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Clin Breast Cancer ; 16(5): 344-348, 2016 10.
Article in English | MEDLINE | ID: mdl-27405796

ABSTRACT

HER2 gene amplification and receptor overexpression is identified in 20% to 25% of human breast cancers. Use of targeted therapy for HER2-amplified breast cancer has led to improvements in disease-free and overall survival in this subset of patients. Neratinib is an oral pan HER inhibitor, that irreversibly inhibits the tyrosine kinase activity of epidermal growth factor receptor (EGFR or HER1), HER2, and HER4, which leads to reduced phosphorylation and activation of downstream signaling pathways. Neratinib is currently being tested in a number of clinical trials for its safety and efficacy in lung cancer, and colorectal, bladder, and breast cancers. In this review we discuss the available phase I, II, and III data for use of neratinib in the metastatic, adjuvant, neoadjuvant, and extended adjuvant settings along with the ongoing clinical trials of neratinib in breast cancer. We also elaborate on the side effect profile of this relatively new drug and provide guidelines for its use in clinical practice.


Subject(s)
Antineoplastic Agents/therapeutic use , Breast Neoplasms/drug therapy , Combined Modality Therapy/methods , Protein Kinase Inhibitors/therapeutic use , Quinolines/therapeutic use , Receptor, ErbB-2/antagonists & inhibitors , Administration, Oral , Antineoplastic Agents/administration & dosage , Antineoplastic Agents/adverse effects , Antineoplastic Combined Chemotherapy Protocols , Breast Neoplasms/metabolism , Breast Neoplasms/pathology , Clinical Trials as Topic , ErbB Receptors/antagonists & inhibitors , Female , Humans , Phosphorylation/drug effects , Practice Guidelines as Topic , Protein Kinase Inhibitors/administration & dosage , Protein Kinase Inhibitors/adverse effects , Quinolines/administration & dosage , Quinolines/adverse effects , Receptor, ErbB-2/metabolism , Receptor, ErbB-4/antagonists & inhibitors , Signal Transduction/drug effects , Treatment Outcome
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