Multi-institutional dosimetric delivery assessment of intracranial stereotactic radiosurgery on different treatment platforms.


Journal

Radiotherapy and oncology : journal of the European Society for Therapeutic Radiology and Oncology
ISSN: 1879-0887
Titre abrégé: Radiother Oncol
Pays: Ireland
ID NLM: 8407192

Informations de publication

Date de publication:
06 2020
Historique:
received: 16 12 2019
revised: 30 04 2020
accepted: 12 05 2020
pubmed: 24 5 2020
medline: 15 4 2021
entrez: 24 5 2020
Statut: ppublish

Résumé

Assessment of dosimetric accuracy of radiosurgery on different treatment platforms. Thirty-three single fraction treatment plans were assessed at thirty centres using an anthropomorphic head phantom with target and brainstem structures. The target being a single irregular shaped target, ~8 cc, 10 mm from the brainstem. The phantom was "immobilised", scanned, planned and treated following the local protocols. EBT-XD films and alanine pellets were used to measure absolute dose, inside both the target and the brainstem, and compared with TPS predicted dose distributions. PTV alanine measurements from gantry-based linacs showed a median percentage difference to the TPS of 0.65%. Cyberknife (CK) had the highest median difference of 2.3% in comparison to the other platforms. GammaKnife (GK) showed the smallest median of 0.3%. Similar trends were observed in the OAR with alanine measurements showing median percentage differences of1.1%, 2.0% and 0.4%, for gantry-based linacs, CK and GK respectively. All platforms showed comparable gamma passing rates between axial and sagittal films. This comparison has highlighted the dosimetric variation between measured and TPS calculated dose for each delivery platform. The results suggest that clinically acceptable agreement with the predicted dose distributions is achievable by all treatment delivery systems.

Sections du résumé

BACKGROUND AND PURPOSE
Assessment of dosimetric accuracy of radiosurgery on different treatment platforms.
MATERIAL AND METHODS
Thirty-three single fraction treatment plans were assessed at thirty centres using an anthropomorphic head phantom with target and brainstem structures. The target being a single irregular shaped target, ~8 cc, 10 mm from the brainstem. The phantom was "immobilised", scanned, planned and treated following the local protocols. EBT-XD films and alanine pellets were used to measure absolute dose, inside both the target and the brainstem, and compared with TPS predicted dose distributions.
RESULTS
PTV alanine measurements from gantry-based linacs showed a median percentage difference to the TPS of 0.65%. Cyberknife (CK) had the highest median difference of 2.3% in comparison to the other platforms. GammaKnife (GK) showed the smallest median of 0.3%. Similar trends were observed in the OAR with alanine measurements showing median percentage differences of1.1%, 2.0% and 0.4%, for gantry-based linacs, CK and GK respectively. All platforms showed comparable gamma passing rates between axial and sagittal films.
CONCLUSIONS
This comparison has highlighted the dosimetric variation between measured and TPS calculated dose for each delivery platform. The results suggest that clinically acceptable agreement with the predicted dose distributions is achievable by all treatment delivery systems.

Identifiants

pubmed: 32445860
pii: S0167-8140(20)30280-2
doi: 10.1016/j.radonc.2020.05.024
pii:
doi:

Types de publication

Journal Article Multicenter Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

153-161

Informations de copyright

Copyright © 2020 Elsevier B.V. All rights reserved.

Auteurs

Alexis Dimitriadis (A)

Faculty of Engineering and Physical Sciences, University of Surrey, Guildford, UK; Radiation Dosimetry Group, National Physical Laboratory, Teddington, UK; Department of Medical Physics, Royal Surrey County Hospital NHS Foundation Trust, Guildford, UK. Electronic address: alex@physicsconsulting.co.uk.

Yatman Tsang (Y)

Radiotherapy Trials Quality Assurance Group, Mount Vernon Hospital, London, UK.

Russell A S Thomas (RAS)

Radiation Dosimetry Group, National Physical Laboratory, Teddington, UK.

Antony L Palmer (AL)

Faculty of Engineering and Physical Sciences, University of Surrey, Guildford, UK; Medical Physics Department, Portsmouth Hospitals NHS Trust, Portsmouth, UK.

David Eaton (D)

Radiotherapy Trials Quality Assurance Group, Mount Vernon Hospital, London, UK.

Jonathan Lee (J)

Radiotherapy Trials Quality Assurance Group, Mount Vernon Hospital, London, UK.

Rushil Patel (R)

Radiotherapy Trials Quality Assurance Group, Mount Vernon Hospital, London, UK.

Ileana Silvestre Patallo (I)

Radiation Dosimetry Group, National Physical Laboratory, Teddington, UK.

Clare Gouldstone (C)

Radiation Dosimetry Group, National Physical Laboratory, Teddington, UK.

Julia A D Snaith (JAD)

Radiation Dosimetry Group, National Physical Laboratory, Teddington, UK.

Karen J Kirkby (KJ)

The Christie NHS Foundation Trust, Manchester, UK; Institute of Cancer Sciences, University of Manchester, UK.

Andrew Nisbet (A)

Radiation Dosimetry Group, National Physical Laboratory, Teddington, UK; University College London, UK.

Catharine H Clark (CH)

Faculty of Engineering and Physical Sciences, University of Surrey, Guildford, UK; Radiation Dosimetry Group, National Physical Laboratory, Teddington, UK; Radiotherapy Trials Quality Assurance Group, Mount Vernon Hospital, London, UK; Department of Medical Physics, Royal Surrey County Hospital NHS Foundation Trust, Guildford, UK.

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