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Systemic therapy for patients with advanced human epidermal growth factor receptor 2-positive breast cancer: American Society of Clinical Oncology clinical practice guideline.
- Source :
-
Journal of clinical oncology : official journal of the American Society of Clinical Oncology [J Clin Oncol] 2014 Jul 01; Vol. 32 (19), pp. 2078-99. Date of Electronic Publication: 2014 May 05. - Publication Year :
- 2014
-
Abstract
- Purpose: To provide evidence-based recommendations to practicing oncologists and others on systemic therapy for patients with human epidermal growth factor receptor 2 (HER2) -positive advanced breast cancer.<br />Methods: The American Society of Clinical Oncology convened a panel of medical oncology, radiation oncology, guideline implementation, and advocacy experts and conducted a systematic literature review from January 2009 to October 2012. Outcomes of interest included overall survival, progression-free survival (PFS), and adverse events.<br />Results: A total of 16 trials met the systematic review criteria. The CLEOPATRA trial found survival and PFS benefits for docetaxel, trastuzumab, and pertuzumab in first-line treatment, and the EMILIA trial found survival and PFS benefits for trastuzumab emtansine (T-DM1) in second-line treatment. T-DM1 also showed a third-line PFS benefit. One trial reported on duration of HER2-targeted therapy, and three others reported on endocrine therapy for patients with HER-positive advanced breast cancer.<br />Recommendations: HER2-targeted therapy is recommended for patients with HER2-positive advanced breast cancer, except for those with clinical congestive heart failure or significantly compromised left ventricular ejection fraction, who should be evaluated on a case-by-case basis. Trastuzumab, pertuzumab, and taxane for first-line treatment and T-DM1 for second-line treatment are recommended. In the third-line setting, clinicians should offer other HER2-targeted therapy combinations or T-DM1 (if not previously administered) and may offer pertuzumab, if the patient has not previously received it. Optimal duration of chemotherapy is at least 4 to 6 months or until maximum response, depending on toxicity and in the absence of progression. HER2-targeted therapy can continue until time of progression or unacceptable toxicities. For patients with HER2-positive and estrogen receptor-positive/progesterone receptor-positive breast cancer, clinicians may recommend either standard first-line therapy or, for selected patients, endocrine therapy plus HER2-targeted therapy or endocrine therapy alone.<br /> (© 2014 by American Society of Clinical Oncology.)
- Subjects :
- Ado-Trastuzumab Emtansine
Anastrozole
Antibodies, Monoclonal, Humanized administration & dosage
Antineoplastic Agents, Hormonal administration & dosage
Breast Neoplasms chemistry
Breast Neoplasms mortality
Breast Neoplasms pathology
Clinical Trials as Topic standards
Comorbidity
Docetaxel
Drug Administration Schedule
Evidence-Based Medicine
Female
Health Status Disparities
Healthcare Disparities
Humans
Lapatinib
Letrozole
Maytansine administration & dosage
Maytansine analogs & derivatives
Nitriles administration & dosage
Quinazolines administration & dosage
Receptors, Estrogen analysis
Receptors, Progesterone analysis
Societies, Medical
Taxoids administration & dosage
Trastuzumab
Treatment Outcome
Triazoles administration & dosage
United States
Antineoplastic Combined Chemotherapy Protocols therapeutic use
Biomarkers, Tumor analysis
Breast Neoplasms drug therapy
Molecular Targeted Therapy methods
Receptor, ErbB-2 analysis
Subjects
Details
- Language :
- English
- ISSN :
- 1527-7755
- Volume :
- 32
- Issue :
- 19
- Database :
- MEDLINE
- Journal :
- Journal of clinical oncology : official journal of the American Society of Clinical Oncology
- Publication Type :
- Academic Journal
- Accession number :
- 24799465
- Full Text :
- https://doi.org/10.1200/JCO.2013.54.0948