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Spots Global Cancer Trial Database for Preventing Anthracycline Cardiovascular Toxicity With Statins (PREVENT)

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Trial Identification

Brief Title: Preventing Anthracycline Cardiovascular Toxicity With Statins (PREVENT)

Official Title: Preventing Anthracycline Cardiovascular Toxicity With Statins (PREVENT)

Study ID: NCT01988571

Interventions

Atorvastatin
Placebo

Study Description

Brief 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.

Detailed 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.

Eligibility

Minimum Age: 21 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Kaiser Permanente Los Angeles Medical Center, Los Angeles, California, United States

MedStar Georgetown University Hospital, Washington, District of Columbia, United States

MedStar Washington Hospital Center, Washington, District of Columbia, United States

Northwestern University, Chicago, Illinois, United States

University of Chicago Comprehensive Cancer Center, Chicago, Illinois, United States

Cancer Center of Kansas-Wichita Medical Arts Tower, Wichita, Kansas, United States

Cancer Center of Kansas - Wichita, Wichita, Kansas, United States

Ochsner Medical Center Jefferson, New Orleans, Louisiana, United States

Tufts Medical Center, Boston, Massachusetts, United States

Spectrum Health at Butterworth Campus, Grand Rapids, Michigan, United States

William Beaumont Hospital-Royal Oak, Royal Oak, Michigan, United States

William Beaumont Hospital - Troy, Troy, Michigan, United States

Saint John's Hospital - Healtheast, Maplewood, Minnesota, United States

Abbott-Northwestern Hospital, Minneapolis, Minnesota, United States

Mayo Clinic in Rochester, Rochester, Minnesota, United States

Park Nicollet Clinic - Saint Louis Park, Saint Louis Park, Minnesota, United States

Regions Hospital, Saint Paul, Minnesota, United States

United Hospital, Saint Paul, Minnesota, United States

Mission Hospital, Asheville, North Carolina, United States

Hope Women's Cancer Centers-Asheville, Asheville, North Carolina, United States

Cone Health Cancer Center at Alamance Regional, Burlington, North Carolina, United States

Novant Health Presbyterian Medical Center, Charlotte, North Carolina, United States

Oncology Specialists of Charlotte, Charlotte, North Carolina, United States

Cone Health Cancer Center, Greensboro, North Carolina, United States

Novant Health Cancer Institute - Huntersville, Huntersville, North Carolina, United States

Southern Oncology Specialists-Huntersville, Huntersville, North Carolina, United States

Novant Health Cancer Institute - Kernersville, Kernersville, North Carolina, United States

Novant Health Cancer Specialists-Matthews, Matthews, North Carolina, United States

Novant Health Forsyth Medical Center, Winston-Salem, North Carolina, United States

Novant Health Oncology Specialists, Winston-Salem, North Carolina, United States

Wake Forest University Health Sciences, Winston-Salem, North Carolina, United States

Columbus Oncology and Hematology Associates Inc, Columbus, Ohio, United States

Doctors Hospital, Columbus, Ohio, United States

Delaware Health Center-Grady Cancer Center, Delaware, Ohio, United States

Genesis Healthcare System Cancer Care Center, Zanesville, Ohio, United States

Geisinger Medical Center, Danville, Pennsylvania, United States

University of Pennsylvania/Abramson Cancer Center, Philadelphia, Pennsylvania, United States

Medical University of South Carolina, Charleston, South Carolina, United States

Prisma Health Cancer Institute - Easley, Easley, South Carolina, United States

Prisma Health Cancer Institute - Butternut, Greenville, South Carolina, United States

Prisma Health Cancer Institute - Faris, Greenville, South Carolina, United States

Prisma Health Cancer Institute - Eastside, Greenville, South Carolina, United States

Prisma Health Cancer Institute - Seneca, Seneca, South Carolina, United States

Centra Lynchburg Hematology-Oncology Clinic Inc, Lynchburg, Virginia, United States

Virginia Cancer Institute, Richmond, Virginia, United States

Virginia Commonwealth University/Massey Cancer Center, Richmond, Virginia, United States

Shenandoah Oncology PC, Winchester, Virginia, United States

Aurora Cancer Care-Southern Lakes VLCC, Burlington, Wisconsin, United States

Aurora Cancer Care-Grafton, Grafton, Wisconsin, United States

Vince Lombardi Cancer Clinic - Oshkosh, Oshkosh, Wisconsin, United States

Aurora Medical Center in Summit, Summit, Wisconsin, United States

Contact Details

Name: Gregory Hundley, MD

Affiliation: Wake Forest University Health Sciences

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

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