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dc.contributor.authorNagpal, SK
dc.contributor.authorKhabra, K
dc.contributor.authorRoss, G
dc.contributor.authorKirby, AM
dc.coverage.spatialEngland
dc.date.accessioned2023-11-23T15:16:51Z
dc.date.available2023-11-23T15:16:51Z
dc.date.issued2023-11-01
dc.identifierS0936-6555(23)00299-6
dc.identifier.citationClinical Oncology, 2023, 35 (11), pp. 736 - 743
dc.identifier.issn0936-6555
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/6072
dc.identifier.eissn1433-2981
dc.identifier.eissn1433-2981
dc.identifier.doi10.1016/j.clon.2023.08.006
dc.identifier.doi10.1016/j.clon.2023.08.006
dc.description.abstractAIMS: The benefit of stereotactic body radiotherapy (SBRT) in metachronous oligometastatic breast cancer (OMBC) has previously been described and its use in current clinical practice is established. The role of SBRT in the management of synchronous OMBC remains uncertain. The aim of this study was to compare outcomes of SBRT-treated synchronous OMBC with those of SBRT-treated metachronous OMBC. MATERIALS AND METHODS: This was a retrospective analysis of consecutive extracranial OMBC patients treated with SBRT at a single institution between 2011 and 2022. Kaplan-Meier methods were used to calculate progression-free survival (PFS), overall survival, local control and distant control. Log-rank tests were used to test any differences. Cox regression was used for univariate and multivariate analyses to identify predictive factors. Toxicity was assessed using Common Terminology Criteria for Adverse Events (CTCAE) version 5. RESULTS: In total, 74 OMBC patients with 113 lesions were analysed. The median follow-up was 20 months (range 0-98). Seventy per cent of patients presented metachronously and 30% synchronously. 30 Gy in three fractions was most commonly prescribed, resulting in a median biologically effective dose (BED at α/β = 10) of 60 Gy (range 35.7-112.5 Gy). Forty-nine per cent of patients switched systemic therapy post-SBRT (median time to switch: 14 months, range 0-79). Two patients (2%) experienced grade 3 acute toxicities with no grade ≥4 toxicities. At 2 years overall survival was 92.4% and PFS 39.0%, local control 85.9% and distant control 37.0%. For metachronous and synchronous disease, respectively, 2-year local control rates were 86.5% and 85.8% and PFS rates were 35.3% and 48.3%. The median PFS of metachronous and synchronous disease were 18 months and 17 months, respectively (P = 0.86). Predictive factors on multivariate analysis were treated site for overall survival, change in systemic therapy post-SBRT for PFS and BED for local control. CONCLUSION: Our data confirm SBRT as a well-tolerated treatment for OMBC with excellent local control rates regardless of metachronous or synchronous presentation. There is no suggestion that survival outcomes are inferior for synchronous disease. Further prospective studies are required to validate this finding.
dc.formatPrint-Electronic
dc.format.extent736 - 743
dc.languageeng
dc.language.isoeng
dc.publisherELSEVIER SCIENCE LONDON
dc.relation.ispartofClinical Oncology
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectBreast
dc.subjectOligometastases
dc.subjectSBRT
dc.subjectStereotactic body radiotherapy
dc.subjectSynchronous
dc.titleTen-Year Outcomes of Stereotactic Body Radiotherapy for Oligometastatic Breast Cancer: Does Synchronous Oligometastatic Breast Cancer Benefit?
dc.typeJournal Article
dcterms.dateAccepted2023-08-21
dc.date.updated2023-11-23T15:14:55Z
rioxxterms.versionAM
rioxxterms.versionofrecord10.1016/j.clon.2023.08.006
rioxxterms.licenseref.startdate2023-11-01
rioxxterms.typeJournal Article/Review
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/37684189
pubs.issue11
pubs.organisational-groupICR
pubs.organisational-groupICR/Primary Group
pubs.organisational-groupICR/Primary Group/ICR Divisions
pubs.organisational-groupICR/Primary Group/ICR Divisions/Radiotherapy and Imaging
pubs.organisational-groupICR/Primary Group/ICR Divisions/Radiotherapy and Imaging/Breast Cancer Radiotherapy
pubs.organisational-groupICR/Primary Group/Royal Marsden Clinical Units
pubs.organisational-groupICR/Primary Group/ICR Divisions/Radiotherapy and Imaging/Breast Cancer Radiotherapy/Breast Cancer Radiotherapy (hon.)
pubs.organisational-groupICR/Primary Group/ICR Divisions/Radiotherapy and Imaging/Uro-oncology Clinical Trials
pubs.publication-statusPublished
pubs.publisher-urlhttp://dx.doi.org/10.1016/j.clon.2023.08.006
pubs.volume35
icr.researchteamUro-oncology Trials
dc.contributor.icrauthorNagpal, Sukhdeep
icr.provenanceDeposited by Mr Arek Surman on 2023-11-23. Deposit type is initial. No. of files: 1. Files: YCLON-S-23-00605 clin onc manuscript draft.pdf


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