Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/18912
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dc.contributor.authorGan, Hui K-
dc.contributor.authorvan den Bent, Martin-
dc.contributor.authorLassman, Andrew B-
dc.contributor.authorReardon, David A-
dc.contributor.authorScott, Andrew M-
dc.date2017-07-04-
dc.date.accessioned2018-09-12T23:37:45Z-
dc.date.available2018-09-12T23:37:45Z-
dc.date.issued2017-11-
dc.identifier.citationNature reviews. Clinical oncology 2017; 14(11): 695-707-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/18912-
dc.description.abstractGlioblastomas are high-grade brain tumours with a poor prognosis and, currently, few available therapeutic options. This lack of effective treatments has been linked to diverse factors, including target selection, tumour heterogeneity and poor penetrance of therapeutic agents through the blood-brain barrier and into tumours. Therapies using monoclonal antibodies, alone or linked to cytotoxic payloads, have proved beneficial for patients with different solid tumours; these approaches are currently being explored in patients with glioblastoma. In this Review, we summarise clinical data regarding antibody-drug conjugates (ADCs) against a variety of targets in glioblastoma, and compare the efficacy and toxicity of targeting EGFR with ADCs versus naked antibodies in order to illustrate key aspects of the use of ADCs in this malignancy. Finally, we discuss the complex challenges related to the biology and mutational changes of glioblastoma that can affect the use of ADC-based therapies in patients with this disease, and highlight potential strategies to improve efficacy.-
dc.language.isoeng-
dc.titleAntibody-drug conjugates in glioblastoma therapy: the right drugs to the right cells.-
dc.typeJournal Article-
dc.identifier.journaltitleNature reviews. Clinical oncology-
dc.identifier.affiliationDana-Farber Cancer Institute, 450 Brookline Avenue, Dana 2134, Boston, Massachusetts 02215, USAen
dc.identifier.affiliationBrain Tumour Centre, Erasmus MC Cancer Institute, Groene Hilledijk 301, 3075 EA Rotterdam, Netherlandsen
dc.identifier.affiliationLa Trobe University School of Cancer Medicine, 145 Studley Road, Heidelberg, Victoria 3084, Australiaen
dc.identifier.affiliationDepartment of Medicine, University of Melbourne, 145 Studley Road, Heidelberg, Victoria 3084, Australiaen
dc.identifier.affiliationDepartment of Neurology & Herbert Irving Comprehensive Cancer Center, Columbia University Medical Center, 161 Fort Washington Avenue, New York, New York 10032, USAen
dc.identifier.affiliationOlivia Newton-John Cancer Research Institute, Heidelberg, Victoria, Australiaen
dc.identifier.affiliationAustin Health, Heidelberg, Victoria, Australia-
dc.identifier.doi10.1038/nrclinonc.2017.95-
dc.identifier.orcid0000-0002-6656-295X-
dc.identifier.pubmedid28675164-
dc.type.austinComparative Study-
dc.type.austinJournal Article-
dc.type.austinReview-
local.name.researcherGan, Hui K
item.openairetypeJournal Article-
item.cerifentitytypePublications-
item.grantfulltextnone-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.languageiso639-1en-
crisitem.author.deptMedical Oncology-
crisitem.author.deptOlivia Newton-John Cancer Wellness and Research Centre-
crisitem.author.deptMolecular Imaging and Therapy-
crisitem.author.deptOlivia Newton-John Cancer Research Institute-
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