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Therapeutic significance of hormone receptor positivity in patients with HER-2 positive breast cancer
I. Kolarova, J. Vanasek, K. Odrazka, B. Melichar, A. Ryska, J. Petera, M. Vosmik, M. Dolezel
Jazyk angličtina Země Česko
Typ dokumentu srovnávací studie, časopisecké články, přehledy
NLK
Directory of Open Access Journals
od 2001
Free Medical Journals
od 1998
Medline Complete (EBSCOhost)
od 2007-06-01
ROAD: Directory of Open Access Scholarly Resources
od 2001
PubMed
31831888
DOI
10.5507/bp.2019.060
Knihovny.cz E-zdroje
- MeSH
- adjuvantní chemoterapie MeSH
- analýza přežití MeSH
- chinoliny terapeutické užití MeSH
- dospělí MeSH
- hodnocení rizik MeSH
- hormonální protinádorové látky aplikace a dávkování MeSH
- invazivní růst nádoru patologie MeSH
- lidé středního věku MeSH
- lidé MeSH
- mastektomie metody MeSH
- nádory prsu genetika mortalita patologie terapie MeSH
- přežití bez známek nemoci MeSH
- prognóza MeSH
- protinádorové látky imunologicky aktivní MeSH
- randomizované kontrolované studie jako téma MeSH
- receptor erbB-2 genetika MeSH
- regulace genové exprese u nádorů MeSH
- staging nádorů MeSH
- trastuzumab terapeutické užití MeSH
- výsledek terapie MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- přehledy MeSH
- srovnávací studie MeSH
Breast cancer with high expression of human epidermal growth factor receptor (HER)-2 represents a biologically and clinically heterogeneous group of neoplastic disorders. Importantly, hormone receptor expression has an effect on biological properties and affects the selection of therapies. On the basis of molecular genetics, four principal subtypes, including luminal A, luminal B, HER2-enriched (HER-2-E), and basal-like can be distinguished. Breast tumors characterized by HER-2 positivity and simultaneous expression of hormone receptors, triple positive breast cancers (TPBC) are of increasing interest owing to the unique biological characteristics associated with complex interactions between HER-2 and hormone receptor signaling pathways. Interactions between hormone receptors and HER-2 explain the decreased efficacy of hormonal therapy in comparison with HER-2-negative patients. The expression of estrogen receptors in HER-2 positive tumors may also be associated with resistance to anti-HER-2 treatment. Multiple available therapeutic options, including hormonal therapy, anti-HER-2 agents and cytotoxic drugs explain favorable prognosis of TPBC. Escalation and de-escalation therapeutic strategies that could result in lower toxicities are being investigated as well as combinations of anti-HER-2 agents with hormonal therapy, immunotherapy, cyclin dependent kinase 4/6 and phosphatidyl inositol-3-kinase inhibitors. Distinction between subtypes of HER-2-positive breast cancer and treatment diversification may result in improved outcomes in TPBC. A response to neoadjuvant therapy may serve in the tailoring of therapy management.
Department of Clinical and Radiation Oncology Pardubice Hospital Pardubice Czech Republic
Department of Oncology 1st Faculty of Medicine Charles University Prague Czech Republic
Department of Oncology and Radiotherapy University Hospital Hradec Kralove Czech Republic
Faculty of Health Studies Pardubice University Pardubice Czech Republic
Institute for Postgraduate Medical Education Prague Czech Republic
Citace poskytuje Crossref.org
Literatura
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- $a Breast cancer with high expression of human epidermal growth factor receptor (HER)-2 represents a biologically and clinically heterogeneous group of neoplastic disorders. Importantly, hormone receptor expression has an effect on biological properties and affects the selection of therapies. On the basis of molecular genetics, four principal subtypes, including luminal A, luminal B, HER2-enriched (HER-2-E), and basal-like can be distinguished. Breast tumors characterized by HER-2 positivity and simultaneous expression of hormone receptors, triple positive breast cancers (TPBC) are of increasing interest owing to the unique biological characteristics associated with complex interactions between HER-2 and hormone receptor signaling pathways. Interactions between hormone receptors and HER-2 explain the decreased efficacy of hormonal therapy in comparison with HER-2-negative patients. The expression of estrogen receptors in HER-2 positive tumors may also be associated with resistance to anti-HER-2 treatment. Multiple available therapeutic options, including hormonal therapy, anti-HER-2 agents and cytotoxic drugs explain favorable prognosis of TPBC. Escalation and de-escalation therapeutic strategies that could result in lower toxicities are being investigated as well as combinations of anti-HER-2 agents with hormonal therapy, immunotherapy, cyclin dependent kinase 4/6 and phosphatidyl inositol-3-kinase inhibitors. Distinction between subtypes of HER-2-positive breast cancer and treatment diversification may result in improved outcomes in TPBC. A response to neoadjuvant therapy may serve in the tailoring of therapy management.
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