Analysis of dose using CBCT and synthetic CT during head and neck radiotherapy: A single centre feasibility study.

ART, adaptive radiotherapy CBCT, Cone Beam Computed Tomography CTV, Clinical Target Volume Cone-beam CT DIR, deformable image registration DVH, dose volume histogram Deformable Dose GTV, Gross Tumour Volume Head and neck cancer IGRT, Image Guided Radiotherapy OAR, Organs at Risk OPSCC, oropharyngeal squamous cell cancer PRV, planning organ at risk volume PTV, Planning Target Volume RT, radiotherapy Radiotherapy SCC, Squamous Cell Carcinoma Synthetic CT TPS, treatment planning system VMAT, volumetric arc therapy pCT, planning Computed Tomography sCT, synthetic Computed Tomography

Journal

Technical innovations & patient support in radiation oncology
ISSN: 2405-6324
Titre abrégé: Tech Innov Patient Support Radiat Oncol
Pays: England
ID NLM: 101762366

Informations de publication

Date de publication:
Jun 2020
Historique:
received: 22 11 2019
revised: 31 01 2020
accepted: 25 02 2020
entrez: 1 4 2020
pubmed: 1 4 2020
medline: 1 4 2020
Statut: epublish

Résumé

The study aimed to assess the suitability of deformable image registration (DIR) software to generate synthetic CT (sCT) scans for dose verification during radiotherapy to the head and neck. Planning and synthetic CT dose volume histograms were compared to evaluate dosimetric changes during the treatment course. Eligible patients had locally advanced (stage III, IVa and IVb) oropharyngeal cancer treated with primary radiotherapy. Weekly CBCT images were acquired post treatment at fractions 1, 6, 11, 16, 21 and 26 over a 30 fraction treatment course. Each CBCT was deformed with the planning CT to generate a sCT which was used to calculate the dose at that point in the treatment. A repeat planning CT2 was acquired at fraction 16 and deformed with the fraction 16 CBCT to compare differences between the calculations mid-treatment. 20 patients were evaluated generating 138 synthetic CT sets. The single fraction mean dose to PTV_HR between the synthetic and planning CT did not vary, although dose to 95% of PTV_HR was smaller at week 6 compared to planning (difference 2.0%, 95% CI (0.8 to 3.1), p = 0.0). There was no statistically significant difference in PRV_brainstem or PRV_spinal cord maximum dose, although greater variation using the sCT calculations was reported. The mean dose to structures based on the fraction 16 sCT and CT2 scans were similar. Synthetic CT provides comparable dose calculations to those of a repeat planning CT; however the limitations of DIR must be understood before it is applied within the clinical setting.

Identifiants

pubmed: 32226833
doi: 10.1016/j.tipsro.2020.02.004
pii: S2405-6324(20)30007-X
pmc: PMC7093804
doi:

Types de publication

Journal Article

Langues

eng

Pagination

21-29

Informations de copyright

© 2020 The Authors.

Déclaration de conflit d'intérêts

The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

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Auteurs

Lisa K Hay (LK)

Department of Clinical Oncology, Beatson West of Scotland Cancer Centre, Glasgow 1053 Great Western Road, Glasgow G12 0YN, United Kingdom.

Claire Paterson (C)

Department of Clinical Oncology, Beatson West of Scotland Cancer Centre, Glasgow 1053 Great Western Road, Glasgow G12 0YN, United Kingdom.

Philip McLoone (P)

Institute of Health & Wellbeing, University of Glasgow, University Ave, Glasgow G12 8QQ, United Kingdom.

Eliane Miguel-Chumacero (E)

Department of Radiotherapy Physics, Beatson West of Scotland Cancer Centre, 1053 Great Western Road, Glasgow G12 0YN, United Kingdom.

Ronan Valentine (R)

Department of Radiotherapy Physics, Beatson West of Scotland Cancer Centre, 1053 Great Western Road, Glasgow G12 0YN, United Kingdom.

Suzanne Currie (S)

Department of Radiotherapy Physics, Beatson West of Scotland Cancer Centre, 1053 Great Western Road, Glasgow G12 0YN, United Kingdom.

Derek Grose (D)

Department of Clinical Oncology, Beatson West of Scotland Cancer Centre, Glasgow 1053 Great Western Road, Glasgow G12 0YN, United Kingdom.

Stefano Schipani (S)

Department of Clinical Oncology, Beatson West of Scotland Cancer Centre, Glasgow 1053 Great Western Road, Glasgow G12 0YN, United Kingdom.

Christina Wilson (C)

Department of Clinical Oncology, Beatson West of Scotland Cancer Centre, Glasgow 1053 Great Western Road, Glasgow G12 0YN, United Kingdom.

Ioanna Nixon (I)

Department of Clinical Oncology, Beatson West of Scotland Cancer Centre, Glasgow 1053 Great Western Road, Glasgow G12 0YN, United Kingdom.

Allan James (A)

Department of Clinical Oncology, Beatson West of Scotland Cancer Centre, Glasgow 1053 Great Western Road, Glasgow G12 0YN, United Kingdom.

Aileen Duffton (A)

Department of Clinical Oncology, Beatson West of Scotland Cancer Centre, Glasgow 1053 Great Western Road, Glasgow G12 0YN, United Kingdom.

Classifications MeSH