Skip to main content
Top
Published in: Breast Cancer Research and Treatment 1/2017

01-07-2017 | Editorial

The relationship between statins and breast cancer prognosis varies by statin type and exposure time: a meta-analysis

Authors: Binliang Liu, Zongbi Yi, Xiuwen Guan, Yi-Xin Zeng, Fei Ma

Published in: Breast Cancer Research and Treatment | Issue 1/2017

Login to get access

Abstract

Purpose

Breast cancer is the most common cancer in females and the leading cause of death worldwide. The effects of statins on breast cancer prognosis have long been controversial; thus, it is important to investigate the relationship between statin type, exposure time, and breast cancer prognosis. This study sought to explore the effect of statins, as well as the different effects of statin solubility and variable follow-up times, on breast cancer prognosis.

Methods

We searched the MEDLINE (via PubMed), EMBASE (via OvidSP), Cochrane Library, and ISI Web of Knowledge databases using combinations of the terms “breast neoplasms[MeSH],” “statins” or “lipid-lowering drug,” “prognosis” or “survival,” or “mortality” or “outcome” with no limit on the publication date. We searched the databases between inception and October 15, 2016. Reference lists of the included studies and relevant reviews were also manually screened. The initial search identified 71 publications, and 7 of these studies, which included a total of 197,048 women, met the selection criteria. Two authors independently screened each study for inclusion and extracted the data. The data were analyzed using Stata/SE 11.0.

Results

Overall statin use was associated with lower cancer-specific mortality and all-cause mortality, although the benefit appeared to be constrained by statin type and follow-up time. Lipophilic statins were associated with decreased breast cancer-specific and all-cause mortality; however, hydrophilic statins were weakly protective against only all-cause mortality and not breast cancer-specific mortality. Of note, one group with more than 4 years of follow-up did not show a significant correlation between statin use and cancer-specific mortality or all-cause mortality, whereas groups with less than 4 years of follow-up still showed the protective effect of statins against cancer-specific mortality and all-cause mortality.

