Abstract
Purpose
The image quality characteristics of two NEMA phantoms with yttrium-90 (90Y) were evaluated on a long axial field-of-view (AFOV) PET/CT. The purpose was to identify the optimized reconstruction setup for the imaging of patients with hepatocellular carcinoma after 90Y radioembolization.
Methods
Two NEMA phantoms were used, where one had a 1:10 sphere to background activity concentration ratio and the second had cold background. Reconstruction parameters used are as follows: iterations 2 to 8, Gaussian filter 2- to 6-mm full-width-at-half-maximum, reconstruction matrices 440 × 440 and 220 × 220, high sensitivity (HS), and ultra-high sensitivity (UHS) modes. 50-, 40-, 30-, 20-, 10-, and 5-min acquisitions were reconstructed. The measurements included recovery coefficients (RC), signal-to-noise ratio (SNR), background variability, and lung error which measures the residual error in the corrections. Patient data were reconstructed with 20-, 10-, 5-, and 1-min time frames and evaluated in terms of SNR.
Results
The RC for the hot phantom was 0.36, 0.45, 0.53, 0.63, 0.68, and 0.84 for the spheres with diameters of 10, 13, 17, 22, 28, and 37 mm, respectively, for UHS 2 iterations, a 220 × 220 matrix, and 50-min acquisition. The RC values did not differ with acquisition times down to 20 min. The SNR was the highest for 2 iterations, measured 11.7, 16.6, 17.6, 19.4, 21.9, and 27.7 while the background variability was the lowest (27.59, 27.08, 27.36, 26.44, 30.11, and 33.51%). The lung error was 18%. For the patient dataset, the SNR was 19%, 20%, 24%, and 31% higher for 2 iterations compared to 4 iterations for 20-, 10-, 5-, and 1-min time frames, respectively.
Conclusions
This study evaluates the NEMA image quality of a long AFOV PET/CT scanner with 90Y. It provides high RC for the smallest sphere compared to other standard AFOV scanners at shorter scan times. The maximum patient SNR was for 2 iterations, 20 min, while 5 min delivers images with acceptable SNR.
Similar content being viewed by others
Explore related subjects
Discover the latest articles, news and stories from top researchers in related subjects.Avoid common mistakes on your manuscript.
Introduction
The procedure of radioembolization with yttrium-90 (90Y) has been increasingly used for treating patients with malignant liver tumors such as hepatocellular carcinoma (HCC) [1,2,3,4,5]. 90Y radioembolization, also known as selective internal radiation therapy (SIRT), utilizes glass or resin microspheres containing 90Y. The spheres can irradiate tumor tissue by locally depositing their energy without significantly affecting the surrounding healthy tissue in the liver. The administration is performed via selected branches of the hepatic artery.
Single-photon emission computed tomography (SPECT) has been regarded the standard for the post-treatment dosimetry validation [6, 7]. However, the 90Y Bremsstrahlung SPECT imaging presents certain challenges [6, 8, 9] such as dominant photon scatter, collimator septal penetration, and limited spatial resolution [10].
Apart for the predominantly emitted beta particles, a rare branch of beta minus of 90Y in its disintegration goes to the first excited state of zirconium-90 (90Zr) where the origin of the beta plus can be explained following a rare monopole transition between the 0 + /0 − states of 90Zr resulting in an internal pair production [11]. Modern positron emission tomography with computed tomography scanners (PET/CTs) can overcome the limitations arising from the low count statistics of the extraordinary small branching ratio (32 ppm) [12] based on their overall higher sensitivity performance. Specifically, for the post-treatment dosimetry evaluation, which is important for assessing the outcome of the irradiation of the tumor lesions, PET has not only been gaining favor but it is strongly recommended for 90Y resin microsphere therapy [13] due to its higher spatial resolution and higher quantitative accuracy compared to SPECT [6, 8, 9, 14,15,16]. The increased use of PET for SIRT imaging has been made possible by the introduction of TOF PET (12, 13), which reduces the noise and serves as an effective sensitivity increaser: such an effect is known to be directly connected to the time resolution of PET scanner [17].
With the recent introduction of long axial field-of-view (LAFOV) scanners, such as the Biograph Siemens Vision Quadra and the uEXPLORER, the sensitivity has increased multiple times compared to the standard axial field-of-view (AFOV) scanners. The peak sensitivity for the Biograph Vision Quadra at the center of the AFOV is 176 cps/kBq which is 2.75 times higher than the Biograph Vision 600 which has a standard AFOV of 26.3 cm [18]. The uEXPLORER with an AFOV of 196 cm provides a peak sensitivity at 174 cps/kBq [19]. In addition, silicon photomultipliers (SiPMs) that have replaced the bulky photomultiplier tubes provide higher overall gain, energy, and timing resolution that further enhance the scanner’s sensitivity.
