Ferdinand Seith1, Holger Schmidt1, Sergios Gatidis1, Ilja Bezrukov2, Christina Schraml1, Christina Pfannenberg1, Christian la Fougère3, Konstanin Nikolaou1, and Nina Schwenzer1
1Radiology, Universitätsklinikum Tübingen, Tübingen, Germany, 2Max-Planck-Institut, Tübingen, Germany, 3Nuclear Medicine, Universitätsklinikum Tübingen, Tübingen, Germany
Synopsis
Attenuation correction (AC) plays a key role in the
quantification of tracer uptake in positron emission tomography (PET), expressed
as standardized uptake value (SUV). The segmentation method is the standard
approach for AC in whole-body PET/magnetic resonance imaging (MRI) that has
been implemented into the software of most vendors. However, this method is
neglecting bone and applies only one single patient-independent attenuation
coefficient for the whole lung. Our study could demonstrate that both,
differences lung density and surrounding bone tissue can have significant
influence on SUV measurement of physiological lung tissue, mostly affecting the
posterior regions.Purpose
In positron emission tomography (PET), the correction
of the AC of 511keV photons on their way through the patients’ body plays a key
role in quantifying the tracer-uptake. However, the signal intensity in MRI is
not related to linear attenuation coefficients (LACs). Thus, several approaches
have been proposed to overcome this drawback. So far, the segmentation method
is the most robust and straight-forward one for whole body imaging and has
therefore been implemented into the software of most vendors [1]. Based on a
T1-weighted sequence, it separates the body into different tissue types (e.g.
background, lung, fat, soft tissue) and assigns every tissue type a predefined
LAC to compute an attenuation map (µ-map). However, bone is routinely not
implemented which can lead to underestimations of SUV in regions with a high
amount of bony tissue [2]. Also, only one
single LAC is defined for the lung tissue. Thus, the aim of this study was to analyze
the accuracy of SUV quantification of the segmentation method in different
regions of the lung in direct comparison to the CT-based AC and to measure the
impact of regional differences of lung density as well as bone tissue.
Material and Methods
21
Patients (9 female, mean age 56.6±13.8 y) with examinations of at least
substantial parts of the lung were examined in a PET/CT
and subsequently in a fully integrated PET/MR (Biograph mMR, Siemens
Healthcare). Acquired PET data from PET/MR were reconstructed using four
different µ-maps: i) a CT-based µ-map (PET_CTAC , gold standard),
ii) a CT-based µ-map in which the LAC of the lung tissue was replaced by the
lung LAC from the MR-based segmentation method (PET_CTAC_MRLUNG); iii)
based on ii), the LAC of bone structures was additionally replaced with the LAC
from the MR-based segmentation method (PET_CTAC_MRLUNG_NOBONE); iv) the μ-map from the vendor-provided MR-based segmentation
method (PET_MRAC). µ-maps were modified using MATLAB. T2-weighted images
as well as MR- and CT-based µ-maps from each patient were rigidly registered to
the corresponding PET data from PET/MRI. 14 ROIs with a diameter of 1cm each
were placed in physiological lung tissue of each patient using PMOD. For each
lung, one ROI was set in the apex, three were set at the level of the hilum
(anterior, middle, posterior) and three were set in the basal lung. The
relative difference of SUVmean between the different PETs was defined as:
(SUVmean (x) - SUVmean (y)) / SUVmean (y).
Results
Table 1 and figure 1 give overviews on the relative
differences of PET reconstructions ii)-iv) in comparison to i). The replacement
of lung tissue in PET_CTAC with LAC from MR (PET_CTAC_MRLUNG)
had no significant effect on the middle lung parts while a relative
overestimation in the anterior parts and an underestimation in the posterior
parts were observed. The additional replacement of bone tissue with soft tissue
from MR (PET_CTAC_MRLUNG_NOBONE) had only very slight effects on the PET
quantification in the anterior and middle parts while there was an additional
increasing of SUV underestimation in the posterior regions. Compared to PET_CTAC_MRLUNG_NOBONE,
a further relative underestimation of SUV in the middle and posterior regions
were found in PET_MRAC. Figure 2 is an example of a subtraction
picture of PET_CTAC and PET_MRAC.
Conclusion
Both, the replacement of lung and bone tissue in the
CT-based µ-map had strongest influence on the posterior lung parts leading to a
relative underestimation. This suggests that the overall resulting deviation of
SUV quantification between PET_MRAC and PET_CTAC is
based on both, differences of lung density (e.g. gravitational dependency) and surrounding
bone tissue. The additional difference between PET_MRAC and PET_CTAC_MRLUNG_NOBONE
might be caused by the algorithm which has not replaced bone tissue completely
in the CT-based µ-map because, according to the literature, the offset LAC was
set to 0.11/cm while soft tissue LAC in PET/MR is set to 0.1/cm.
Discussion
Using the segmentation method for AC in PET/MR systems
leads to deviations of SUV in physiological lung tissue, mostly affecting the
posterior lung parts. Differences in lung density and the relative high amount
of surrounding bone tissue in those regions (spine and costovertebral joints)
seem to be strongly influencing factors. This has to be taken into account when
comparing SUVs from PET/CT and PET/MR.
Acknowledgements
No acknowledgement found.References
1. Martinez-Moller, A.,
et al., Tissue classification as a
potential approach for attenuation correction in whole-body PET/MRI: evaluation
with PET/CT data. J Nucl Med, 2009. 50(4): p. 520-6.
2. Hofmann, M., et al., MRI-based attenuation correction for
whole-body PET/MRI: quantitative evaluation of segmentation- and atlas-based
methods. J Nucl Med, 2011. 52(9): p. 1392-9.