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  3. Treatment planning comparison in the PROTECT-trial randomising proton versus photon beam therapy in oesophageal cancer: Results from eight European centres.
 

Treatment planning comparison in the PROTECT-trial randomising proton versus photon beam therapy in oesophageal cancer: Results from eight European centres.

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BORIS DOI
10.48350/176376
Date of Publication
July 2022
Publication Type
Article
Division/Institute

Universitätsklinik fü...

Contributor
Hoffmann, Lone
Mortensen, Hanna
Shamshad, Muhammad
Berbee, Maaike
Bizzocchi, Nicola
Bütof, Rebecca
Canters, Richard
Defraene, Gilles
Ehmsen, Mai Lykkegaard
Fiorini, Francesca
Haustermans, Karin
Hulley, Ryan
Korevaar, Erik W
Clarke, Matthew
Makocki, Sebastian
Muijs, Christina T
Murray, Luke
Nicholas, Owen
Nordsmark, Marianne
Radhakrishna, Ganesh
Thomas, Melissa
Troost, Esther G C
Vilches-Freixas, Gloria
Visser, Sabine
Weber, Damien Charles
Universitätsklinik für Radio-Onkologie
Møller, Ditte Sloth
Subject(s)

600 - Technology::610...

Series
Radiotherapy and oncology
ISSN or ISBN (if monograph)
0167-8140
Publisher
Elsevier
Language
English
Publisher DOI
10.1016/j.radonc.2022.04.029
PubMed ID
35513132
Uncontrolled Keywords

Anatomical changes In...

Description
PURPOSE

To compare dose distributions and robustness in treatment plans from eight European centres in preparation for the European randomized phase-III PROTECT-trial investigating the effect of proton therapy (PT) versus photon therapy (XT) for oesophageal cancer.

MATERIALS AND METHODS

All centres optimized one PT and one XT nominal plan using delineated 4DCT scans for four patients receiving 50.4 Gy (RBE) in 28 fractions. Target volume receiving 95% of prescribed dose (V95%iCTVtotal) should be >99%. Robustness towards setup, range, and respiration was evaluated. The plans were recalculated on a surveillance 4DCT (sCT) acquired at fraction ten and robustness evaluation was performed to evaluate the effect of respiration and inter-fractional anatomical changes.

RESULTS

All PT and XT plans complied with V95%iCTVtotal >99% for the nominal plan and V95%iCTVtotal >97% for all respiratory and robustness scenarios. Lung and heart dose varied considerably between centres for both modalities. The difference in mean lung dose and mean heart dose between each pair of XT and PT plans was in median [range] 4.8 Gy [1.1;7.6] and 8.4 Gy [1.9;24.5], respectively. Patients B and C showed large inter-fractional anatomical changes on sCT. For patient B, the minimum V95%iCTVtotal in the worst-case robustness scenario was 45% and 94% for XT and PT, respectively. For patient C, the minimum V95%iCTVtotal was 57% and 72% for XT and PT, respectively. Patient A and D showed minor inter-fractional changes and the minimum V95%iCTVtotal was >85%.

CONCLUSION

Large variability in dose to the lungs and heart was observed for both modalities. Inter-fractional anatomical changes led to larger target dose deterioration for XT than PT plans.
Handle
https://boris-portal.unibe.ch/handle/20.500.12422/116515
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FileFile TypeFormatSizeLicensePublisher/Copright statementContent
1-s2.0-S0167814022002353-main.pdftextAdobe PDF2.95 MBAttribution (CC BY 4.0)publishedOpen
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