Systemic therapy for patients with advanced human epidermal growth factor receptor 2-positive breast cancer: American Society of Clinical Oncology clinical practice guideline

J Clin Oncol. 2014 Jul 1;32(19):2078-99. doi: 10.1200/JCO.2013.54.0948. Epub 2014 May 5.

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.

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.

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.

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.

Publication types

  • Practice Guideline
  • Research Support, Non-U.S. Gov't
  • Review
  • Systematic Review

MeSH terms

  • Ado-Trastuzumab Emtansine
  • Anastrozole
  • Antibodies, Monoclonal, Humanized / administration & dosage
  • Antineoplastic Agents, Hormonal / administration & dosage
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use*
  • Biomarkers, Tumor / analysis*
  • Breast Neoplasms / chemistry
  • Breast Neoplasms / drug therapy*
  • 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
  • Molecular Targeted Therapy / methods*
  • Nitriles / administration & dosage
  • Quinazolines / administration & dosage
  • Receptor, ErbB-2 / analysis*
  • Receptors, Estrogen / analysis
  • Receptors, Progesterone / analysis
  • Societies, Medical
  • Taxoids / administration & dosage
  • Trastuzumab
  • Treatment Outcome
  • Triazoles / administration & dosage
  • United States

Substances

  • Antibodies, Monoclonal, Humanized
  • Antineoplastic Agents, Hormonal
  • Biomarkers, Tumor
  • Nitriles
  • Quinazolines
  • Receptors, Estrogen
  • Receptors, Progesterone
  • Taxoids
  • Triazoles
  • Lapatinib
  • Maytansine
  • Docetaxel
  • Anastrozole
  • Letrozole
  • ERBB2 protein, human
  • Receptor, ErbB-2
  • pertuzumab
  • Trastuzumab
  • Ado-Trastuzumab Emtansine