Eva Oberacker1, Katharina Paul1, Lukas Winter1, Celal Oezerdem1, Antje Els1, Andreas Pohlmann1, Laura Boehmert1, Stefanie Kox1, Min-Chi Ku1, Till Huelnhagen1, Oliver Stachs2, Jens Heufelder3,4, Andreas Weber3,4, and Thoralf Niendorf1,5
1Berlin Ultrahigh Field Facility (B.U.F.F.), Max Delbrück Center for Molecular Medicine in the Helmholtz Association, Berlin, Germany, 2Department of Ophthalmology, University of Rostock, Rostock, Germany, 3Department of Ophthalmology, Charité University Medicine, Berlin, Germany, 4BerlinProtonen, Helmholtz Zentrum Berlin, Berlin, Germany, 5Experimental and Clinical Research Center (ECRC), a joint cooperation between the Charité Medical Faculty and the Max Delbrück Center for Molecular Medicine in the Helmholtz Association, Berlin, Germany
Synopsis
This
work examines the MR safety of intraocular tantalum markers used in proton beam
therapy of uveal melanoma. RF power deposition induced heating was studied
using electromagnetic field and temperature simulations. Magnetic
force acting on the marker was investigated and image artifacts were assessed. Minor local increase of RF power deposition was observed
for SAR0.075g but not detectable for SAR1g. Measurements
showed no detectable magnetic attraction of the implant. FSE based imaging showed only small artifacts barely exceeding the thickness of the
sclera. Our studies indicate that intraocular tantalum markers do not
constitute a per se contraindication
for 7.0T MRI.Purpose
A growing
number of reports refer to MRI of the eye segments and their masses
1,2.
Ocular MRI holds the potential to provide guidance during diagnostic assessment
and proton beam therapy of uveal melanoma
3. Patients scheduled for
proton beam therapy undergo implantation of metallic markers which are
essential for tumor localization, treatment planning and patient positioning
for proton irradiation
3. This work examines the MR safety of
intraocular tantalum markers used for proton beam therapy of uveal melanoma.
Methods
RF power
deposition induced heating was studied using electromagnetic field(EMF) and
temperature(Pin=1W peak power, t=60s) simulations(Sim4Life V2.0,ZMT,Zurich,Switzerland).
E-field coupling was investigated for a tantalum marker implant with a button
like geometry(Fig.1a). Alternatively, a disk with the same shape and outer
dimensions was employed to generalize and simplify the setup. To approximate
the in vivo situation with a given size and shape of the eyeball, the tantalum
implants were placed in an agarose phantom at a distance of 15-30mm from its
surface. A bowtie electric dipole antenna was used for RF transmission. This
approach ensures defined E-field vectors in relation to the implant with the
E-field lines being in parallel with the antenna4. Disk rotations
between 0° and 90° parallel and perpendicular to the electric field lines were
investigated. A high resolution meshbox(resolution (0.05mm)³, size 10x10x10mm³)
was defined around the device under investigation(DUI). SAR
distribution for various averaging masses(m<1g) was calculated to approach the
temperature distribution in the purely SAR dominated linear heating regime. Meeting
this criterion, SAR was
evaluated locally(SAR0.075g, cube size (4.2mm)³) and for 1g mass
averages(cube size (9.8mm)³).
Magnetic force acting on the marker was investigated with the
deflection angle method5(Fig.1b). An USP9-0 suture was used to meet
the restriction msuture< 1%mimplant5. The
holder was positioned at the entrance of the magnet bore(B0≈1.5T,$$$\nabla$$$B0≈3.5T/m).
Image
artifacts were investigated at 7.0T(Magnetom,Siemens Healthcare,Erlangen,Germany)
and 9.4T(Biospec 94/20 USR,Bruker Biospin,Ettlingen,Germany). At 7.0T, a six-channel
transceiver array tailored for ophthalmic MRI was employed2 with a
cylindrical phantom including two spherical holders accommodating an agarose
phantom eye(Fig.1c) and ex-vivo pig eyes(Fig.1d). At 9.4T, a 35mm quadrature volume resonator
was used. Gradient echo(GRE) and a fast spin echo(FSE) imaging(caption Fig.3)
was applied. Three ocular tantalum markers were sutured to the sclera of the pig
eye resembling the positioning of the markers in proton beam therapy(Fig.1d).
Results
Peak SAR0.075g
(Pin=1 W peak power accepted at port) obtained for the disk accords
very well with max SAR0.075g observed for the tantalum implant(Fig.1a).
SAR1g clipped peak SAR due to the averaging volume size being
significantly larger than the implant (9.8mm vs. 2.5mm;Fig.1). SAR0.075g
showed an exponential decay with increasing distance between the RF antenna and
the implant(R²=1;Fig.1b). A linear correlation(R²=1) was found between SAR0.075g(W)
with the implant being present and SAR0.075g(W/O) without the presence of the implant(Fig.1d). When changing the effective conductive length by rotating
the disk perpendicular to the E-field lines a cosine dependence of SAR0.075g(W)(γ)
on the rotation angle was obtained(R²=0.95;Fig.1e,f). Rotation along the
E-field lines did not influence the effective conductive length and hence showed
no clear angular dependence(Fig.1g). Our simulations demonstrated that SAR0.075g(W)
in presence of the implant can be simply described by SAR0.075g(W/O)
without the presence of the implant: $$SAR_{0.075g(W)}(γ)=1.1·(0.04·cos(2γ)+0.96)·SAR_{0.075g(W/O)}(0°)+0.1$$
Maximum SAR0.075g(W)=1.9W/kg of the DUI was inferior to maximum SAR0.075g=2.57W/kg
located at the phantom surface. Thermal simulations confirmed a larger temperature
increase at the phantom surface(ΔTmax=36.7mK) then at the disk edges(ΔTdisk=18mK)
after approximately 2s of heating(Fig.1h). Presence of the disk caused
additional heating of δT=1.2mK versus the empty phantom.
Magnetic deflection angle measurement showed no detectable attraction
of the implant towards the scanner bore, staying well below the 45° reference
point5.
GRE imaging showed severe
susceptibility artifacts around the implant(Fig.3a,b,d,e). FSE images were less affected(Fig.3c,f).
Ex-vivo eye imaging(Fig.4) confirmed the strong artifacts in GRE. FSE was less
prone to susceptibility artifacts with the artifact towards the vitreous humor
barely exceeding the thickness of the sclera.
Discussion and conclusion
Minor local
increase of RF power deposition was observed for SAR
0.075g(W) but not
detectable for SAR
1g. Our studies indicate that intraocular tantalum
markers commonly used for proton beam therapy do not constitute a
per se contraindication for 7.0T MRI.
Strict rejection of subjects with tantalum markers from 7.0T MRI is not
justified. Imaging can be conditionally performed after collection of
substantial safety information and evaluation of the detailed exposure scenario(RF
coil/type and position of implant). This opens the road to high spatial
resolution ultrahigh field MRI of patients equipped with tantalum markers who
could benefit from MR guided diagnostics, proton therapy beam treatment and response
monitoring of ocular masses.
Acknowledgements
No acknowledgement found.References
[1] Paul, K. et al., Invest Radiol, 2015
[2] Graessl, A. et al., Invest Radiol, 2014
[3] Höcht, S. et al., Strahlenther Onkol, 2004
[4] Winter, L. et al., Magn Res Med, 2014
[5] ASTM International, F2052-15
[6] International Electrotechnical Commission, 2002