Clinical trial

A Phase II Trial of Doxil, Carboplatin and Bevacizumab in Triple Negative Previously Untreated Metastatic Breast Cancer

Name
040702
Description
The purpose of this research study is to look at the effectiveness of a combination of doxil, carboplatin and bevacizumab on metastatic breast cancer. The type of breast cancer being studied is negative for a protein called HER2/neu and for estrogen receptors (ER) and progesterone receptors (PR). HER2/neu, ER and PR are part of a family of receptors found on both cancer and normal cells. This family of receptors is important for cell growth and is found in many tumor types.This study is being conducted for the following research purposes:· To find out what effects, if any, the study drug has on metastatic breast cancer. For instance, will the study drug cause the tumor(s) to shrink or stop growing?· To test the safety of the study drugs and to see what affects it has. For instance, are there any side effects? If so, what kind of side effects does the study drug cause? How severe are the side effects, and how often do they occur?· To see if the study drugs have any effect on keeping the disease from getting worse.
Trial arms
Trial start
2008-05-16
Estimated PCD
2015-07-12
Trial end
2015-09-25
Status
Completed
Phase
Early phase I
Treatment
Doxil
Doxil 30 mg/m2 will be administered on Day 1 of each 28-day cycle.
Arms:
Doxil, Carboplatin and Bevacizumab
Carboplatin
Carboplatin 30 mg/m2 will be administered on Day 1 of each 28-day cycle.
Arms:
Doxil, Carboplatin and Bevacizumab
Bevacizumab
Bevacizumab 10 mg/kg will be administered on Day 1 immediately following chemotherapy and alone on Day 15 of each 28-day cycle.
Arms:
Doxil, Carboplatin and Bevacizumab
Other names:
Avastin
Size
31
Primary endpoint
Progression Free Survival (PFS) After Treatment With Doxil, Carboplatin and Bevacizumab in Patients With ER, PR, HER2neu Negative Metastatic Breast Cancer
Two Years
Eligibility criteria
Inclusion Criteria: 1. Women with previously untreated metastatic breast cancer, ER/PR/HER2/neu negative. 2. Age \>= 18 3. ECOG performance status \<= 2 4. Normal organ and marrow function 5. Normal cardiac function as evidenced by LVEF within institutional normal limits Exclusion Criteria: 1. History of hypersensitivity reactions to doxil or bevacizumab 2. Myocardial infarct or unstable angina within 6 months before enrollment 3. Prior anthracycline dose exceeding 360 mg/m2 for doxorubicin (including DOXIL) or 720 mg/m2 for epirubicin. 4. Proteinuria
Protocol
{'studyType': 'INTERVENTIONAL', 'phases': ['PHASE2'], 'designInfo': {'allocation': 'NA', 'interventionModel': 'SINGLE_GROUP', 'primaryPurpose': 'TREATMENT', 'maskingInfo': {'masking': 'NONE'}}, 'enrollmentInfo': {'count': 31, 'type': 'ACTUAL'}}
Updated at
2023-02-08

1 organization

3 drugs

1 indication

Drug
R-CHOP
Indication
Breast Cancer
Drug
AN0025