Elena S Diaz1, Beth Y Karlan, Andrew J Li. 1. Department of Obstetrics and Gynecology, Division of Gynecologic Oncology, Cedars-Sinai Medical Center, Los Angeles, CA 90048, USA. Elena.Diaz@cshs.org
Abstract
OBJECTIVE: Stress may promote ovarian cancer progression through mechanisms including autonomic nervous system mediators such as norepinephrine and epinephrine. Beta blockers, used to treat hypertension, block production of these adrenergic hormones, and have been associated with prolonged survival in several malignancies. We sought to determine the association between beta blocker use and epithelial ovarian cancer (EOC) disease progression and survival. METHODS: We performed an institutional retrospective review of patients with EOC treated between 1996 and 2006. Patients underwent cytoreductive surgery followed by platinum-based chemotherapy. Women were considered beta blocker users if these medications were documented on at least two records more than 6 months apart. Statistical tests included Fisher's exact, Kaplan-Meier, and Cox regression analyses. RESULTS: 248 met inclusion criteria. 68 patients used antihypertensives, and 23 used beta blockers. Median progression-free survival for beta blocker users was 27 months, compared with 17 months for non-users (p=0.05). Similarly, overall disease-specific survival was longer for beta blocker users (56 months) compared with non-users (48 months, p=0.02, hazard ratio=0.56). Multivariate analysis identified beta blocker use as an independent positive prognostic factor, after controlling for age, stage, grade, and cytoreduction status (p=0.03). Overall survival remained longer for beta blocker users (56 months) when compared with hypertensive patients on other medications (34 months) and patients without hypertension (51 months) (p=0.007). CONCLUSIONS: In this cohort of patients with EOC, beta blocker use was associated with a 54% reduced chance of death compared with that of non-users.
OBJECTIVE: Stress may promote ovarian cancer progression through mechanisms including autonomic nervous system mediators such as norepinephrine and epinephrine. Beta blockers, used to treat hypertension, block production of these adrenergic hormones, and have been associated with prolonged survival in several malignancies. We sought to determine the association between beta blocker use and epithelial ovarian cancer (EOC) disease progression and survival. METHODS: We performed an institutional retrospective review of patients with EOC treated between 1996 and 2006. Patients underwent cytoreductive surgery followed by platinum-based chemotherapy. Women were considered beta blocker users if these medications were documented on at least two records more than 6 months apart. Statistical tests included Fisher's exact, Kaplan-Meier, and Cox regression analyses. RESULTS: 248 met inclusion criteria. 68 patients used antihypertensives, and 23 used beta blockers. Median progression-free survival for beta blocker users was 27 months, compared with 17 months for non-users (p=0.05). Similarly, overall disease-specific survival was longer for beta blocker users (56 months) compared with non-users (48 months, p=0.02, hazard ratio=0.56). Multivariate analysis identified beta blocker use as an independent positive prognostic factor, after controlling for age, stage, grade, and cytoreduction status (p=0.03). Overall survival remained longer for beta blocker users (56 months) when compared with hypertensivepatients on other medications (34 months) and patients without hypertension (51 months) (p=0.007). CONCLUSIONS: In this cohort of patients with EOC, beta blocker use was associated with a 54% reduced chance of death compared with that of non-users.
Authors: Julie J Ruterbusch; Rouba Ali-Fehmi; Sara H Olson; Shawnita Sealy-Jefferson; Benjamin A Rybicki; Sharon Hensley-Alford; Mohamed A Elshaikh; Arthur R Gaba; Daniel Schultz; Adnan R Munkarah; Michele L Cote Journal: Am J Obstet Gynecol Date: 2014-06-19 Impact factor: 8.661
Authors: Lois M Ramondetta; Wei Hu; Premal H Thaker; Diana L Urbauer; Gary B Chisholm; Shannon N Westin; Yunjie Sun; Pedro T Ramirez; Nicole Fleming; Sunil K Sahai; Alpa M Nick; Jesusa M G Arevalo; Thomas Dizon; Robert L Coleman; Steve W Cole; Anil K Sood Journal: Gynecol Oncol Date: 2019-07-25 Impact factor: 5.482
Authors: Tianyi Huang; Shelley S Tworoger; Jonathan L Hecht; Megan S Rice; Anil K Sood; Laura D Kubzansky; Elizabeth M Poole Journal: Cancer Epidemiol Biomarkers Prev Date: 2016-09-01 Impact factor: 4.254
Authors: Jason W-L Eng; Chelsey B Reed; Kathleen M Kokolus; Rosemarie Pitoniak; Adam Utley; Mark J Bucsek; Wen Wee Ma; Elizabeth A Repasky; Bonnie L Hylander Journal: Nat Commun Date: 2015-03-10 Impact factor: 14.919
Authors: Marisa Coelho; Cátia Soares-Silva; Daniela Brandão; Franca Marino; Marco Cosentino; Laura Ribeiro Journal: J Cancer Res Clin Oncol Date: 2016-10-05 Impact factor: 4.553
Authors: Kathleen M Kokolus; Ying Zhang; Jeffrey M Sivik; Carla Schmeck; Junjia Zhu; Elizabeth A Repasky; Joseph J Drabick; Todd D Schell Journal: Oncoimmunology Date: 2017-12-21 Impact factor: 8.110