Neratinib as adjuvant therapy in patients with HER2 positive breast cancer: expert opinion

Author:

Caputo Roberta1,Buono Giuseppe1ORCID,Lauro Vincenzo Di1ORCID,Cianniello Daniela1,Arx Claudia Von1ORCID,Pensabene Matilde1ORCID,Pagliuca Martina23ORCID,Pacilio Carmen1,Rella Francesca Di1,Verrazzo Annarita124,Martinelli Claudia4,Nuzzo Francesco1ORCID,Laurentiis Michelino De1ORCID

Affiliation:

1. Department of Breast & Thoracic Oncology, Division of Breast Medical Oncology, Istituto Nazionale Tumori IRCCS ‘Fondazione G. Pascale,’ Naples, Italy

2. Clinical & Translational Oncology, Scuola Superiore Meridionale, Naples, Italy

3. U981 Molecular Predictors & New Targets in Oncology, Gustave Roussy, Villejuif, France

4. Department of Clinical Medicine & Surgery, University of Naples Federico II, Naples, Italy

Abstract

Neratinib is a tyrosine kinase receptor inhibitor used in the extended adjuvant therapy of early-stage breast cancer. After adjuvant trastuzumab therapy, neratinib reduces the risk of recurrence and, if taken within 1 year from trastuzumab, significantly improves the invasive disease-free survival of patients with early-stage human epidermal growth factor receptor-2 positive (HER2+) breast cancer with no increased risk of long-term toxicity. Diarrhea, the most common adverse event associated with neratinib use, deters some clinicians from prescribing this drug. However, neratinib-related toxicity is predictable, short-lived, mostly limited to the first month of treatment and can be managed with dose-escalation and prophylactic strategies. Thus, close surveillance and prompt management, relying on supportive care and administration schedule modification, allows discontinuation of treatment to be avoided.

Publisher

Future Medicine Ltd

Subject

Cancer Research,Oncology,General Medicine

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