Clinical Trials Directory

Trials / Unknown

UnknownNCT06304896

Colchicine Versus Beta-blockers, Angiotensin-converting Enzyme Inhibitors, and Statins for Prevention of Chemotherapy-Induced Cardiomyopathy

Status
Unknown
Phase
Phase 1
Study type
Interventional
Enrollment
150 (estimated)
Sponsor
Arab Contractors Medical Centre · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

BASiC-CIC Trial is a multicenter, double-blinded, randomized, placebo-controlled clinical trial to investigate whether repurposing colchicine or a combination of beta-blockers, angiotensin-converting enzyme (ACE) inhibitors, and statins will be effective as a prophylactic treatment for the prevention of chemotherapy-induced cardiomyopathy, reduction of major adverse cardiovascular events, and all-cause mortality.

Detailed description

The 2021 European Society of Cardiology (ESC) guidelines recommend that the treatment with angiotensin-converting enzyme inhibitors (ACEi) and a beta-blocker (preferably carvedilol) should be considered in cancer patients developing left ventricle systolic dysfunction, defined as a 10% or more decrease in left ventricular ejection fraction (LVEF) from baseline value or a value lower than 50%, during anthracycline chemotherapy. This statement has a class of recommendation of II with a level of evidence B, which means that the weight of evidence/opinion is in favor of the usefulness of these treatments. The statement recommends starting the dual treatment after echocardiographic evidence of cardiac affection. Therefore, whether pre-treatment with these dual cardio-protective agents will protect the patient's heart from the toxic effects of the chemotherapeutic intervention is unclear. Additionally, The 2022 ACC/AHA/HFSA American guidelines recommend that in asymptomatic patients with cancer therapy-related cardiomyopathy (ejection fraction\<50%), angiotensin-receptor blocker (ARBs)and beta-blockers are reasonable to prevent progression to heart failure and improve cardiac function. The statement also recommends starting the dual treatment after echocardiographic evidence of cardiac affection. However, these guidelines state that in patients at risk of cancer therapy-related cardiomyopathy, initiation of beta blockers and ACEi/ARB for the primary prevention of drug-induced cardiomyopathy is of uncertain benefit and further clinical research is an unmet need. Accordingly, the effectiveness of preemptive use of ACEi-ARB and/or selected beta-blockers (such as carvedilol and nebivolol) in reducing the risk of cancer therapy-related cardiomyopathy has been investigated in a number of small clinical trials, with conflicting findings. Additionally, statins have pleiotropic therapeutic effects that range from endothelial stabilization to suppression of inflammation. However, its role in decreasing disease morbidity (repeated hospitalization) in established chronic heart failure is also uncertain. On the other hand, colchicine is an immunomodulator that accumulates in the white blood cells and affects them in a variety of ways including decreasing motility, mobilization, and adhesion. Generally, colchicine appears to inhibit multiple proinflammatory mechanisms, while enabling increased levels of anti-inflammatory mediators. In a randomized trial involving patients with chronic coronary disease, the risk of cardiovascular events was significantly lower among those who received 0.5 mg of colchicine once daily than among those who received a placebo. Accordingly, colchicine can reduce the risk of cardiovascular events in patients with chronic coronary artery disease, but its efficacy in improving the functional status in patients with established chronic heart failure is also uncertain. While the use of this immunomodulatory agent in established heart failure is uncertain, its effectiveness in the prophylactic reduction of chemotherapy-induced cardiomyopathy in patients with normal pre-treatment ejection fraction has not been investigated. Accordingly, 150 enrolled cancer patients who are candidates for guideline-directed anthracycline-based chemotherapy with or without the anti-HER2 trastuzumab at the time of presentation, will undergo the following: * General and Local cardiac examination. * CBC. * Chemistry Panel including KFTs, LFTs. * Serum electrolytes levels. * Baseline resting surface 12 leads ECG followed by serial recording (monthly for a total of 6 months). * Baseline Echocardiography followed by serial imaging every 2 months for a total of 6 months. * Baseline serum BNP test/NT-proBNP followed by serial testing every 2 months for a total of 6 months.

Conditions

Interventions

TypeNameDescription
DRUGCarvedilolCarvedilol 6.25 mg oral tablets. Prescribed: Twice daily PO with 200 mL of water.
DRUGRamiprilRamipril 2.5 mg oral capsules. Prescribed: Once daily PO with 200 mL of water.
DRUGRosuvastatinRosuvastatin 20 mg oral tablets. Prescribed: Once daily PO with 200 mL of water.
DRUGColchicineColchicine 0.6 mg oral tablets/capsules. Prescribed: Once daily PO with 200 mL of water.
DRUGPlaceboPlacebo oral capsules. Prescribed: Once daily PO with 200 mL of water.

Timeline

Start date
2024-05-01
Primary completion
2025-05-01
Completion
2025-12-01
First posted
2024-03-12
Last updated
2024-03-12

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT06304896. Inclusion in this directory is not an endorsement.