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BIOMARKER:

HER-2 negative + HR positive + ESR1 wild-type

i
Other names: ERBB2, CD340, HER-2, HER2, NEU, NGL, V-erb-b2 avian erythroblastic leukemia viral oncogene homolog 2
Entrez ID:
Associations
Trials
7d
Oral selective estrogen receptor degraders in hormone receptor-positive, HER2-negative advanced breast cancer: a systematic review and meta-analysis. (PubMed, Breast Cancer Res Treat)
Pooled randomized evidence supports a clinically meaningful benefit of oral SERDs over standard ET after endocrine progression in HR + /HER2-ABC, with the strongest and most consistent efficacy observed in ESR1-mutated disease.
Clinical • Retrospective data • Review • Journal
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HER-2 (Human epidermal growth factor receptor 2) • ER (Estrogen receptor)
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HR positive • HER-2 negative • ESR1 mutation • HR positive + HER-2 negative • HER-2 negative + HR positive + ESR1 mutation • HER-2 negative + HR positive + ESR1 wild-type
6ms
Co-clinical trial targeting ER, FGFR and CDK4/6 in resistant hormone-positive breast cancer with FGFR alterations. (PubMed, NPJ Precis Oncol)
Using patient-derived organoids (PDOs), we demonstrated that FGFR-amplified PDOs respond to fulvestrant, palbociclib, and rogaratinib only when PIK3CA and ESR1 are wild-type. Toxicity was manageable and consistent with prior data. Our findings highlight biomarker-driven approaches as essential for refining FGFR-targeted strategies in this resistant population.
Journal
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HER-2 (Human epidermal growth factor receptor 2) • ER (Estrogen receptor) • PIK3CA (Phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha) • FGFR1 (Fibroblast growth factor receptor 1) • FGFR (Fibroblast Growth Factor Receptor) • CDK4 (Cyclin-dependent kinase 4)
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HR positive • HER-2 negative • HR positive + HER-2 negative • HER-2 negative + HR positive + ESR1 wild-type
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Ibrance (palbociclib) • fulvestrant • rogaratinib (BAY 1163877)