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Systemic Therapy for Estrogen Receptor–Positive, HER2-Negative Breast Cancer
Abstract
ER-positive, HER2-negative breast cancer, which accounts for about 70% of all breast cancers, is heterogeneous. Antiestrogen therapy is the cornerstone of systemic therapy, and its efficacy depends on such factors as grade, Ki-67 labeling, and progesterone receptor expression.
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“CDK4/6 inhibitors, such as palbociclib, ribociclib and abemaciclib, are effective in the treatment of some cancers, particularly oestrogen receptor-positive breast cancers147.”
From The current state of the art and future trends in RAS-targeted cancer therapies (2022) · cites this paper as [147]
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Metadata
- Authors
- Burstein, H. J.
- Affiliations
- Brigham and Women's Hospital (US)
- Corresponding author
- Burstein, Harold J.
- ORCID
- Burstein, Harold J.
- Venue
- New England Journal of Medicine
- Publisher
- Massachusetts Medical Society
- Published
- 2020-12-24
- Volume
- 383
- Issue
- 26
- Pages
- 2557-2570
- ISSN
- 0028-4793 (ISSN-L)
- 1533-4406
- OpenAlex
- W3116128628
- Cited by
- 316
- References
- 106
- Citations by year
- 2026: 51 · 2025: 53 · 2024: 67 · 2023: 62 · 2022: 53 · 2021: 30
- FWCI
- 3.70
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- New England Journal of Medicine (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Breast Cancer Treatment Studies
- Health Sciences › Medicine › Oncology › Advanced Breast Cancer Therapies
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Endocrinology › Estrogen and related hormone effects
- Keywords
- estrogen receptor-positive breast cancer, HER2-negative breast cancer, systemic therapy, antiestrogen therapy, breast cancer heterogeneity, progesterone receptor expression, tumor grade
- MeSH terms
- Breast Neoplasms, Female, Humans, Prognosis, Receptors, Estrogen, Chemotherapy, Adjuvant, Erb-b2 Receptor Tyrosine Kinases, Receptor, ErbB-2, Neoadjuvant Therapy, Selective Estrogen Receptor Modulators, Estrogen Receptor Antagonists
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