Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/20501
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dc.contributor.authorChia, Puey Ling-
dc.contributor.authorScott, Andrew M-
dc.contributor.authorJohn, Thomas-
dc.date2019-03-27-
dc.date.accessioned2019-04-02T01:07:32Z-
dc.date.available2019-04-02T01:07:32Z-
dc.date.issued2019-03-27-
dc.identifier.citationExpert opinion on drug delivery 2019; 16(4): 441-451-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/20501-
dc.description.abstractMalignant 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.isoeng-
dc.subjectEGFR overexpression-
dc.subjectepidermal growth factor receptor (EGFR)-
dc.subjectmalignant mesothelioma-
dc.subjecttargeted therapies-
dc.titleEpidermal growth factor receptor (EGFR)-targeted therapies in Mesothelioma.-
dc.typeJournal Article-
dc.identifier.journaltitleExpert opinion on drug delivery-
dc.identifier.affiliationFaculty of Medicine, University of Melbourne, Melbourne, Australiaen
dc.identifier.affiliationSchool of Cancer Medicine, La Trobe University, Melbourne, Australiaen
dc.identifier.affiliationDepartment of Molecular Imaging and Therapy, Austin Health, The University of Melbourne, Heidelberg, Victoria, Australiaen
dc.identifier.affiliationDepartment of Medical Oncology, Austin Health, Heidelberg, Victoria, Australiaen
dc.identifier.affiliationOlivia Newton-John Cancer Research Institute, Heidelberg, Victoria, Australiaen
dc.identifier.doi10.1080/17425247.2019.1598374-
dc.identifier.orcid0000-0002-6656-295X-
dc.identifier.pubmedid30916586-
dc.type.austinJournal Article-
local.name.researcherChia, Puey Ling
item.languageiso639-1en-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
item.openairetypeJournal Article-
crisitem.author.deptOlivia Newton-John Cancer Research Institute-
crisitem.author.deptMolecular Imaging and Therapy-
crisitem.author.deptOlivia Newton-John Cancer Research Institute-
crisitem.author.deptOlivia Newton-John Cancer Research Institute-
crisitem.author.deptMedical Oncology-
crisitem.author.deptOlivia Newton-John Cancer Wellness and Research Centre-
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