Evolution of anti-HER2 therapies for cancer treatment
Sagun Parakh1, Hui K Gan1, Adam C Parslow2
1Tumour Targeting Laboratory, Olivia Newton-John Cancer Research Institute, Melbourne, Australia; Department of Medical Oncology, Olivia Newton-John Cancer and Wellness Centre, Austin Health, Heidelberg, Melbourne, Australia; School of Cancer Medicine, La Trobe University, Melbourne, Australia.
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.
Insights
HER2-targeted therapies, including monoclonal antibodies and tyrosine kinase inhibitors, improve cancer patient survival. Overcoming resistance and personalizing treatment remain challenges, but molecular imaging and novel antibody conjugates offer future promise.
Area of Science:
- Oncology
- Molecular Biology
- Immunotherapy
Background:
- HER2-directed therapies (monoclonal antibodies, TKIs) have improved outcomes for cancer patients.
- ErbB receptor family biology insights have advanced treatment strategies.
- Current HER2 therapies show success but face challenges in personalization and resistance.
Purpose of the Study:
- To review the benefits and challenges of HER2-directed therapies.
- To explore the role of molecular imaging in assessing HER2 expression and treatment response.
- To discuss novel therapeutic strategies for HER2-overexpressing tumors.
Main Methods:
- Review of existing literature on HER2-targeted therapies.
- Discussion of molecular imaging techniques using radiolabeled HER2 antibodies (pertuzumab, trastuzumab).
- Exploration of antibody-drug conjugates and cellular immunotherapy combinations.
Main Results:
- HER2-directed therapies improve survival and quality of life in responsive patients.
- Molecular imaging allows quantitative assessment of HER2 expression and drug delivery.
- Novel approaches like antibody conjugates and immunotherapy show potential for improved treatment.
Conclusions:
- Personalizing HER2 therapy and overcoming resistance are critical unmet needs.
- Molecular imaging offers non-invasive predictive and prognostic capabilities.
- Future research in novel conjugates and immunotherapy promises enhanced therapeutic responses and reduced toxicity.
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