Copenhagen, Denmark
Onsite/Online

ESTRO 2022

Session Item

Saturday
May 07
16:55 - 17:55
Poster Station 2
08: Advances in radiotherapy planning & techniques
Madalyne Day, Switzerland
Poster Discussion
RTT
Feasibility of magnetic resonance-guided stereotactic ablative body radiotherapy of liver cancer
Vikneswary Batumalai, Australia
PD-0334

Abstract

Feasibility of magnetic resonance-guided stereotactic ablative body radiotherapy of liver cancer
Authors:

Maddison Picton1, Vikneswary Batumalai1, David Crawford2, Claire Pagulayan3, Louise Hogan2, Urszula Jelen2, Conrad Loo2, Nicole Dunkerley2, Lori Geddes2, Sandy Sampaio2, Monique Heinke2, Tania Twentyman2, Michael Jameson2, Jeremy de Leon2

1GenesisCare, Radiation Therapy , Sydney, Australia; 2GenesisCare, Radiation Therapy, Sydney, Australia; 3GensisCare, Radiation Therapy, Sydney, Australia

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Purpose or Objective

Stereotactic ablative body radiotherapy (SABR) is an effective treatment method for liver cancer. However, tumour motion and proximity of organs at risk (OAR) can be a limiting factor when delivering high doses of radiation. Magnetic resonance (MR) guided adaptive radiotherapy (MRgART) can improve the accuracy and dose coverage of tumour volumes. This study assessed the feasibility of MRgART for liver cancer. 

Material and Methods

Five patients with liver cancer were treated with MRgART. Image sequencing included a T2 Navigated scan which produced images at expiration. A balance turbo fast field echo (BTFFE) image was also acquired every fraction to measure liver motion for the ITV margin. All plans were prescribed to 50Gy in 5 fractions. Plans were adapted in real time for every fraction with treatment time and dosimetric criteria recorded.

Results

Median patient age was 61 years (range 54-85 years).  Twenty-five fractions (adapted plans) were delivered to a total of five patients. Dosimetric parameters are summarised in Table 1. Median dose to 98% of the gross tumour volume and planning target volume were 52.4 Gy and 46.5 Gy, respectively. OAR targets were met for all twenty-five fractions. The median time from ‘patient set-up’ to ‘beam-off’ time was 49.3 minutes (range 39.2-57.0 minutes). All patients completed treatment with no interruptions.

Conclusion

Our early experience suggests that MRgART for liver cancer is feasible and safe with acceptable dosimetric parameters and treatment time. We continue to collect data and evidence on patient and clinician reported outcome, safety and tolerability of MRgART.