Copenhagen, Denmark
Onsite/Online

ESTRO 2022

Session Item

RTT treatment planning, OAR and target definitions
Poster (digital)
RTT
Initial experience delivering stereotactic radiotherapy to a gluteal metastasis on a 1.5T MR Linac
Phil Fendall Amaro, United Kingdom
PO-1877

Abstract

Initial experience delivering stereotactic radiotherapy to a gluteal metastasis on a 1.5T MR Linac
Authors:

Phil Teles Amaro1, Lisa McDaid1, Lucy Davies1, Lee Whiteside1, Abigael Clough1, Corinne Faivre-Finn2,3, Jacqui Parker1, Rachael Bailey1, Rebecca Benson1, Claire Nelder1, Eleanor Pitt1, Cynthia Eccles1,4, Cathryn Crockett2, Ahmed Salem2, Ananya Choudhury2,5

1The Christie NHS Foundation Trust, Radiotherapy, Manchester, United Kingdom; 2The Christie NHS Foundation Trust, Clinical Oncology, Manchester, United Kingdom; 3University of Manchester, Radiation Oncology, Manchester, United Kingdom; 4University of Manchester, Medicine and health, Manchester, United Kingdom; 5University of Manchester, Cancer Sciences, Manchester, United Kingdom

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Purpose or Objective

This work reports on our initial experience delivering stereotactic ablative radiotherapy (SABR) to a gluteal metastasis on a 1.5T Elekta Unity MR Linac (MRL) (Elekta AB. Stockholm, Sweden).

Material and Methods

A patient with non-small cell lung cancer (NSCLC) was found to have an 8mm right-sided gluteal oligometastasis on staging FDG PET-CT (stage IVa, oligometastatic disease). Discussion at local SABR multi-disciplinary team (MDT) highlighted challenges in localising the sub-centimetre gluteal metastasis on cone-beam CT (CBCT) imaging, therefore a referral was made for treatment on the MRL within the ethically approved, imaging study PRIMER (Clinicaltrials.gov NCT02973828).

A preliminary MR scan was performed to ensure the lesion was identifiable. Vendor approved MR sequences (Table 1) were used to determine lesion conspicuity as, ultimately, only these sequences are sanctioned for clinical use on the Unity MRL. A further spectrally selective attenuated inversion recovery (SPAIR) sequence was performed to suppress fat signal and provide further confidence in disease visibility. The patient then underwent CT and MR planning scans (pCT and pMR respectively), positioned supine with arms on thorax and pelvis immobilised with knee and foot step. pCT was performed for the provision of electron density data to inform treatment planning.

pCT and pMR image sets were imported into the Monaco treatment planning system (v 5.40.01, Elekta AB. Stockholm, Sweden) for target volume and organ at risk (OAR) delineation and a prescription of 30Gy in 3 fractions was planned. The T2 SPAIR sequence was co-registered with the 6 minute T2 3D Tra sequence to further aid target delineation.

Results

Delivery of SABR (30Gy in 3 fractions over 6 days) to a gluteal oligometastasis was successfully completed on the Unity MRL following the Adapt to Position (ATP) workflow. Target visualisation on pMR was superior to pCT, in which the 8mm lesion was barely visible (Figure 1). Consensus review showed that the 6 minute T2 3D Tra sequence provided superior confidence in target visibility and was therefore used for planning and daily plan adaptation/verification. Median treatment time was 52:08 (range 49:19 - 57:16). The patient did not report any adverse effects.  



Conclusion

We have successfully completed SABR delivery to a sub-centimetre oligometastasis within the right gluteus medius muscle on the Elekta Unity MRL following the ATP workflow, a first at our institution. This would not have been possible on a conventional linac due to the poor soft-tissue contrast associated with CT and CBCT imaging. Workflows have been established that will facilitate a future MR guided, soft tissue tumour service.