Clinical Study of Nab-paclitaxel Plus Carboplatin Versus Nab-paclitaxel Plus Capecitabine in the Treatment of Advanced Triple-negative Breast Cancer

Who is this study for? Adult women with advanced triple negative breast cancer
Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

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
Participation Requirements
Sex: Female
Minimum Age: 18
Maximum Age: 70
Healthy Volunteers: f
View:

• 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);

• Eastern Cooperative Oncology Group (ECOG) performance status less than or equal to one;

• Patients with life expectancy of at least 3 months;

• Bone marrow function:neutrophils (≥1.5×10\^9/L), platelets (≥100×10\^9/L), hemoglobin (≥90 g/L);

• Renal and hepatic function: Serum creatinine≤ 1.5×institutional upper limit of normal (ULN); AST and ALT ≤ 2.5 × ULN; Total bilirubin≤1.5×ULN, or patients with Gilbert's syndrome ≤ 2.5 × ULN;

• Patients had good compliance with the planned treatment, understood the research process and written informed consent.

Locations
Other Locations
China
The Fourth Hospital of Hebei Medical University
RECRUITING
Shijiazhuang
Contact Information
Primary
Cuizhi Geng, M.D.
gengcuizhi@hotmail.com
0311-6669 6310
Time Frame
Start Date: 2019-11-20
Estimated Completion Date: 2028-09-20
Participants
Target number of participants: 414
Treatments
Experimental: Nab-paclitaxel + Carboplatin
Nab-paclitaxel given IV at 125 mg/m\^2 on days 1, 8 and carboplatin given IV at AUC 5 on days 1 every 21 days x 6 cycles; Maintenance therapy: Capecitabine 1000 mg/m\^2 bid, d1-14; every 21 days, until disease progression or intolerable toxicity;
Experimental: Nab-paclitaxel + Capecitabine
Nab-paclitaxel given IV at 125 mg/m\^2 on days 1, 8 and capecitabine given IV at 1000 mg/m\^2 bid, d1-14 every 21 days x 6 cycles; Maintenance therapy: Capecitabine 1000 mg/m\^2 bid, d1-14; every 21 days, until disease progression or intolerable toxicity;
Related Therapeutic Areas
Sponsors
Collaborators: CSPC Ouyi Pharmaceutical Co., Ltd., Beijing 302 Hospital
Leads: Hebei Medical University Fourth Hospital

This content was sourced from clinicaltrials.gov

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