Sorafenib and Anastrozole in Treating Postmenopausal Women With Metastatic Breast Cancer

NCT ID: NCT00217399

Last Updated: 2014-05-28

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1/PHASE2
• Total Enrollment: 35 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2005-06-30
• Study Completion Date: 2013-01-31

Brief Summary

Sorafenib may stop the growth of tumor cells by blocking blood flow to the tumor and by blocking some of the enzymes needed for cell growth. Estradiol can cause the growth of breast cancer. Hormone therapy using anastrozole may fight breast cancer by blocking the use of estradiol by the tumor cells. Sometimes when hormone therapy is given, it does not stop the growth of tumor cells. The tumor is said to be resistant to hormone therapy. Giving sorafenib together with anastrozole may reduce drug resistance and allow the tumor cells to be killed. This phase I/II trial is studying the side effects and best dose of sorafenib when given in combination with anastrozole and to see how well they work in treating postmenopausal women with metastatic breast cancer.

Detailed Description

PRIMARY OBJECTIVES:

I. Determine the clinical benefit rate of sorafenib in combination with anastrazole in women with estrogen receptor- and/or progesterone receptor-positive metastatic breast cancer.

II. Determine the recommended phase II dose of sorafenib when administered with anastrozole in these patients.

SECONDARY OBJECTIVES:

I. Determine the toxic effects of this regimen in these patients. II. Determine the changes in Raf-MAPK and VEGF-signaling pathways in tumor tissue and stroma before and after treatment with this regimen in these patients.

OUTLINE: This is a multicenter, dose-escalation study of sorafenib.

PHASE I: Patients receive oral sorafenib twice daily and oral anastrozole once daily on days 1-28.

Courses repeat every 28 days in the absence of disease progression or unacceptable toxicity. Cohorts of 3-6 patients receive escalating doses of sorafenib until the maximum tolerated dose (MTD) is determined. The MTD is defined as the dose preceding that at which 2 of 6 patients experience dose-limiting toxicity. A minimum of 6 patients are treated at the MTD.

PHASE II: Patients receive sorafenib at the MTD and anastrozole as in phase I.

After completion of study treatment, patients are followed every 4-8 weeks.

Conditions

Recurrent Breast Cancer; Stage IV Breast Cancer

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Treatment

PHASE I: Patients receive oral sorafenib twice daily and oral anastrozole once daily on days 1-28.

Courses repeat every 28 days in the absence of disease progression or unacceptable toxicity. Cohorts of 3-6 patients receive escalating doses of sorafenib until the MTD is determined. The MTD is defined as the dose preceding that at which 2 of 6 patients experience dose-limiting toxicity. A minimum of 6 patients are treated at the MTD.

PHASE II: Patients receive sorafenib at the MTD and anastrozole as in phase I.

Group Type: EXPERIMENTAL

sorafenib tosylate

Intervention Type: DRUG

Given orally

anastrozole

Intervention Type: DRUG

Given orally

Interventions

sorafenib tosylate

Given orally

Intervention Type: DRUG

anastrozole

Given orally

Intervention Type: DRUG

Other Intervention Names

BAY 43-9006; BAY 43-9006 Tosylate Salt; BAY 54-9085; Nexavar; SFN; ANAS; Arimidex; ICI-D1033

Eligibility Criteria

Inclusion Criteria

• Histologically or cytologically confirmed breast cancer
• Metastatic disease
• Measurable disease, defined as >=1 unidimensionally measurable lesion, including >= 1 of the following:

• Lesion >= 10 mm on CT scan (5 mm sections)
• Lesion >= 20 mm on CT scan or MRI (10 mm sections)
• Bone disease that is >= 10 mm on MRI
• Lytic bone lesions that are >= 10 mm on CT scan (with 5 mm sections) OR >= 20 mm on plain film or CT scan (with 10 mm sections)
• Lesion >= 10 mm on physical exam
• Patients must have received >= 1 prior aromatase inhibitor in either the adjuvant or metastatic setting and must have had either disease recurrence or disease progression on a prior aromatase inhibitor therapy
• No brain metastases diagnosed within the past 6 months OR previously untreated brain metastases
• Estrogen receptor-positive and/or progesterone receptor-positive, defined as > 1% staining by immunohistochemistry or > 10 fmol/mg of protein by radio-ligand dextran-coated steroid binding assay
• Postmenopausal, as defined by 1 of the following:

• Prior bilateral oophorectomy
• No menses for >= 12 months in patients with an intact uterus
• Follicle-stimulating hormone (FSH) in postmenopausal range in patients < 60 years of age who have had a prior hysterectomy or have been amenorrheic for >= 3 months
• Age >= 60 years
• Pre- or perimenopausal patients receiving monthly injections of goserelin at a dose of 3.6 mg are eligible
• ECOG 0-2
• More than 3 months
• Absolute neutrophil count >= 1,500/mm3 Platelet count >= 100,000/mm3 No bleeding diathesis
• Bilirubin =< 1.5 times upper limit of normal (ULN AST and ALT =< 2.5 times ULN
• Systolic blood pressure (BP) < 150 mm Hg and diastolic BP < 100 mm Hg on at least one reading prior to study entry No uncontrolled hypertension
• None of the following within the past 6 months:

• Symptomatic congestive heart failure
• Unstable angina pectoris
• Myocardial infarction
• Cardiac arrhythmia with hemodynamic compromise
• Not pregnant or nursing
• Able to swallow oral medication
• No known HIV positivity
• No ongoing or active infection
• No psychiatric illness or social situation that would preclude study compliance
• No other active invasive malignancy within the past 5 years except nonmelanoma skin cancer or treated carcinoma in situ of the cervix
• No other uncontrolled illness
• More than 4 weeks since prior chemotherapy
• No more than 2 prior chemotherapy regimens for metastatic disease
• At least 8 weeks since prior anastrozole therapy
• Concurrent steroids allowed if dose is stable
• More than 4 weeks since prior radiotherapy
• More than 4 weeks since prior major surgery
• Recovered from prior therapy
• No prior sorafenib
• No concurrent therapeutic anticoagulation
• Concurrent prophylactic anticoagulation (i.e., low-dose warfarin) for venous or arterial access devices allowed provided PT and PTT are =< 1.5 times ULN
• No concurrent agents that may interact with sorafenib, including any of the following:

• Hypericum perforatum (St. John's wort)
• Rifampin
• P450 CYP3A4 enzyme-inducing anticonvulsants (e.g., phenytoin, carbamazepine, or phenobarbital)
• No other concurrent investigational agents

Exclusion Criteria

• estrogen receptor status unknown
• history of myocardial infarction within 6 months
• performance status 3
• performance status 4
• premenopausal
• progesterone receptor status unknown
• HIV positive

• Minimum Eligible Age: 18 Years
• Eligible Sex: FEMALE
• Accepts Healthy Volunteers: No

Sponsors

National Cancer Institute (NCI)

NIH

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Claudine Isaacs

Role: PRINCIPAL_INVESTIGATOR

Lombardi Comprehensive Cancer Center at Georgetown University

Locations

Lombardi Comprehensive Cancer Center at Georgetown University

Washington D.C., District of Columbia, United States

Countries

United States

Other Identifiers

NCI-2009-00069

Identifier Type: REGISTRY

Identifier Source: secondary_id

CDR0000440067

Identifier Type: -

Identifier Source: secondary_id

2004-251

Identifier Type: -

Identifier Source: secondary_id

2004-251

Identifier Type: OTHER

Identifier Source: secondary_id

6584

Identifier Type: OTHER

Identifier Source: secondary_id

NCI-2009-00069

Identifier Type: -

Identifier Source: org_study_id