Conclusions

Although statins can reduce breast cancer patient mortality, the benefit appears to be constrained by statin type and follow-up time. Lipophilic statins showed a strong protective function in breast cancer patients, whereas hydrophilic statins only slightly improved all-cause mortality. Finally, the protective effect of statins could only be observed in groups with less than 4 years of follow-up. These findings are meaningful in clinical practice, although some conclusions contradict conventional wisdom and will thus require further exploration.
Literature
1.
go back to reference Vicente GG, José EGM, Vicente PC (2016) Overview of guidelines for the management of dyslipidemia: EU perspectives. Vasc Health Risk Manag 12:357–369CrossRef Vicente GG, José EGM, Vicente PC (2016) Overview of guidelines for the management of dyslipidemia: EU perspectives. Vasc Health Risk Manag 12:357–369CrossRef
2.
go back to reference Ferlay J et al (2015) Cancer incidence and mortality worldwide: sources, methods and major patterns in GLOBOCAN 2012. Int J Cancer 136(5):E359–E386CrossRefPubMed Ferlay J et al (2015) Cancer incidence and mortality worldwide: sources, methods and major patterns in GLOBOCAN 2012. Int J Cancer 136(5):E359–E386CrossRefPubMed
3.
go back to reference Borgquist S et al (2016) Statin use and breast cancer risk in the nurses’ health study. Cancer Epidemiol Biomark Prev 25(1):201–206CrossRef Borgquist S et al (2016) Statin use and breast cancer risk in the nurses’ health study. Cancer Epidemiol Biomark Prev 25(1):201–206CrossRef
6.
go back to reference Anothaisintawee T et al (2016) Effect of lipophilic and hydrophilic statins on breast cancer risk in Thai women: a cross-sectional study. J Cancer 7(9):1163–1168CrossRefPubMedPubMedCentral Anothaisintawee T et al (2016) Effect of lipophilic and hydrophilic statins on breast cancer risk in Thai women: a cross-sectional study. J Cancer 7(9):1163–1168CrossRefPubMedPubMedCentral
7.
go back to reference Schlienger RG, Meier CR (2003) HMG-CoA reductase inhibitors in osteoporosis. Drugs Aging 20(5):321–336CrossRefPubMed Schlienger RG, Meier CR (2003) HMG-CoA reductase inhibitors in osteoporosis. Drugs Aging 20(5):321–336CrossRefPubMed
8.
go back to reference Wu Q et al (2015) Statin use and breast cancer survival and risk: a systematic review and meta-analysis. Oncotarget 6(40):42988PubMedPubMedCentral Wu Q et al (2015) Statin use and breast cancer survival and risk: a systematic review and meta-analysis. Oncotarget 6(40):42988PubMedPubMedCentral
9.
go back to reference Manthravadi S, Shrestha A, Madhusudhana S (2016) Impact of statin use on cancer recurrence and mortality in breast cancer: a systematic review and meta-analysis. Int J Cancer 139(6):1281–1288CrossRefPubMed Manthravadi S, Shrestha A, Madhusudhana S (2016) Impact of statin use on cancer recurrence and mortality in breast cancer: a systematic review and meta-analysis. Int J Cancer 139(6):1281–1288CrossRefPubMed
11.
go back to reference Cardwell CR et al (2015) Statin use after diagnosis of breast cancer and survival: a population-based cohort study. Epidemiology 26(1):68–78CrossRefPubMed Cardwell CR et al (2015) Statin use after diagnosis of breast cancer and survival: a population-based cohort study. Epidemiology 26(1):68–78CrossRefPubMed
13.
go back to reference Nickels S et al (2013) Mortality and recurrence risk in relation to the use of lipid-lowering drugs in a prospective breast cancer patient cohort. Plos One 8(9):e75088CrossRefPubMedPubMedCentral Nickels S et al (2013) Mortality and recurrence risk in relation to the use of lipid-lowering drugs in a prospective breast cancer patient cohort. Plos One 8(9):e75088CrossRefPubMedPubMedCentral
14.
go back to reference Chae YK et al (2011) Reduced risk of breast cancer recurrence in patients using ACE inhibitors, ARBs, and/or Statins. Cancer Investig 29(9):585–593CrossRef Chae YK et al (2011) Reduced risk of breast cancer recurrence in patients using ACE inhibitors, ARBs, and/or Statins. Cancer Investig 29(9):585–593CrossRef
15.
go back to reference Ceacareanu AC et al (2011) Statin treatment use in diabetic patients with breast cancer: a potential C-reactive protein mediated benefit in ASCO Breast Cancer Symposium Ceacareanu AC et al (2011) Statin treatment use in diabetic patients with breast cancer: a potential C-reactive protein mediated benefit in ASCO Breast Cancer Symposium
17.
go back to reference Wulaningsih W et al (2015) Prediagnostic serum glucose and lipids in relation to survival in breast cancer patients: a competing risk analysis. BMC Cancer 15(1):913CrossRefPubMedPubMedCentral Wulaningsih W et al (2015) Prediagnostic serum glucose and lipids in relation to survival in breast cancer patients: a competing risk analysis. BMC Cancer 15(1):913CrossRefPubMedPubMedCentral
20.
go back to reference Park YH et al (2013) Statin induces inhibition of triple negative breast cancer (TNBC) cells via PI3 K pathway. Biochem Biophys Res Commun 439(2):275–279CrossRefPubMed Park YH et al (2013) Statin induces inhibition of triple negative breast cancer (TNBC) cells via PI3 K pathway. Biochem Biophys Res Commun 439(2):275–279CrossRefPubMed
21.
22.
23.
24.
go back to reference Gauthaman K, Fong CY, Bongso A (2009) Statins, stem cells, and cancer. J Cell Biochem 106(6):975–983CrossRefPubMed Gauthaman K, Fong CY, Bongso A (2009) Statins, stem cells, and cancer. J Cell Biochem 106(6):975–983CrossRefPubMed
26.
go back to reference Seeger H, Wallwiener D, Mueck AO (2003) Statins can inhibit proliferation of human breast cancer cells in vitro. Exp Clin Endocrinol Diabetes 111(1):47–48CrossRefPubMed Seeger H, Wallwiener D, Mueck AO (2003) Statins can inhibit proliferation of human breast cancer cells in vitro. Exp Clin Endocrinol Diabetes 111(1):47–48CrossRefPubMed
27.
go back to reference Campbell MJ (2006) Breast cancer growth prevention by statins. Can Res 66(17):8707–8714CrossRef Campbell MJ (2006) Breast cancer growth prevention by statins. Can Res 66(17):8707–8714CrossRef
28.
go back to reference Nezasa K et al (2000) Uptake of HMG-CoA reductase inhibitor ZD4522 into hepatocytes and distribution into liver and other tissues of the rat. Atherosclerosis 151(1):39CrossRef Nezasa K et al (2000) Uptake of HMG-CoA reductase inhibitor ZD4522 into hepatocytes and distribution into liver and other tissues of the rat. Atherosclerosis 151(1):39CrossRef
29.
go back to reference Kiener PA et al (2001) Stimulation of inflammatory responses in vitro and in vivo by lipophilic HMG-CoA reductase inhibitors. Int Immunopharmacol 1(1):105–118CrossRefPubMed Kiener PA et al (2001) Stimulation of inflammatory responses in vitro and in vivo by lipophilic HMG-CoA reductase inhibitors. Int Immunopharmacol 1(1):105–118CrossRefPubMed
Metadata
Title
The relationship between statins and breast cancer prognosis varies by statin type and exposure time: a meta-analysis
Authors
Binliang Liu
Zongbi Yi
Xiuwen Guan
Yi-Xin Zeng
Fei Ma
Publication date
01-07-2017
Publisher
Springer US
Published in
Breast Cancer Research and Treatment / Issue 1/2017
Print ISSN: 0167-6806
Electronic ISSN: 1573-7217
DOI
https://doi.org/10.1007/s10549-017-4246-0

Other articles of this Issue 1/2017

Breast Cancer Research and Treatment 1/2017 Go to the issue
Webinar | 19-02-2024 | 17:30 (CET)

Keynote webinar | Spotlight on antibody–drug conjugates in cancer

Antibody–drug conjugates (ADCs) are novel agents that have shown promise across multiple tumor types. Explore the current landscape of ADCs in breast and lung cancer with our experts, and gain insights into the mechanism of action, key clinical trials data, existing challenges, and future directions.

Dr. Véronique Diéras
Prof. Fabrice Barlesi
Developed by: Springer Medicine