Literature DB >> 33441781

Beta-blockers have no impact on survival in pancreatic ductal adenocarcinoma prior to cancer diagnosis.

Anthony Yang1, Haley M Zylberberg1, Sheila D Rustgi1, Sunil P Amin2, Ariel Bar-Mashiah1, Paolo Boffetta3, Aimee L Lucas4.   

Abstract

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.

Entities:  

Year:  2021        PMID: 33441781      PMCID: PMC7807087          DOI: 10.1038/s41598-020-79999-0

Source DB:  PubMed          Journal:  Sci Rep        ISSN: 2045-2322            Impact factor:   4.379


  33 in total

1.  Metformin Improves Survival in Patients with Pancreatic Ductal Adenocarcinoma and Pre-Existing Diabetes: A Propensity Score Analysis.

Authors:  S Amin; G Mhango; J Lin; A Aronson; J Wisnivesky; P Boffetta; Aimee L Lucas
Journal:  Am J Gastroenterol       Date:  2016-07-19       Impact factor: 10.864

2.  Cancer statistics, 2018.

Authors:  Rebecca L Siegel; Kimberly D Miller; Ahmedin Jemal
Journal:  CA Cancer J Clin       Date:  2018-01-04       Impact factor: 508.702

3.  Chronic stress accelerates pancreatic cancer growth and invasion: a critical role for beta-adrenergic signaling in the pancreatic microenvironment.

Authors:  Corina Kim-Fuchs; Caroline P Le; Matthew A Pimentel; David Shackleford; Davide Ferrari; Eliane Angst; Frédéric Hollande; Erica K Sloan
Journal:  Brain Behav Immun       Date:  2014-03-17       Impact factor: 7.217

4.  Beta-Blocker Drug Use and Survival among Patients with Pancreatic Adenocarcinoma.

Authors:  Ruzan Udumyan; Scott Montgomery; Fang Fang; Henrik Almroth; Unnur Valdimarsdottir; Anders Ekbom; Karin E Smedby; Katja Fall
Journal:  Cancer Res       Date:  2017-05-04       Impact factor: 12.701

5.  Selective β2-AR Blockage Suppresses Colorectal Cancer Growth Through Regulation of EGFR-Akt/ERK1/2 Signaling, G1-Phase Arrest, and Apoptosis.

Authors:  Chih-Chien Chin; Jhy-Ming Li; Kam-Fai Lee; Yun-Ching Huang; Kuan-Chieh Wang; Hsiao-Ching Lai; Chih-Chung Cheng; Yi-Hung Kuo; Chung-Sheng Shi
Journal:  J Cell Physiol       Date:  2015-09-01       Impact factor: 6.384

6.  β2-adrenergic antagonists suppress pancreatic cancer cell invasion by inhibiting CREB, NFκB and AP-1.

Authors:  Dong Zhang; Qing-Yong Ma; Heng-Tong Hu; Min Zhang
Journal:  Cancer Biol Ther       Date:  2010-07-01       Impact factor: 4.742

7.  Stress hormone-mediated invasion of ovarian cancer cells.

Authors:  Anil K Sood; Robert Bhatty; Aparna A Kamat; Charles N Landen; Liz Han; Premal H Thaker; Yang Li; David M Gershenson; Susan Lutgendorf; Steven W Cole
Journal:  Clin Cancer Res       Date:  2006-01-15       Impact factor: 12.531

Review 8.  Intercepting neoplastic progression in lung malignancies via the beta adrenergic (β-AR) pathway: implications for anti-cancer drug targets.

Authors:  Hussein A N Al-Wadei; Mohammad F Ullah; Mohammed H Al-Wadei
Journal:  Pharmacol Res       Date:  2012-04-02       Impact factor: 7.658

9.  The association of statin use after cancer diagnosis with survival in pancreatic cancer patients: a SEER-medicare analysis.

Authors:  Christie Y Jeon; Stephen J Pandol; Bechien Wu; Galen Cook-Wiens; Roberta A Gottlieb; C Noel Bairey Merz; Noel Bairey Merz; Marc T Goodman
Journal:  PLoS One       Date:  2015-04-01       Impact factor: 3.240

10.  Beta-adrenergic receptors are expressed across diverse cancers.

Authors:  Steven L Rains; Clarissa N Amaya; Brad A Bryan
Journal:  Oncoscience       Date:  2017-08-23
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