Beta-blockers Have No Impact on Survival in Pancreatic Ductal Adenocarcinoma Prior to Cancer Diagnosis
Authors
Affiliations
Previous studies have suggested that β-adrenergic signaling may regulate the growth of various cancers. The aim of our study is to investigate the association between the incidental use of beta-blockers for various conditions on the overall survival of patients with pancreatic ductal adenocarcinoma (PDAC). Patients with histologically-confirmed PDAC between 2007 and 2011 were extracted from Surveillance, Epidemiology, and End Results registry (SEER)-Medicare linked database. Kaplan Meier and multivariable Cox Proportional-Hazard models were used to examine the association between beta-blocker usage before diagnosis and overall survival adjusting for appropriate confounders. As an additional analysis we also examined continuous beta-blocker use before and after diagnosis. From 2007 to 2011, 13,731 patients were diagnosed with PDAC. Of these, 7130 patients had Medicare Part D coverage in the 6-month period before diagnosis, with 2564 (36%) of these patients using beta-blockers in this period. Patients receiving beta-blockers had a mean survival time of 5.1 months compared to 6 months for non-users (p < 0.01). In multivariable analysis, beta-blockers usage was not associated with improved survival (Hazard Ratio (HR) 1.04, 95%, Confidence Interval (CI) 0.98-1.1, p = 0.2). When patients were stratified by conditions with indications for beta-blocker usage, such as hypertension, coronary artery disease and cardiac arrhythmia, differences in survival were insignificant compared to non-users in all groups (p > 0.05). After stratification by receptor selectivity, this lack of association with survival persisted (p > 0.05 for all). As a subgroup analysis, looking at patients with continuous Medicare Part D coverage who used beta-blockers in the 6-month period before and after cancer diagnosis, we identified 7085 patients, of which 1750 (24.7%) had continuous beta blocker use. In multivariable analysis, continuous beta-blockers usage was associated with improved survival (Hazard Ratio (HR) 0.86, 95%, Confidence Interval (CI) 0.8-0.9, p < 0.01). Beta-blocker usage before diagnosis does not confer a survival advantage in patients with PDAC, though continuous use before and after diagnosis did confer a survival advantage. Prospective studies into the mechanism for this advantage are needed.
Clinical Evaluation of the Pancreatic Cancer Microenvironment: Opportunities and Challenges.
Szczepanski J, Rudolf M, Shi J Cancers (Basel). 2024; 16(4).
PMID: 38398185 PMC: 10887250. DOI: 10.3390/cancers16040794.
Beta-blocker adjunct therapy as a prospective anti-metastatic with cardio-oncologic regulation.
Nair S, Benny S, Jose W, Aneesh T P Clin Exp Metastasis. 2024; 41(1):9-24.
PMID: 38177715 DOI: 10.1007/s10585-023-10258-y.
Targeting the Cancer-Neuronal Crosstalk in the Pancreatic Cancer Microenvironment.
Capodanno Y, Hirth M Int J Mol Sci. 2023; 24(19).
PMID: 37834436 PMC: 10573820. DOI: 10.3390/ijms241914989.
Bozec A, Brugel M, Djerada Z, Ayad M, Perrier M, Carlier C Front Pharmacol. 2023; 14:1137791.
PMID: 37274119 PMC: 10235451. DOI: 10.3389/fphar.2023.1137791.
The connection between innervation and metabolic rearrangements in pancreatic cancer through serine.
Dong M, Cao L, Cui R, Xie Y Front Oncol. 2022; 12:992927.
PMID: 36582785 PMC: 9793709. DOI: 10.3389/fonc.2022.992927.