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dc.contributor.authorSundahl, N
dc.contributor.authorBrand, D
dc.contributor.authorParker, C
dc.contributor.authorDearnaley, D
dc.contributor.authorTree, A
dc.contributor.authorPathmanathan, A
dc.contributor.authorSuh, Y-E
dc.contributor.authorVan As, N
dc.contributor.authorEeles, R
dc.contributor.authorKhoo, V
dc.contributor.authorHuddart, R
dc.contributor.authorMurray, J
dc.coverage.spatialIreland
dc.date.accessioned2024-08-21T12:35:40Z
dc.date.available2024-08-21T12:35:40Z
dc.date.issued2024-07-01
dc.identifierARTN 100800
dc.identifierS2405-6308(24)00077-6
dc.identifier.citationClinical and Translational Radiation Oncology, 2024, 47 pp. 100800 -en_US
dc.identifier.issn2405-6308
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/6366
dc.identifier.eissn2405-6308
dc.identifier.eissn2405-6308
dc.identifier.doi10.1016/j.ctro.2024.100800
dc.identifier.doi10.1016/j.ctro.2024.100800
dc.description.abstractBACKGROUND: Moderately hypofractionated radiotherapy regimens or stereotactic body radiotherapy (SBRT) are standard of care for localised prostate cancer. However, some patients are unable or unwilling to travel daily to the radiotherapy department and do not have access to, or are not candidates for, SBRT. For many years, The Royal Marsden Hospital NHS Foundation Trust has offered a weekly ultra-hypofractionated radiotherapy regimen to the prostate (36 Gy in 6 weekly fractions) to patients unable/unwilling to travel daily. METHODS: The current study is a retrospective analysis of all patients with non-metastatic localised prostate cancer receiving this treatment schedule from 2010 to 2015. RESULTS: A total of 140 patients were included in the analysis, of whom 86 % presented with high risk disease, with 31 % having Gleason Grade Group 4 or 5 disease and 48 % T3 disease or higher. All patients received hormone treatment, and there was often a long interval between start of hormone treatment and start of radiotherapy (median of 11 months), with 34 % of all patients having progressed to non-metastatic castrate-resistant disease prior to start of radiotherapy. Median follow-up was 52 months. Median progression-free survival (PFS) and overall survival (OS) for the whole group was 70 months and 72 months, respectively. PFS and OS in patients with hormone-sensitive disease at time of radiotherapy was not reached and 75 months, respectively; and in patients with castrate-resistant disease at time of radiotherapy it was 20 months and 61 months, respectively. CONCLUSION: Our data shows that a weekly ultra-hypofractionated radiotherapy regimen for prostate cancer could be an option in those patients for whom daily treatment or SBRT is not an option.
dc.formatElectronic-eCollection
dc.format.extent100800 -
dc.languageeng
dc.language.isoengen_US
dc.publisherELSEVIER IRELAND LTDen_US
dc.relation.ispartofClinical and Translational Radiation Oncology
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/en_US
dc.subjectProstate cancer
dc.subjectRadiotherapy
dc.subjectUltra-hypofractionation
dc.titleWeekly ultra-hypofractionated radiotherapy in localised prostate cancer.en_US
dc.typeJournal Article
dcterms.dateAccepted2024-05-25
dc.date.updated2024-08-21T10:50:47Z
rioxxterms.versionVoRen_US
rioxxterms.versionofrecord10.1016/j.ctro.2024.100800en_US
rioxxterms.licenseref.startdate2024-07-01
rioxxterms.typeJournal Article/Reviewen_US
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/38872938
pubs.organisational-groupICR
pubs.organisational-groupICR/Primary Group
pubs.organisational-groupICR/Primary Group/ICR Divisions
pubs.organisational-groupICR/Primary Group/ICR Divisions/Closed research teams
pubs.organisational-groupICR/Primary Group/ICR Divisions/Genetics and Epidemiology
pubs.organisational-groupICR/Primary Group/ICR Divisions/Genetics and Epidemiology/Oncogenetics
pubs.organisational-groupICR/Primary Group/ICR Divisions/Radiotherapy and Imaging
pubs.organisational-groupICR/Primary Group/ICR Divisions/Radiotherapy and Imaging/Oncogenetics
pubs.organisational-groupICR/Primary Group/ICR Divisions/Radiotherapy and Imaging/Stereotactic and Precision Body Radiotherapy
pubs.organisational-groupICR/Primary Group/ICR Divisions/Radiotherapy and Imaging/Clinical Academic Radiotherapy (Huddart)
pubs.organisational-groupICR/Primary Group/Royal Marsden Clinical Units
pubs.organisational-groupICR/Primary Group/ICR Divisions/Closed research teams/Clinical Academic Radiotherapy (Dearnaley)
pubs.organisational-groupICR/Students
pubs.organisational-groupICR/Students/PhD and MPhil
pubs.organisational-groupICR/Students/PhD and MPhil/17/18 Starting Cohort
pubs.publication-statusPublished online
pubs.publisher-urlhttp://dx.doi.org/10.1016/j.ctro.2024.100800
pubs.volume47
icr.researchteamStereotactic Radiotheren_US
icr.researchteamClinic Acad RT Dearnaleyen_US
icr.researchteamOncogeneticsen_US
icr.researchteamClinic Acad RT Huddarten_US
dc.contributor.icrauthorBrand, Douglas
dc.contributor.icrauthorDearnaley, David
dc.contributor.icrauthorEeles, Rosalind
dc.contributor.icrauthorHuddart, Robert
dc.contributor.icrauthorMurray, Julia
icr.provenanceDeposited by Miss Fay Allen (impersonating Prof Ros Eeles) on 2024-08-21. Deposit type is initial. No. of files: 1. Files: 36 in 6 manuscript submission_ctRO_resubmission_clean.docx
icr.provenanceDeposited by Mr Arek Surman (impersonating Dr Doug Brand) on 2024-08-21. Deposit type is subsequent. No. of files: 1. Files: 1-s2.0-S2405630824000776-main.pdf


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