However, the Biograph Vision Quadra has similar timing and spatial resolution to the Biograph Vision 600 since they both use SiPM detectors based on same technology [18]. A study has already evaluated National Electrical Manufacturers Association (NEMA) body phantom [20] datasets acquired on an uEXPLORER and has shown that the SNR for the smaller spheres, with diameters 13 mm and 10 mm, was higher compared to Biograph mCT PET/CT which has an AFOV of 21.8 cm and a sensitivity of 9.6 cps/kBq [21]. In this work, 90Y datasets of two NEMA body phantoms, acquired on a LAFOV PET/CT scanner with an AFOV of 106 cm, were reconstructed with different parameters as well as acquisition times and evaluated in terms of image quality metrics, like mean contrast recovery coefficient (RCmean) and signal-to-noise ratio (SNR). Taking advantage of the higher overall sensitivity of the scanner compared to scanners with standard AFOV (15–30 cm), the purpose is to define the optimal reconstruction setup that provides maximum SNR and high RCmean as well as minimizing scan time for patient comfort.
Materials and methods
Scanner
A Biograph Vision Quadra PET/CT scanner (Siemens Healthineers, Knoxville, TN, USA) was used which employs silicon photomultiplier-based detectors with 3.2 × 3.2 × 20.0 mm lutetium-oxoorthosilicate crystals [18]. The Biograph Vision Quadra has 32 detector rings, each one with 38 detector blocks, which provide an AFOV of 106 cm. The data were acquired using the complete AFOV, in ultra-high sensitivity (UHS) mode, with the maximum ring distance (MRD) of 322 crystals (MRD 322). In addition to this UHS mode, images were also reconstructed using the high sensitivity (HS) mode that was the default reconstruction before UHS was available, with a maximum ring distance of only 85 crystals (MRD 85) [18].
Specifically, the Biograph Vision Quadra records all possible lines of response (LORs) using MRD 322, with an acceptance angle of 52 degrees. In the first version of the reconstruction software (VR10), also named high-sensitivity mode, images are reconstructed with LORs spanning an MRD of 85 crystal rings (MRD 85). This MRD is comparable to the Biograph Vision 600 MRD of 79 [22], corresponding to an acceptance angle for axial LOR of about 18°. The MRD metric refers to the number of crystals in the LOR’s axial extent and includes the gaps between blocks. In MRD 85 mode, the Vision Quadra does not use all the possible LORs between scintillating crystals for image reconstruction. In short, UHS has maximum ring difference of 322; HS has maximum ring difference of 85. UHS has acceptance angle of 54 degrees whereas HS has 18 degrees. The data is always acquired with full ring difference; HS and UHS are just different reconstructions [18].
The overall system sensitivity is 176 cps/kBq for UHS and 83 cps/kBq for HS mode, while the time-of-flight (TOF) is 230 ps and 228 ps, respectively [18]. Furthermore, an improved 3D scatter correction algorithm is utilized, where the full 3D scatter profile is estimated based on the residuals between measured and modeled data [23]. In this novel approach, the 2D measured data along with the 2D single scatter simulation (SSS) model-based scatter was used to provide the non-scattered true image estimate. Since the single and multiple scatter in oblique angles for LAFOV scanners is more prominent, the scatter for these segments was computed as the residual between the measured net trues and the non-scattered true estimate.
Attenuation correction was based on the CT data.
Phantom preparation
Two NEMA International Electrotechnical Commission (IEC) body phantoms (Data Spectrum Corp.) were used, with 6 fillable spheres with inner diameters of 10, 13, 17, 22, 28, and 37 mm [20]. The background volume of one of the phantoms was filled with distilled water and activity (hot phantom) while the other one was filled with non-radioactive distilled water (cold phantom). The background volumes of both phantoms (9829 ml and 9762 ml, respectively) were weighted with the lung and sphere inserts placed inside the phantoms. The first phantom was filled at ~ 1:10 of its whole volume capacity plus twice the volume of the spheres inserts, and the whole activity was infused in that volume. After shaking the phantom for homogeneity, another syringe was used to extract enough volume from the background to fill the spheres inserts of both phantoms. For the purposes of our study, liquid [90Y]-yttrium citrate, in 0.5 M hydrochloric acid to prevent adhesion to the plastic phantom walls, was used for convenience, to fill the spheres and the background of the hot phantom, instead of microspheres. The activity was measured with a well-type dose calibrator (ISOMED 2010). The calibrator satisfies the Swiss regulatory requirements and was calibrated by the Swiss Federal Institute of Metrology (METAS) [24]. The drawn activity, by an automatic injector, was measured 1309.48 MBq while the residual activity in the syringe was 0.1 MBq. Therefore, the background activity concentration of the hot phantom was ~ 0.13 MBq/ml and the spheres’ activity concentration for both phantoms was ~ 1.3 MBq/ml. The phantom was filled the day before the scan and left to decay to represent the average injected activities at the clinic of around 1 GBq (background and spheres’ activity concentration at 0.1 and 1.0 MBq/ml, respectively at the time of the scan).
