Can Statins Influence the Outcome of Patients with Triple Negative Breast Cancer?

Based on a paper titled “Association of statin use with clinical outcomes in patients with Triple- Negative Breast Cancer” 

Original paper: Nowakowska M, Lei X, Thompson M, Shaitelman S, Wehner M, Woodward W et al. Association of statin use with clinical outcomes in patients with triple-negative breast cancer. Journal of Clinical Oncology. 2021;39(15_suppl):523-523.

By: Murielle Nsiela 

Statins are groups of drugs used to reduce the amount of cholesterol found in the blood. They achieve this by inhibiting a substance required by the body to make cholesterol; this substance has shown to be upregulated in different types of cancers, including breast cancer[1]

Statins have been shown to exhibit more than one beneficial effect in cell migration, proliferation, and survival, which are all enhanced during a process whereby normal cells turn into cancerous cells[2]. Furthermore, statins may help treat breast cancer, including the most aggressive types such as triple-negative breast cancer (TNBC)[3]. TNBC makes up 10 to 20% of breast cancer and is more aggressive with fewer treatment options and worse outcomes[4]. Therefore, it has been suggested that statins target essential pathways associated with TNBC in addition to increasing the cancer cell death rate [5],[6],[7]

There have been conflicting outcomes concerning whether statins improve the outcome of breast cancer. Some studies have shown a link between statin intake and better outcomes for patients with breast cancer [8],[9],[10]. In contrast, other studies have found the contrary [11]. However, the research carried out by this clinical study aimed to investigate the relationship between the commencement of statin therapy in the twelve months after the patient has been diagnosed with breast cancer. They examined the outcome of women with stage one, two and three breast cancer and focused on breast cancer-specific survival (BCSS) and overall survival (OS) in patients with TNBC. The study involved women aged 66 years and older.

Within the study, 23,192 patients with stage one to three breast cancer met the standards to be included in the study. However, only 2,281 patients were given statins one year after being diagnosed. The results showed a statistically significant relationship between statins and better BCSS and OS in patients with TNBC. Further analysis indicated that women with early-stage TNBC are more likely to have a better outcome with statin intake. However, there was no association between BCSS or OS with patients that did not have TNBC. In addition, the study examined the type and intensity of statin used concerning women with and without TNBC. 

Regarding individuals with TNBC, there was statistical significance with L- statins and improved OS. Furthermore, the study suggested that using high-intensity statins provided the most substantial effect on OS in TNBC patients. Conversely, patients with no TNBC did not show much benefit from using statins [12].

In conclusion, there have been studies supporting and providing evidence for the association between statin intake and better survival for patients with TNBC. However, some worldwide studies have also shown conflicting evidence that it is not statistically significant. 

Although the use of statins for TNBC treatment may be unclear, this study shows potential for their use in the future. The clinical data indicates that there is a possibility that statins can be used as therapy for patients with TNBC, which supports other studies as well.

References

  1. Ehmsen S, Pedersen MH, Wang G, et al. Increased cholesterol bio-synthesis is a key characteristic of breast cancer stem cells influencing patient outcome. Cell Rep. 2019;27:3927- 3938.e6
  2. Beckwitt CH, Brufsky A, Oltvai ZN, Wells A. Statin drugs to reduce breast cancer recurrence and mortality. Breast Cancer Res. 2018;20:144
  3. Van Wyhe RD, Rahal OM, Woodward WA. Effect of statins on breast cancer recurrence and mortality: a review. Breast Cancer (Dove Med Press). 2017;9:559- 565.
  4. Yao H, He G, Yan S, et al. Triple- negative breast cancer: is there a treat-ment on the horizon? Oncotarget.  2017;8:1913- 1924
  5. Bjarnadottir O, Romero Q, Bendahl PO, et al. Targeting HMG- CoA reductase with statins in a window- of- opportunity breast cancer trial. Breast Cancer Res Treat. 2013;138:499- 508.
  6. Jung HH, Lee SH, Kim JY, Ahn JS, Park YH, Im YH. Statins affect ETS1- overexpressing triple- negative breast cancer cells by restoring DUSP4 deficiency. Sci Rep. 2016;6:33035.
  7. Liu H, Song Y, Qiu H, et al. Downregulation of FOXO3a by DNMT1 promotes breast cancer stem cell properties and tumorigenesis. Cell Death Differ. 2020;27:966- 983.
  8. Ahern TP, Pedersen L, Tarp M, et al. Statin prescriptions and breast cancer recurrence risk: a Danish nationwide prospective cohort study. J Natl Cancer Inst.  2011;103:1461- 1468.
  9. Murtola TJ, Visvanathan K, Artama M, Vainio H, Pukkala E. Statin use and breast cancer survival: a nationwide cohort study from Finland. PLoS One. 2014;9:e110231.
  10. Borgquist S, Broberg P, Tojjar J, Olsson H. Statin use and breast cancer survival— a Swedish nationwide study. BMC Cancer. 2019;19:54
  11. Cardwell CR, Hicks BM, Hughes C, Murray LJ. Statin use after diag-nosis of breast cancer and survival: a population- based cohort study. Epidemiology.  2015;26:68- 78
  12. Nowakowska M, Lei X, Thompson M, Shaitelman S, Wehner M, Woodward W et al. Association of statin use with clinical outcomes in patients with triple-negative breast cancer. Journal of Clinical Oncology. 2021;39(15_suppl):523-523.
This content is purely informational and isn’t medical guidance. It shouldn’t replace professional medical counsel. Always consult your physician regarding treatment risks and benefits. See our editorial standards for more details.

Get our health newsletter

Get daily health and wellness advice from our medical team.
Your privacy is important to us. Any information you provide to this website may be placed by us on our servers. If you do not agree do not provide the information.

Murielle Nsiela

MSc Graduate in Medical Engineering - Bachelor's degree, Pharmaceutical Science, Keele University, Staffordshire UK

MSc in Medical Engineering Design, Keele University Modules included: Advanced engineering applications, Engineering for medical applications report, Bioreactors and Growth environment, Creative engineering design, Experimental research methodology and research projects



BSc (Hons) Pharmaceutical Science, Technology and Business, Keele University Modules included: Core topics in pharmaceutical science, Laboratory studies - tabletting and liposomes report, applied Pharmaceutical Science 2, Pharmaceutical research project

Leave a Reply

Your email address will not be published. Required fields are marked *

my.klarity.health presents all health information in line with our terms and conditions. It is essential to understand that the medical information available on our platform is not intended to substitute the relationship between a patient and their physician or doctor, as well as any medical guidance they offer. Always consult with a healthcare professional before making any decisions based on the information found on our website.
Klarity is a citizen-centric health data management platform that enables citizens to securely access, control and share their own health data. Klarity Health Library aims to provide clear and evidence-based health and wellness related informative articles. 
Email:
Klarity / Managed Self Ltd
Alum House
5 Alum Chine Road
Westbourne Bournemouth BH4 8DT
VAT Number: 362 5758 74
Company Number: 10696687

Phone Number:

 +44 20 3239 9818