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18F-FDG-PET in guided dose-painting with intensity modulated radiotherapy in oropharyngeal tumours: A phase I study (FiGaRO).
Michaelidou, A; Adjogatse, D; Suh, Y; Pike, L; Thomas, C; Woodley, O; Rackely, T; Palaniappan, N; Jayaprakasam, V; Sanchez-Nieto, B; Evans, M; Barrington, S; Lei, M; Guerrero Urbano, T.
Afiliación
  • Michaelidou A; Department of Clinical Oncology, Guy's and St Thomas' NHS Foundation Trust, London, UK; King's College London and Guy's and St Thomas' PET Centre, School of Biomedical Engineering and Imaging Sciences, King's College London, King's Health Partners, London, UK; Kent Oncology Centre, Maidstone and Tun
  • Adjogatse D; Department of Clinical Oncology, Guy's and St Thomas' NHS Foundation Trust, London, UK; King's College London and Guy's and St Thomas' PET Centre, School of Biomedical Engineering and Imaging Sciences, King's College London, King's Health Partners, London, UK.
  • Suh Y; Department of Clinical Oncology, Guy's and St Thomas' NHS Foundation Trust, London, UK; King's College London and Guy's and St Thomas' PET Centre, School of Biomedical Engineering and Imaging Sciences, King's College London, King's Health Partners, London, UK; Department of Clinical Oncology, Royal
  • Pike L; King's College London and Guy's and St Thomas' PET Centre, School of Biomedical Engineering and Imaging Sciences, King's College London, King's Health Partners, London, UK.
  • Thomas C; Department of Medical Physics, Guy's and St Thomas' NHS Foundation Trust, London, UK; King's College London and Guy's and St Thomas' PET Centre, School of Biomedical Engineering and Imaging Sciences, King's College London, King's Health Partners, London, UK.
  • Woodley O; Medical Physics Department, Velindre University NHS Trust, Cardiff, UK.
  • Rackely T; Department of Oncology, Velindre University NHS Trust, Cardiff, UK.
  • Palaniappan N; Department of Oncology, Velindre University NHS Trust, Cardiff, UK.
  • Jayaprakasam V; Wales Research and Diagnostic PET Imaging Centre, Cardiff, UK.
  • Sanchez-Nieto B; Institute of Physics, Pontificia Universidad Católica de Chile, Santiago, Chile.
  • Evans M; Department of Oncology, Velindre University NHS Trust, Cardiff, UK.
  • Barrington S; King's College London and Guy's and St Thomas' PET Centre, School of Biomedical Engineering and Imaging Sciences, King's College London, King's Health Partners, London, UK.
  • Lei M; Department of Clinical Oncology, Guy's and St Thomas' NHS Foundation Trust, London, UK.
  • Guerrero Urbano T; Department of Clinical Oncology, Guy's and St Thomas' NHS Foundation Trust, London, UK. Electronic address: Teresa.GuerreroUrbano@gstt.nhs.uk.
Radiother Oncol ; 155: 261-268, 2021 02.
Article en En | MEDLINE | ID: mdl-33161013
ABSTRACT
BACKGROUND AND

PURPOSE:

The FiGaRO trial assessed the feasibility and safety of using an FDG-PET-based dose-painting technique to deliver a radiotherapy (RT) boostto the FDG-avid primary tumour in patients with locally advanced high and intermediate risk oropharyngeal cancer. MATERIALS AND

METHOD:

Patients underwent a planning 18FDG-PET-CT scan, immobilised in the treatment position, after one cycle of induction chemotherapy. The volume of persistent FDG-avidity in the primary tumour was escalated to 71.5 Gy in30 fractions delivered using a simultaneous integrated boost Intensity Modulated RT (SIB-IMRT) technique. RT was delivered with concomitant Cisplatin following 2 cycles of induction chemotherapy. The primary outcome was the incidence of grade ≥ 3 late mucosal toxicity 12 months post-treatment, with an excess rate of >10% regarded as unacceptable.

RESULTS:

Twenty-nine patients were included and twenty-four were treated between 2014 and 2018, in two UK centres. Median follow-up was 36 months (range 4-56 months). Pre-defined planning target volume objectives and organ at risk dose constraints were met in all cases. There were no incidents of acute grade 4 toxicity. There were 4 cases of grade ≥ 3 mucosal toxicity at 12 months post-treatment (19.1%). There were no cases of persistent mucosal ulceration at 12 months. Overall survival at 3-years was 87.5%, 92.9% for intermediate and 70.0% for high risk patients.

CONCLUSION:

Late toxicity rates, although higher than anticipated, are comparable to contemporary published data for standard dose chemo-IMRT. Results suggest improved 3y survival rates for high risk patients. This approach merits further investigation. ClinicalTrials.gov Identifier NCT02953197.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Neoplasias Orofaríngeas / Radioterapia de Intensidad Modulada Límite: Humans Idioma: En Año: 2021 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Neoplasias Orofaríngeas / Radioterapia de Intensidad Modulada Límite: Humans Idioma: En Año: 2021 Tipo del documento: Article