Prostate Cancer Clinical Trial

Statin Therapy Versus Placebo Prior to Prostatectomy

Summary

This is a randomized trial comparing the effect of oral simvastatin versus placebo on targets of the mevalonate pathway in men undergoing a prostatectomy as planned management for prostate cancer. Observed tissue effects will be correlated with changes in serum cholesterol and low-density lipoprotein.

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Full Description

Prostate cancer patients that have chosen to undergo a prostatectomy as their primary treatment option will be recruited to this trial. Forty-four subjects will be randomized to either placebo or simvastatin (40 mg po/day) for 4 weeks prior to surgery. Serum samples will be obtained at baseline and immediately prior to prostatectomy. At prostatectomy, cancerous and benign prostate tissue will be microdissected and cryopreserved. Archival prostatectomy tissues will be used to construct tissue microarrays containing matched benign and malignant sections. The effect of HMG-CoA reductase inhibition on lipid raft cholesterol content and targets of prenylation will be determined. The incidence of apoptosis will be determined along with protein levels of mediators of apoptosis. Lastly the effect of statin therapy on cellular markers of proliferation will be determined.

Previously, we studied the effect of statin use on the risk of prostate cancer detection in a case-control study at the Portland VA Medical Center. Statin use was associated with a 62% reduction in cancer odds-risk (OR = 0.38, 95% CI 0.21-0.69). Although these epidemiologic and laboratory findings have generated enthusiasm for the study of statins in prostate cancer, no studies have examined the biologic effects of statins on prostate cancer in humans.

Hypothesis: Statin therapy prior to prostatectomy will successfully target the mevalonate pathway in the human prostate and this intervention will favorably alter tumor biomarker status.

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Eligibility Criteria

Inclusion Criteria:

Histologically confirmed prostatic adenocarcinoma with Gleason 5 to 7 (3+4 = 7 accepted, not 4 + 3 = 7)
Radical prostatectomy chosen as primary treatment for prostate cancer
Age 18 years or older
Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1

Exclusion Criteria:

Other preoperative or prior treatment directed at prostate cancer (i.e., Radiation, hormonal therapy, cryotherapy)
Significant active medical illness which in the opinion of the investigator would preclude protocol treatment
History of or active liver disease or abnormal results of the baseline liver function test (> 2 x normal)

Current use of:

simvastatin
lovastatin
other HMG-CoA inhibitors
lipid-lowering agents
Amiodarone
Cholestyramine
Cholestyramine and colestipol (bile acid sequestrants)
Clofibrate and fenofibrate
Cyclosporine
CYP3A4 inhibitors
Danazol
Diltiazem
Gemfibrozil
Niacin ( 1 g/day)
Verapamil and Warfarin
Known allergy or sensitivity to ingredients in simvastatin

Study is for people with:

Prostate Cancer

Estimated Enrollment:

42

Study ID:

NCT00572468

Recruitment Status:

Completed

Sponsor:

VA Office of Research and Development

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There are 2 Locations for this study

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Durham VA Medical Center, Durham, NC
Durham North Carolina, 27705, United States
VA Medical Center, Portland
Portland Oregon, 97201, United States

How clear is this clinincal trial information?

Study is for people with:

Prostate Cancer

Estimated Enrollment:

42

Study ID:

NCT00572468

Recruitment Status:

Completed

Sponsor:


VA Office of Research and Development

How clear is this clinincal trial information?

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