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Current status of hormone therapy in patients with hormone receptor positive (HR+) advanced breast cancer
- Source :
- Breast (Edinburgh, Scotland). 23(6)
- Publication Year :
- 2014
-
Abstract
- The natural history of HR+ breast cancer tends to be different from hormone receptor-negative disease in terms of time to recurrence, site of recurrence and overall aggressiveness of the disease. The developmental strategies of hormone therapy for the treatment of breast cancer have led to the classes of selective estrogen receptor modulators, selective estrogen receptor downregulators, and aromatase inhibitors. These therapeutic options have improved breast cancer outcomes in the metastatic setting, thereby delaying the need for chemotherapy. However, a subset of hormone receptor-positive breast cancers do not benefit from endocrine therapy (intrinsic resistance), and all HR+ metastatic breast cancers ultimately develop resistance to hormonal therapies (acquired resistance). Considering the multiple pathways involved in the HR network, targeting other components of pathologically activated intracellular signaling in breast cancer may prove to be a new direction in clinical research. This review focuses on current and emerging treatments for HR+ metastatic breast cancer.
- Subjects :
- Oncology
CA15-3
Selective Estrogen Receptor Modulators
medicine.medical_specialty
Antineoplastic Agents, Hormonal
medicine.medical_treatment
Estrogen receptor
Breast Neoplasms
Anastrozole
Breast cancer
Internal medicine
Nitriles
medicine
Humans
Neoplasm Metastasis
skin and connective tissue diseases
Fulvestrant
Estradiol
business.industry
Aromatase Inhibitors
Cancer
General Medicine
Triazoles
medicine.disease
Metastatic breast cancer
Tamoxifen
Receptors, Estrogen
Hormone receptor
Drug Resistance, Neoplasm
Hormonal therapy
Surgery
Female
Hormone therapy
business
Receptors, Progesterone
Subjects
Details
- ISSN :
- 15323080
- Volume :
- 23
- Issue :
- 6
- Database :
- OpenAIRE
- Journal :
- Breast (Edinburgh, Scotland)
- Accession number :
- edsair.doi.dedup.....0c918540fd124a2bfc2df27d08280d83