Show simple item record

dc.contributor.authorSyndikus, I
dc.contributor.authorCruickshank, C
dc.contributor.authorStaffurth, J
dc.contributor.authorTree, A
dc.contributor.authorHenry, A
dc.contributor.authorNaismith, O
dc.contributor.authorMayles, H
dc.contributor.authorSnelson, N
dc.contributor.authorHassan, S
dc.contributor.authorBrown, S
dc.contributor.authorPorta, N
dc.contributor.authorGriffin, C
dc.contributor.authorHall, E
dc.date.accessioned2020-10-12T09:54:57Z
dc.date.issued2020-11-01
dc.identifier.citationClinical and translational radiation oncology, 2020, 25 pp. 22 - 28
dc.identifier.issn2405-6308
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/4137
dc.identifier.eissn2405-6308
dc.identifier.doi10.1016/j.ctro.2020.08.003
dc.description.abstract•PIVOTALboost evaluates benefits/toxicity of pelvic node RT and focal boost dose escalation.•Unfavourable intermediate/high risk and bulky local disease are most likely to benefit.•Functional MRI imaging is used to select patients for different types of dose escalation.•HDR brachytherapy or focal dose escalation with IMRT are used as options.•Training and support is provided to reduce variations of contouring and radiotherapy planning.•The trial is recruiting patients in 38 radiotherapy centres through the UK.
dc.formatElectronic-eCollection
dc.format.extent22 - 28
dc.languageeng
dc.language.isoeng
dc.publisherELSEVIER IRELAND LTD
dc.rights.urihttps://creativecommons.org/licenses/by/4.0
dc.titlePIVOTALboost: A phase III randomised controlled trial of prostate and pelvis versus prostate alone radiotherapy with or without prostate boost (CRUK/16/018).
dc.typeJournal Article
dcterms.dateAccepted2020-08-24
rioxxterms.versionofrecord10.1016/j.ctro.2020.08.003
rioxxterms.licenseref.urihttps://creativecommons.org/licenses/by/4.0
rioxxterms.licenseref.startdate2020-11
rioxxterms.typeJournal Article/Review
dc.relation.isPartOfClinical and translational radiation oncology
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/Clinical Studies
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies/Clinical Trials & Statistics Unit
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies/ICR-CTSU Urology and Head and Neck Trials Team
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/Clinical Studies
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies/Clinical Trials & Statistics Unit
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies/ICR-CTSU Urology and Head and Neck Trials Team
pubs.publication-statusPublished
pubs.volume25
pubs.embargo.termsNot known
icr.researchteamClinical Trials & Statistics Unit
icr.researchteamICR-CTSU Urology and Head and Neck Trials Team
dc.contributor.icrauthorCruickshank, Clare
dc.contributor.icrauthorBrown, Stephanie
dc.contributor.icrauthorPorta, Nuria
dc.contributor.icrauthorGriffin, Clare
dc.contributor.icrauthorHall, Emma


Files in this item

Thumbnail

This item appears in the following collection(s)

Show simple item record

https://creativecommons.org/licenses/by/4.0
Except where otherwise noted, this item's license is described as https://creativecommons.org/licenses/by/4.0