dc.contributor.author | Wilkinson, MJ | |
dc.contributor.author | Smith, HG | |
dc.contributor.author | Pencavel, TD | |
dc.contributor.author | Mansfield, DC | |
dc.contributor.author | Kyula-Currie, J | |
dc.contributor.author | Khan, AA | |
dc.contributor.author | McEntee, G | |
dc.contributor.author | Roulstone, V | |
dc.contributor.author | Hayes, AJ | |
dc.contributor.author | Harrington, KJ | |
dc.date.accessioned | 2016-08-26T15:16:56Z | |
dc.date.issued | 2016-09-15 | |
dc.identifier.citation | International journal of cancer, 2016, 139 (6), pp. 1414 - 1422 | |
dc.identifier.issn | 0020-7136 | |
dc.identifier.uri | https://repository.icr.ac.uk/handle/internal/76 | |
dc.identifier.eissn | 1097-0215 | |
dc.identifier.doi | 10.1002/ijc.30162 | |
dc.description.abstract | The 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.format | Print-Electronic | |
dc.format.extent | 1414 - 1422 | |
dc.language | eng | |
dc.language.iso | eng | |
dc.publisher | WILEY | |
dc.rights.uri | https://creativecommons.org/licenses/by/4.0 | |
dc.subject | Extremities | |
dc.subject | Cell Line, Tumor | |
dc.subject | Animals | |
dc.subject | Humans | |
dc.subject | Rats | |
dc.subject | Sarcoma | |
dc.subject | Disease Models, Animal | |
dc.subject | Recurrence | |
dc.subject | Melphalan | |
dc.subject | Antineoplastic Agents | |
dc.subject | Combined Modality Therapy | |
dc.subject | Radiotherapy | |
dc.subject | Tumor Burden | |
dc.subject | Transduction, Genetic | |
dc.subject | Apoptosis | |
dc.subject | Genetic Vectors | |
dc.subject | Male | |
dc.subject | Chemotherapy, Cancer, Regional Perfusion | |
dc.subject | Oncolytic Virotherapy | |
dc.subject | Oncolytic Viruses | |
dc.subject | Caspase 3 | |
dc.subject | Proton Therapy | |
dc.title | Isolated 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.type | Journal Article | |
dcterms.dateAccepted | 2016-04-15 | |
rioxxterms.versionofrecord | 10.1002/ijc.30162 | |
rioxxterms.licenseref.uri | https://creativecommons.org/licenses/by/4.0 | |
rioxxterms.licenseref.startdate | 2016-09 | |
rioxxterms.type | Journal Article/Review | |
dc.relation.isPartOf | International journal of cancer | |
pubs.issue | 6 | |
pubs.notes | No 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-status | Published | |
pubs.volume | 139 | |
pubs.embargo.terms | No embargo | |
icr.researchteam | Sarcoma and Melanoma Surgery | |
icr.researchteam | Targeted Therapy | |
dc.contributor.icrauthor | Mansfield, David | |
dc.contributor.icrauthor | Roulstone, Victoria | |
dc.contributor.icrauthor | Harrington, Kevin | |