Expired Study
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Boston, Massachusetts 02114


Purpose:

The purpose of this research study is to determine the effects of the combination of bevacizumab, vinorelbine, and trastuzumab on participants and their cancer.


Study summary:

- Participants will receive bevacizumab intravenously every 2 weeks. They will also receive trastuzumab and vinorelbine intravenously once a week. Therefore, treatments will alternate between receiving all three drugs (1st week, third week, fifth week, etc.) and receiving only trastuzumab and vinorelbine (2nd week, fourth week, sixth week, etc.) A treatment cycle lasts four weeks. - During all treatment cycles a physical exam will be performed and the participant will be asked general health and specific questions about any problems they are experiencing. - X-ray, CT scans, and/or MRI scans will be performed every 8 weeks (every 2 cycles) in order to assess the effect of the study treatment on the participants cancer. These tests are considered standard of care in patients receiving chemotherapy. - Once a week blood counts will be performed and at least every 4 weeks, chemistry and other tests to measure any additional effect of the study drug and disease status will be checked. These tests are also considered standard of care for patients receiving chemotherapy. - At the beginning of the study and at the 4- and 8-week time point, additional blood will be drawn in order to conduct research blood tests to measure the presence of cancer cells in the blood. - A urine test and MUGA scan or echocardiogram will be done every 8 weeks while the participant in on the study. - Participants can remain on the research study as long as the study treatment appears to be working and they are not experiencing unacceptable side effects.


Criteria:

Inclusion Criteria: - Histologically or cytologically confirmed invasive breast cancer, with metastatic disease. - HER2-positive tumor - Measurable disease defined as at least one lesion that can be accurately measured in at least one dimension as 20mm or greater with conventional techniques or as 10mm or greater with spiral CT scan - 18 years of age or older - Life expectancy of more than 12 weeks - ECOG Performance Status of 0 or 1 - Normal organ and marrow function as outlined in the protocol - Left ventricular ejection fraction 50% or greater as determined by RVG or echocardiogram within 30 days prior to initiation of protocol therapy - Patients with stable or previously treated CNS metastases are eligible for study participation, provided there is no history of clinically significant CNS bleeding - Men and women of child-bearing potential must agree to use adequate contraception prior to study entry and for the duration of study participation COHORT A: - No prior chemotherapy for treatment of metastatic breast cancer - May NOT have received prior treatment with trastuzumab for recurrent or metastatic breast cancer - No prior vinorelbine for treatment of breast cancer - No prior bevacizumab for treatment of breast cancer - May have received prior radiation therapy and/or any number of lines of hormonal therapy - Prior trastuzumab therapy in the adjuvant setting is also allowed, providing that relapse occured at least 12 months following the last dose - Must have recovered from all reversible toxicities related to prior therapy and may not have any pre-existing treatment-related toxicities in excess of Grade 1. Patients must have stopped prior radiation therapy at least 7 days prior to beginning protocol treatment COHORT B: - One prior line of chemotherapy for treatment of metastatic breast cancer or recurrence of breast cancer within 12 months of completion of adjuvant trastuzumab - No prior vinorelbine for treatment of breast cancer - No prior bevacizumab for treatment of breast cancer - May have received prior radiation therapy and/or any number of lines of hormonal therapy - Must have recovered from all reversible toxicities related to prior therapy and may not have any pre-existing treatment-related toxicities in excess of Grade 1. Patients must have stopped prior radiation therapy at least 7 days prior to beginning protocol treatment Exclusion Criteria: - Patients who have had chemotherapy within 14 days prior to entering the study, ot those who have not recovered adequately from adverse events due to agents administered earlier - Concurrent radiation therapy - History of Grade 3 or 4 allergic reactions attributed to compounds of similar chemical or biologic composition as the agents used in this study - Prior therapy with bevacizumab or vinorelbine - Current, recent (within 4 weeks of the first infusion of this study), or planned participation in an experimental drug study other than a Genentech-sponsored bevacizumab cancer study - Inadequately controlled hypertension - Prior history of hypertensive crisis of hypertensive encephalopathy - NHYA Grade II or greater congestive heart failure - History of myocardial infarction of unstable angina within 6 months prior to study enrollment - History of stroke or transient ischemic attack within 6 months prior to study enrollment - Progressive or untreated CNS metastases - Significant vascular disease within 6 months prior to study enrollment - Symptomatic peripheral vascular disease - Evidence of bleeding diathesis or coagulopathy - Major surgical procedure, open biopsy, or significant traumatic injury within 28 days prior to study enrollment or anticipation of need for major surgical procedure during the course of the study - Core biopsy or other minor surgical procedure, excluding placement of vascular access device, within 7 days prior to study enrollment - History of abdominal fistula, gastrointestinal perforation, or intra-abdominal abscess within 6 months prior to study enrollment - Serious non-healing wound, active ulcer, or untreated bone fracture - Proteinuria at screening - Pregnant or lactating - Current and ongoing treatment with full-dose warfarin or its equivalent


