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MRI commissioning of 1.5T MR-linac systems - a multi-institutional study.

Rob H N Tijssen ,
Marielle E P Philippens ,
Eric S Paulson ,
Markus Glitzner ,
Brige Chugh ,
Andreas Wetscherek ,
Michael Dubec ,
Jihong Wang ,
Uulke A van der Heide

Abstract

MATERIALS & METHODS

Here we describe a comprehensive commissioning protocol, which contains standard MRI performance measurements as well as dedicated hybrid tests that specifically assess the interactions between the Linac and the MRI system. The commissioning results of four MR-linac systems are presented in a multi-center study.

CONCLUSION

Our results highlight the importance of dedicated hybrid commissioning tests and the ability to compare the machines between institutes at this very early stage of clinical introduction. Until formal guidelines and tolerances are defined the tests described in this study may be used as a practical guideline. Moreover, the multi-center results provide initial bench mark data for future MR-linac installations.

RESULTS

Although the four systems showed similar performance in all the standard MRI performance tests, some differences were observed relating to the hybrid character of the systems. Field homogeneity measurements identified differences in the gantry shim configuration, which was later confirmed by the vendor.

BACKGROUND

Magnetic Resonance linear accelerator (MR-linac) systems represent a new type of technology that allows for online MR-guidance for high precision radiotherapy (RT). Currently, the first MR-linac installations are being introduced clinically. Since the imaging performance of these integrated MR-linac systems is critical for their application, a thorough commissioning of the MRI performance is essential. However, guidelines on the commissioning of MR-guided RT systems are not yet defined and data on the performance of MR-linacs are not yet available.

More about this publication

Radiotherapy and oncology : journal of the European Society for Therapeutic Radiology and Oncology

Volume 132
Pages 114-120
Publication date 01-03-2019

Full text links

Publisher website (DOI) 10.1016/j.radonc.2018.12.011
Europe PubMed Central 30825959
Pubmed 30825959

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