Scan
Both phantoms were positioned on the bed around the center with a 10-cm gap between them. A helical CT scan was acquired for the PET attenuation correction with the following parameters: 80 kV tube voltage, 39 modulated mAs tube current, 38.4 mm total collimation width, 5 mm slice thickness, and a pitch 0.8. The reconstruction matrix for the CT images was 512 × 512 with 644 slices, and the voxel dimensions were 1.523 × 1.523 × 1.600 mm3. Following the CT, the PET acquisition was performed with a total acquisition time of 50 min. The AFOV covered both phantoms. The voxel dimensions were 3.30 × 3.30 × 1.65 mm3. The scanner had been calibrated before for 90Y and a calibration factor was used for normalizing the data. The data were decay corrected to the injection time.
Reconstruction
All of the data were reconstructed with TOF, point spread function (PSF) recovery, and ordered subset expectation maximization (OSEM). Then, the list-mode data were reconstructed with different parameters. The images were generated with iteration numbers from 2 to 8 with 5 subsets, a Gaussian filter of 2–6 mm full width at half maximum (FWHM), a matrix size of 440 × 440 and 220 × 220, and reconstructions with HS and UHS. Furthermore, images, except for the full-data 50-min acquisition, were generated using the first 40, 30, 20, 10, and 5 min of the list-mode data. In total, there were 840 reconstructed image datasets (Table 1). To test the performance of the product of iterations and subsets on RCmean at low count statistics, the phantom data for the 5-min acquisition were also reconstructed with 10 iterations and 1 subset.
Analysis
The analysis was performed for both hot and cold phantoms. Volume-of-interest (VOI) masks were manually drawn on both phantom PET images using itk-SNAP, an open-source software [25], centered on the slice where the smallest sphere was best visualized. These included spherical VOIs over the 6 spheres, 10 background VOIs with the same size as the biggest sphere VOI, 5 background VOIs with similar sizes to the smaller spheres, and a VOI placed on the lung insert with a diameter size of 30 mm. The performance characteristic analysis includes the RCmean for all fillable spheres, lung error, i.e., the percentage counts in the lung, background variability [26], and signal-to-noise ratio. Similar to the NEMA standard, but using VOIs instead of regions-of-interest (ROIs), the RCmean was defined as:
where SS,j is the average counts in the VOI for sphere j, Sb,j is the average of the background VOI counts for sphere j, as,j is the activity concentration in the hot spheres, and ab,j is the activity concentration in the background.
For the cold phantom, the recovery coefficients of the spheres were calculated as before, without normalization to the background concentration. The SNR was calculated as the ratio of the measured VOI mean signal of each sphere to the corresponding background VOI standard deviation.
The percent background variability for each sphere was calculated as the ratio of the spheres’ VOI standard deviation to the background VOI mean signal. The lung error was calculated as the ratio of the lung insert VOI mean signal to the average of the ten 37-mm-diameter background VOI mean signals. Image viewing was performed on syngo.via (Siemens Healthineers, Chicago, IL, USA).
Patient data
One male patient of 70 years old, diagnosed with HCC and pulmonary metastatic colorectal cancer injected with 1.1 GBq activity, received a PET scan on a Biograph Vision Quadra after 90Y resin microsphere radioembolization. The images were reconstructed using the clinical protocol with 4 iterations and 5 subsets, a 2-mm FWHM Gaussian filter, a 440 × 440 reconstruction matrix, and an acquisition time of 20 min. Data were reconstructed also with 2 iterations and a 220 × 220 reconstruction matrix, based on the phantom data evaluation. The list-mode data were also rebinned and reconstructed using 1-, 5-, and 10-min frames. The SNR was defined as the mean VOI signal of the lesion with the highest uptake concentration to the liver’s background VOI standard deviation. The coefficient of variation (COV) which is the background variation was defined as the ratio of the liver’s background VOI standard deviation to the liver’s background VOI mean signal.
Statistical analysis
The uncertainties of the RCmean results were based on the standard deviation of the mean. The statistical significance of the difference between the results was performed using the two-tailed paired t-test with a p value < 0.05.
Results
Due to the huge number of reconstructed datasets, only the results regarding the clinically optimum trade-off between the RCmean and SNR values are listed. A summary of the maximum and minimum values can be found in Table 2. All other results can be seen on the figures.
