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One versus three weeks hypofractionated whole breast radiotherapy for early breast cancer treatment: the FAST-Forward phase III RCT.
Brunt, Adrian Murray; Haviland, Joanne S; Wheatley, Duncan A; Sydenham, Mark A; Bloomfield, David J; Chan, Charlie; Cleator, Suzy; Coles, Charlotte E; Donovan, Ellen; Fleming, Helen; Glynn, David; Goodman, Andrew; Griffin, Susan; Hopwood, Penelope; Kirby, Anna M; Kirwan, Cliona C; Nabi, Zohal; Patel, Jaymini; Sawyer, Elinor; Somaiah, Navita; Syndikus, Isabel; Venables, Karen; Yarnold, John R; Bliss, Judith M.
Affiliation
  • Brunt AM; School of Medicine, University of Keele and University Hospitals of North Midlands, Staffordshire, UK.
  • Haviland JS; Clinical Trials and Statistics Unit (ICR-CTSU), The Institute of Cancer Research, London, UK.
  • Wheatley DA; Clinical Trials and Statistics Unit (ICR-CTSU), The Institute of Cancer Research, London, UK.
  • Sydenham MA; Department of Oncology, Royal Cornwall Hospital NHS Trust, Truro, UK.
  • Bloomfield DJ; Clinical Trials and Statistics Unit (ICR-CTSU), The Institute of Cancer Research, London, UK.
  • Chan C; Sussex Cancer Centre, Brighton and Sussex University Hospitals, Brighton, UK.
  • Cleator S; Women's Health Clinic, Nuffield Health Cheltenham Hospital, Cheltenham, UK.
  • Coles CE; Department of Oncology, Imperial Healthcare NHS Trust, London, UK.
  • Donovan E; Department of Oncology, University of Cambridge, Cambridge, UK.
  • Fleming H; Centre for Vision, Speech and Signal Processing, University of Surrey, Guildford, UK.
  • Glynn D; Clinical and Translational Radiotherapy Research Group, National Cancer Research Institute, London, UK.
  • Goodman A; Centre for Health Economics, University of York, York, UK.
  • Griffin S; Oncology Unit, Torbay Hospital, Devon, UK.
  • Hopwood P; Centre for Health Economics, University of York, York, UK.
  • Kirby AM; Clinical Trials and Statistics Unit (ICR-CTSU), The Institute of Cancer Research, London, UK.
  • Kirwan CC; Department of Radiotherapy, The Royal Marsden NHS Foundation Trust, Sutton, UK and Division of Radiotherapy and Imaging, The Institute of Cancer Research, London, UK.
  • Nabi Z; Division of Cancer Sciences, University of Manchester, Manchester, UK.
  • Patel J; RTQQA, Mount Vernon Cancer Centre, Middlesex, UK.
  • Sawyer E; Clinical Trials and Statistics Unit (ICR-CTSU), The Institute of Cancer Research, London, UK.
  • Somaiah N; Comprehensive Cancer Centre, King's College London, London, UK.
  • Syndikus I; Department of Radiotherapy, The Royal Marsden NHS Foundation Trust, Sutton, UK and Division of Radiotherapy and Imaging, The Institute of Cancer Research, London, UK.
  • Venables K; Clatterbridge Cancer Centre, Clatterbridge Hospital NHS Trust, Cheshire, UK.
  • Yarnold JR; RTQQA, Mount Vernon Cancer Centre, Middlesex, UK.
  • Bliss JM; Department of Radiotherapy, The Royal Marsden NHS Foundation Trust, Sutton, UK and Division of Radiotherapy and Imaging, The Institute of Cancer Research, London, UK.
Health Technol Assess ; 27(25): 1-176, 2023 Nov.
Article in En | MEDLINE | ID: mdl-37991196
Patients diagnosed with early breast cancer are often recommended to have radiotherapy after surgery because research has shown that it lowers the risk of the cancer returning. However, it may cause some short- and long-term side effects. Previous clinical trials showed that the same, or even better, outcomes with a lower total dose of radiotherapy given in fewer, larger daily doses compared with older historical treatment schedules. The National Institute for Health and Care Research Health Technology Assessment Programme-funded FAST-Forward Trial aimed to see whether the number of doses could be reduced further without reducing the beneficial effects of radiotherapy. Between November 2011 and June 2014, 4096 patients agreed to take part in the FAST-Forward Main Trial testing three schedules of radiotherapy to the breast. Standard treatment given on 15 days over 3 weeks (Control Group) was compared with two different lower dose schedules where treatment was given on 5 days over 1 week (lower dose Test Groups). An additional 469 patients entered a sub-study where the gland area under the arm also received radiotherapy (Nodal Sub-Study). Main Trial 5-year results reported in April 2020 showed that the number of patients whose cancer had returned in the treated breast was low in all groups: around 2 in 100 (2.1%) for the Control Group, and 1.7% in the higher dose and 1.4% in the lower dose Test Groups. The majority of reported side effects assessed by patients and doctors up to 5 years after radiotherapy were mild for all treatment groups. Patients in the Control Group and in the lower dose Test Group experienced similar levels of side effects. More side effects were reported in the higher dose Test Group, although differences were small. Overall, the FAST-Forward findings suggest that the lower dose 1-week schedule gave similar results in terms of the cancer returning and side effects to the standard 3-week treatment and this schedule can now be used to help treat future patients.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Breast Neoplasms Type of study: Systematic_reviews Limits: Female / Humans Language: En Journal: Health Technol Assess Journal subject: PESQUISA EM SERVICOS DE SAUDE / TECNOLOGIA MEDICA Year: 2023 Type: Article Affiliation country: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Breast Neoplasms Type of study: Systematic_reviews Limits: Female / Humans Language: En Journal: Health Technol Assess Journal subject: PESQUISA EM SERVICOS DE SAUDE / TECNOLOGIA MEDICA Year: 2023 Type: Article Affiliation country: United kingdom