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https://ahro.austin.org.au/austinjspui/handle/1/20501
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DC Field | Value | Language |
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dc.contributor.author | Chia, Puey Ling | - |
dc.contributor.author | Scott, Andrew M | - |
dc.contributor.author | John, Thomas | - |
dc.date | 2019-03-27 | - |
dc.date.accessioned | 2019-04-02T01:07:32Z | - |
dc.date.available | 2019-04-02T01:07:32Z | - |
dc.date.issued | 2019-03-27 | - |
dc.identifier.citation | Expert opinion on drug delivery 2019; 16(4): 441-451 | - |
dc.identifier.uri | https://ahro.austin.org.au/austinjspui/handle/1/20501 | - |
dc.description.abstract | Malignant mesothelioma (MM) is an aggressive malignancy arising from the mesothelial cells lining the pleura and other serosal membranes. It is associated with an extremely poor prognosis and has limited therapeutic options. Areas covered: Epidermal growth factor receptor (EGFR) is known to be highly over-expressed in mesothelioma with reported EGFR overexpression between 44 to 97%. Given this, several anti-EGFR agents have been trialled in mesothelioma. In this review, we provide an overview of the current available data on anti-EGFR therapies in MM and future directions of investigation with these targeted agents in MM. Expert opinion: While many anti-EGFR therapies have failed to show significant efficacy in the management of MM, the pathway is biologically active and its abrogation preclinically points towards it being a valid target. Towards targeting the pathway, many novel EGFR based therapies are still being investigated. Current ongoing research of interest in MM include EGFR targeted nanotechnology approach for drug delivery, antibodies targeting the extracellular EGFR and potentially anti-EGFR antibody drug conjugates. | - |
dc.language.iso | eng | - |
dc.subject | EGFR overexpression | - |
dc.subject | epidermal growth factor receptor (EGFR) | - |
dc.subject | malignant mesothelioma | - |
dc.subject | targeted therapies | - |
dc.title | Epidermal growth factor receptor (EGFR)-targeted therapies in Mesothelioma. | - |
dc.type | Journal Article | - |
dc.identifier.journaltitle | Expert opinion on drug delivery | - |
dc.identifier.affiliation | Faculty of Medicine, University of Melbourne, Melbourne, Australia | en |
dc.identifier.affiliation | School of Cancer Medicine, La Trobe University, Melbourne, Australia | en |
dc.identifier.affiliation | Department of Molecular Imaging and Therapy, Austin Health, The University of Melbourne, Heidelberg, Victoria, Australia | en |
dc.identifier.affiliation | Department of Medical Oncology, Austin Health, Heidelberg, Victoria, Australia | en |
dc.identifier.affiliation | Olivia Newton-John Cancer Research Institute, Heidelberg, Victoria, Australia | en |
dc.identifier.doi | 10.1080/17425247.2019.1598374 | - |
dc.identifier.orcid | 0000-0002-6656-295X | - |
dc.identifier.pubmedid | 30916586 | - |
dc.type.austin | Journal Article | - |
local.name.researcher | Chia, Puey Ling | |
item.languageiso639-1 | en | - |
item.fulltext | No Fulltext | - |
item.grantfulltext | none | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
item.cerifentitytype | Publications | - |
item.openairetype | Journal Article | - |
crisitem.author.dept | Olivia Newton-John Cancer Research Institute | - |
crisitem.author.dept | Molecular Imaging and Therapy | - |
crisitem.author.dept | Olivia Newton-John Cancer Research Institute | - |
crisitem.author.dept | Olivia Newton-John Cancer Research Institute | - |
crisitem.author.dept | Medical Oncology | - |
crisitem.author.dept | Olivia Newton-John Cancer Wellness and Research Centre | - |
Appears in Collections: | Journal articles |
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