Ovarian Cancer Survival: How Peri-Operative Beta Blockers Impact Outcomes
"A closer look at the surprising effects of selective and nonselective beta-blockers on ovarian cancer patients' survival and recurrence rates."
Ovarian cancer remains a significant health challenge for women, necessitating continuous research into treatment strategies and factors influencing survival rates. Recent preclinical studies have explored the role of adrenergic agonists in promoting tumor growth and invasiveness in ovarian cancer, specifically through the beta-2 adrenergic receptor. These findings have prompted investigations into whether beta-blockers, commonly prescribed medications that counteract these adrenergic effects, could impact epithelial ovarian cancer (EOC) survival.
Beta-blockers are primarily used to manage conditions such as hypertension, anxiety, and heart conditions by blocking the effects of adrenaline and noradrenaline. The use of these medications in the context of cancer treatment has been a topic of interest due to their potential to influence cancer progression and outcomes. However, clinical results have been conflicting, leading researchers to delve deeper into understanding the nuances of beta-blocker usage and its effects on cancer patients.
To address these uncertainties, a study was conducted to examine the association between peri-operative beta-blockade and clinical outcomes in EOC patients. The study retrospectively reviewed patient data to assess the impact of beta-blocker use on overall survival (OS) and progression-free survival (PFS), considering the timing of beta-blocker administration relative to surgery. The results of this research shed light on the complex interplay between beta-blockers and ovarian cancer progression, providing valuable insights for clinicians and patients alike.
Selective vs. Nonselective: Understanding the Impact of Beta-Blocker Type

The study utilized a cox survival model to evaluate the outcomes of women who took selective beta-blockers (SBBs) during the peri-operative period. The results indicated a concerning trend: women who used SBBs were four times more likely to die compared to non-users, as indicated by an adjusted hazard ratio (HR) of 5.82 (95% CI 1.17-28.91, p=0.031). This finding suggests that SBB usage around the time of surgery may have a detrimental effect on overall survival.
- Selective Beta-Blockers (SBBs): Usage during the peri-operative period was associated with a fourfold increase in the likelihood of death compared to non-users.
- Nonselective Beta-Blockers (NSBBs): No significant difference in progression-free survival was observed between users and non-users.
- Recurrence of Disease: SBB users were four times more likely to experience disease recurrence compared to non-users.
Future Directions and Clinical Implications
The study's findings suggest that peri-operative SBB use is associated with poorer overall survival, while any SBB use is linked to poorer progression-free survival in patients with EOC. While preclinical studies might hint at survival benefits, the current clinical data indicates a potential harm from SBB use, underscoring the necessity for further investigation. Future research should aim to clarify the underlying mechanisms and explore alternative strategies to improve outcomes for women with ovarian cancer.