Evangelia Kaza1, Bret Nicholson2, Kevin Anderson2, Jesse Drake2, Alex Marques1, Steven Hatch1, Jeremy Bredfeldt1, Martin King1, and Atchar Sudhyadhom1
1Radiation Oncology, Brigham and Women's Hospital, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA, United States, 2Diacor Inc, West Valley City, UT, United States
Synopsis
MR conditional stirrups would be beneficial in MR-guided
gynecological and prostate brachytherapy but have not been clinically
available. Evaluation of a prototype Diacor MR conditional board and stirrups
system revealed no significant projectile or heating risks at 3T. The maximum
temperature measured on its metallic surfaces after scanning was 22 ⁰C, relating to a 3 ⁰C increase. The
stainless steel blades of the stirrup joints caused signal cancellation
artifacts which extended radially up to 23cm on phantom images. On volunteer
scans, artifacts were observed in posterior hip areas only. Pelvic organ
visualization was considered suitable for brachytherapy treatment planning.
Introduction
MRI is increasingly employed for image guidance
in gynecological and prostate brachytherapy in conjunction with CT, which is generally
required for interstitial catheter reconstruction1. Differences in patient
position between the two examinations can cause registration errors which may
translate to radiation delivery errors. Recent advances in detecting brachytherapy
applicators, seeds and needles on MR images2-4 present the opportunity
to eliminate CT and consequently MR-CT misregistration. MR conditional stirrups
would benefit the current MR-CT procedure by preserving patient position and would
enable MR-only brachytherapy treatment planning workflows by allowing
applicator or needle adjustments. To date, they have not been clinically available.
This work evaluated a prototype MR conditional board and stirrups system for
heating and artifacts during 3T MRI.Methods
A prototype Diacor Zephyr HDR Hoverboard with MR-tek 350 stirrups
was tested with a handheld magnet for attractive forces before being laid on a
3T Siemens Vida couch. Surface temperature was assessed at 13 locations along
the device using a Fluke 62 Max non-contact infrared thermometer initially, and
after each phantom test A-C (figure 1): A) A 24cm diameter spherical phantom on
the hoverboard mat simulated the pelvis. One 1900ml cylindrical phantom was
placed superiorly and one anteriorly to the sphere. B) The sphere flanked by
both bottles covered the entire space between the stirrup joints, with the
bottles touching the joints’ blades. C) The sphere was placed between the mat
and a 5300ml cylindrical phantom. Clinical and research sequences with increased
coverage (table 1) were acquired to determine the minimum artifact-free area in
test A, and artifact extent in tests B-C. Ambient temperature was measured independently
using the dedicated exam room thermometer at various timepoints throughout the
study.
D) Two consented healthy female volunteers were scanned on the
hoverboard using brachytherapy protocols (table 1). MR images were evaluated
for artifacts and pelvic organs visualization.
For all scans, receiving coils were: body 18 long (top), biomatrix
spine 32 (bottom).Results
No parts of the
assessed board and stirrups posed projectile risks at 3T. Temperature difference
between phantom tests and baseline ranged from -0.6 ⁰C to 3.3 ⁰C (figure
2). The largest temperature increase of 3.3 ⁰C was observed after 27 minutes of MR acquisition for the vinyl covered
aluminum joint of the stirrup (test A). The overall maximum measured
temperature was 22 ⁰C for the aluminum gas spring rail
mount after 15 minutes of continuous scanning, 3 ⁰C higher than the average room
temperature (test C). Non-metallic parts of the hoverboard and stirrups, and those
further from isocenter, demonstrated the least warming.
The shortest observed artifact-free length on the spherical
phantom was 18cm in superior-inferior direction for the VIBE and BEAT sequence
with TRUFI contrast on test A, and 17cm in right-left direction on the VIBE
images of test B. The maximum artifact extent measured from the stirrup blades
was 18cm for the VIBE sequence of test B and 23cm on the test C STIR images
(figure 3).
The board with mounted stirrups bearing volunteers fit well inside
the 70cm bore MR scanner. The fully clothed volunteers reported feeling no
warming at stirrup contact during the 45 minutes long examination. MR signal
cancellation caused by the stirrups metallic plate was observed only on
posterior hip areas and was most prominent on the T2-weighted STIR and TSE
images (figure 4). A radiation oncologist deemed pelvic organ visibility adequate
for treatment planning contour generation. Discussion
Phantom tests
revealed a maximum temperature increase of 3.3 ⁰C on the surface of metallic
components of the board and stirrups after a total MR scan duration of 27
minutes. The highest measured temperature of 22 ⁰C was far below the lowest cutaneous
thermal injury threshold of 44 ⁰C determined for exposure longer than
3 hours5. Therefore, the assessed device is not expected to pose
thermal injury risks upon contact during or after 3T MRI.
The wide variety of MR sequences used for the phantom and
volunteer scans covers most clinical brachytherapy protocols. The employed
phantoms provide uniform signal across their volume under ideal imaging
conditions. Their placement aimed to represent a patient’s torso in test A, and
to assess the entire space between the largest metallic stirrup components in
tests B and C. Artifacts caused by the presence of metal were identifiable as
characteristic dark areas on the phantom images. The main artifact sources were the stainless
steel blades on the inner side of the stirrups, causing signal voids that extended
up to 23cm radially on STIR images. Metal artifact measurements on phantoms may
prove useful to inform protocol sequence selection and to optimize patient
positioning on the hoverboard.
Signal cancellation artifacts were also identified on volunteer scans,
but they were confined in the posterior hip or leg area and did not affect
genitourinary or gastrointestinal organ visualization. Thus, overall image
quality was considered suitable for treatment planning purposes. Conclusion
The evaluated Diacor Zephyr HDR
Hoverboard and stirrups presented no MR safety risks at 3T. Although metal
artifacts were observed closer to the stirrup joints on MR images, brachytherapy
areas of interest in the pelvis remained unaffected. The device was considered suitable
for clinical use in MR-guided brachytherapy. Acknowledgements
No acknowledgement found.References
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