Basic Trial Information
Trial Description
     Summary
     Further Trial Information
     Eligibility Criteria
Trial Contact Information

Basic Trial Information

Trial Description

Summary

RATIONALE: Chemoprevention is the use of certain drugs to keep cancer from forming, growing, or coming back. The use of simvastatin and anastrozole may stop cancer from forming, growing, or coming back in patients with invasive breast cancer, ductal carcinoma in situ, or a high risk of breast cancer.

PURPOSE: This phase II trial is studying how well giving simvastatin together with anastrozole works in treating postmenopausal women with invasive breast cancer, ductal carcinoma in situ, or a high risk of breast cancer.

Further Study Information

OBJECTIVES:

Primary

• Assess the effects of concurrent anastrozole and simvastatin on anastrozole's steady-state concentration in postmenopausal women with history of invasive breast cancer or ductal carcinoma in situ or at high risk for developing breast cancer.

Secondary

• Study the effect of concurrent simvastatin and anastrozole on estrogen suppression in these patients.

OUTLINE: This is a pilot study.

Patients continue to receive oral anastrozole once daily (as prior to study entry). They also receive oral simvastatin once daily for 14-18 days in the absence of unacceptable toxicity or diagnosis of new or recurrent breast cancer.

Patients undergo blood sample collection at baseline and after study therapy for analysis of anastrozole and hormone (estradiol and estrogen) concentrations.

PROJECTED ACCRUAL: A total of 20 patients will be accrued for this study.

Eligibility Criteria

DISEASE CHARACTERISTICS:

• Meets any of the following criteria:

• History of invasive breast cancer

• History of ductal carcinoma in situ

• At high risk for breast cancer, defined as being on anastrozole for chemoprevention of breast cancer

• Receiving anastrozole for ≥ 30 days as adjuvant breast cancer treatment or for prevention of breast cancer

• No active breast cancer with known metastatic involvement

• Hormone receptor status not specified

PATIENT CHARACTERISTICS:

• Female

• Postmenopausal

• ECOG performance status 0-2

• AST and ALT ≤ 3 times upper limit of normal

• Creatinine clearance ≥ 30 mL/min

• No active liver disease

• No prior hypersensitivity to any HMG-CoA reductase inhibitor or any of its components

• No daily alcohol use of > 3 standard drinks/day

• A standard drink is defined as 10 g of alcohol, which is equivalent to 285 mL of beer, 530 mL of light beer, 100 mL of wine, or 30 mL of liquor

PRIOR CONCURRENT THERAPY:

• See Disease Characteristics

• No cholesterol-lowering drug, including a statin, within the past 3 months

• No selective estrogen receptor modulator (SERM) within the past 3 months

• No other hormone therapy within the past 3 months

• No prior estrogen and/or progesterone hormone replacement therapy that lasted for ≥ 5 years

• Vaginal estrogen preparations allowed

• No other concurrent statin or cholesterol-lowering drug

• No other concurrent SERM

• No other concurrent hormone therapy

• No other concurrent investigational drugs

• No concurrent CYP3A4 inhibitors, including itraconazole, ketoconazole, erythromycin, clarithromycin, telithromycin, HIV protease inhibitors, nefazodone, or cyclosporine

• No concurrent chemotherapy or biological agents

• No concurrent daily grapefruit juice > 8 oz/day

• No other concurrent anticancer agents or therapies

Trial Contact Information

Trial Lead Organizations/Sponsors

Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins

Vered Stearns

Principal Investigator

Link to the current ClinicalTrials.gov record.
NLM Identifer NCT00354640
Information obtained from ClinicalTrials.gov on January 18, 2012

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