First-line Nab-paclitaxel Plus Cisplatin Plus Carilizumab in mTNBC Patients
Primary Purpose
Breast Cancer
Status
Recruiting
Phase
Phase 2
Locations
China
Study Type
Interventional
Intervention
nab-paclitaxel plus cisplatin plus carilizumab (AP+PD-1)
Sponsored by
About this trial
This is an interventional treatment trial for Breast Cancer
Eligibility Criteria
Inclusion Criteria:
- Female patients aged 18-70 years who had
- Metastatic TNBC. ER, PgR, and HER2 status were determined locally by immunohistochemistry (IHC) of patient primary or metastatic tumor sections. Metastatic disease was confirmed by clinical, imaging, histological or cytological measures.
- Patients were required to receive no previous chemotherapy or targeted therapy for metastatic triple-negative breast cancer.
- Patients who had received adjuvant/neoadjuvant therapy were required an interval for at least 6 months after stop of chemotherapy before the enrollment.
- At least one measurable lesion according to RECIST 1.1,
- ECOG performance status ≤ 1
- Life expectancy of more than 12 weeks
- Adequate organ and bone marrow function.
Exclusion Criteria:
- Patient of childbearing potential but unwilling to receive contraception.
- Radiation therapy of axial bone within 4 weeks before enrollment.
- Previous treatment with PD-1 antibody, PD-L1 antibody and CTLA-4 antibody.
- Patients have active autoimmune diseases.
- Patients who need systemic corticosteroids (> 10 mg prednisone/d) or other immunosuppressive drugs within 14 days before enrollment or during the study period.
- Symptomatic central nervous system (CNS) disease (patients with asymptomatic treated CNS metastases were permitted)
- Other malignant diseases within the past 5 years (patients with basal cell skin carcinoma and cervical carcinoma in situ were permitted)
- Uncontrolled infection.
Sites / Locations
- Fudan University Shanghai Cancer CenterRecruiting
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
nab-paclitaxel plus cisplatin plus carilizumab (AP+PD-1)
Arm Description
Nab-paclitaxel 125 mg/m2,ivgtt,d1, 8 Cisplatin 75 mg/m2,ivgtt,d1 Carilizumab 200mg, ivgtt,d1,q2w
Outcomes
Primary Outcome Measures
PFS
Progression free survival
Adverse events
Number of participants with treatment-related adverse events as assessed by Common Terminology Criteria for Adverse Events version 4.0 (CTCAE v4.0)
Secondary Outcome Measures
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT04537286
Brief Title
First-line Nab-paclitaxel Plus Cisplatin Plus Carilizumab in mTNBC Patients
Official Title
A Prospective, Single-arm, Open-Label, Phase II Study of Nab-paclitaxel Plus Cisplatin Plus Carilizumab as First-line Treatment in Patients With Metastatic Triple-negative Breast Cancer
Study Type
Interventional
2. Study Status
Record Verification Date
February 2023
Overall Recruitment Status
Recruiting
Study Start Date
August 25, 2020 (Actual)
Primary Completion Date
September 15, 2023 (Anticipated)
Study Completion Date
October 15, 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Fudan University
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
To evaluate the efficacy and safety of nab-paclitaxel plus cisplatin plus carilizumab as first-line treatment in patients with metastatic triple-negative breast cancer.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Breast Cancer
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
90 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
nab-paclitaxel plus cisplatin plus carilizumab (AP+PD-1)
Arm Type
Experimental
Arm Description
Nab-paclitaxel 125 mg/m2,ivgtt,d1, 8 Cisplatin 75 mg/m2,ivgtt,d1 Carilizumab 200mg, ivgtt,d1,q2w
Intervention Type
Drug
Intervention Name(s)
nab-paclitaxel plus cisplatin plus carilizumab (AP+PD-1)
Intervention Description
Nab-paclitaxel 125 mg/m2,ivgtt,d1, 8 Cisplatin 75 mg/m2,ivgtt,d1 Carilizumab 200mg, ivgtt,d1,q2w
Primary Outcome Measure Information:
Title
PFS
Description
Progression free survival
Time Frame
6 weeks
Title
Adverse events
Description
Number of participants with treatment-related adverse events as assessed by Common Terminology Criteria for Adverse Events version 4.0 (CTCAE v4.0)
Time Frame
6 weeks
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Female patients aged 18-70 years who had
Metastatic TNBC. ER, PgR, and HER2 status were determined locally by immunohistochemistry (IHC) of patient primary or metastatic tumor sections. Metastatic disease was confirmed by clinical, imaging, histological or cytological measures.
Patients were required to receive no previous chemotherapy or targeted therapy for metastatic triple-negative breast cancer.
Patients who had received adjuvant/neoadjuvant therapy were required an interval for at least 6 months after stop of chemotherapy before the enrollment.
At least one measurable lesion according to RECIST 1.1,
ECOG performance status ≤ 1
Life expectancy of more than 12 weeks
Adequate organ and bone marrow function.
Exclusion Criteria:
Patient of childbearing potential but unwilling to receive contraception.
Radiation therapy of axial bone within 4 weeks before enrollment.
Previous treatment with PD-1 antibody, PD-L1 antibody and CTLA-4 antibody.
Patients have active autoimmune diseases.
Patients who need systemic corticosteroids (> 10 mg prednisone/d) or other immunosuppressive drugs within 14 days before enrollment or during the study period.
Symptomatic central nervous system (CNS) disease (patients with asymptomatic treated CNS metastases were permitted)
Other malignant diseases within the past 5 years (patients with basal cell skin carcinoma and cervical carcinoma in situ were permitted)
Uncontrolled infection.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Biyun Wang, Professor
Phone
+8613701748410
Email
pro_wangbiyun@163.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Biyun Wang, Professor
Organizational Affiliation
Fudan University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Fudan University Shanghai Cancer Center
City
Shanghai
State/Province
Shanghai
ZIP/Postal Code
200032
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Biyun Wang, Professor
Phone
+8613701748410
Email
pro_wangbiyun@163.com
12. IPD Sharing Statement
Plan to Share IPD
No
IPD Sharing Plan Description
Shared patient information is not allowed by study center.
Learn more about this trial
First-line Nab-paclitaxel Plus Cisplatin Plus Carilizumab in mTNBC Patients
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