Hot phantom
The lower matrix (220 × 220) exhibited similar RCmean for the two largest spheres compared to the higher matrix (440 × 440) while higher values were present for the 4 smaller spheres (6 to 31%). In addition, HS provided significantly higher RCmean values for the 4 smaller spheres (5 to 29%) compared to the UHS for all iterations setups. UHS provided higher SNR for both the lower and the higher reconstruction matrices compared to HS (220 × 220: 20 to 13% from the largest to the smallest sphere, 440 × 440: 23 to 15%). The lower matrix with UHS provided, respectively, 6 to 13% higher SNR compared to the higher matrix (Fig. 1). There was no difference between 2 and 4 iterations.
For 2-mm FWHM Gaussian filter and 50-min acquisition the RCmean was lowest for 2 iterations (0.84, 0.68, 0.63, 0.53, 0.45, and 0.36). Figure 2 shows axial slices of the hot phantom for all iterations and with the HS and UHS reconstruction modes as well as UHS maximum intensity projections (MIPs). The noise becomes more prominent with increasing number of iterations for both modes, especially from the 4 iteration and on. UHS however delivers higher SNR compared to the HS. On the MIPs, the noise distribution is better visualized on the background as well. The smallest sphere is discernible for any number of iterations.
For the 5-min acquisition, the RCmean for the spheres was 0.97, 0.74, 0.72, 0.47, 0.44, and 0.22 for 2 iterations. Figure 3 shows the RCmean trend for all spheres against number of iterations, reconstructed times and Gaussian filter for both phantoms. It is worth mentioning that the drop in RCmean, while it is smoother for the hot phantom below the 17-mm sphere, is steeper for the cold phantom. Figure 4 shows that from 4 iterations, higher RCmean values converge and reach a plateau for all spheres. In addition, RCmean values are comparable from 50 min down to 20 min for all spheres and even down to 10 min for the bigger spheres.
The SNR was found to be highest for UHS 2 iterations, 50-min acquisition, with 6-mm FWHM Gaussian filter (49.51, 38.83, 33.76, 29.67, 26, and 17.57). Figure 5 shows axial slices for both phantoms and the MIPs for all reconstructed times from 50 down to 5 min. All spheres are visualized for all reconstructed times. The noise gets really prominent in the 5-min reconstruction. For 2-mm FWHM Gaussian filter, which is more clinically relevant due to sharper images, the SNR for 2 iterations was 27.76, 21.86, 19.42, 17.64, 16.62, and 11.65 (for HS 22.13, 17.36, 15.72, 13.57, 13.24, and 10.2). UHS provides 22.5%, 22.9%, 21.1%, 26.0%, 22.6%, and 13.2% increase in SNR compared to HS. The SNR for the UHS 20-min acquisition was 39.9%, 43.6%, 45%, 35%, 46%, and 44.4% less, than for the 50-min acquisition. The SNR diagrams can be found in Fig. 6.
The percent background variability for UHS 50-min acquisition was lowest for all the spheres, from the largest to the smallest, for the 2 iterations with 2-mm FWHM Gaussian filtering (27.59, 27.08, 27.36, 26.44, 30.11, and 33.51%). For the same parameters but with HS reconstruction, the percent background variability was 35.00, 36.05, 33.99, 33.41, 35.97, and 36.18% for 2 iterations. For the UHS 5-min acquisition, the percent background variability for 2 iterations and 2-mm FWHM Gaussian filter was 99.54, 95.72, 93.78, 75.5, 111.99, and 70.48%. Lung error was measured 18% (HS: 19%).
The RCmean with 10 iterations and 1 subset for 5-min acquisition was 1.07, 0.88, 0.84, 0.46, 0.47, and 0.27 in contrast to 0.97, 0.74, 0.72, 0.47, 0.44, and 0.22 for 2 iterations for the biggest to the smallest sphere. Due to the longer convergence with 10 iterations, the RCmean values were higher than with 2 iterations (except for the 17-mm sphere), and the difference was statistically significant (p < 0.05).
Cold phantom
The RCmean was the lowest for 2 iterations and 50-min acquisition (0.86, 0.67, 0.59, 0.47, 0.46, and 0.26). Figure 7 shows the axial slices with HS and UHS for the cold phantom. Once again, the noise becomes higher after the 4 iteration, and all spheres are well visualized for all iteration numbers. The lower matrix with UHS provided higher SNR compared to the higher matrix (37 to 29% for the largest to the smallest sphere). UHS showed higher SNR to HS for both matrices (220 × 220: 55 to 51%, 440 × 440: 59 to 57%). For the 5-min acquisition, the RCmean for the spheres was 0.80, 0.53, 0.48, 0.37, 0.31, and 0.10 for 2 iterations (Fig. 3).
