Breast Cancer Clinical Trial
The Effect of Simvastatin on Breast Cancer Cell Growth in Women With Stage I-II Breast Cancer
Summary
The purpose of this pilot phase II trial is to identify the molecular and genetic mechanisms by which statins influence breast cancer cell proliferation. Simvastatin may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth and reduce the aggressiveness of breast cancer cells.
Full Description
PRIMARY OBJECTIVES:
I. Evaluate the relationship between short-term use of oral simvastatin on change in expression of Ki-67 as a candidate biomarker of breast tumor proliferation among women with clinical stage 1 or 2- primary invasive breast cancer.
II. Evaluate the relationship between short-term use of oral simvastatin on changes in other candidate predictive markers of breast tumor proliferation (cyclin D1 and P27), changes in a marker of apoptosis (cleaved caspase-3 [CC3]), changes in a marker of inflammation (c-reactive protein [CRP]) and as novel additional biomarkers changes in the composition of the plasma membrane (lipid rafts) and changes in activation of signaling markers (phosphorylation [p]Akt, pMAPK, pEGFR, PHER2).
III. To conduct exploratory analyses comparing the effect of statins on breast tumor proliferation and apoptosis in groups defined by tumor expression of hydroxymethylglutaryl co-enzyme A (CoA) reductase (HMG-CoA), estrogen receptor (ER)/progesterone receptor (PR) status, HER2neu, and tumor grade.
OUTLINE:
Patients receive simvastatin orally (PO) daily for 2-4 weeks in the absence of disease progression or unacceptable toxicity.
Eligibility Criteria
Inclusion Criteria:
Provision of informed consent prior to any study specific procedures
Histologic confirmation of invasive breast cancer with any measures of ER, PR and HER2neu
Clinical stage I or II breast cancer for which there will be at least a 2 week period of time between diagnosis and definitive surgery
Performance status (Eastern Cooperative Oncology Group [ECOG] 0-1)
Not currently pregnant during the study; participants will be informed that the use of contraceptive pills is contraindicated because it may interfere with the study drug and it may be harmful to the woman who has been diagnosed with breast cancer
Exclusion Criteria:
Plans for administration of neoadjuvant chemotherapy or hormonal therapy
Insufficient tissue on diagnostic core breast biopsy for analysis
Previous or concurrent malignancy (with the exception of non-melanomatous skin cancer)
Severe gastrointestinal disorder
Current use of statins or fibrates for any time during the 3 months prior to the study
Proven hypersensitivity to statins
White blood cell (WBC) < 3,500/mm^3
Platelet (Plt) < 120,000/mm^3
Hemoglobin (HgB) < 10 g/dL
Aspartate aminotransferase (AST) > 45 U/L
Alanine aminotransferase (ALT) > 45 U/L
Creatinine > 1.5 mg/dL
Bilirubin > 1.15 mg/dL
Creatine kinase measurement (CPK) > or = 250 mg/dL
Central nervous system (CNS) diseases and major psychiatric diseases or inability to comply to the protocol procedures
Active infections
Cardiac failure, class I-IV
Current anticoagulant or antiplatelet aggregation therapy
Mitral and/or tricuspid valvopathy or valvular prosthesis; angina; severe arterial hypertension; chronic and/or paroxysmal atrial fibrillation; previous myocardial infarction
Current lactation
Check Your Eligibility
Let’s see if you might be eligible for this study.
What is your age and gender ?
There is 1 Location for this study
Detroit Michigan, 48201, United States
How clear is this clinincal trial information?

Please confirm you are a US based health care provider:
Yes, I am a health care Provider No, I am not a health care providerSign Up Now.
Take Control of Your Disease Journey.
Sign up now for expert patient guides, personalized treatment options, and cutting-edge insights that can help you push for the best care plan.