Breast Cancer Clinical Trial

Preventing Anthracycline Cardiovascular Toxicity With Statins (PREVENT)

Summary

The purpose of this research study is to see if Atorvastatin (Lipitor) 40 mg by mouth daily decreases the chance of developing heart problems in individuals receiving adjuvant anthracycline-based chemotherapy for breast cancer of lymphoma.

View Full Description

Full Description

PRIMARY OBJECTIVES:

Specific Aim 1:

To determine if Atorvastatin(Lipitor) administration preserves left ventricular ejection fraction (LVEF) 24 months after initiation of Anthracycline-based adjuvant therapy for adjuvant treatment of breast cancer or lymphoma.

Specific Aim 2:

To determine if baseline to 6-month differences in LVEF predict baseline to 24-month differences in LVEF after Anthracycline-based adjuvant therapy and concomitant atorvastatin therapy.

To achieve these aims, we will perform a double-blind, placebo-controlled, randomized clinical trial of 0 or 40 mg of atorvastatin/day in 278 individuals scheduled to receive Anthracycline-based chemotherapy for treatment of Stage I-III breast cancer or lymphoma Stage I-IV with a projected > 2 year life expectancy. We will use innovative noninvasive magnetic resonance imaging (MRI) procedures to accurately measure LVEF. In addition, we will measure left ventricle (LV) volumes, myocardial strain, fibrosis, aortic pulse wave velocity (PWV) and wall thickness, all factors that can influence LVEF by altering LV pre-load, after-load, and contractility.19,20 Advanced serum biomarkers will be measured that assess for the presence of oxidative/nitrosative stress, systemic inflammation and circulating neurohormones that also may influence LVEF.

This study will test a new clinical paradigm to manage breast cancer: primary prevention of Anthracycline-based adjuvant therapy-related LV dysfunction using pre-treatment with low-cost statins. In addition, this trial will be the first systematic collection of data regarding the mechanism(s) and time course by which LV dysfunction and subsequent chronic heart failure (CHF) evolve in individuals given Anthracycline-based chemotherapy for breast cancer or lymphoma. These data will be useful to physicians trying to determine the optimal cardiac protection strategies when administering adjuvant chemotherapeutic regimens to their breast cancer or lymphoma patients. The objective of this research is to use inexpensive medications to preserve cardiovascular (CV) health and thereby improve overall survival in the growing number of breast cancer and lymphoma patients.

SECONDARY OBJECTIVES

Specific Aim 1:

To document the effect of Atorvastatin (Lipitor) on cognitive function using a battery of neurocognitive tests (HVLT, Rey-osterrieth Figure, controlled oral word association test (COWA), Trail-making Parts A and B, Digit Span and Grooved Pegboard) in breast cancer and lymphoma patients receiving an anthracycline.

Specific Aim 2:

To document the effect of Atorvastatin(Lipitor) on self-reported quality of life using validated questionnaires (PROMIS including: General form, Cog Concerns, Cog Abilities, Fatigue, Pain intensity and interference, Sleep Disturbance, Physical Functioning and Social Functioning) in breast cancer and lymphoma patients receiving an anthracycline.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Stage I-III breast cancer (including inflammatory and newly diagnosed recurrent breast cancer) or lymphoma Stage I-IV. (Patients should have a > 2 year life expectancy)
Scheduled to receive adjuvant chemotherapy with an Anthracycline (doxorubicin and epirubicin)
21 years of age or older
LVEF > 50% (Most recent within the last 5 years)
Prior administration of anthracyclines is acceptable if therapy was completed > 6 months prior to study enrollment
Patients that are receiving or have received chemotherapy regimens are allowed
Able to hold breath for 10 seconds
Prior cancers allowed if no evidence of disease in last 5 years
Eastern Cooperative Oncology Group (ECOG) 0 or 1

Exclusion Criteria:

Prior use of lipid-lowering therapy within the last 6 months
Current postmenopausal hormone-replacement therapy
Uncontrolled hypertension (systolic blood pressure >190 mm Hg or diastolic blood pressure >100 mm Hg)
Scheduled to receive neoadjuvant chemotherapy with an anthracycline
No active liver disease allowed
Uncontrolled hypothyroidism
Recent history (within past 3 years) of alcohol or drug abuse, inflammatory conditions such as lupus or inflammatory bowel disease, use of immunosuppressant agents, or another medical condition that might compromise safety or the successful completion of the study.
Patients with ferromagnetic cerebral aneurysm clips or other intraorbital/intracranial metal;pacemakers, defibrillators, functioning neurostimulator devices or other implanted electronic devices.
Unstable angina; significant ventricular arrhythmias (>20 premature ventricular complexes (PVCs)/min due to gating difficulty) atrial fibrillation with uncontrolled ventricular response; coronary artery disease; acute myocardial infarction within 28 days
Current use of Cytochrome P450 (CYP3A4) inhibitors. These include Clarithromycin, HIV protease inhibitors, Itraconazole, grapefruit juice, Cyclosporine, Rifampin or Digoxin
Current or history of hepatic dysfunction
Unable to provide informed consent
Claustrophobia
Planning to move within 24 months of trial enrollment
Pregnant or breast-feeding

Study is for people with:

Breast Cancer

Phase:

Phase 2

Estimated Enrollment:

279

Study ID:

NCT01988571

Recruitment Status:

Completed

Sponsor:

Wake Forest University Health Sciences

Check Your Eligibility

Let’s see if you might be eligible for this study.

