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Optimising patient positioning for accelerated partial breast radiotherapy with the Integrated Magnetic Resonance Linear Accelerator

Optimising patient positioning for accelerated partial breast radiotherapy with the Integrated Magnetic Resonance Linear Accelerator

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ANZCTR
Registry ID
ACTRN12624000679583
Acronym
OPRAH - MRL
Enrollment
4
Registered
2024-05-28
Start date
2024-01-09
Completion date
2025-01-31
Last updated
2024-06-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

The aim of this study is to compare the benefits and limitations of different positioning options for early breast cancer patients who are suitable for partial breast treatment on the Magnetic Resonance integrated Linac. Who is it for? You may be eligible for this study if you are a female age 40 or older, with early stage breast cancer and suitable for accelerated partial breast radiotherapy. Study details Participants will receive both a supine (on your back) and prone (on your tummy) scan in the MRI and a CT scan in the ideal treatment position (supine OR prone) as per our usual standard of care. Participants will then be asked to complete a short (10-15 mins) anonymous survey on an electronic platform to ask about their experience of the MRI scan and whether they have a preference for the supine or prone position. There are no changes to standard treatments for participants. It is hoped that the findings from this study will streamline the simulation process for APBI patients and help us to determine who would benefit from which position without needing to complete both scans. It is also hoped that this information can be used across our other treatment machines to benefit patients who may not be able to have an MRI scan to work out the best position for them.

Interventions

After completing the standard of care planning MRI scans, participants will be asked to complete a short (10-15 mins) anonymous survey on an electronic platform to ask about their experience of the MRI scan and whether they have a preference for the supine or prone position. Participants will be asked to indicate their agreement with a statement on a Likert scale, and have the opportunity to provide answers to open- ended questions, There are no changes to standard treatments for participants.

Sponsors

Jenna Dean, ONJ Centre, Austin Health
Lead SponsorIndividual

Eligibility

Sex/Gender
All
Age
40 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Eligible for accelerated partial breast radiotherapy as per the ASTRO favorable and Cautionary Guidelines 2. Informed consent

Exclusion criteria

1. Contraindications to MRI after screening 2. Patient unable to lay in treatment position for greater than 45 minutes 3. Patient unable to meet physical requirements of supine and prone scans

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 5, 2026