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dc.contributor.authorWeller, A
dc.contributor.authorO'Brien, MER
dc.contributor.authorAhmed, M
dc.contributor.authorPopat, S
dc.contributor.authorBhosle, J
dc.contributor.authorMcDonald, F
dc.contributor.authorYap, TA
dc.contributor.authorDu, Y
dc.contributor.authorVlahos, I
dc.contributor.authordeSouza, NM
dc.date.accessioned2017-07-13T13:20:35Z
dc.date.issued2016-05-01
dc.identifier.citationEuropean journal of cancer (Oxford, England : 1990), 2016, 59 pp. 65 - 78
dc.identifier.issn0959-8049
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/693
dc.identifier.eissn1879-0852
dc.identifier.doi10.1016/j.ejca.2016.02.017
dc.description.abstractTherapeutic options in locally advanced non-small cell lung cancer (NSCLC) have expanded in the past decade to include a palate of targeted interventions such as high dose targeted thermal ablations, radiotherapy and growing platform of antibody and small molecule therapies and immunotherapies. Although these therapies have varied mechanisms of action, they often induce changes in tumour architecture and microenvironment such that response is not always accompanied by early reduction in tumour mass, and evaluation by criteria other than size is needed to report more effectively on response. Functional imaging techniques, which probe the tumour and its microenvironment through novel positron emission tomography and magnetic resonance imaging techniques, offer more detailed insights into and quantitation of tumour response than is available on anatomical imaging alone. Use of these biomarkers, or other rational combinations as readouts of pathological response in NSCLC have potential to provide more accurate predictors of treatment outcomes. In this article, the robustness of the more commonly available positron emission tomography and magnetic resonance imaging biomarker indices is examined and the evidence for their application in NSCLC is reviewed.
dc.formatPrint-Electronic
dc.format.extent65 - 78
dc.languageeng
dc.language.isoeng
dc.publisherELSEVIER SCI LTD
dc.subjectHumans
dc.subjectCarcinoma, Non-Small-Cell Lung
dc.subjectLung Neoplasms
dc.subjectAntineoplastic Agents
dc.subjectRadiopharmaceuticals
dc.subjectObserver Variation
dc.subjectPositron-Emission Tomography
dc.subjectMagnetic Resonance Imaging
dc.subjectCatheter Ablation
dc.subjectTreatment Outcome
dc.subjectImmunotherapy
dc.subjectCell Proliferation
dc.subjectCell Hypoxia
dc.subjectForecasting
dc.subjectMolecular Targeted Therapy
dc.subjectTumor Microenvironment
dc.subjectMultimodal Imaging
dc.subjectBiomarkers, Tumor
dc.subjectPositron Emission Tomography Computed Tomography
dc.titleMechanism and non-mechanism based imaging biomarkers for assessing biological response to treatment in non-small cell lung cancer.
dc.typeJournal Article
dcterms.dateAccepted2016-02-18
rioxxterms.versionofrecord10.1016/j.ejca.2016.02.017
rioxxterms.licenseref.startdate2016-05
rioxxterms.typeJournal Article/Review
dc.relation.isPartOfEuropean journal of cancer (Oxford, England : 1990)
pubs.notesNot known
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 Therapeutics
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Cancer Therapeutics/Medicine Drug Development Unit (de Bono)
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies/Medicine Drug Development Unit (de Bono)
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies/Thoracic Oncology
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies/Thoracic Oncology/Thoracic Oncology (hon.)
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies/Treatment of thoracic tumours
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies/Treatment of thoracic tumours/Treatment of thoracic tumours (hon.)
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging/Lung Radiotherapy
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging/Magnetic Resonance
pubs.organisational-group/ICR/Primary Group/Royal Marsden Clinical Units
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 Therapeutics
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Cancer Therapeutics/Medicine Drug Development Unit (de Bono)
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies/Medicine Drug Development Unit (de Bono)
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies/Thoracic Oncology
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies/Thoracic Oncology/Thoracic Oncology (hon.)
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies/Treatment of thoracic tumours
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies/Treatment of thoracic tumours/Treatment of thoracic tumours (hon.)
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging/Lung Radiotherapy
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging/Magnetic Resonance
pubs.organisational-group/ICR/Primary Group/Royal Marsden Clinical Units
pubs.publication-statusPublished
pubs.volume59
pubs.embargo.termsNot known
icr.researchteamMedicine Drug Development Unit (de Bono)
icr.researchteamThoracic Oncology
icr.researchteamTreatment of thoracic tumours
icr.researchteamLung Radiotherapy
icr.researchteamMagnetic Resonance
dc.contributor.icrauthorWeller, Alexander
dc.contributor.icrauthordeSouza, Nandita


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