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Platinum Rechallenge in Patients With Platinum-sensitive mTNBC

Primary Purpose

Metastatic Breast Cancer

Status
Recruiting
Phase
Phase 2
Locations
China
Study Type
Interventional
Intervention
Vinorelbine
DDP
Sponsored by
Fudan University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Metastatic Breast Cancer

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  1. Females with age between 18 and 70 years old
  2. Performance status no more than 2
  3. Life expectancy longer than 3 months
  4. Histological proven unresectable recurrent or advanced breast cancer
  5. Triple-negative for estrogen receptor (ER), progestogen receptor (PR), and human epithelial receptor-2 (HER2) by immunohistochemistry (ER <1%, PR <1% and Her2 negative). A negative Her2 gene amplification should be verified by FISH test for those patients with Her2 (2+).
  6. Patients must have progressed after 1or 2 prior chemotherapy regimens for metastatic disease, cis/carbo-platin pretreated only 1 previous line prior to randomisation. Platinum sensitive in this study is defined as complete or partial or stable disease following completion (a minimum of 4 treatment cycles) of previous platinum-based chemotherapy and disease progression greater than 3 months after completion of their last dose of platinum chemotherapy (last dose).
  7. At least one measurable disease according to the response evaluation criteria in solid tumor (RECIST 1.1)
  8. Radiation therapy within 4 weeks prior to enrollment
  9. All patients enrolled are required to have adequate hematologic, hepatic, and renal function
  10. Be able to understand the study procedures and sign informed consent.

Exclusion Criteria:

  1. Patients had prior treatment with vinorelbine
  2. Pregnant or lactating women, women of child-bearing potential, unwilling to use adequate contraceptive protection during the process of the study
  3. Patients with symptomatic central nervous system metastases are not permitted, except for those with stable and asymptomatic brain metastases who have completed cranial irradiation, and have at least one measurable lesion outside the brain. Radiotherapy should be completed within 4 weeks prior to the registration
  4. Treatment with an investigational product within 4 weeks before the first treatment
  5. Severe cardiopulmonary insufficiency, severe hepatic and renal dysfunction
  6. Uncontrolled serious infection
  7. Other active malignancies (including other hematologic malignancies) or other malignancies, except for cured nonmelanoma skin cancer or cervical intraepithelial neoplasia.

Sites / Locations

  • Fudan University Cancer HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Vinorelbine Plus DDP

Vinorelbine

Arm Description

Vinorelbine:25 mg/m2, D1, D8 every 21 days DDP:75 mg/m2, D1 every 21 days

Vinorelbine:30 mg/m2, D1, D8 every 21 days

Outcomes

Primary Outcome Measures

Progression Free Survival (PFS)

Secondary Outcome Measures

Objective Response Rate (ORR)
Number of Participants with Adverse Events as a Measure of Safety and Tolerability
Overall Survival (OS)

Full Information

First Posted
November 16, 2015
Last Updated
April 19, 2022
Sponsor
Fudan University
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1. Study Identification

Unique Protocol Identification Number
NCT02607215
Brief Title
Platinum Rechallenge in Patients With Platinum-sensitive mTNBC
Official Title
Platinum Retreated in Second- or Third-line Patients With Platinum Sensitive Metastatic Triple Negative Breast Cancer (Randomised, Phase II, NPN Trial)
Study Type
Interventional

2. Study Status

Record Verification Date
April 2022
Overall Recruitment Status
Recruiting
Study Start Date
November 2015 (undefined)
Primary Completion Date
December 2022 (Anticipated)
Study Completion Date
December 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Fudan University

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Platinum Retreated in Patients with Platinum Sensitive mTNBC
Detailed Description
Platinum Retreated in Second- or Third-line Patients with Platinum Sensitive Metastatic Triple Negative Breast Cancer (randomised, phase II, NPN trial)

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Metastatic Breast Cancer

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
84 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Vinorelbine Plus DDP
Arm Type
Experimental
Arm Description
Vinorelbine:25 mg/m2, D1, D8 every 21 days DDP:75 mg/m2, D1 every 21 days
Arm Title
Vinorelbine
Arm Type
Active Comparator
Arm Description
Vinorelbine:30 mg/m2, D1, D8 every 21 days
Intervention Type
Drug
Intervention Name(s)
Vinorelbine
Other Intervention Name(s)
NVB
Intervention Description
25 mg/m2, D1, D8
Intervention Type
Drug
Intervention Name(s)
DDP
Intervention Description
75 mg/m2, D1
Primary Outcome Measure Information:
Title
Progression Free Survival (PFS)
Time Frame
6 weeks
Secondary Outcome Measure Information:
Title
Objective Response Rate (ORR)
Time Frame
6 weeks
Title
Number of Participants with Adverse Events as a Measure of Safety and Tolerability
Time Frame
6 weeks
Title
Overall Survival (OS)
Time Frame
From date of randomization until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 100 months

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: Females with age between 18 and 70 years old Performance status no more than 2 Life expectancy longer than 3 months Histological proven unresectable recurrent or advanced breast cancer Triple-negative for estrogen receptor (ER), progestogen receptor (PR), and human epithelial receptor-2 (HER2) by immunohistochemistry (ER <1%, PR <1% and Her2 negative). A negative Her2 gene amplification should be verified by FISH test for those patients with Her2 (2+). Patients must have progressed after 1or 2 prior chemotherapy regimens for metastatic disease, cis/carbo-platin pretreated only 1 previous line prior to randomisation. Platinum sensitive in this study is defined as complete or partial or stable disease following completion (a minimum of 4 treatment cycles) of previous platinum-based chemotherapy and disease progression greater than 3 months after completion of their last dose of platinum chemotherapy (last dose). At least one measurable disease according to the response evaluation criteria in solid tumor (RECIST 1.1) Radiation therapy within 4 weeks prior to enrollment All patients enrolled are required to have adequate hematologic, hepatic, and renal function Be able to understand the study procedures and sign informed consent. Exclusion Criteria: Patients had prior treatment with vinorelbine Pregnant or lactating women, women of child-bearing potential, unwilling to use adequate contraceptive protection during the process of the study Patients with symptomatic central nervous system metastases are not permitted, except for those with stable and asymptomatic brain metastases who have completed cranial irradiation, and have at least one measurable lesion outside the brain. Radiotherapy should be completed within 4 weeks prior to the registration Treatment with an investigational product within 4 weeks before the first treatment Severe cardiopulmonary insufficiency, severe hepatic and renal dysfunction Uncontrolled serious infection Other active malignancies (including other hematologic malignancies) or other malignancies, except for cured nonmelanoma skin cancer or cervical intraepithelial neoplasia.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Xichun Hu, MD, PhD
Phone
64175590
Ext
5006
Email
huxicun@gmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Zhonghua Wang, MD
Phone
64175590
Ext
5000
Email
zhonghuawang95@hotmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Xichun Hu, MD, PhD
Organizational Affiliation
Fudan University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Fudan University Cancer Hospital
City
Shanghai
ZIP/Postal Code
200032
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Xichun Hu, MD,PhD
Phone
64175590
Ext
5006
Email
huxicun@gmail.com
First Name & Middle Initial & Last Name & Degree
Zhonghua Wang, MD
Phone
64175590
Ext
5000
Email
zhonghuawang95@hotmail.com

12. IPD Sharing Statement

Learn more about this trial

Platinum Rechallenge in Patients With Platinum-sensitive mTNBC

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