The SNR was the highest for UHS 2 iterations, 50-min acquisition, with 6-mm FWHM Gaussian filter (564.00, 361.27, 306.54, 233.08, 206.83, and 115.37). For 2-mm FWHM Gaussian filter, which provides higher resolution, the SNR for 2 iterations was 327.86, 255.27, 222.68, 178.26, 174.60, and 100.47. The SNR for the 5-min acquisition was 305.84, 203.09, 183.55, 139.75, 117.83, and 36.89. For the HS mode, the SNR for 2 iterations, 50-min acquisition, and a 2-mm FWHM Gaussian filter was 217.62, 172.25, 147.47, 120.79, 125.80, and 75.78 (Fig. 6).
The percent background variability for UHS 50-min acquisition was the lowest for 2 iterations 27.59, 27.08, 27.36, 26.44, 30.11, and 33.51% (HS: 115.14, 123.05, 126.9, 78.78, 121.35, and 66.19%). For the UHS 5-min acquisition, it was measured 603.38, 701.46, 454.39, 406.59, 263.51, and 145.73%. Lung error was measured 120% for 2 iterations, 50 min with 2-mm FWHM Gaussian filtering (334% for 5-min reconstruction).
The 10 iterations and 1 subset produced the following RCmean for a 5-min acquisition: 0.78, 0.54, 0.45, 0.4, 0.35, and 0.12 in contrast to 0.8, 0.53, 0.48, 0.37, 0.31, and 0.1 for the 2 iterations and 5 subsets for the biggest to the smallest sphere. The difference was not statistically significant (p < 0.05).
Statistical analysis
UHS and HS did not present significant differences regarding the RCmean values of the spheres, even though HC produced consistently higher RCmean values to UHS. RCmean values for all spheres did not exhibit significant differences between reconstructed times of 50 and 10 min for UHS 2 iterations (between 50 and 20 min for 8 iterations), while for the 5 bigger spheres, the RCmean does not show significant differences between 2 and 4 iterations; 4 iterations provide significantly higher RCmean for the smallest sphere for 20 min and below. The hot and cold phantoms presented similar RCmean values for all spheres except for the smallest one where RCmean was significantly higher in the hot phantom (0.36) than in the cold phantom (0.26).
Patient data
As a convention, the values presented are in the following sequence: 20-, 10-, 5-, and 1-min reconstruction times. The SNR with UHS, for 2 iterations, was 19%, 20%, 24%, and 31% higher compared to 4 iterations (Fig. 8). The reconstruction with 2 iterations and UHS produced 2%, 10%, 17%, and 61% higher SNR compared to HS. Between reconstruction matrices of 220 × 220 and 440 × 440, the SNR percentage difference was lower than 10% for all reconstruction times for 2 iterations and UHS. The background liver VOI mean did not show any differences between 2 and 4 iterations for both UHS and HS. The COV was measured 6%, 15%, 16%, and 22% lower for UHS to HS for 2 iterations and 13%, 22%, 20%, and 26% for 4 iterations. The COV was 31%, 38%, 48%, and 64% lower for UHS 2 iterations compared to 4 iterations. The reconstruction with UHS 220 × 220 matrix exhibited 6%, 5%, 7%, and 16% lower COV compared to the 440 × 440 matrix.
Discussion
In this study, the acquired NEMA body phantom datasets were reconstructed with different parameters like mode (UHS and HS), matrix (440 × 440 and 220 × 220), number of iterations (2–8), Gaussian FWHM filter (2–6 mm), and reconstructed times based on list-mode data rebinning (40, 30, 20, 10, and 5 min and the full acquired data of 50 min). The image quality was evaluated in terms of RCmean, background variability, lung error, and SNR. One patient dataset was reconstructed as well with 20-, 10-, 5-, and 1-min time frames and 2 iterations based on the evaluation of the phantom results.
The images reconstructed with a 220 × 220 matrix presented consistently a higher SNR (6% for the biggest sphere and 13% for the smallest sphere on average) than the images reconstructed with a 440 × 440 matrix, while the latter exhibited higher RCmean values for all spheres.
In addition, the images with higher Gaussian FWHM filter resulted in higher SNR and higher loss of RCmean values, as expected. UHS provided lower background variability and thus higher SNR (on average 5% for the largest sphere and 10% for the smallest sphere). The best reconstruction setup was deemed to be the 2 iterations, with 2-mm FWHM Gaussian filter. Twenty minutes seem to be the optimal acquisition time with 10 min seeming feasible as well, with minimal loss of SNR.
For the comparison of RCmean values for various scanners below, some studies use the NEMA RCmean definition while other follow the recommendations of the European Association of Nuclear Medicine (EANM) and EANM Research Ltd. (EARL). The RCmean based on EARL is measured by drawing a VOI at 50% of the maximum pixel value corrected for background uptake [27]. Therefore, comparison may not be reliable since the NEMA takes into account all voxels of the VOI placed on a sphere, so it produces smoother RCmean values. In any case, the EARL RCmean values favor the other systems so the NEMA analysis described above provides conservative values.
