This study, called "ROSUBREAST", is a multicenter, double-blind, randomized clinical trial evaluating whether rosuvastatin (20 mg daily) can protect the heart in women with breast cancer receiving anthracycline-based chemotherapy. A total of 400 participants will be randomly assigned to receive either rosuvastatin or placebo for 12 months. The main goal is to determine whether rosuvastatin can prevent cancer treatment-related cardiac dysfunction (CTRCD), defined as a significant drop in heart pumping function. The study will also assess changes in cardiac strain, blood biomarkers, symptoms of heart failure, quality of life, and possible side effects.
Introduction: Anthracycline-induced cardiotoxicity significantly threatens the long-term cardiac health of breast cancer patients undergoing chemotherapy. Statins have shown potential cardioprotective effects without compromising cancer treatment efficacy. The ROSUBREAST study aims to evaluate the efficacy of rosuvastatin in preventing CTRCD in breast cancer patients receiving anthracycline-based chemotherapy. Methods: This multicenter, two-arm, double-blinded, superiority, parallel-group, randomized, placebo controlled clinical trial will be conducted across seven oncocardiology centers in Iran. A total of 400 participants will be enrolled and will be randomly assigned in a 1:1 ratio to receive either rosuvastatin (20 mg daily) or no intervention for 12 months. The primary endpoint is the incidence of CTRCD, defined as a ≥10% reduction in left ventricular ejection fraction (LVEF) to below the lower normal limit (53%). Secondary endpoints include changes in Global Longitudinal Strain (GLS), biomarkers (Troponin, NT-proBNP, hsCRP), and development of heart failure (HF). Ancillary endpoints are quality-of-life assessments and adverse effects of treatment. Conclusion: The ROSUBREAST study seeks to provide evidence on the cardioprotective role of rosuvastatin in breast cancer patients undergoing anthracycline-based chemotherapy, potentially informing clinical guidelines and improving patient outcomes.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
QUADRUPLE
Enrollment
400
Consumption of rosuvastatin 20mg tablets every day
consumption of placebo tablets similar to rosuvastatin 20mg
Motahari Breast Cancer Clinic
Shiraz, Fars, Iran
Kowsar Hospital, Fars Heart Foundation
Shiraz, Fars, Iran
Toba Oncology Department, Mazandaran University of Medical Sciences
Sari, Mazandaran, Iran
Modarres Hospital, Shahid Beheshti University of Medical Sciences
Tehran, Tehran Province, Iran
Rajaee Hospital, Iran University of Medical Sciences
Tehran, Tehran Province, Iran
Sina Hospital, Tehran University of Medical Sciences
Tehran, Tehran Province, Iran
Taleghani Hospital, Shahid Beheshti University of Medical Sciences
Tehran, Tehran Province, Iran
CTRCD (cancer treatment-related cardiac dysfunction)
CTRCD is defined as a reduction of ≥10 percentage points in LVEF by echocardiography to \<53% or a \>15% relative decline in global longitudinal strain (GLS) compared with baseline strain.
Time frame: 12 months after randomization
changes in LVEF
Time frame: 3, 6, and 12 months after randomization
changes in Global Longitudinal Strain (GLS)
Time frame: 3, 6, and 12 months after randomization
changes in Troponin level
Time frame: 3, 6, and 12 months after randomization
changes in N-terminal pro b-type Natriuretic Peptide (NT-proBNP) level
Time frame: 3, 6, and 12 months after randomization
changes in High-sensitivity C-reactive Protein (hsCRP) level
Time frame: 3, 6, and 12 months after randomization
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