Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/16162
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dc.contributor.authorParakh, Sagun-
dc.contributor.authorParslow, Adam C-
dc.contributor.authorGan, Hui K-
dc.contributor.authorScott, Andrew M-
dc.date2015-12-19-
dc.date.accessioned2016-08-26T00:18:21Z-
dc.date.available2016-08-26T00:18:21Z-
dc.date.issued2016-
dc.identifier.citationExpert Opinion on Drug Delivery 2016; 13(3): 401-419en_US
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/16162-
dc.description.abstractINTRODUCTION: Antibody-conjugated therapies (ACTs) combine the specificity of monoclonal antibodies to target cancer cells directly with highly potent payloads, often resulting in superior efficacy and/or reduced toxicity. This represents a new approach to the treatment of cancer. There have been highly promising clinical trial results using this approach with improvements in linker and payload technology. The breadth of current trials examining ACTs in haematological malignancies and solid tumours indicate the potential for clinical impact. AREAS COVERED: This review will provide an overview of ACTs currently in clinical development as well as the principles of antibody delivery and types of payloads used, including cytotoxic drugs, radiolabelled isotopes, nanoparticle-based siRNA particles and immunotoxins. EXPERT OPINION: The focus of much of the clinical activity in ACTs has, understandably, been on their use as a monotherapy or in combination with standard of care drugs. This will continue, as will the search for better targets, linkers and payloads. Increasingly, as these drugs enter routine clinical care, important questions will arise regarding how to optimise ACT treatment approaches, including investigation of resistance mechanisms, biomarker and patient selection strategies, understanding of the unique toxicities of these drugs, and combinatorial approaches with standard therapies as well as emerging therapeutic agents like immunotherapy.en_US
dc.subjectAntibody-conjugated therapiesen_US
dc.subjectImmunotoxinsen_US
dc.subjectRadioimmunotherapyen_US
dc.subjectsiRNAen_US
dc.titleAntibody-mediated delivery of therapeutics for cancer therapyen_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleExpert Opinion on Drug Deliveryen_US
dc.identifier.affiliationAustin Health, Heidelberg, Victoria, Australiaen_US
dc.identifier.affiliationTumour Targeting Laboratory, Olivia Newton-John Cancer Research Institute, Heidelberg, Victoria, Australiaen_US
dc.identifier.affiliationDepartment of Medical Oncology, Olivia Newton-John Cancer and Wellness Centre, Austin Health, Heidelberg, Victoria, Australiaen_US
dc.identifier.affiliationSchool of Cancer Medicine, La Trobe University, Bundoora, Victoria, Australiaen_US
dc.identifier.affiliationDepartment of Molecular Imaging and Therapy, Austin Health, Heidelberg, Victoria, Australiaen_US
dc.identifier.affiliationDepartment of Medicine, University of Melbourne, Melbourne, Victoria, Australiaen_US
dc.identifier.pubmedurihttps://pubmed.ncbi.nlm.nih.gov/26654403en_US
dc.identifier.doi10.1517/17425247.2016.1124854en_US
dc.type.contentTexten_US
dc.identifier.orcid0000-0002-6656-295Xen_US
dc.type.austinJournal Articleen_US
local.name.researcherGan, Hui K
item.openairetypeJournal Article-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.cerifentitytypePublications-
crisitem.author.deptMedical Oncology-
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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