Cardioprotective Effects of Nebivolol Versus Placebo in Patients Undergoing Chemotherapy With Anthracyclines (CONTROL Trial)
试验速览
- 阶段
- 3 期
- 状态
- 进行中(未招募)
- 入组人数
- 80
- 试验地点
- 1
- 主要终点
- Left Ventricular Ejection Fraction reduction assessed by Cardiac Magnetic Resonance
研究概览
简要总结
As the cancer-related prognosis improves thanks to recent advances in cancer-targeted therapies, the prognostic burden of chemotherapy-related complications - including cardiotoxicity - is increasingly recognised. So far, the evidence supporting pharmacological preventive strategies in cardio-oncology has been inconsistent and conflicting, and there is a clear need for well-designed trials with novel interventions. In this study, by using cardiac magnetic resonance, the investigators want to assess if a commonly used beta-blocker with a unique pharmacological profile, i.e. nebivolol, can prevent cardiac dysfunction in patients with breast cancer or diffuse large B-cell lymphoma undergoing chemotherapy with anthracyclines.
详细描述
During the last decades, major efforts have been made in the field of cancer therapy to improve prognosis and quality of life of patients treated with any sort of chemotherapy. Cardiotoxicity represents one of the most relevant adverse effects of chemotherapy, primarily in patients treated with anthracyclines. The potential protective role of cardiovascular medications in the prevention of cardiotoxicity associated with anthracyclines chemotherapy is still a matter of debate since evidence in this field are scarce and largely inconclusive. Indeed, prior studies were often limited by a non-blinded design or an echocardiography-based assessment of left ventricular ejection fraction (with a relevant inter and intra-operator variability). The primary objective of the trial is to evaluate the cardioprotective effects of the betablocker nebivolol in an individually randomized, parallel, placebo-controlled, double-blinded (patient, treating physician, investigator, outcomes assessor, statistician), superiority trial in patients with a solid tumor (i.e., breast cancer) or a hematologic malignancy (i.e., diffuse large B cell lymphoma) who have a normal cardiac function as assessed by echocardiography and will receive anthracyclines as part of their first-line chemotherapy program. Indeed, recent evidence suggests that anthracycline cardiotoxicity seems mainly due to an anthracycline-induced dysregulation of mitochondrial activity and metabolism in cardiomyocytes. Nebivolol has a distinctive profile among beta-blockers, with the unique power of increasing the nitric oxide bioavailability. Nebivolol-induced nitric oxide release has shown favourable effects in terms of antioxidant activity, cardiac neo-angiogenesis, mitochondrial and endothelial protection. On this basis, the individually randomized, parallel, placebo-controlled, double-blinded (patient, treating physician, investigator, outcomes assessor, statistician), superiority CONTROL trial will assess the cardioprotective effects of a commonly used betablocker (nebivolol) in patients with baseline normal left ventricular systolic function receiving anthracycline chemotherapy as first-line chemotherapy for breast cancer or diffuse large B-cell lymphoma. The assessment of left ventricular ejection fraction and related endpoints will be performed with cardiac magnetic resonance.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Prevention
- 盲法
- Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
盲法说明
Patients, treating physicians, investigators, and outcome assessors are masked to the allocated treatment.
入排标准
- 年龄范围
- 18 Years 至 —(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Age ≥18 years
- •Established histologic diagnosis of breast cancer or diffuse large B-cell lymphoma
- •Planned chemotherapy with anthracyclines
- •left ventricular ejection fraction ≥55% (assessed by echocardiography)
- •Ability to provide informed consent
排除标准
- •Known intolerance/contraindications to betablocker therapy
- •History of coronary artery disease
- •History of cardiomyopathy
- •History of heart failure
- •Ongoing treatment with betablockers for other indications
- •Heart rate at baseline <60 beats per minute
- •Arterial blood pressure at baseline <100/60 mmHg
- •Contraindications to undergo cardiac magnetic resonance (e.g., non-compatible pacemakers or metallic prosthesis)
- •Pregnancy or lactation
- •Current participation to another study
研究组 & 干预措施
Nebivolol
nebivolol, capsule, 5 mg once daily, for 12 months
干预措施: Nebivolol (Drug)
Placebo
placebo, capsule, once daily, for 12 months
干预措施: Placebo (Drug)
结局指标
主要结局
Left Ventricular Ejection Fraction reduction assessed by Cardiac Magnetic Resonance
时间窗: from baseline to 12 months
The primary endpoint is defined as Left Ventricular Ejection Fraction (LVEF) reduction (unit of measurement: %) assessed by Cardiac Magnetic Resonance at 12 months of follow-up. LVEF reduction is defined as the difference between LVEF at baseline and LVEF at 12 months follow-up (LVEF reduction = Baseline LVEF - 12 months LVEF).
次要结局
- Myocardial fibrosis assessed by Cardiac Magnetic Resonance(at 12-month follow-up)
- Myocardial edema assessed by Cardiac Magnetic Resonance(at 12-month follow-up)
- Right ventricular ejection fraction assessed by Cardiac Magnetic Resonance(at 12-month follow-up)
- Left ventricular end-diastolic volume assessed by Cardiac Magnetic Resonance(at different timepoints (1-month, 6-month, 12-months))
- Left ventricular end-systolic volume assessed by Cardiac Magnetic Resonance(at different timepoints (1-month, 6-month, 12-months))
- Serum N-terminal-pro hormone B-type natriuretic peptide (NT-proBNP)(at different timepoints (1-month, 6-month, 12-months))
- Left ventricular ejection fraction assessed by Cardiac Magnetic Resonance(at 12-month follow-up)
- Left ventricular mass assessed by Cardiac Magnetic Resonance(at different timepoints (1-month, 6-month, 12-months))
- Left ventricular ejection fraction assessed by Echocardiography(at different timepoints (1-month, 6-month, 12-months))
- Left ventricular diastolic function assessed by Echocardiography(at different timepoints (1-month, 6-month, 12-months))
- Right ventricular systolic function assessed by Echocardiography(at different timepoints (1-month, 6-month, 12-months))
- Left ventricular end-diastolic volume assessed by Echocardiography(at different timepoints (1-month, 6-month, 12-months))
- Serum troponin(at different timepoints (1-month, 6-month, 12-months))
- Serum B-type natriuretic peptide (BNP)(at different timepoints (1-month, 6-month, 12-months))
- All-cause mortality(at 12-month follow-up)
- Left ventricular end-systolic volume assessed by Echocardiography(at different timepoints (1-month, 6-month, 12-months))
- Myocardial infarction(at 12-month follow-up)
- Hospitalization for heart failure(at 12-month follow-up)
- Cardiovascular mortality(at 12-month follow-up)
- Cerebrovascular events(at 12-month follow-up)
研究者
Giulio Stefanini
Professor
Humanitas Hospital, Italy
