Risk of cardiovascular disease in breast cancer patients receiving aromatase inhibitors vs. tamoxifen: A systematic review and meta-analysis

被引:21
作者
Yu, Qiuyan [1 ]
Xu, Yueping [1 ]
Yu, Enguang [1 ]
Zheng, Zhufeng [1 ]
机构
[1] Jiaxing Hosp Tradit Chinese Med, Dept Nursing, 1501 Zhongshan East Rd, Jiaxing 314001, Zhejiang, Peoples R China
关键词
aromatase inhibitors; breast cancer; cardiovascular disease; endocrine therapy; tamoxifen; ADJUVANT ENDOCRINE THERAPY; POSTMENOPAUSAL WOMEN; DRUG-THERAPY; ANASTROZOLE; ESTROGEN; OUTCOMES; EVENTS; TRENDS; HEART;
D O I
10.1111/jcpt.13598
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
What is known and objective Breast cancer is one of the leading causes of morbidity and mortality in women worldwide. In order to reduce the risks of its recurrence, endocrine therapies, such as tamoxifen and aromatase inhibitors are commonly administered. Despite having a similar efficacy in preventing breast cancer recurrence, these drugs differ in terms of instigating cardiovascular morbidities. Recent randomized controlled trials and cohort studies provide inconclusive evidence of the cardiovascular risks associated with the administration of these endocrine therapies. This present review and meta-analysis evaluates the comparative cardiovascular adverse event outcomes in breast cancer patients receiving tamoxifen and aromatase inhibitors. To evaluate the comparative cardiovascular adverse outcomes, such as venous thromboembolism, heart failure, angina, myocardial infarction and stroke in patients with breast cancer receiving tamoxifen and aromatase inhibitors. Methods A systematic search of the academic literature was performed according to the PRISMA guidelines across five databases, including Web of Science, EMBASE, CENTRAL, Scopus, and MEDLINE. A random-effect meta-analysis was conducted to compare the cardiovascular adverse events (i.e. venous thromboembolism, heart failure, angina, myocardial infarction, stroke) in breast cancer patients treated with tamoxifen and aromatase inhibitors. Results and discussion From 993 studies, 20 eligible studies were identified, with 174,142 female breast cancer patients (mean age: 67.4 +/- 3.8 years). A meta-analysis revealed insignificantly (p > 0.05) higher risks of venous thromboembolism (Odds ratio, 95% CI: 1.70, 0.91-3.18) in patients treated with tamoxifen as compared to aromatase inhibitors. We also observed insignificantly higher risks of stroke (0.93, 0.45-1.91), angina (0.77, 0.12-4.59), myocardial infarction (0.74, 0.30-1.79), and heart failure (0.81, 0.22-2.91) in patients receiving aromatase inhibitors as compared to tamoxifen. What is new and conclusions The study provides evidence regarding the comparative cardiovascular adverse outcomes between breast cancer patients consuming tamoxifen and aromatase inhibitors. The study reports an insignificant increase in the events of stroke, angina, myocardial infarction, and heart failure in breast cancer patients treated with aromatase inhibitors as compared to tamoxifen. The study also reports that tamoxifen treatment is associated with an insignificant increase in the events of venous thromboembolism as compared to treatment with aromatase inhibitors.
引用
收藏
页码:575 / 587
页数:13
相关论文
共 58 条
  • [1] The risk of myocardial infarction with aromatase inhibitors relative to tamoxifen in post-menopausal women with early stage breast cancer
    Abdel-Qadir, Husam
    Amir, Eitan
    Fischer, Hadas D.
    Fu, Longdi
    Austin, Peter C.
    Harvey, Paula J.
    Rochon, Paula A.
    Lee, Douglas S.
    Anderson, Geoffrey M.
    [J]. EUROPEAN JOURNAL OF CANCER, 2016, 68 : 11 - 21
  • [2] Abo-Touk Niveen A, 2010, J Egypt Natl Canc Inst, V22, P79
  • [3] [Anonymous], What is Breast Cancer?
  • [4] A systematic comparison of software dedicated to meta-analysis of causal studies
    Bax, Leon
    Yu, Ly-Mee
    Ikeda, Noriaki
    Moons, Karel G. M.
    [J]. BMC MEDICAL RESEARCH METHODOLOGY, 2007, 7 (1)
  • [5] Disease-Related Outcomes With Long-Term Follow-Up: An Updated Analysis of the Intergroup Exemestane Study
    Bliss, Judith M.
    Kilburn, Lucy S.
    Coleman, Robert E.
    Forbes, John F.
    Coates, Alan S.
    Jones, Stephen E.
    Jassem, Jacek
    Delozier, Thierry
    Andersen, Jorn
    Paridaens, Robert
    van de Velde, Cornelis J. H.
    Lonning, Per E.
    Morden, James
    Reise, Justine
    Cisar, Laura
    Menschik, Thomas
    Coombes, R. Charles
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2012, 30 (07) : 709 - 717
  • [6] Switching to anastrozole versus continued tamoxifen treatment of early breast cancer. Updated results of the Italian tamoxifen anastrozole (ITA) trial
    Boccardo, F.
    Rubagotti, A.
    Guglielmini, P.
    Fini, A.
    Paladini, G.
    Mesiti, M.
    Rinaldini, M.
    Scali, S.
    Porpiglia, M.
    Benedetto, C.
    Restuccia, N.
    Buzzi, F.
    Franchi, R.
    Massidda, B.
    Distante, V.
    Amadori, D.
    Sismondi, P.
    [J]. ANNALS OF ONCOLOGY, 2006, 17 : VII10 - VII14
  • [7] Meta-analysis of vascular and neoplastic events associated with tamoxifen
    Braithwaite, RS
    Chlebowski, RT
    Lau, J
    George, S
    Hess, R
    Col, NF
    [J]. JOURNAL OF GENERAL INTERNAL MEDICINE, 2003, 18 (11) : 937 - 947
  • [8] Buzdar AU., 2007, ENDOCRINE THERAPIES
  • [9] Aromatase inhibitors for breast cancer in postmenopausal women
    Campos, SM
    [J]. ONCOLOGIST, 2004, 9 (02) : 126 - 136
  • [10] CDC Breast Cancer, 2020, WHAT IS BREAST CANC