Metastatic or recurrent breast cancer
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1) Institutional review board (IRB) approval for research and transportation of breast cancer samples 2) Availability to obtain surgical specimen or core needle biopsy sample of breast cancer
Exclusion criteria
Exclusion criteria: 1) Patients not adequate for participation in this study at doctors' discretion. 2) Patients not obtained informed consentnot obtained informed consent
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Correlation between the bio-marker and clinical efficacy, i.e. PFS: progression free survival, of each patient who has participated in SELECT BC trial | — |
Secondary
| Measure | Time frame |
|---|---|
| Correlation between the bio-marker and clinical efficacy, i.e. TTF:Time to Treatment Failure, OS:Overall survival, and DCR:Disease control rate, of each patient who has participated in SELECT BC trial | — |
Countries
Japan
Contacts
Public Health Research Foundation Comprehensive Support Project for Oncology Research