Travis Salzillo1, Yao Ding1, and Jihong Wang1
1MD Anderson Cancer Center, Houston, TX, United States
Synopsis
Keywords: New Devices, Motion Correction, Biofeedback
Motivation: Biofeedback during radiotherapy simulation and treatment on conventional linacs improves the accuracy and reproducibility of patient alignment, especially those using breath-hold. However, commercial devices cannot operate in MR environments.
Goal(s): The goal of this study was to develop an MR-compatible biofeedback device and test its utility in volunteer studies.
Approach: The device consists of a single-board computer and addressable LED strip, which was automatically controlled by tracking anatomic motion in CINE MR images.
Results: Initial volunteer studies using the device in an MR linac demonstrated that biofeedback-guided breath-hold resulted in more accurate and consistent target alignment compared to self-guided breath-hold.
Impact: MR-compatible biofeedback devices can facilitate and improve
breath-hold techniques for MR-guided radiotherapy simulation and treatment. Furthermore,
incorporation of CINE MR images to measure changes in internal anatomy improves
target alignment relative to existing devices that use surface imaging.
Introduction
For tumors in the thoracic and abdominal cavities,
respiratory motion can greatly impact radiotherapy efficacy and side effects
due to the reduced dose to the target and increased dose to nearby normal
tissue. To mitigate the effects of motion, breath-hold techniques are routinely
implemented, where the patient holds their breath and expands their diaphragm
to a reproducible level while the linac beam is on. Biofeedback devices, which
are used to indicate the accuracy of the breath-hold to the patient, have
proven successful at improving accuracy and reproducibility of breath-hold
techniques1-3. However, commercial biofeedback devices cannot be
used in MR-guided simulations and treatments due to the high magnetic field and
enclosure of the patient in the MRI bore. The goal of this study was to develop
a biofeedback device that could operate in the MR environment and guide a
patient’s breath-hold based on anatomic motion measured in CINE MR images. Methods
The development of this device comprised of both software
and hardware components. For the software component, several open-source
motion tracking algorithms were adapted and tested for both computational speed
and tracking accuracy. These included Normalized Cross Correlation (NCC),
Mutual Information (MI), and Kernalized Correlation Filter (KCF)4.
For the hardware component, several configurations of a video grabber,
single-board computer, strip of addressable light-emitting diodes (LED), and
shielded fiber optic cables were tested for operability in the MR-Linac vault
and operation latency.
With an operational prototype, volunteer studies were
conducted, following institutional review board policy, to test the device’s ability
to guide breath-holds. Consenting volunteers were imaged with CINE MRI and
asked to perform a series of breath-holds. The resultant anatomic displacement
over time was measured for self-guided and biofeedback-guided breath-holds. Results
Among the three tracking algorithms, KCF had both the lowest
computation time (12.36 ms) and highest average correlation coefficient (0.65)
between calculated displacement and actual displacement. Thus, this algorithm
was incorporated into python script, whose output was used in a modified
open-source script to control the LED strip. The hardware was made operational
by running the script on a single-board computer. CINE MR images were inputted
via HDMI cable and processed, and the resultant voltage and data signal was
outputted via general-purpose input/output pins on the computer. These signals
were transmitted via shielded fiber optic cables into the MRI vault and
integrated with the LED strip to control individual unit illumination and
color. The LED strip was attached to the superior side of the inside of the MR
linac bore. No impact on MR signal acquisition or image quality was observed
during the operation of the LED strip. The measured end-to-end latency between
CINE frame update and LED strip illumination was approximately 800 ms.
Volunteers are still being recruited for the in vivo analysis,
but a sample of one volunteer’s self-guided and biofeedback-guided breath-hold
is illustrated in the associated figure. The biofeedback-guided breath-hold
resulted in a smaller median anatomic displacement (2 vs. 10 pixels), which was
more stable (0-2 pixels vs. 8-12 pixels) compared to the self-guided
breath-hold.DIscussion
The developed biofeedback device can reliably operate in a high magnetic field within the enclosed
MRI bore. Because the device extracts frames from CINE MR, the motion
of the actual target can be directly measured, rather than a surrogate such as the patient surface. This is achieved with no additional radiation dose unlike
fluoroscopy-based real-time imaging. One
drawback of the device is the 800 ms latency, which is higher than many
biofeedback devices. However, for the purposes of assessing breath-hold
accuracy, this is acceptable.
Another feature of this device is that it is highly
customizable. The tracking algorithm can be easily replaced since only the
tracking output is used as the input for the LED illumination. The displacement
tolerance resulting in a change in LED illumination can be any number of pixels
and in any direction, and the color and number of illuminated LED units can be
customized. The CINE MR images were extracted from the console via screen
grabber, so this device can be installed at any MR console that displays CINE
MR images in real-time. Thus, in addition to testing the device at an MR linac,
it will also be deployed at an MR simulator to help guide breath-holds during
simulation imaging for treatment planning. Conclusion
A prototype MR-compatible biofeedback device was
successfully constructed and tested in the MR linac environment. Initial
volunteer testing demonstrates promising results that the device can
effectively guide patient breath-holds to improve target alignment during
MR-guided radiotherapy simulation and treatment. Acknowledgements
No acknowledgement found.References
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