Impact of beta blockers on epithelial ovarian cancer survival

被引:142
作者
Diaz, Elena S. [1 ]
Karlan, Beth Y. [1 ]
Li, Andrew J. [1 ]
机构
[1] Cedars Sinai Med Ctr, Dept Obstet & Gynecol, Div Gynecol Oncol, Los Angeles, CA 90048 USA
关键词
Ovarian cancer; Beta blockers; Adrenergic hormones; ENDOTHELIAL GROWTH-FACTOR; BREAST-CANCER; CARCINOMA CELLS; STRESS; METASTASIS; DEPRESSION; ANGIOGENESIS; MECHANISMS; EXPRESSION; PATHWAYS;
D O I
10.1016/j.ygyno.2012.07.102
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
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. (C) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:375 / 378
页数:4
相关论文
共 33 条
[1]
Al-Wadei HA, 2009, ANTI-CANCER DRUG, V20, P477
[2]
Opinion - The influence of bio-behavioural factors on tumour biology: pathways and mechanisms [J].
Antoni, MH ;
Lutgendorf, SK ;
Cole, SW ;
Dhabhar, FS ;
Sephton, SE ;
McDonald, PG ;
Stefanek, M ;
Sood, AK .
NATURE REVIEWS CANCER, 2006, 6 (03) :240-248
[3]
Beta Blockers and Breast Cancer Mortality: A Population-Based Study [J].
Barron, Thomas I. ;
Connolly, Roisin M. ;
Sharp, Linda ;
Bennett, Kathleen ;
Visvanathan, Kala .
JOURNAL OF CLINICAL ONCOLOGY, 2011, 29 (19) :2635-2644
[4]
Perioperative use of β-blockers and COX-2 inhibitors may improve immune competence and reduce the risk of tumor metastasis [J].
Benish, Marganit ;
Bartal, Inbal ;
Goldfarb, Yael ;
Levi, Ben ;
Avraham, Roi ;
Raz, Amiram ;
Ben-Eliyahu, Shamgar .
ANNALS OF SURGICAL ONCOLOGY, 2008, 15 (07) :2042-2052
[5]
Catecholamines Regulate Tumor Angiogenesis [J].
Chakroborty, Debanjan ;
Sarkar, Chandrani ;
Basu, Biswarup ;
Dasgupta, Partha Sarathi ;
Basu, Sujit .
CANCER RESEARCH, 2009, 69 (09) :3727-3730
[6]
Molecular Pathways: Beta-Adrenergic Signaling in Cancer [J].
Cole, Steven W. ;
Sood, Anil K. .
CLINICAL CANCER RESEARCH, 2012, 18 (05) :1201-1206
[7]
De Giorgi V, 2011, J CLIN ONCOL S, V29
[8]
Control of adhesion-dependent cell survival by focal adhesion kinase [J].
Frisch, SM ;
Vuori, K ;
Ruoslahti, E ;
ChanHui, PY .
JOURNAL OF CELL BIOLOGY, 1996, 134 (03) :793-799
[9]
DISRUPTION OF EPITHELIAL CELL-MATRIX INTERACTIONS INDUCES APOPTOSIS [J].
FRISCH, SM ;
FRANCIS, H .
JOURNAL OF CELL BIOLOGY, 1994, 124 (04) :619-626
[10]
Cardiovascular alterations and autonomic imbalance in an experimental model of depression [J].
Grippo, AJ ;
Moffitt, JA ;
Johnson, AK .
AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, 2002, 282 (05) :R1333-R1341