Trastuzumab in Combination With Vinorelbine or Taxane-Based Chemotherapy in Patients With Metastatic Breast Cancer

Breast Cancer Clinical Trial

Official title:

A Randomized Phase III Study of Trastuzumab (Herceptin) in Combination With Either Vinorelbine (Navelbine), or Taxane-based Chemotherapy in Patients With HER2 Overexpressing Metastatic Breast Cancer

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00146549
• Other study ID #: 01-087
• Status: Completed
• Phase: Phase 3
• First received: September 2, 2005
• Last updated: October 30, 2009
• Start date: August 2001
• Est. completion date: December 2007

Study information

• Verified date: October 2009
• Source: Dana-Farber Cancer Institute
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Institutional Review Board
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to compare two different combinations of chemotherapy with trastuzumab as initial treatment for HER2 positive advanced breast cancer. Half of the patients will receive trastuzumab in combination with a taxane form of chemotherapy (either paclitaxel or docetaxel), while the other group will receive trastuzumab in combination with vinorelbine.

Description:

• All patients will receive trastuzumab then be randomized into one of two arms. Arm A:

Trastuzumab in combination with weekly vinorelbine and Arm B: Trastuzumab in combination with a weekly taxane-based regimen, either paclitaxel or docetaxel, chosen at the discretion of the investigator.

• Treatment is administered on an outpatient basis. Trastuzumab is administered weekly. There is a one-time loading dose for the first week of the first cycle. For that initial treatment, only, the trastuzumab dose is 4mg/kg. The dose for all subsequent weekly trastuzumab treatments is 2mg/kg.

• Arm A: vinorelbine is administered every week and the dose is adjusted based on the absolute neutrophil count for that week. Vinorelbine is given after trastuzumab.

• Arm B: Either paclitaxel given weekly (dose bases on absolute neutrophil count) or docetaxel given on weeks 1,2,3,5,6,7 of each 8-week cycle (dose based upon absolute neutrophil count). Patients on paclitaxel will also receive dexamethasone, diphenhydramine and ranitidine to help prevent allergic or hypersensitivity reactions. Patients on docetaxel will receive dexamethasone to help reduce fluid retention or edema.

• Every 8 weeks the patients cancer will be re-evaluated to see if the treatment is working. If the treatment appears to be working, treatment will continue. Standard radiological testing (x-rays, CT scan, radioactive drug scans, or MRI's) will be used to follow the disease treatment.

• Heart function will be measured after 16 weeks to be sure it is safe to continue treatment.

• Every 8 weeks, patients' will be asked to complete a brief written survey that asks about symptoms and side effects.

• Patients' will remain on the treatment as long as there is no disease progression or unacceptable side effects.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 250
• Est. completion date: December 2007
• Est. primary completion date: August 2007
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Histologically or cytologically confirmed invasive breast cancer, with stage IV disease

• Tumors must be HER2 overexpressing

• Measurable disease, defined as a least one lesion that can be accurately measured in at least one dimension

• 18 years of age or older

• Life expectancy of greater than 6 months

• ECOG performance status of 0-2

• ANC count > 1,500/mm3

• Platelets > 100,000/mm3

• Total bilirubin < 1.5 mg/dl

• AST/ALT < 115 U/I

• Creatinine < 2.0 mg/dl

• Glucose < 200 mg/dl

• LVEF > 50%

Exclusion Criteria:

• Prior chemotherapy or prior trastuzumab therapy for metastatic breast cancer

• Concurrent hormonal therapy, chemotherapy, or radiation treatments

• Pregnant or lactating women

• Known brain metastases or leptomeningeal carcinomatosis

• History of grade 3 or 4 allergic reactions attributed to compounds of similar chemical or biologic composition to the agents in this study

• Pre-existing neuropathy from any cause in excess of grade 1

• Uncontrolled intercurrent illness

• History of other non-breast cancer malignancy except for carcinoma in situ of the cervix or non-melanoma skin cancer

• Patients taking macrolide antibiotics, ketoconazole, or AZT

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Breast Cancer
• Breast Neoplasms
• Stage IV Breast Cancer

Intervention

Drug:
• Trastuzumab

• Vinorelbine

• Paclitaxel

• Docetaxel

Locations

Country	Name	City	State
United States	Dana-Farber Cancer Institute	Boston	Massachusetts
United States	Massachusetts General Hospital	Boston	Massachusetts

Sponsors (5)

Lead Sponsor	Collaborator
Dana-Farber Cancer Institute	Brigham and Women's Hospital, GlaxoSmithKline, Massachusetts General Hospital, North Shore Medical Center

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	To compare the overall response rate for patients receiving trastuzumab in combination with either vinorelbine or taxane-based chemotherapy.
Secondary	Characterization of the time to disease progression and time to treatment failure for patients receiving trastuzumab with either vinorelbine or taxane-based chemotherapy
Secondary	Characterization of side effects for both treatments
Secondary	analysis of quality of life for patients receiving either treatment.