Robustness assessment of clinical adaptive proton and photon radiotherapy for oesophageal cancer in the model-based approach

dc.accessRightsAnonymous*
dc.contributor.authorVisser, Sabine
dc.contributor.authorO. Ribeiro, Cássia
dc.contributor.authorDieters, Margriet
dc.contributor.authorMul, Veronique E.
dc.contributor.authorNiezink, Anne G.H.
dc.contributor.authorvan der Schaaf, Arjen
dc.contributor.authorLangendijk, Johannes A.
dc.contributor.authorKorevaar, Erik W.
dc.contributor.authorBoth, Stefan
dc.contributor.authorMuijs, Christina T.
dc.contributor.authorKnopf, Antje
dc.date.accessioned2023-05-09T11:25:17Z
dc.date.available2023-05-09T11:25:17Z
dc.date.issued2022-12
dc.description.abstractPurpose In the Netherlands, oesophageal cancer (EC) patients are selected for intensity modulated proton therapy (IMPT) using the expected normal tissue complication probability reduction (ΔNTCP) when treating with IMPT compared to volumetric modulated arc therapy (VMAT). In this study, we evaluate the robustness of the first EC patients treated with IMPT in our clinic in terms of target and organs-at-risk (OAR) dose with corresponding NTCP, as compared to VMAT. Materials and Methods For 20 consecutive EC patients, clinical IMPT and VMAT plans were created on the average planning 4DCT. Both plans were robustly evaluated on weekly repeated 4DCTs and if target coverage degraded, replanning was performed. Target coverage was evaluated for complete treatment trajectories with and without replanning. The planned and accumulated mean lung dose (MLD) and mean heart dose (MHD) were additionally evaluated and translated into NTCP. Results Replanning in the clinic was performed more often for IMPT (15x) than would have been needed for VMAT (8x) (p = 0.11). Both adaptive treatments would have resulted in adequate accumulated target dose coverage. Replanning in the first week of treatment had most clinical impact, as anatomical changes resulting in insufficient accumulated target coverage were already observed at this stage. No differences were found in MLD between the planned dose and the accumulated dose. Accumulated MHD differed from the planned dose (p < 0.001), but since these differences were similar for VMAT and IMPT (1.0 and 1.5 Gy, respectively), the ΔNTCP remained unchanged. Conclusion Following an adaptive clinical workflow, adequate target dose coverage and stable OAR doses with corresponding NTCPs was assured for both IMPT and VMAT.en_US
dc.identifier.doi10.1016/j.radonc.2022.11.001
dc.identifier.issn0167-8140
dc.identifier.urihttps://irf.fhnw.ch/handle/11654/34920
dc.identifier.urihttps://doi.org/10.26041/fhnw-4840
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.relation.ispartofRadiotherapy and Oncologyen_US
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/en_US
dc.subjectIMPTen_US
dc.subjectVMATen_US
dc.subjectRobustnessen_US
dc.subjectOesophageal canceren_US
dc.subjectDose accumulationen_US
dc.subjectModel-based approachen_US
dc.subject.ddc600 - Technik, Medizin, angewandte Wissenschaftenen_US
dc.titleRobustness assessment of clinical adaptive proton and photon radiotherapy for oesophageal cancer in the model-based approachen_US
dc.type01A - Beitrag in wissenschaftlicher Zeitschrift*
dc.volume177en_US
dspace.entity.typePublication
fhnw.InventedHereNoen_US
fhnw.IsStudentsWorknoen_US
fhnw.ReviewTypeAnonymous ex ante peer review of a complete publicationen_US
fhnw.affiliation.hochschuleHochschule für Life Sciences FHNWde_CH
fhnw.affiliation.institutInstitut für Medizintechnik und Medizininformatikde_CH
fhnw.openAccessCategoryHybriden_US
fhnw.pagination197-204en_US
fhnw.publicationStatePublisheden_US
relation.isAuthorOfPublication7c92bfb0-ba14-40c5-8233-6f259dffa6d2
relation.isAuthorOfPublication.latestForDiscovery7c92bfb0-ba14-40c5-8233-6f259dffa6d2
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