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Beta-blocker usage after malignant melanoma diagnosis and survival: a population-based nested case-control study
C McCourt1, H G Coleman, L J Murray
1Department of Dermatology, Belfast Health and Social Care Trust, Belfast, Northern Ireland; Cancer Epidemiology and Health Services Research Group, Centre for Public Health, Institute of Clinical Sciences-B, Royal Victoria Hospital Site, Queen's University Belfast, Grosvenor Road, Belfast, BT12 6BJ, Northern Ireland.
Beta-blocker use after malignant melanoma diagnosis did not reduce the risk of melanoma-specific death in a UK study. This research found no significant association between beta-blocker prescriptions and survival outcomes for melanoma patients.
Area of Science:
- Oncology
- Pharmacology
- Epidemiology
Background:
- Beta-blockers exhibit potential antiangiogenic and antimigratory properties.
- Prior studies suggested a survival benefit for malignant melanoma patients using beta-blockers.
Purpose of the Study:
- To evaluate the association between post-diagnosis beta-blocker use and melanoma-specific mortality.
- Investigated risk of death in a population-based cohort of malignant melanoma patients.
Main Methods:
- Nested case-control study using UK Clinical Practice Research Datalink data (1998-2010).
- Matched patients with melanoma-specific death (cases) to four controls based on diagnosis year, age, and sex.
- Conditional logistic regression analyzed beta-blocker prescribing data from general practitioners.
Main Results:
- 20.2% of cases and 20.3% of controls received beta-blockers post-diagnosis.
- No significant association found between post-diagnosis beta-blocker use and melanoma-specific death (OR 0.99, 95% CI 0.68-1.42).
- Adjusted analysis and subgroup analyses (beta-blocker types, dosage, all-cause mortality) showed no significant associations.
Conclusions:
- Beta-blocker use following a malignant melanoma diagnosis was not linked to a reduced risk of death from melanoma.
- Findings contrast with some previous studies, indicating no survival benefit in this UK population-based cohort.
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