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Evolution of anti-HER2 therapies for cancer treatment
Institution:1. Instituto de Biología Molecular y Celular del Cáncer-CSIC, CIBERONC and IBSAL, Salamanca, Spain;2. Centro Nacional de Investigaciones Oncológicas (CNIO), Madrid, Spain;3. Experimental Therapeutics Unit, Hospital Clínico San Carlos, Madrid, Spain;4. CIBERONC and Centro Regional de Investigaciones Biomedicas (CRIB), Castilla La Mancha University, Albacete, Spain;1. Breast and Gynecologic Cancer Research, Sarah Cannon Research Institute and Tennessee Oncology, Nashville, TN, USA;2. Division of Hematology/Oncology, Mays Cancer Center, UT Health San Antonio, San Antonio, TX, USA;3. Wilmot Cancer Institute, University of Rochester Medical Center, Rochester, NY, USA;4. Department of Hematology/Oncology, West Cancer Center and Research Institute and University of Tennessee Health Science Center, Germantown, TN, USA;5. Oncology Hematology Care, Cincinnati, OH, USA;6. F. Hoffmann-La Roche Ltd, Basel, Switzerland;7. Product Development Oncology, Genentech Inc, South San Francisco, CA, USA;8. Product Development Safety, Genentech Inc, South San Francisco, CA, USA;9. Biostatistics, IQVIA-RDS India Pvt Ltd, Mumbai, Maharashtra, India;10. Oncology Biomarker Development, Genentech Inc, South San Francisco, CA, USA;11. Department of Medicine, University of Pittsburgh Medical Center Hillman Cancer Center, Pittsburgh, PA, USA
Abstract:The development of HER2-directed monoclonal antibodies and tyrosine kinase inhibitors have provided benefits to cancer patients, as well as produced many insights into the biology of the ErbB receptor family. Current therapies based on ErbB family members have resulted in improved overall survival with associated improvements in quality of life for the cancer patients that respond to treatment. Compared to monotherapy using either two antibodies to block the HER2 receptor blockade or combinatorial approaches with HER2 antibodies and standard therapies has provided additional benefits. Despite the therapeutic success of existing HER2 therapies, personalising treatment and overcoming resistance to these therapies remains a significant challenge. The heterogeneous intra-tumoural HER2 expression and lack of fully predictive and prognostic biomarkers remain significant barriers to improving the use of HER2 antibodies. Imaging modalities using radiolabelled pertuzumab and trastuzumab allow quantitative assessment of intra-tumoural HER2 expression, HER2 antibody saturation and the success of different drug delivery systems to be assessed. Molecular imaging with HER2 antibodies has the potential to be a non-invasive, predictive and prognostic technique capable of influencing therapeutic decisions, predicting response and failure of treatments as well as providing insights into receptor recycling and signalling. Similarly, conjugating HER2 antibodies with novel toxic payloads or combining HER2 antibodies with cellular immunotherapy provide exciting new opportunities for the management of tumours overexpressing HER2. Future research will lead to higher therapeutic responses, lower toxicities and providing insight into the mechanisms of resistance to HER2-targeted treatments.
Keywords:HER2  Monoclonal antibodies  Trastuzumab  Pertuzumab  T-DM1  Imaging
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