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Beta-adrenergic receptor blockade in angiosarcoma: Which beta-blocker to choose?
Alaa Embaby1, Lisanne van Merendonk2, Neeltje Steeghs1
1Department of Medical Oncology and Clinical Pharmacology, The Netherlands Cancer Institute-Antoni van Leeuwenhoek, Amsterdam, Netherlands.
Abstract:
Beta-blockers are currently studied to improve therapeutic options for patients with angiosarcoma. However, most of these patients have no cardiovascular co-morbidity and it is therefore crucial to discuss the most optimal pharmacological properties of beta-blockers for this population. To maximize the possible effectiveness in angiosarcoma, the use of a non-selective beta-blocker is preferred based on in vitro data. To minimize the risk of cardiovascular adverse events a beta-blocker should ideally have intrinsic sympathomimetic activity or vasodilator effects, e.g. labetalol, pindolol or carvedilol. However, except for one case of carvedilol, only efficacy data of propranolol is available. In potential follow-up studies labetalol, pindolol or carvedilol can be considered to reduce the risk of cardiovascular adverse events.
Insights
Non-selective beta-blockers show promise for angiosarcoma treatment. Drugs with intrinsic sympathomimetic activity or vasodilator effects, like labetalol, may reduce cardiovascular risks in patients without heart conditions.
Area of Science:
- Pharmacology
- Oncology
- Cardiology
Background:
- Angiosarcoma treatment options are limited.
- Beta-blockers are being investigated as a novel therapeutic strategy for angiosarcoma.
- Most angiosarcoma patients lack cardiovascular comorbidities, necessitating careful drug selection.
Purpose of the Study:
- To determine the optimal pharmacological properties of beta-blockers for angiosarcoma treatment.
- To identify beta-blockers that maximize efficacy while minimizing cardiovascular adverse events in angiosarcoma patients.
Main Methods:
- Review of in vitro data regarding beta-blocker effectiveness in angiosarcoma.
- Analysis of pharmacological properties, including intrinsic sympathomimetic activity and vasodilator effects.
- Examination of existing clinical data on beta-blocker use in angiosarcoma.
Main Results:
- Non-selective beta-blockers are preferred for maximizing potential effectiveness in angiosarcoma based on in vitro data.
- Beta-blockers with intrinsic sympathomimetic activity or vasodilator effects (e.g., labetalol, pindolol, carvedilol) are suggested to minimize cardiovascular risks.
- Currently, only propranolol has available efficacy data, with one reported case of carvedilol use.
Conclusions:
- Non-selective beta-blockers are a promising avenue for angiosarcoma therapy.
- Labetalol, pindolol, or carvedilol are potential candidates for future studies to mitigate cardiovascular adverse events.
- Further research is needed to evaluate the efficacy and safety of specific beta-blockers in angiosarcoma patients without cardiovascular comorbidities.
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