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Studying Metabolic Brain Connectivity Using 2-Deoxy-2-[18F]Fluoro-D-Glucose Dynamic Positron Emission Tomography at the Single-subject Level
Published on: January 24, 2025
In ®Entresto we trust
Massimiliano Camilli1, Marco Giuseppe Del Buono1, Pierantonio Menna2
1Department of Cardiovascular and Thoracic Sciences, Catholic University of the Sacred Heart, Rome, Italy.
Insights
Sacubitril/Valsartan effectively treats heart failure with reduced ejection fraction (HFrEF). This study suggests its potential benefit in cancer patients with therapy-induced HFrEF, a group previously excluded from trials.
Area of Science:
- Cardio-Oncology
- Pharmacology
- Heart Failure Management
Background:
- Heart failure with reduced ejection fraction (HFrEF) is a significant concern in cancer patients.
- Cancer therapies, such as anthracyclines, can induce cardiotoxicity leading to HFrEF.
- Patients with cancer therapy-induced HFrEF were excluded from pivotal Sacubitril/Valsartan trials.
Purpose of the Study:
- To evaluate the efficacy and safety of Sacubitril/Valsartan (S/V) in patients with HFrEF caused by cancer therapy.
- To establish the value of S/V in this specific, vulnerable patient subgroup.
Main Methods:
- Retrospective analysis of a small cohort of cancer patients with HFrEF.
- Patients primarily included women with breast cancer treated with anthracyclines.
- Assessment of S/V treatment effects on cardiac function and clinical outcomes.
Main Results:
- Limited data suggest Sacubitril/Valsartan shows encouraging effects in this population.
- Results appear consistent with prior studies on S/V in broader HFrEF populations.
- No major adverse events related to S/V were highlighted in this small group.
Conclusions:
- Sacubitril/Valsartan may be a valuable treatment option for cancer patients with therapy-induced HFrEF.
- Further prospective studies are warranted to confirm these preliminary findings.
- This research supports the consideration of S/V in cardio-oncology practice.
Abstract:
Sacubitril/Valsartan (S/V) is a novel and remarkably effective opportunity to treat heart failure with reduced ejection fraction (HFrEF). However, patients with HFrEF induced by cancer therapy were a priori excluded from the registration study. The value of S/V in this important subgroup of patients needs to be firmly established. In this issue of Cardio-Oncology, Gregorietti et al. report on the effects of S/V in a small group of cancer patients, primarily women with breast cancer treated with anthracyclines. The data are limited but seem to confirm the encouraging results of prior studies, paving the way to foster the use of S/V in cardio-oncology patients and hopefully, to design ad hoc prospective studies in this highly vulnerable population.
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