A study comparing the Biograph mCT PET/CT (overall sensitivity 8.1 cps/kBq with an AFOV of 16.2 cm and 540 ps TOF [28]) and Biograph mMR PET/MR scanners with a 1:4 sphere to background ratio showed the highest RCmean for the 37-mm sphere at 0.60 for mCT and slightly lower for mMR [29]. For the smallest sphere, 10 mm, the RCmean was 0.20 for the mCT and slightly lower for the mMR. The reconstruction parameters used were as follows: 400 × 400 reconstruction matrix for mCT, 344 × 344 for mMR, 2 mm Gaussian FWHM filter, 3 iterations, and 21 subsets for both scanners, PSF TOF for the mCT, and only PSF for the mMR. The sphere activity concentration was around 1 MBq/ml.
Maughan et al. showed RCmean values from 0.75 down to 0.30 with an 1:8 sphere to background activity concentration ratio, for the non-TOF Biograph mMR (overall sensitivity 15 cps/kBq [30]) with an AFOV of 25.6 cm [31]. The sphere activity concentration was 2.16 MB/ml, the scan was a 30-min single-bed acquisition, and the reconstruction parameters were PSF 3 iterations, 21 subsets with 5-mm FWHM Gaussian filter.
Kunnen et al. presented RCmean values between 0.87 and 0.45 again with an 1:8 sphere to background activity concentration for Biograph Vision Edge 600 [32]. The scanner has an overall sensitivity of 16.4 cps/kBq and an AFOV of 26.1 cm [33]. The sphere concentration ratio was 2 MBq/ml, and the data were acquired during a 30-min two-bed acquisition. The reconstruction parameters were PSF TOF, 2 iterations, 5 subsets, no Gaussian post-filter, and a reconstruction matrix of 220 × 220. The RCmean definition followed the NEMA standard.
Scott et al. evaluated the GE Discovery 710 PET/CT (General Electric, WA, USA) scanner with an overall sensitivity 7.25 cps/kBq and an AFOV of 15 cm [34] with an 1:8 sphere to background activity concentration ratio that provided the highest RCmean of 0.73 for the 37-mm sphere and 0.39 for the 17-mm sphere, for a 30-min two-bed acquisition [35]. The two smallest spheres (13 mm and 10 mm) were not taken into consideration due to high uncertainties in the measurements. In this study, the reconstruction used a Bayesian penalized likelihood reconstruction algorithm (Q. Clear, GE Healthcare) in full convergence so iterations and subsets do not apply.
Another study with the Signa PET/MR (General Electric, WA, USA), with overall sensitivity of 21 cps/kBq and an AFOV of 25 cm [36], showed RCmean values ranging from 0.80 down to 0.27 with a 1:4 sphere to background ratio, 0.75 MBq/ml sphere concentration, a 60-min single-bed acquisition, and images reconstructed with TOF2 iterations, 28 subsets, and 4-mm FWHM Gaussian filter [37]. The Biograph Vision Quadra shows improved contrast recovery coefficients for the smaller spheres, compared to PET/CT systems with standard AFOV. The smallest sphere is clearly visible even in the 5-min scan, although at the expense of increased noise, suggesting that scans shorter than 20 min could be clinically feasible without loss of diagnostic accuracy of small lesions. Some of the scanners with standard AFOV could not discern the smallest sphere at all or could only depict them with an acquisition time of at least 30 min and at least double activity concentration than in the study described here. Another good point to note here is that the other studies used at least an 1:8 sphere to background activity concentration while the study with the Biograph Vision Quadra used even less at 1:10 that could further have an effect on lowering the RCmean values for all spheres.
For the patient data UHS delivers better image quality with higher SNR at the low count statistics of the 5-min acquisition compared to HS while it delivers a mediocre improvement with 20-min acquisition. Reconstruction with 2 iterations provides improved image quality with lower noise and higher SNR compared to the standard protocol with 4 iterations. In general, after 4 iterations, noise levels become more prominent. For post-treatment dosimetry validation where quantification of lesions is essential, 4 iterations could be the better reconstruction parameter since it can deliver higher recovery coefficients, but 2 iterations could be better for small lesion detectability. However, in this study, we prioritized the SNR, this is why we reconstructed the patient data also with 2 iterations. A future study that would also evaluate the quantification and dosimetric quantities could establish the optimal trade-off of reconstruction parameters between the SNR and RCmean. Furthermore, it seems that based on the size of the spheres, the reconstruction parameter, like number of iterations that delivers improved SNR and RCmean, varies. This is in accordance with another phantom study that used a digital photon counting PET for optimizing reconstruction parameters [38] and showed that depending on the size of the sphere a different number of iterations and subsets should be used for more accurate quantification [38]. For the smallest spheres, for example, a number of iterations even higher than 4 could be justified as long as noise level is acceptable. In the end, the image quality depends on the density of the patient and the injected activity of 90Y.
