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Towards the clinical implementation of intensity-modulated proton therapy for thoracic indications with moderate motion: Robust optimised plan evaluation by means of patient and machine specific information

Authors :
Arturs Meijers
M. Dieters
Johannes A. Langendijk
Antje Knopf
S. Visser
Robin Wijsman
Nanna M. Sijtsema
Erik W Korevaar
Christina T. Muijs
Stefan Both
Cássia O. Ribeiro
R Melissa Anakotta
Guided Treatment in Optimal Selected Cancer Patients (GUTS)
Damage and Repair in Cancer Development and Cancer Treatment (DARE)
Source :
Radiotherapy and Oncology, 157, 210-218. ELSEVIER IRELAND LTD
Publication Year :
2020

Abstract

Purpose Compared to volumetric modulated arc therapy (VMAT), clinical benefits are anticipated when treating thoracic tumours with intensity-modulated proton therapy (IMPT). However, the current concern of plan robustness as a result of motion hampers its wide clinical implementation. To define an optimal protocol to treat lung and oesophageal cancers, we present a comprehensive evaluation of IMPT planning strategies, based on patient 4DCTs and machine log files. Materials and methods For ten lung and ten oesophageal cancer patients, a planning 4DCT and weekly repeated 4DCTs were collected. For these twenty patients, the CTV volume and motion were assessed based on the 4DCTs. In addition to clinical VMAT plans, layered rescanned 3D and 4D robust optimised IMPT plans (IMPT_3D and IMPT_4D respectively) were generated, and approved clinically, for all patients. The IMPT plans were then delivered in dry runs at our proton facility to obtain log files, and subsequently evaluated through our 4D robustness evaluation method (4DREM). With this method, for each evaluated plan, fourteen 4D accumulated scenario doses were obtained, representing 14 possible fractionated treatment courses. Results From VMAT to IMPT_3D, nominal Dmean(lungs-GTV) decreased 2.75 ± 0.56 GyRBE and 3.76 ± 0.92 GyRBE over all lung and oesophageal cancer patients, respectively. A more pronounced reduction was verified for Dmean(heart): 5.38 ± 7.36 GyRBE (lung cases) and 9.51 ± 2.25 GyRBE (oesophagus cases). Target coverage robustness of IMPT_3D was sufficient for 18/20 patients. Averaged dose in critical structures over all 4DREM scenarios changed only slightly for both IMPT_3D and IMPT_4D. Relative to IMPT_3D, no gain in IMPT_4D was observed. Conclusion The dosimetric superiority of IMPT over VMAT has been established. For most thoracic tumours, our IMPT_3D planning protocol showed to be robust and clinically suitable. Nevertheless, accurate patient positioning and adapting to anatomical variations over the course of treatment remain compulsory.

Details

ISSN :
18790887 and 01678140
Volume :
157
Database :
OpenAIRE
Journal :
Radiotherapy and oncology : journal of the European Society for Therapeutic Radiology and Oncology
Accession number :
edsair.doi.dedup.....edaf323f8978d52660cb5b7e94c2aa3e