Operable breast cancer(stage I-III)
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1)Clinical trial(s) started after July 2010. 2)Principal investigator(s) in each trial agree with participation in this study. 3)Abraxane-containing regimen was used for neoadjuvant chemotherapy in naive operable breast cancer patients. 4)Registered in UMIN with ethical review. 5)Clinical trials in which more than 10 patients participated. 6)Clinical trials that have already been completed (unpublished data are available). 7)To submit the data, each researcher was authorized by each research ethics committee.
Exclusion criteria
Exclusion criteria: Patients who are unwilling to participate in this study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| pCR: pathological complete response | — |
Secondary
| Measure | Time frame |
|---|---|
| Adverse events(>=G3) RDI(Relative dose intensity for Abraxane) | — |
Countries
Japan,Asia(except Japan)
Contacts
Japan Breast Cancer Research Group (JBCRG) Head office