Breast Cancer
Conditions
Keywords
Breast cancer, Neo-adjuvant chemotherapy, Proteomic, Histological response
Brief summary
The scope of the trial is to identify proteomic signatures correlated with tumor response to neo-adjuvant chemotherapy.
Interventions
Taken at different times : inclusion, at the cycle 4 and at the cycle 6 during the neoadjuvant chemotherapy
Biopsy at the moment of inclusion, before neoadjuvant chemotherapy
Surgery after neoadjuvant chemotherapy
Sponsors
Study design
Eligibility
Inclusion criteria
* Women aged more than 18 years * Histologically proven breast carcinoma * Neo-adjuvant chemotherapy with anthracyclines and/or taxanes * No prior chemotherapy * Written informed consent
Exclusion criteria
* Metastatic disease
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Proteomic analysis by SELDI-TOF on the tumor biopsy and blood samples Histological response according To Chevallier and Sataloff | 6 months |
Secondary
| Measure | Time frame |
|---|---|
| Correlation with node invasion | 6 months |
| Correlation with basal, luminal phenotypes, HER2 status or hormonal status | 6 months |
| Correlation with the response measured by ultrasound after chemotherapy | After 3 and 5 months |
Countries
France
Contacts
Centre Oscar Lambret