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dc.contributor.authorBrunt, AM
dc.contributor.authorHaviland, JS
dc.contributor.authorSydenham, M
dc.contributor.authorAgrawal, RK
dc.contributor.authorAlgurafi, H
dc.contributor.authorAlhasso, A
dc.contributor.authorBarrett-Lee, P
dc.contributor.authorBliss, P
dc.contributor.authorBloomfield, D
dc.contributor.authorBowen, J
dc.contributor.authorDonovan, E
dc.contributor.authorGoodman, A
dc.contributor.authorHarnett, A
dc.contributor.authorHogg, M
dc.contributor.authorKumar, S
dc.contributor.authorPassant, H
dc.contributor.authorQuigley, M
dc.contributor.authorSherwin, L
dc.contributor.authorStewart, A
dc.contributor.authorSyndikus, I
dc.contributor.authorTremlett, J
dc.contributor.authorTsang, Y
dc.contributor.authorVenables, K
dc.contributor.authorWheatley, D
dc.contributor.authorBliss, JM
dc.contributor.authorYarnold, JR
dc.date.accessioned2020-04-02T10:21:50Z
dc.date.issued2020-10-01
dc.identifier.citationJournal of clinical oncology : official journal of the American Society of Clinical Oncology, 2020, 38 (28), pp. 3261 - 3272
dc.identifier.issn0732-183X
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/3569
dc.identifier.eissn1527-7755
dc.identifier.doi10.1200/jco.19.02750
dc.description.abstractPURPOSE: Previous studies of hypofractionated adjuvant whole-breast radiotherapy for early breast cancer established a 15- or 16-fraction (fr) regimen as standard. The FAST Trial (CRUKE/04/015) evaluated normal tissue effects (NTE) and disease outcomes after 5-fr regimens. Ten-year results are presented. METHODS: Women ≥ 50 years of age with low-risk invasive breast carcinoma (pT1-2 pN0) were randomly assigned to 50 Gy/25 fr (5 weeks) or 30 or 28.5 Gy in 5 once-weekly fr of 6.0 or 5.7 Gy. The primary end point was change in photographic breast appearance at 2 and 5 years; secondary end points were physician assessments of NTE and local tumor control. Odds ratios (ORs) from longitudinal analyses compared regimens. RESULTS: A total of 915 women were recruited from 18 UK centers (2004-2007). Five-year photographs were available for 615/862 (71%) eligible patients. ORs for change in photographic breast appearance were 1.64 (95% CI, 1.08 to 2.49; P = .019) for 30 Gy and 1.10 (95% CI, 0.70 to 1.71; P = .686) for 28.5 Gy versus 50 Gy. α/β estimate for photographic end point was 2.7 Gy (95% CI, 1.5 to 3.9 Gy), giving a 5-fr schedule of 28 Gy (95% CI, 26 to 30 Gy) estimated to be isoeffective with 50 Gy/25 fr. ORs for any moderate/marked physician-assessed breast NTE (shrinkage, induration, telangiectasia, edema) were 2.12 (95% CI, 1.55 to 2.89; P < .001) for 30 Gy and 1.22 (95% CI, 0.87 to 1.72; P = .248) for 28.5 Gy versus 50 Gy. With 9.9 years median follow-up, 11 ipsilateral breast cancer events (50 Gy: 3; 30 Gy: 4; 28.5 Gy: 4) and 96 deaths (50 Gy: 30; 30 Gy: 33; 28.5 Gy: 33) have occurred. CONCLUSION: At 10 years, there was no significant difference in NTE rates after 28.5 Gy/5 fr compared with 50 Gy/25 fr, but NTE were higher after 30 Gy/5 fr. Results confirm the published 3-year findings that a once-weekly 5-fr schedule of whole-breast radiotherapy can be identified that appears to be radiobiologically comparable for NTE to a conventionally fractionated regimen.
dc.formatPrint-Electronic
dc.format.extent3261 - 3272
dc.languageeng
dc.language.isoeng
dc.publisherAMER SOC CLINICAL ONCOLOGY
dc.rights.urihttps://creativecommons.org/licenses/by/4.0
dc.titleTen-Year Results of FAST: A Randomized Controlled Trial of 5-Fraction Whole-Breast Radiotherapy for Early Breast Cancer.
dc.typeJournal Article
dcterms.dateAccepted2020-03-30
rioxxterms.versionofrecord10.1200/jco.19.02750
rioxxterms.licenseref.urihttps://creativecommons.org/licenses/by/4.0
rioxxterms.licenseref.startdate2020-10
rioxxterms.typeJournal Article/Review
dc.relation.isPartOfJournal of clinical oncology : official journal of the American Society of Clinical Oncology
pubs.issue28
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
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.publication-statusPublished
pubs.volume38
pubs.embargo.termsNot known
icr.researchteamClinical Trials & Statistics Unit
dc.contributor.icrauthorHaviland, Joanne
dc.contributor.icrauthorSydenham, Mark
dc.contributor.icrauthorBliss, Judith
dc.contributor.icrauthorYarnold, John


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