Myriam Jaarsma-Coes1, Megan Schuurmans2, Kilany Hassan2, Eleftheria Astreinidou3, Marina Marinkovic4, Femke Peters3, and Jan-Willem Beenakker1
1Radiology & Ophthalmology, Leiden University Medical Center, Leiden, Netherlands, 2Radiology, Leiden University Medical Center, Leiden, Netherlands, 3Radiotherapy, Leiden University Medical Center, Leiden, Netherlands, 4Ophthalmology, Leiden University Medical Center, Leiden, Netherlands
Synopsis
MRI
is becoming a new important imaging modality for ocular tumours. The
acquisition of the MR-images for therapy planning are acquired in supine
position, but proton beam radiotherapy is performed with the patient in sitting
position. By performing scans in supine and in flexed position, we found that
this change in gravity direction produces no substantial changes (<0.3mm) in
eye and tumour shape. Our results indicate that supinely acquired MR images can
be used to accurately plan proton beam radiotherapy of ocular tumours.
Introduction
Uveal
melanoma (UM) is the most common primary malignant intraocular tumour1,2.
Proton beam irradiation (PBT) is often the therapy of choice for large tumours,
as well as tumours in close proximity to the optic nerve. Conventionally 2D
ultrasound imaging is used to plan the radiotherapy, but recently 3D MRI is
proposed for PBT treatment planning3,4,5. However, while PBT is
performed with the patient in sitting position, the acquisition of the MR-images
is performed in supine position (figure 1). This change in gravity direction potentially
changes the shape of the eye and tumour. As even small geometrical deformation
can lead to over- or underdose to the tumour and surrounding healthy tissues,
we used MRI to investigate and quantify the effect of different patient
positions on the shape of the eye and tumour.Methods
Seven
volunteers and one UM patient were scanned with closed eyes in two positions on
a 3T Philips MRI scanner with a 47mm surface coil after giving informed consent.
One set of images was acquired in supine position, while a second set was acquired
in flexed position, mimicking the patient sitting upright for PBT (figure 1).
Additionally, two volunteers were scanned twice in the supine position to
assess the reproducibility. For the healthy subjects, the analyses were
performed on 3D T2-weighted images (turbo spin echo, TR/TE: 2500ms/285ms, voxel
size: 0.9mm isotropic, echo train length: 130, NSA: 2, time:3
min) as these provide optimal contrast to differentiate the sclera,
while for the UM patients a post-contrast T1 (TR/TE:350ms/9.4ms, voxel size:
1.0mm isotropic, scan time: 3 min) was used to differentiate between UM and
retinal detachment.
The two scans were registered and subsequently the sclera, or if applicable tumour, were segmented (figure 2) using Elastix 4.9.09 in Mevislab 3.0.2 (MeVis Medical Solutions AG, Bremen, Germany). After registration the sclera, lens and tumour were segmented using Subdivision Surfaces controlled by the maximal gradient magnitude6. This method is independent of signal amplitude which is valuable as the signal amplitude varies per MRI scan. For the UM patient only the tumour-vitreous border could be accurately compared, as the fast retinal wash-out of the contrast agent changed the appearance of the eye-wall between both acquisitions (figure 3).
Results
A
masked registration was performed in all scans,
to accommodate a potentially rotated eye within moved head, after which the
eye-wall or tumour were successfully segmented. Figure 2 (middle) shows the result of
the registration and subsequent segmentation for one of the subjects. In
healthy controls the median difference between the supine and flexed scans was
0.1mm (95th percentile (P): 0.3mm), which is in the order of the
reproducibility of the method (95th P: 0.3mm), figure 4. The slightly larger
difference in eye-shapes of subjects 5 was caused by eye-motion artefacts. In
the UM patient we found a median UM difference of the tumour of 0.1mm (95th P:
0.4mm) (figure 3 & 4).Discussion
The
small differences in eye shapes of the healthy eyes are probably mainly caused
by small registration errors due to the high rotational symmetry of the eye. As
the tumour breaks this symmetry, a more accurate registration was possible for
the UM-patient, explaining the lower median difference in tumour shapes. As
there is approximately 10 minutes between the acquisition of the supine and
flexed MR-images, the washout of the Gd-contrast agent might result in an
artificial change in tumour shape. A T2-weighted sequence would be less
sensitive to this effect, but on T2 the tumour is often difficult to
discriminate from retinal detachment. For all subjects motion artefacts are
another cause of artificial differences, as these blur the anatomical
boundaries. Nevertheless, we can conclude that the changes in eye and/or tumour
shape between sitting and supine position are less than 0.3mm, which is
significantly better than accuracy of the conventional Ultrasonic techniques,
which have a reproducibility of 0.6mm7. We are currently expanding
the number of UM patients to confirm our findings for other tumour shapes. Conclusion
No significant deformations in eye and
tumour shape were detected, indicating that that supinely acquired MR images of the
eye can be used to accurately plan proton beam therapy of eye tumours. Acknowledgements
The authors thank Berend Stoel, Niels Dekker and
Denis Shamonin (LKEB, LUMC) fort their help with image registration and
Emmanuelle Fleury (Erasmus MC) for discussions on MR-based therapy planning of
UM. This work is part of the research program Protons4Vision with project
number 14654 which is financed by the Netherlands Organization for Scientific
Research (NWO).References
1. Singh AD, Turell ME, Topham AK. Uveal
melanoma: Trends in incidence, treatment, and survival. Ophthalmology.
2011. doi:10.1016/j.ophtha.2011.01.040
2.
Chang AE, Karnell LH, Menck HR. The national cancer data base report on
cutaneous and noncutaneous melanoma: A summary of 84,836 cases from the past
decade. Cancer. 1998.
doi:10.1002/(SICI)1097-0142(19981015)83:8<1664::AID-CNCR23>3.0.CO;2-G
3. Beenakker JWM, Ferreira TA, Soemarwoto KP, et
al. Clinical evaluation of ultra-high-field MRI for three-dimensional
visualisation of tumour size in uveal melanoma patients, with direct relevance
to treatment planning. Magn Reson Mater Physics, Biol Med. 2016.
doi:10.1007/s10334-016-0529-4
4. De Graaf P,
Göricke S, Rodjan F, et al. Guidelines
for imaging retinoblastoma: Imaging principles and MRI standardization. Pediatr Radiol. 2012.
doi:10.1007/s00247-011-2201-5
5. Nguyen HG, Sznitman R, Maeder P,
et al. Personalized
Anatomic Eye Model From T1-Weighted Volume Interpolated Gradient Echo Magnetic
Resonance Imaging of Patients With Uveal Melanoma. Int J Radiat Oncol
Biol Phys. 2018.
6. Kitslaar PH, van’t Klooster R, Staring M, Lelieveldt BPF, van der Geest
RJ. Segmentation
of branching vascular structures using adaptive subdivision surface fitting.
In: Medical Imaging 2015: Image Processing. Vol 9413. International
Society for Optics and Photonics; 2015:94133Z.
7. Char
DH, Kroll S, Stone RD, Harrie R, Kerman B. Ultrasonographic measurement of
uveal melanoma thickness: interobserver variability. Br J Ophthalmol.
1990;74:183–185. doi: 10.1136/bjo.74.3.183.