Luminal breast cancer: from biology to treatment
- PMID: 23881035
- DOI: 10.1038/nrclinonc.2013.124
Luminal breast cancer: from biology to treatment
Abstract
Oestrogen receptor (ER)-positive--or luminal--tumours represent around two-thirds of all breast cancers. Luminal breast cancer is a highly heterogeneous disease comprising different histologies, gene-expression profiles and mutational patterns, with very varied clinical courses and responses to systemic treatment. Despite adjuvant endocrine therapy and chemotherapy treatment for patients at high risk of relapse, both early and late relapses still occur, a fact that highlights the unmet medical needs of these patients. Ongoing research aims to identify those patients who can be spared adjuvant chemotherapy and who will benefit from extended adjuvant hormone therapy. This research also aims to explore the role of adjuvant bisphosphonates, to interrogate new agents for targeting minimal residual disease, and to address endocrine resistance. Data from next-generation sequencing studies have given us new insight into the biology of luminal breast cancer and, together with advances in preclinical models and the availability of newer targeted agents, have led to the testing of rationally chosen combination treatments in clinical trials. However, a major challenge will be to make sense of the large amount of patient genomic data that is becoming increasingly available. This analysis will be critical to our understanding how intertumour and intratumour heterogeneity can influence treatment response and resistance.
Similar articles
-
Proliferation and estrogen signaling can distinguish patients at risk for early versus late relapse among estrogen receptor positive breast cancers.Breast Cancer Res. 2013;15(5):R86. doi: 10.1186/bcr3481. Breast Cancer Res. 2013. PMID: 24060333 Free PMC article.
-
Adjuvant chemotherapy in luminal breast cancers.Breast. 2011 Oct;20 Suppl 3:S128-31. doi: 10.1016/S0960-9776(11)70309-5. Breast. 2011. PMID: 22015279 Review.
-
Adjuvant endocrine therapy alone in patients with node-positive, luminal A type breast cancer.Medicine (Baltimore). 2017 Jun;96(22):e6777. doi: 10.1097/MD.0000000000006777. Medicine (Baltimore). 2017. PMID: 28562530 Free PMC article.
-
Current issues with luminal subtype classification in terms of prediction of benefit from endocrine therapy in early breast cancer.Histopathology. 2018 Oct;73(4):545-558. doi: 10.1111/his.13523. Epub 2018 May 28. Histopathology. 2018. PMID: 29603357 Review.
-
Current and future status of adjuvant therapy for breast cancer.Cancer. 2003 Feb 1;97(3 Suppl):880-6. doi: 10.1002/cncr.11124. Cancer. 2003. PMID: 12548590 Review.
Cited by
-
A deep learning based holistic diagnosis system for immunohistochemistry interpretation and molecular subtyping.Neoplasia. 2024 Feb 26;50:100976. doi: 10.1016/j.neo.2024.100976. Online ahead of print. Neoplasia. 2024. PMID: 38412576 Free PMC article.
-
p66ShcA promotes malignant breast cancer phenotypes by alleviating energetic and oxidative stress.Redox Biol. 2024 Apr;70:103028. doi: 10.1016/j.redox.2024.103028. Epub 2024 Jan 5. Redox Biol. 2024. PMID: 38211442 Free PMC article.
-
Targeting the Tumor Microenvironment in Breast Cancer: Prognostic and Predictive Significance and Therapeutic Opportunities.Int J Mol Sci. 2023 Nov 26;24(23):16771. doi: 10.3390/ijms242316771. Int J Mol Sci. 2023. PMID: 38069096 Free PMC article. Review.
-
AI-enabled routine H&E image based prognostic marker for early-stage luminal breast cancer.NPJ Precis Oncol. 2023 Nov 15;7(1):122. doi: 10.1038/s41698-023-00472-y. NPJ Precis Oncol. 2023. PMID: 37968376 Free PMC article.
-
'Social' versus 'asocial' cells-dynamic competition flux balance analysis.NPJ Syst Biol Appl. 2023 Oct 28;9(1):53. doi: 10.1038/s41540-023-00313-5. NPJ Syst Biol Appl. 2023. PMID: 37898597 Free PMC article.
References
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
