STOP-CA (Statins TO Prevent the Cardiotoxicity From Anthracyclines)
Overview
- Phase
- Phase 2
- Intervention
- Placebo
- Conditions
- Heart Failure
- Sponsor
- Massachusetts General Hospital
- Enrollment
- 300
- Locations
- 4
- Primary Endpoint
- The Percentage of Individuals in Each Group With a Significant Decline in the LVEF.
- Status
- Completed
- Last Updated
- 11 months ago
Overview
Brief Summary
This research study will test whether atorvastatin, a drug commonly prescribed for reducing cholesterol levels, can protect the heart during chemotherapy with doxorubicin. Atorvastatin is from a family of medications that are commonly called "statins"
Detailed Description
This research study is a Phase II clinical trial. Phase II clinical trials test the effectiveness of a drug and determine whether the investigational drug works in treating a specific disease. "Investigational" means that the drug is being studied. The chemotherapy drug that the participant have been scheduled to be treated with, Doxorubicin, has been associated with the development of heart failure in some patients. This research study is testing whether Atorvastatin can protect the hearts of patients being treated with Doxorubicin and can reduce cardiac injury and the risk of heart failure. Atorvastatin is not approved by the FDA (the U.S. Food and Drug Administration) for use to reduce the cardiac injury after Doxorubicin. Atorvastatin is approved by the FDA for lowering cholesterol and for reducing the risk of heart attack and stroke. The heart is a muscle that pumps blood and Atorvastatin may protect the heart by preserving cardiac muscle function. The investigators will test whether atorvastatin protects the heart using a combination of imaging tests on the participants heart, blood tests, and stress testing. The imaging tests will involve an echocardiogram (an echo) and cardiac magnetic resonance (CMR), a type of magnetic resonance imaging (MRI) scan.
Investigators
Tomas G. Neilan, MD
MD
Massachusetts General Hospital
Eligibility Criteria
Inclusion Criteria
- •\> 18 years of age
- •All patients with newly diagnosed NHL and HL
- •Scheduled to receive anthracycline-based therapy
Exclusion Criteria
- •Statin use or Statin use is indicated based on guidelines
- •Pregnancy or breastfeeding
- •Unable to provide informed consent
- •Unexplained persistent elevation of transaminases (\>3 times upper limits of normal)
- •Concomitant use of cyclosporine
- •Renal failure: estimated glomerular filtration \<45 mL/min/1.73 m2
- •Contraindication to a CMR (metallic object, severe claustrophobia, pacemaker, vascular clip
- •LVEF of \<50% at baseline
Arms & Interventions
Placebo
Placebo will be administered at a pre determined dose The drug is taken by mouth, once a day (evening)
Intervention: Placebo
Atorvastatin
Atorvastatin will be administered at a pre determined dose The drug is taken by mouth, once a day (evening)
Intervention: Atorvastatin
Outcomes
Primary Outcomes
The Percentage of Individuals in Each Group With a Significant Decline in the LVEF.
Time Frame: 12 months
To determine if the administration of statins is associated with a lower percentage of individuals who experience a significant decline in the LVEF at 12 months. The primary outcome was the percentage of participants with an absolute decline in left ventricular ejection fraction (LVEF) of\>10% from prior to chemotherapy to a final value of \<55% over 12 months.
Secondary Outcomes
- The Percentage of Participants in Each Group With New Onset Heart Failure.(2 years)
- Myocardial Extracellular Volume by Cardiac MRI.(1 Year)
- Global Longitudinal Strain (GLS)(1 year)