The smallest sphere was better visible in the hot phantom compared to the cold phantom. This could be explained because the background activity in the hot phantom minimizes the partial volume effect in uptake areas near the spatial resolution limit. The impact of the different reconstruction parameters was the same for both phantoms.
The optimal reconstruction protocol to maximize the SNR, based on the phantom-based evaluation, appears to be 2 iterations with 2-mm FWHM Gaussian filter, with a reconstruction matrix of 220 × 220 and using the UHS mode. The acquisition time with 20 min delivers high SNR and resolution images, comparable to the 50-min acquisition. The results show that 10 min seems to be clinically feasible as well, even though noise starts to become more apparent, but more testing with clinical data is required.
Except for the standardized analysis based on RCmean or SNR on optimizing the reconstruction parameters for 90Y post-treatment dosimetry validation, another approach is to evaluate the dose volume histograms (DVH) of the spheres of a NEMA body phantom. A study has already used this method and showed that by minimizing the errors in DVH, joint optimization of iterations and filtering for 90Y volumetric quantification can be achieved [39]. The DVH method was used also to evaluate patient data for pre-treatment dosimetry plan based on Technetium-99 m (99mTc) macroaggregated albumin (MAA) SPECT/CT [40].
PET can provide images with higher resolution and more accurate quantification compared to SPECT, thus setting itself a better candidate imaging method for post-treatment dosimetry evaluation. In particular, the LAFOV PET/CT could further boost the involvement of PET in 90Y post-treatment clinical practice by providing quantitative images with high SNR at reduced scan times, improving the whole patient throughput. As expected, the applications of the Biograph Vision Quadra in 90Y SIRT imaging benefits from the combination of increased sensitivity due to LAFOV and the noise reduction due to very good time resolution (about 230 ps).
In conclusion, the NEMA phantom-based evaluation for 90Y imaging with the Biograph Vision Quadra provides images with higher recovery coefficient values for the smallest spheres than any other commercial PET/CT with standard AFOV as well as high SNR for all spheres at significantly reduced scanned times. Specifically, the reconstruction with UHS, 2 iterations, 2-mm FWHM Gaussian filter, and a reconstruction matrix of 220 × 220 seems to provide the highest SNR while 4 iterations and higher could be optimal for small lesion quantification for post-treatment 90Y validation, given however that the increased noise level that comes with higher number of iterations is acceptable. Scan times of only 10 min provide images with an acceptable SNR loss, but more testing for clinical validation is required.
References
Williams SJ, Rilling WS, White SB. Quality of life and cost considerations: Y-90 radioembolization. Semin Intervent Radiol. 2021;38:482–7. https://doi.org/10.1055/s-0041-1735570.
Peynircioglu B, Cil B, Bozkurt F, Aydemir E, Ugur O, Balkanci F. Radioembolization for the treatment of unresectable liver cancer: initial experience at a single center. Diagn Interv Radiol. 2010;16:70–8. https://doi.org/10.4261/1305-3825.DIR.2693-09.1.
Ahmadzadehfar H, Biersack HJ, Ezziddin S. Radioembolization of liver tumors with yttrium-90 microspheres. Semin Nucl Med. 2010;40:105–21. https://doi.org/10.1053/j.semnuclmed.2009.11.001.
Braat AJ, Smits ML, Braat MN, van den Hoven AF, Prince JF, de Jong HW, et al. (9)(0)Y hepatic radioembolization: an update on current practice and recent developments. Journal of nuclear medicine: official publication, Society of Nuclear Medicine. 2015;56:1079–87. https://doi.org/10.2967/jnumed.115.157446.
Levi Sandri GB, Ettorre GM, Giannelli V, Colasanti M, Sciuto R, Pizzi G, et al. Trans-arterial radio-embolization: a new chance for patients with hepatocellular cancer to access liver transplantation, a world review. Translational gastroenterology and hepatology. 2017;2:98. https://doi.org/10.21037/tgh.2017.11.11.
Tafti BA, Padia SA. Dosimetry of Y-90 microspheres utilizing Tc-99m SPECT and Y-90 PET. Semin Nucl Med. 2019;49:211–7. https://doi.org/10.1053/j.semnuclmed.2019.01.005.
Dezarn WA, Cessna JT, DeWerd LA, Feng W, Gates VL, Halama J, et al. Recommendations of the American Association of Physicists in Medicine on dosimetry, imaging, and quality assurance procedures for 90Y microsphere brachytherapy in the treatment of hepatic malignancies. Med Phys. 2011;38:4824–45. https://doi.org/10.1118/1.3608909.
