About this trial
This is a multi-center , open-lable clinical trial. Triple-negative breast cancer (TNBC) is a term applied to breast cancer cases that have \<1% expression of the estrogen receptor (ER) and the progesterone receptor (PR) and do not over express HER2. TNBC is diagnosed in 15-20% of breast cancer cases and tends to occur in younger women and have biologically more aggressive high grade disease.
The purpose of this study is to assess the efficacy and safety of the following two combinations: i) nab-paclitaxel+carboplatin; ii) nab-paclitaxel+capecitabine in subjects with advanced TNBC and up to one prior line of systemic treatment for metastatic disease. Maintenance therapy with capecitabine after completion of combination chemotherapy.
Eligibility criteria
Qualifiers
Females with age between 18 to 70 years old;
Histologically confirmed triple negative breast cancer;
No more than one-line prior treatment for locally advanced or metastatic breast cancer;
Have at least one measurable lesion as per the RECIST criteria (version 1.1);
Disqualifiers
Patients with heart disease above grade II (including grade II) identified by New York Heart Association (NYHA) scores;
Brain metastasis;
Recurrence or metastasis within 6 months after capecitabine withdrawal;
Recurrence or metastasis within 6 months after platinum withdrawal;
Trial design
Treatments tested in this trial
- Nab-paclitaxel + Carboplatin
- Nab-paclitaxel + Capecitabine
Treatment groups
Sponsors and collaborators
Hebei Medical University Fourth Hospital
Lead sponsor
Beijing 302 Hospital
Collaborator
CSPC Ouyi Pharmaceutical Co., Ltd.
Collaborator