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Radiation Planning Assistant - A Streamlined, Fully Automated Radiotherapy Treatment Planning System
Published on: April 11, 2018
Improving fiducial and prostate capsule visualization for radiotherapy planning using MRI
Angela U Pathmanathan1,2, Maria A Schmidt1,2, Douglas H Brand1,2
1The Royal Marsden Hospital NHS Foundation Trust, London, UK.
T2*-weighted MRI sequences accurately depict prostate anatomy and fiducial markers, improving radiotherapy accuracy. This single sequence enhances contouring consistency and fiducial marker identification in treatment planning.
Area of Science:
- Radiotherapy
- Medical Imaging
- Prostate Cancer Treatment
Background:
- Fiducial markers (FM) are crucial for accurate radiotherapy (RT) delivery in prostate cancer.
- Assessing geometric integrity and contouring consistency is vital for RT planning.
Purpose of the Study:
- To evaluate the geometric accuracy and contouring consistency of T2*-weighted (T2*W) MRI sequences for prostate radiotherapy.
- To determine if T2*W sequences alone can visualize fiducial markers and delineate the prostate.
Main Methods:
- Ten patients from the PACE trial underwent CT, T2-weighted (T2W), and T2*W MRI.
- Three clinicians contoured the prostate on each imaging set.
- Interobserver variability was assessed using Monaco ADMIRE.
- Geometric accuracy and marker positioning were tested using specialized objects.
Main Results:
- T2*W MRI demonstrated significantly lower interobserver variability in prostate contouring compared to CT.
- All fiducial markers were visible in T2*W images (29/30 correctly identified), versus only 3/30 in T2W images.
- MRI showed minimal geometric distortion (<0.375 mm in-plane displacements), with symmetric signal loss around markers.
Conclusions:
- Prostate T2*W MRI sequences are geometrically accurate and provide consistent prostate contours.
- T2*W imaging effectively identifies fiducial markers and enables prostate delineation.
- This single sequence is suitable for use in mixed MR-CT workflows for radiotherapy planning.
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