» Articles » PMID: 31630379

Advances in Endocrine-Based Therapies for Estrogen Receptor-Positive Metastatic Breast Cancer

Overview
Journal Drugs
Specialty Pharmacology
Date 2019 Oct 21
PMID 31630379
Citations 30
Authors
Affiliations
Soon will be listed here.
Abstract

Approximately 70% of breast cancers are estrogen-receptor positive. Tamoxifen and aromatase inhibitors have been the mainstay of endocrine therapy and have improved breast cancer survival. However, a large number of patients experience disease recurrence either during or following completion of endocrine therapy. Recent improvements in our understanding of the various mechanisms underlying the development of endocrine resistance have led to a dramatic change in the landscape of current endocrine treatment with the introduction of new drugs targeting molecular pathways involved in endocrine resistance. Over the past years we have witnessed the use of combination endocrine therapy with mammalian target of rapamycin antagonists, whilst most recently the introduction of cyclin-dependent kinase 4/6 inhibitors has significantly improved response to endocrine therapy. Whilst not a formal systematic review, this article will provide historical background and summarise key clinical trials and current strategies in both first-line and second-line endocrine therapy.

Citing Articles

Targeting estrogen-regulated system x promotes ferroptosis and endocrine sensitivity of ER+ breast cancer.

Cao J, Zhou T, Wu T, Lin R, Huang J, Shi D Cell Death Dis. 2025; 16(1):30.

PMID: 39833180 PMC: 11756422. DOI: 10.1038/s41419-025-07354-0.


The present and future of the Cancer Dependency Map.

Arafeh R, Shibue T, Dempster J, Hahn W, Vazquez F Nat Rev Cancer. 2024; 25(1):59-73.

PMID: 39468210 DOI: 10.1038/s41568-024-00763-x.


Obesity-Senescence-Breast Cancer: Clinical Presentation of a Common Unfortunate Cycle.

Engin A, Engin A Adv Exp Med Biol. 2024; 1460:821-850.

PMID: 39287873 DOI: 10.1007/978-3-031-63657-8_27.


Effects of Curcumin and Estrogen Receptor Alpha in Luminal Breast Cancer Cells.

Palacios-Navarro L, Crispin L, Munoz J, Calaf G Diagnostics (Basel). 2024; 14(16).

PMID: 39202273 PMC: 11353822. DOI: 10.3390/diagnostics14161785.


A narrative review of the clinical development of CDK4/6 inhibitor abemaciclib in breast cancer.

Yang L, Chen Y, Wang N, Han W Transl Breast Cancer Res. 2024; 3:4.

PMID: 38751545 PMC: 11093002. DOI: 10.21037/tbcr-21-36.


References
1.
Thangavel C, Dean J, Ertel A, Knudsen K, Aldaz C, Witkiewicz A . Therapeutically activating RB: reestablishing cell cycle control in endocrine therapy-resistant breast cancer. Endocr Relat Cancer. 2011; 18(3):333-45. PMC: 3624623. DOI: 10.1530/ERC-10-0262. View

2.
Smith I, Dowsett M . Aromatase inhibitors in breast cancer. N Engl J Med. 2003; 348(24):2431-42. DOI: 10.1056/NEJMra023246. View

3.
Im S, Lu Y, Bardia A, Harbeck N, Colleoni M, Franke F . Overall Survival with Ribociclib plus Endocrine Therapy in Breast Cancer. N Engl J Med. 2019; 381(4):307-316. DOI: 10.1056/NEJMoa1903765. View

4.
Nishimura R, Osako T, Okumura Y, Tashima R, Toyozumi Y, Arima N . Changes in the ER, PgR, HER2, p53 and Ki-67 biological markers between primary and recurrent breast cancer: discordance rates and prognosis. World J Surg Oncol. 2011; 9:131. PMC: 3214885. DOI: 10.1186/1477-7819-9-131. View

5.
Milani A, Geuna E, Mittica G, Valabrega G . Overcoming endocrine resistance in metastatic breast cancer: Current evidence and future directions. World J Clin Oncol. 2014; 5(5):990-1001. PMC: 4259959. DOI: 10.5306/wjco.v5.i5.990. View