What is your age and gender ?

Submit

There are 48 Locations for this study

See Locations Near You

Kaiser Permanente Los Angeles Medical Center
Los Angeles California, 90027, United States
MedStar Georgetown University Hospital
Washington District of Columbia, 20007, United States
MedStar Washington Hospital Center
Washington District of Columbia, 20010, United States
Northwestern University
Chicago Illinois, 60611, United States
University of Chicago Comprehensive Cancer Center
Chicago Illinois, 60637, United States
Cancer Center of Kansas-Wichita Medical Arts Tower
Wichita Kansas, 67208, United States
Cancer Center of Kansas - Wichita
Wichita Kansas, 67214, United States
Ochsner Medical Center Jefferson
New Orleans Louisiana, 70121, United States
Tufts Medical Center
Boston Massachusetts, 02111, United States
Spectrum Health at Butterworth Campus
Grand Rapids Michigan, 49503, United States
William Beaumont Hospital-Royal Oak
Royal Oak Michigan, 48073, United States
William Beaumont Hospital - Troy
Troy Michigan, 48085, United States
Saint John's Hospital - Healtheast
Maplewood Minnesota, 55109, United States
Abbott-Northwestern Hospital
Minneapolis Minnesota, 55407, United States
Mayo Clinic in Rochester
Rochester Minnesota, 55905, United States
Park Nicollet Clinic - Saint Louis Park
Saint Louis Park Minnesota, 55416, United States
Regions Hospital
Saint Paul Minnesota, 55101, United States
United Hospital
Saint Paul Minnesota, 55102, United States
Mission Hospital
Asheville North Carolina, 28801, United States
Hope Women's Cancer Centers-Asheville
Asheville North Carolina, 28816, United States
Cone Health Cancer Center at Alamance Regional
Burlington North Carolina, 27215, United States
Novant Health Presbyterian Medical Center
Charlotte North Carolina, 28204, United States
Oncology Specialists of Charlotte
Charlotte North Carolina, 28207, United States
Cone Health Cancer Center
Greensboro North Carolina, 27403, United States
Novant Health Cancer Institute - Huntersville
Huntersville North Carolina, 28078, United States
Southern Oncology Specialists-Huntersville
Huntersville North Carolina, 28078, United States
Novant Health Cancer Institute - Kernersville
Kernersville North Carolina, 27284, United States
Novant Health Cancer Specialists-Matthews
Matthews North Carolina, 28105, United States
Novant Health Forsyth Medical Center
Winston-Salem North Carolina, 27103, United States
Novant Health Oncology Specialists
Winston-Salem North Carolina, 27103, United States
Wake Forest University Health Sciences
Winston-Salem North Carolina, 27157, United States
Columbus Oncology and Hematology Associates Inc
Columbus Ohio, 43214, United States
Doctors Hospital
Columbus Ohio, 43228, United States
Delaware Health Center-Grady Cancer Center
Delaware Ohio, 43015, United States
Genesis Healthcare System Cancer Care Center
Zanesville Ohio, 43701, United States
Geisinger Medical Center
Danville Pennsylvania, 17822, United States
University of Pennsylvania/Abramson Cancer Center
Philadelphia Pennsylvania, 19104, United States
Medical University of South Carolina
Charleston South Carolina, 29425, United States
Prisma Health Cancer Institute - Easley
Easley South Carolina, 29640, United States
Prisma Health Cancer Institute - Butternut
Greenville South Carolina, 29605, United States
Prisma Health Cancer Institute - Faris
Greenville South Carolina, 29605, United States
Prisma Health Cancer Institute - Eastside
Greenville South Carolina, 29615, United States
Prisma Health Cancer Institute - Seneca
Seneca South Carolina, 29672, United States
Centra Lynchburg Hematology-Oncology Clinic Inc
Lynchburg Virginia, 24501, United States
Virginia Cancer Institute
Richmond Virginia, 23230, United States
Virginia Commonwealth University/Massey Cancer Center
Richmond Virginia, 23298, United States
Shenandoah Oncology PC
Winchester Virginia, 22601, United States
Aurora Cancer Care-Southern Lakes VLCC
Burlington Wisconsin, 53105, United States
Aurora Cancer Care-Grafton
Grafton Wisconsin, 53024, United States
Vince Lombardi Cancer Clinic - Oshkosh
Oshkosh Wisconsin, 54904, United States
Aurora Medical Center in Summit
Summit Wisconsin, 53066, United States

How clear is this clinincal trial information?

Study is for people with:

Breast Cancer

Phase:

Phase 2

Estimated Enrollment:

279

Study ID:

NCT01988571

Recruitment Status:

Completed

Sponsor:


Wake Forest University Health Sciences

How clear is this clinincal trial information?

×

Introducing, the Journey Bar

Use this bar to access information about the steps in your cancer journey.

Please confirm you are a US based health care provider:

Yes, I am a health care Provider No, I am not a health care provider