Nab-paclitaxel Based Regimens VS Paclitaxel Based Regimens in Neoadjuvant Treatment for TNBC

Triple Negative Breast Cancer Clinical Trial

Official title:

Albumin Bound (Nab)-Paclitaxel Combined With Carboplatin Versus Paclitaxel Combined With Carboplatin Followed by Epirubicin and Cyclophosphamide as Neoadjuvant Treatment for Participants With Triple Negative Breast Cancer (TNBC)

Clinical Trial Details — Status: Withdrawn

Administrative data

• NCT number: NCT04067102
• Other study ID #: TNBC-NEO
• Status: Withdrawn
• Phase: N/A
• Start date: May 10, 2019
• Est. completion date: May 2026

Study information

• Verified date: July 2021
• Source: Hebei Medical University Fourth Hospital
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

To evaluate the efficacy and safety of P nab-paclitaxel combined with carboplatin versus paclitaxel combined with carboplatin followed by epirubicin and cyclophosphamide in the neoadjuvant treatment of triple negative breast cancer.

Recruitment information / eligibility

• Status: Withdrawn
• Enrollment: 0
• Est. completion date: May 2026
• Est. primary completion date: May 2021
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 18 Years to 70 Years

Eligibility

Inclusion Criteria:

• Female, aged = 18 yrs and =70 yrs;

• Histological confirmation of Unilateral primary invasive breast cancer, cT2-4NanyM0, planning to receive neoadjuvant chemotherapy;

• The expression of ER<10%,PR <10% and Her-2 negative by immunohistochemical, if HER2 expression ++, further FISH test confirmed no amplification of Her-2 gene;

• ECOG performance status 0-1;

• LVEF=55%;

• Bone marrow function: neutrophils = 1.5×109/L, platelets = 100×109/L, hemoglobin = 90 g/L;

• Liver and renal function:Serum creatinine = 1.5x ULN;Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) = 2.5x ULN;Total bilirubin = 1.5x ULN or when patients with Gilbert's syndrome = 2.5x ULN;

• The patient has good compliance with the planned treatment, understands the research process of the study and signs a written informed consent form.

Exclusion Criteria:

• Cytotoxic chemotherapy, endocrine therapy or radiation therapy for any reason;

• New York Heart Association (NYHA) score identifies patients with heart disease above grade II (including grade II);

• Patients with severe systemic infections or other serious illnesses;

• Patients known to be allergic or intolerant to chemotherapeutic drugs or their excipients;

• Combined with other malignant tumors or had malignant tumors other than breast cancer in the past 5 years, except for cervical carcinoma in situ and non-melanoma skin cancer that have been fully treated;

• Women of childbearing age who are pregnant or lactating and who refuse to take appropriate contraceptive measures during the trial;

• Participated in other experimental studies within 30 days before the first dose of study drug administration

• Researchers judged patients who were unsuitable for this study.

Related Conditions & MeSH terms

• Breast Neoplasms
• Triple Negative Breast Cancer
• Triple Negative Breast Neoplasms

Intervention

Drug:
• Albumin bound (nab)-paclitaxel combined with carboplatin followed by epirubicin and cyclophosphamide
Paclitaxel for injection (albumin binding)260mg/m2,I.v., d1;carboplatin AUC=5, I.v., d1; 21 days in one cycle, 4 cycles in total.Continue the protocol when evaluated as CR/PR/SD at the second cycle, Terminate the protocol paclitaxel (albumin binding) combined with carboplatin when evaluated as PD at the second cycle,and use the EC protocol in advance or decide the next treatment
• paclitaxel combined with carboplatin followed by epirubicin and cyclophosphamide
Paclitaxel 175mg/m2, I.v., d1; Carboplatin injection AUC 5, I.v., d1; 21 days in one cycle, 4 cycles in total.Continue the protocol when evaluated as CR/PR/SD at the second cycle, Terminate the protocol paclitaxel (albumin binding) combined with carboplatin when evaluated as PD at the second cycle,and use the EC protocol in advance or decide the next treatment protocol by the researcher

Locations

Country	Name	City	State
China	Fourth Hospital of Hebei Medical University	Shijiazhuang	Hebei

Sponsors (1)

Lead Sponsor	Collaborator
Hebei Medical University Fourth Hospital

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	pathologic complete response(pCR)	pCR is defined as no histologic evidence of invasive tumor cells in the surgical breast specimen, axillary nodes, or sentinel node identified after neoadjuvant chemotherapy (ypT0/Tis ypN0)	6 months
Secondary	Objective Response Rate (ORR)	Percentage of Participants Who Achieve Complete Response (CR) or Partial Response (PR)	3 months
Secondary	Disease-free survival(DFS)	Disease-free survival refers to the time from surgical resection of breast cancer to clinically confirmed local recurrence, distant metastasis, second primary tumor diagnosis, or patient death.	5 years
Secondary	Overall survival(OS)	Overall survival is defined as the length of time from random assignment to death or to last contact.	5 years
Secondary	adverse events(AEs)	AEs are evaluated according to National Cancer Institute Common Terminology Criteria for Adverse Events v4.03.	until 28 days after the last study drug administration