Endocrine therapy for hormone receptor-positive metastatic breast cancer: American Society of Clinical Oncology Guideline Journal Article


Authors: Rugo, H. S.; Rumble, R. B.; Macrae, E.; Barton, D. L.; Connolly, H. K.; Dickler, M. N.; Fallowfield, L.; Fowble, B.; Ingle, J. N.; Jahanzeb, M.; Johnston, S. R. D.; Korde, L. A.; Khatcheressian, J. L.; Mehta, R. S.; Muss, H. B.; Burstein, H. J.
Article Title: Endocrine therapy for hormone receptor-positive metastatic breast cancer: American Society of Clinical Oncology Guideline
Abstract: Purpose To develop recommendations about endocrine therapy for women with hormone receptor (HR) -positive metastatic breast cancer (MBC). Methods The American Society of Clinical Oncology convened an Expert Panel to conduct a systematic review of evidence from 2008 through 2015 to create recommendations informed by that evidence. Outcomes of interest included sequencing of hormonal agents, hormonal agents compared with chemotherapy, targeted biologic therapy, and treatment of premenopausal women. This guideline puts forth recommendations for endocrine therapy as treatment for women with HR-positive MBC. Recommendations Sequential hormone therapy is the preferential treatment for most women with HR-positive MBC. Except in cases of immediately life-threatening disease, hormone therapy, alone or in combination, should be used as initial treatment. Patients whose tumors express any level of hormone receptors should be offered hormone therapy. Treatment recommendations should be based on type of adjuvant treatment, disease-free interval, and organ function. Tumor markers should not be the sole criteria for determining tumor progression; use of additional biomarkers remains experimental. Assessment of menopausal status is critical; ovarian suppression or ablation should be included in premenopausal women. For postmenopausal women, aromatase inhibitors (AIs) are the preferred first-line endocrine therapy, with or without the cyclin-dependent kinase inhibitor palbociclib. As second-line therapy, fulvestrant should be administered at 500 mg with a loading schedule and may be administered with palbociclib. The mammalian target of rapamycin inhibitor everolimus may be administered with exemestane to postmenopausal women with MBC whose disease progresses while receiving nonsteroidal AIs. Among patients with HR-positive, human epidermal growth factor receptor 2-positive MBC, human epidermal growth factor receptor 2-targeted therapy plus an AI can be effective for those who are not chemotherapy candidates. (C) 2016 by American Society of Clinical Oncology
Keywords: first-line therapy; placebo-controlled trial; double-blind; growth-factor receptor; phase-iii trial; progression-free survival; postmenopausal; nonsteroidal aromatase inhibitor; fulvestrant 500 mg; japanese women; everolimus plus exemestane
Journal Title: Journal of Clinical Oncology
Volume: 34
Issue: 25
ISSN: 0732-183X
Publisher: American Society of Clinical Oncology  
Date Published: 2016-09-01
Start Page: 3069
End Page: 3103
Language: English
ACCESSION: WOS:000382470100019
DOI: 10.1200/jco.2016.67.1487
PROVIDER: wos
PUBMED: 27217461
Notes: Article -- Source: Wos
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  1. Maura N Dickler
    238 Dickler