Study is Available At:


Original ID:

07-214


NCT ID:

NCT00670982


Secondary ID:


Study Acronym:


Brief Title:

Bevacizumab in Combination With Vinorelbine and Trastuzumab for HER2-Positive, Metastatic Breast Cancer


Official Title:

Phase 2 Study of Bevacizumab in Combination With Vinorelbine and Trastuzumab for HER2-Positive, Metastatic Breast Cancer


Overall Status:

Active, not recruiting


Study Phase:

Phase 2


Genders:

Both


Minimum Age:

18 Years


Maximum Age:

N/A


Quick Facts

Healthy Volunteers
Oversight Has DMC
Study Is FDA Regulated
Study Is Section 801
Has Expanded Access

Study Source:

Dana-Farber Cancer Institute


Oversight Authority:

United States: Institutional Review Board


Reasons Why Stopped:


Study Type:

Interventional


Study Design:

Endpoint Classification: Safety/Efficacy Study, I


Number of Arms:

1


Number of Groups:

0


Total Enrollment:

65


Enrollment Type:

Anticipated


Overall Contact Information

Official Name:Harold J. Burstein, MD, PhD
Principal Investigator
Dana-Farber Cancer Institute

Study Dates

Start Date:May 2008
Primary Completion Date:May 2011
Primary Completion Type:Anticipated
Verification Date:February 2011
Last Changed Date:February 26, 2011
First Received Date:April 29, 2008

Study Outcomes

Outcome Type:Primary Outcome
Measure:Determination of proportion of patients alive and without progression of disease at 1 year from start of protocol-based therapy.
Time Frame:2 years
Safety Issues:False
Outcome Type:Secondary Outcome
Measure:Determination of objective response rate, time to progression and overall survival.
Time Frame:5 years
Safety Issues:False
Outcome Type:Secondary Outcome
Measure:Characterization of the side effects related to concurrent administration of trastuzumab, vinorelbine, and bevacizumab
Time Frame:3 years
Safety Issues:True

Study Interventions

Intervention Type:Drug
Name:bevacizumab
Description:Given intravenously every 2 weeks
Other Name:Avastin
Intervention Type:Drug
Name:vinorelbine
Description:Given intravenously once a week
Other Name:Navelbine
Intervention Type:Drug
Name:trastuzumab
Description:Given intravenously once a week
Other Name:Herceptin

Study Arms

There are no available Study Arms

Study Agencies

Agency Class:Other
Agency Type:Lead Sponsor
Agency Name:Dana-Farber Cancer Institute
Agency Class:Other
Agency Type:Collaborator
Agency Name:Brigham and Women's Hospital

Sample and Retention Information

There are no available Sample and Retention Information

Study References

There are no available Study References

Data Source: ClinicalTrials.gov

Date Processed: November 18, 2019

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