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Evaluation of plan quality in radiotherapy planning with an MR-linac.

Agustinus J A J van de Schoot ,
Wouter van den Wollenberg ,
Casper Carbaat ,
Peter de Ruiter ,
Marlies E Nowee ,
Floris Pos ,
Baukelien van Triest ,
Jan-Jakob Sonke ,
Tomas M Janssen

Abstract

MATERIALS & METHODS

Data of eight rectal and eight prostate cancer patients, who received radiotherapy on a conventional CBCT-integrated linac, were selected. Clinically acquired CTs and associated delineations of target volumes and organs-at-risk (OARs) were used for MR-linac treatment planning in Monaco. To investigate treatment planning software bias 'quasi MR-linac plans' were generated in Pinnacle3 by mimicking MR-linac specific beam characteristics. MR-linac, quasi MR-linac, and clinical plans were compared and differences in target and OAR doses assessed. Differences in plan complexity were determined by the number of segments and monitor units.

CONCLUSIONS

This study demonstrates the feasibility of creating high-quality MR-linac treatment plans. The results supported the clinical introduction of an MR-linac.

RESULTS

Compared to clinical plans, MR-linac plans showed a statistically significant decrease in plan homogeneity, an increase in PTV Dmean (prostate: 0.6 Gy; rectum: 0.8 Gy) and D1% (prostate: 1.9 Gy; rectum: 2.0 Gy), and increases in OAR dose. Quasi MR-linac plans were comparable to MR-linac plans with respect to OAR dose and plan homogeneity. For rectal cancer an increase was seen in PTV Dmean (0.12 Gy) and D1% (0.5 Gy) compared to regular MR-linac plans. All created plans were clinically equivalent to current clinical practice.

BACKGROUND & PURPOSE

Clinical introduction of magnetic resonance (MR)-guided radiotherapy involves treatment planning while taking into account machine-specific characteristics. Our aim was to investigate the feasibility of high-quality MR-linac treatment planning for an MR-linac and to benchmark MR-linac plan quality (IMRT) against current clinical practice (VMAT).

More about this publication

Physics and imaging in radiation oncology

Volume 10
Pages 19-24
Publication date 01-04-2019

Full text links

Publisher website (DOI) 10.1016/j.phro.2019.04.004
Europe PubMed Central 33458263
Pubmed 33458263

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