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Thalidomide Plus Chemotherapy Versus Chemotherapy Alone for Advanced Breast Cancer

Primary Purpose

Metastatic Breast Cancer

Status
Unknown status
Phase
Phase 2
Locations
China
Study Type
Interventional
Intervention
Thalidomide
Physician's choice chemotherapy
Sponsored by
Zhejiang Cancer Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Metastatic Breast Cancer

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)FemaleDoes not accept healthy volunteers
  1. inclusion criteria:

    • Women >/= 18 and < 65 years of age .
    • Histologically or cytologically confirmed breast cancer with evidence of metastatic disease. (Note: the participant must be recovered from any clinically significant toxicity thereof last therapy.)
    • ECOG performance status 0-2.
    • Adequate bone marrow, kidney and liver function.
    • ER/PR breast cancer positive patients must have received and progressed on at least one endocrine therapy (adjuvant or metastatic), or have disease that the treating physician believes to be inappropriate for endocrine therapy.
  2. exclusion criteria:

    • Prior treatment with thalidomide.
    • Patients with HER2 positive disease.
    • Untreated and/or uncontrolled brain metastases.
    • Prior malignancy unless curatively treated and disease-free for > 5 years prior to study entry. Prior adequately treated non-melanoma skin cancer, in situ cancer of the cervix, DCIS or stage I grade 1 endometrial cancer allowed.
    • Known HIV (Human Immunodeficiency Virus) infection.
    • Pregnant or breast-feeding women.
    • Bilateral invasive breast cancer.
    • Cardiac and thrombotic disease or risk for same as judged by Investigator.
    • Other serious illness or medical conditions such as (partial list- review with Investigator) history of significant neurologic or psychiatric disorders that would prohibit the understanding and giving of informed consent, active uncontrolled infection, active peptic ulcer, unstable diabetes mellitus or subjects with symptomatic, intrinsic lung disease resulting in dyspnea at rest.

Sites / Locations

  • Zhejiang Cancer HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

thalidomide plus chemotherapy

chemotherapy

Arm Description

thalidomide tablet 100mg qn po

Physician's choice chemotherapy. No constraints of the choice of chemotherapy drugs and regimens.

Outcomes

Primary Outcome Measures

Progression free survival(PFS)
PFS is defined as the months that from the anticipation of the clinical-trial to the progress of breast cancer.

Secondary Outcome Measures

Overall survival(OS)
OS is defined as the months that from the anticipation of the clinical-trial to the death of patients.

Full Information

First Posted
December 13, 2015
Last Updated
January 5, 2016
Sponsor
Zhejiang Cancer Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT02649101
Brief Title
Thalidomide Plus Chemotherapy Versus Chemotherapy Alone for Advanced Breast Cancer
Official Title
Thalidomide Plus Chemotherapy Versus Chemotherapy Alone: A Phase II Study in Advanced Breast Cancer
Study Type
Interventional

2. Study Status

Record Verification Date
January 2016
Overall Recruitment Status
Unknown status
Study Start Date
October 2015 (undefined)
Primary Completion Date
June 2017 (Anticipated)
Study Completion Date
October 2017 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Zhejiang Cancer Hospital

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Sixty advanced breast cancer patients are planed to enrolled in this clinical trial. Forty patients are enrolled into thalidomide plus chemotherapy group. Twenty patients are enrolled into chemotherapy alone group. There is no restriction on chemotherapy regimen and lines.
Detailed Description
The study compares the combination of thalidomide and chemotherapy with chemotherapy alone for the treatment of stage IV breast cancer. Efficacy and safety of the chemotherapy-thalidomide combination will be evaluated. Assessing the isolated effects of thalidomide in a setting where pre and post treatment serum specimens can be obtained will provide essential information about the mechanisms by which vascular endothelial growth factor(VEGF) inhibition affects tumor growth, and represents an ideal opportunity to evaluate the molecular effects of thalidomide on breast tumor.

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
60 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
thalidomide plus chemotherapy
Arm Type
Experimental
Arm Description
thalidomide tablet 100mg qn po
Arm Title
chemotherapy
Arm Type
Active Comparator
Arm Description
Physician's choice chemotherapy. No constraints of the choice of chemotherapy drugs and regimens.
Intervention Type
Drug
Intervention Name(s)
Thalidomide
Other Intervention Name(s)
Contergan
Intervention Description
Thalidomide tablet 100mg qn po.
Intervention Type
Drug
Intervention Name(s)
Physician's choice chemotherapy
Other Intervention Name(s)
no other name
Intervention Description
Investigators will declare no constraint of regimens.
Primary Outcome Measure Information:
Title
Progression free survival(PFS)
Description
PFS is defined as the months that from the anticipation of the clinical-trial to the progress of breast cancer.
Time Frame
Change from Baseline RECIST at 6 months was assessed every 6 weeks up to 24 weeks. Data collection is from date of randomization until the date of first documented progression assessed up to 6 months.
Secondary Outcome Measure Information:
Title
Overall survival(OS)
Description
OS is defined as the months that from the anticipation of the clinical-trial to the death of patients.
Time Frame
Survival assessed every 8 weeks up to 100 months following objective disease progression. Data collection is from date of randomization until the date of death from any cause, assessed up to 100 months.

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
inclusion criteria: Women >/= 18 and < 65 years of age . Histologically or cytologically confirmed breast cancer with evidence of metastatic disease. (Note: the participant must be recovered from any clinically significant toxicity thereof last therapy.) ECOG performance status 0-2. Adequate bone marrow, kidney and liver function. ER/PR breast cancer positive patients must have received and progressed on at least one endocrine therapy (adjuvant or metastatic), or have disease that the treating physician believes to be inappropriate for endocrine therapy. exclusion criteria: Prior treatment with thalidomide. Patients with HER2 positive disease. Untreated and/or uncontrolled brain metastases. Prior malignancy unless curatively treated and disease-free for > 5 years prior to study entry. Prior adequately treated non-melanoma skin cancer, in situ cancer of the cervix, DCIS or stage I grade 1 endometrial cancer allowed. Known HIV (Human Immunodeficiency Virus) infection. Pregnant or breast-feeding women. Bilateral invasive breast cancer. Cardiac and thrombotic disease or risk for same as judged by Investigator. Other serious illness or medical conditions such as (partial list- review with Investigator) history of significant neurologic or psychiatric disorders that would prohibit the understanding and giving of informed consent, active uncontrolled infection, active peptic ulcer, unstable diabetes mellitus or subjects with symptomatic, intrinsic lung disease resulting in dyspnea at rest.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
lei lei, master
Phone
+8613750802564
Email
leilei1241@163.com
First Name & Middle Initial & Last Name or Official Title & Degree
xiaojia wang, doctor
Phone
+8613906500190
Email
wangxj@zjcc.org.cn
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
xiaojia wang, doctor
Organizational Affiliation
Director
Official's Role
Study Chair
Facility Information:
Facility Name
Zhejiang Cancer Hospital
City
Hangzhou
State/Province
Zhejiang
ZIP/Postal Code
310022
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Xiaojia Wang, PHD
Phone
86 13906500190
Email
wxiaojia0803@163.com
First Name & Middle Initial & Last Name & Degree
Jian Huang, Doctor
Phone
86 13588048995
Email
huang_jian22@aliyun.com
First Name & Middle Initial & Last Name & Degree
Xiaojia Wang, PHD

12. IPD Sharing Statement

Plan to Share IPD
Undecided

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Thalidomide Plus Chemotherapy Versus Chemotherapy Alone for Advanced Breast Cancer

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