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dc.contributor.authorWilkinson, MJ
dc.contributor.authorSmith, HG
dc.contributor.authorPencavel, TD
dc.contributor.authorMansfield, DC
dc.contributor.authorKyula-Currie, J
dc.contributor.authorKhan, AA
dc.contributor.authorMcEntee, G
dc.contributor.authorRoulstone, V
dc.contributor.authorHayes, AJ
dc.contributor.authorHarrington, KJ
dc.date.accessioned2016-08-26T15:16:56Z
dc.date.issued2016-09-15
dc.identifier.citationInternational journal of cancer, 2016, 139 (6), pp. 1414 - 1422
dc.identifier.issn0020-7136
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/76
dc.identifier.eissn1097-0215
dc.identifier.doi10.1002/ijc.30162
dc.description.abstractThe management of locally advanced or recurrent extremity sarcoma often necessitates multimodal therapy to preserve a limb, of which isolated limb perfusion (ILP) is a key component. However, with standard chemotherapeutic agents used in ILP, the duration of response is limited. Novel agents or treatment combinations are urgently needed to improve outcomes. Previous work in an animal model has demonstrated the efficacy of oncolytic virotherapy when delivered by ILP and, in this study, we report further improvements from combining ILP-delivered oncolytic virotherapy with radiation and surgical resection. In vitro, the combination of radiation with an oncolytic vaccinia virus (GLV-1h68) and melphalan demonstrated increased cytotoxicity in a panel of sarcoma cell lines. The effects were mediated through activation of the intrinsic apoptotic pathway. In vivo, combinations of radiation, oncolytic virotherapy and standard ILP resulted in delayed tumour growth and prolonged survival when compared with standard ILP alone. However, local disease control could only be secured when such treatment was combined with surgical resection, the timing of which was crucial in determining outcome. Combinations of oncolytic virotherapy with surgical resection and radiation have direct clinical relevance in extremity sarcoma and represent an exciting prospect for improving outcomes in this pathology.
dc.formatPrint-Electronic
dc.format.extent1414 - 1422
dc.languageeng
dc.language.isoeng
dc.publisherWILEY
dc.rights.urihttps://creativecommons.org/licenses/by/4.0
dc.subjectExtremities
dc.subjectCell Line, Tumor
dc.subjectAnimals
dc.subjectHumans
dc.subjectRats
dc.subjectSarcoma
dc.subjectDisease Models, Animal
dc.subjectRecurrence
dc.subjectMelphalan
dc.subjectAntineoplastic Agents
dc.subjectCombined Modality Therapy
dc.subjectRadiotherapy
dc.subjectTumor Burden
dc.subjectTransduction, Genetic
dc.subjectApoptosis
dc.subjectGenetic Vectors
dc.subjectMale
dc.subjectChemotherapy, Cancer, Regional Perfusion
dc.subjectOncolytic Virotherapy
dc.subjectOncolytic Viruses
dc.subjectCaspase 3
dc.subjectProton Therapy
dc.titleIsolated limb perfusion with biochemotherapy and oncolytic virotherapy combines with radiotherapy and surgery to overcome treatment resistance in an animal model of extremity soft tissue sarcoma.
dc.typeJournal Article
dcterms.dateAccepted2016-04-15
rioxxterms.versionofrecord10.1002/ijc.30162
rioxxterms.licenseref.urihttps://creativecommons.org/licenses/by/4.0
rioxxterms.licenseref.startdate2016-09
rioxxterms.typeJournal Article/Review
dc.relation.isPartOfInternational journal of cancer
pubs.issue6
pubs.notesNo embargo
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Cancer Biology
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Cancer Biology/Targeted Therapy
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging/Sarcoma and Melanoma Surgery
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging/Targeted Therapy
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Cancer Biology
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Cancer Biology/Targeted Therapy
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging/Sarcoma and Melanoma Surgery
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging/Targeted Therapy
pubs.publication-statusPublished
pubs.volume139
pubs.embargo.termsNo embargo
icr.researchteamSarcoma and Melanoma Surgery
icr.researchteamTargeted Therapy
dc.contributor.icrauthorMansfield, David
dc.contributor.icrauthorRoulstone, Victoria
dc.contributor.icrauthorHarrington, Kevin


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