
- emergency
Sites / Locations
- Institut Paoli CalmettesRecruiting
- Hôpital Sainte-MusseRecruiting
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
breast cancer
Arm Description
blood and tumor sample
Outcomes
Primary Outcome Measures
molecular alteration in breast cancer
gene expression level
Secondary Outcome Measures
relation between molecular alteration and clinical and histological characteristics
hazard ratio between molecular alteration and clinical and histological characteristics
Full Information
NCT ID
NCT01521676
First Posted
December 22, 2011
Last Updated
September 1, 2017
Sponsor
Institut Paoli-Calmettes
1. Study Identification
Unique Protocol Identification Number
NCT01521676
Brief Title
Predictive Clinical and Biological Parameters in Breast Cancer
Acronym
BC-BIO
Official Title
Research of Predictive Clinical and Biological Parameters in Breast Cancer
Study Type
Interventional
2. Study Status
Record Verification Date
September 2017
Overall Recruitment Status
Recruiting
Study Start Date
December 2010 (undefined)
Primary Completion Date
December 2019 (Anticipated)
Study Completion Date
December 2029 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Institut Paoli-Calmettes
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Research of predictive clinical and biological factors in breast cancer :
genomic, proteomic, mutation
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Breast Cancer
Keywords
breast cancer
7. Study Design
Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
750 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
breast cancer
Arm Type
Experimental
Arm Description
blood and tumor sample
Intervention Type
Genetic
Intervention Name(s)
molecular alteration
Intervention Description
research of molecular alteration
Primary Outcome Measure Information:
Title
molecular alteration in breast cancer
Description
gene expression level
Time Frame
average of 4 weeks after diagnosis
Secondary Outcome Measure Information:
Title
relation between molecular alteration and clinical and histological characteristics
Description
hazard ratio between molecular alteration and clinical and histological characteristics
Time Frame
up to 3 years
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
breast cancer
age > 18
signed informed consent
Exclusion Criteria:
emergency
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Dominique GENRE, MD
Phone
33491223778
Email
drci.up@ipc.unicancer.fr
First Name & Middle Initial & Last Name or Official Title & Degree
Jihane PAKRADOUNI, PharmD PhD
Phone
33491223778
Email
drci.up@ipc.unicancer.fr
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Carole TARPIN, MD
Organizational Affiliation
Institut Paoli-Calmettes
Official's Role
Principal Investigator
Facility Information:
Facility Name
Institut Paoli Calmettes
City
Marseille
ZIP/Postal Code
13009
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Carole TARPIN, MD
Phone
33491223778
Email
drci.up@ipc.unicancer.fr
First Name & Middle Initial & Last Name & Degree
Carole TARPIN, MD
Facility Name
Hôpital Sainte-Musse
City
Toulon
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Frédéric VIRET, MD
Email
frederic.viret@ch-toulon.fr
12. IPD Sharing Statement
Citations:
PubMed Identifier
27765906
Citation
Goncalves A, Bertucci F, Guille A, Garnier S, Adelaide J, Carbuccia N, Cabaud O, Finetti P, Brunelle S, Piana G, Tomassin-Piana J, Paciencia M, Lambaudie E, Popovici C, Sabatier R, Tarpin C, Provansal M, Extra JM, Eisinger F, Sobol H, Viens P, Lopez M, Ginestier C, Charafe-Jauffret E, Chaffanet M, Birnbaum D. Targeted NGS, array-CGH, and patient-derived tumor xenografts for precision medicine in advanced breast cancer: a single-center prospective study. Oncotarget. 2016 Nov 29;7(48):79428-79441. doi: 10.18632/oncotarget.12714.
Results Reference
derived
Links:
URL
http://www.institutpaolicalmettes.fr
Description
official web site of the sponsor
Learn more about this trial
Predictive Clinical and Biological Parameters in Breast Cancer
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