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dc.contributor.authorJayson, GC
dc.contributor.authorZhou, C
dc.contributor.authorBacken, A
dc.contributor.authorHorsley, L
dc.contributor.authorMarti-Marti, K
dc.contributor.authorShaw, D
dc.contributor.authorMescallado, N
dc.contributor.authorClamp, A
dc.contributor.authorSaunders, MP
dc.contributor.authorValle, JW
dc.contributor.authorMullamitha, S
dc.contributor.authorBraun, M
dc.contributor.authorHasan, J
dc.contributor.authorMcEntee, D
dc.contributor.authorSimpson, K
dc.contributor.authorLittle, RA
dc.contributor.authorWatson, Y
dc.contributor.authorCheung, S
dc.contributor.authorRoberts, C
dc.contributor.authorAshcroft, L
dc.contributor.authorManoharan, P
dc.contributor.authorScherer, SJ
dc.contributor.authorDel Puerto, O
dc.contributor.authorJackson, A
dc.contributor.authorO'Connor, JPB
dc.contributor.authorParker, GJM
dc.contributor.authorDive, C
dc.date.accessioned2020-08-12T14:46:00Z
dc.date.issued2018-11-07
dc.identifier.citationNature communications, 2018, 9 (1), pp. 4672 - ?
dc.identifier.issn2041-1723
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/3941
dc.identifier.eissn2041-1723
dc.identifier.doi10.1038/s41467-018-07174-1
dc.description.abstractOncological use of anti-angiogenic VEGF inhibitors has been limited by the lack of informative biomarkers. Previously we reported circulating Tie2 as a vascular response biomarker for bevacizumab-treated ovarian cancer patients. Using advanced MRI and circulating biomarkers we have extended these findings in metastatic colorectal cancer (n = 70). Bevacizumab (10 mg/kg) was administered to elicit a biomarker response, followed by FOLFOX6-bevacizumab until disease progression. Bevacizumab induced a correlation between Tie2 and the tumor vascular imaging biomarker, Ktrans (R:-0.21 to 0.47) implying that Tie2 originated from the tumor vasculature. Tie2 trajectories were independently associated with pre-treatment tumor vascular characteristics, tumor response, progression free survival (HR for progression = 3.01, p = 0.00014; median PFS 248 vs. 348 days p = 0.0008) and the modeling of progressive disease (p < 0.0001), suggesting that Tie2 should be monitored clinically to optimize VEGF inhibitor use. A vascular response is defined as a 30% reduction in Tie2; vascular progression as a 40% increase in Tie2 above the nadir. Tie2 is the first, validated, tumor vascular response biomarker for VEGFi.
dc.formatElectronic
dc.format.extent4672 - ?
dc.languageeng
dc.language.isoeng
dc.publisherNATURE PUBLISHING GROUP
dc.rights.urihttps://creativecommons.org/licenses/by/4.0
dc.subjectHumans
dc.subjectColorectal Neoplasms
dc.subjectDisease Progression
dc.subjectNeovascularization, Pathologic
dc.subjectReceptor, TIE-2
dc.subjectAngiogenesis Inhibitors
dc.subjectAngiopoietin-2
dc.subjectVascular Endothelial Growth Factor A
dc.subjectPrognosis
dc.subjectDisease-Free Survival
dc.subjectModels, Biological
dc.subjectAdult
dc.subjectAged
dc.subjectMiddle Aged
dc.subjectFemale
dc.subjectMale
dc.subjectKaplan-Meier Estimate
dc.subjectBiomarkers, Tumor
dc.subjectBevacizumab
dc.titlePlasma Tie2 is a tumor vascular response biomarker for VEGF inhibitors in metastatic colorectal cancer.
dc.typeJournal Article
dcterms.dateAccepted2018-10-04
rioxxterms.versionofrecord10.1038/s41467-018-07174-1
rioxxterms.licenseref.urihttps://creativecommons.org/licenses/by/4.0
rioxxterms.licenseref.startdate2018-11-07
rioxxterms.typeJournal Article/Review
dc.relation.isPartOfNature communications
pubs.issue1
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/Radiotherapy and Imaging
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging/Quantitative Biomedical Imaging
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/Radiotherapy and Imaging
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging/Quantitative Biomedical Imaging
pubs.publication-statusPublished
pubs.volume9
pubs.embargo.termsNot known
icr.researchteamQuantitative Biomedical Imaging
dc.contributor.icrauthorO'Connor, James Patrick


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