Elschot M, Vermolen BJ, Lam MG, de Keizer B, van den Bosch MA, de Jong HW. Quantitative comparison of PET and Bremsstrahlung SPECT for imaging the in vivo yttrium-90 microsphere distribution after liver radioembolization. PLoS ONE. 2013;8: e55742. https://doi.org/10.1371/journal.pone.0055742.
Roshan HR, Azarm A, Mahmoudian B, Islamian JP. Advances in SPECT for optimizing the liver tumors radioembolization using yttrium-90 microspheres. World journal of nuclear medicine. 2015;14:75–80. https://doi.org/10.4103/1450-1147.157120.
Elschot M, Nijsen JF, Dam AJ, de Jong HW. Quantitative evaluation of scintillation camera imaging characteristics of isotopes used in liver radioembolization. PLoS ONE. 2011;6: e26174. https://doi.org/10.1371/journal.pone.0026174.
Bé MM, E. Browne, V. Chechev, V. Chisté, R. Dersch, C. Dulieu, R.G. Helmer, N. Kuzmenco, A.L. Nichols ES. Table of radionuclides. Pavillon de Breteuil, F-92310 Sevres: Bureau International des Poids et Mesures; 2010.
Dryak P, Solc J. Measurement of the branching ratio related to the internal pair production of Y-90. Applied radiation and isotopes: including data, instrumentation and methods for use in agriculture, industry and medicine. 2020;156: 108942. https://doi.org/10.1016/j.apradiso.2019.108942.
Levillain H, Bagni O, Deroose CM, Dieudonne A, Gnesin S, Grosser OS, et al. International recommendations for personalised selective internal radiation therapy of primary and metastatic liver diseases with yttrium-90 resin microspheres. Eur J Nucl Med Mol Imaging. 2021;48:1570–84. https://doi.org/10.1007/s00259-020-05163-5.
Lhommel R, Goffette P, Van den Eynde M, Jamar F, Pauwels S, Bilbao JI, et al. Yttrium-90 TOF PET scan demonstrates high-resolution biodistribution after liver SIRT. Eur J Nucl Med Mol Imaging. 2009;36:1696. https://doi.org/10.1007/s00259-009-1210-1.
Willowson KP, Tapner M, Team QI, Bailey DL. A multicentre comparison of quantitative (90)Y PET/CT for dosimetric purposes after radioembolization with resin microspheres: the QUEST Phantom Study. Eur J Nucl Med Mol Imaging. 2015;42:1202–22. https://doi.org/10.1007/s00259-015-3059-9.
Kubik A, Budzynska A, Kacperski K, Maciak M, Kuc M, Piasecki P, et al. Evaluation of qualitative and quantitative data of Y-90 imaging in SPECT/CT and PET/CT phantom studies. PLoS ONE. 2021;16: e0246848. https://doi.org/10.1371/journal.pone.0246848.
Eriksson L, Conti M. Randoms and TOF gain revisited. Phys Med Biol. 2015;60:1613–23. https://doi.org/10.1088/0031-9155/60/4/1613.
Prenosil GA, Sari H, Furstner M, Afshar-Oromieh A, Shi K, Rominger A, et al. Performance characteristics of the Biograph Vision Quadra PET/CT system with long axial field of view using the NEMA NU 2–2018 Standard. Journal of nuclear medicine : official publication, Society of Nuclear Medicine. 2021. https://doi.org/10.2967/jnumed.121.261972.
Spencer BA, Berg E, Schmall JP, Omidvari N, Leung EK, Abdelhafez YG, et al. Performance evaluation of the uEXPLORER total-body PET/CT scanner based on NEMA NU 2–2018 with additional tests to characterize PET scanners with a long axial field of view. Journal of nuclear medicine : official publication, Society of Nuclear Medicine. 2021;62:861–70. https://doi.org/10.2967/jnumed.120.250597.
Kim Greer C. NEMA IEC body phantom set user’s manual. In: Cooperation DS, editor.; 2002–2008.
Costa G, Spencer B, Omidvari N, Foster C, Rusnak M, Hunt H, et al. Radioembolization dosimetry with total-body (90)Y PET. Journal of nuclear medicine: official publication, Society of Nuclear Medicine. 2022;63:1101–7. https://doi.org/10.2967/jnumed.121.263145.
Carlier T, Ferrer L, Conti M, Bodet-Milin C, Rousseau C, Bercier Y, et al. From a PMT-based to a SiPM-based PET system: a study to define matched acquisition/reconstruction parameters and NEMA performance of the Biograph Vision 450. EJNMMI physics. 2020;7:55. https://doi.org/10.1186/s40658-020-00323-w.
Bal H, Panin VY, Schaefferkoetter J, Cabello J, Conti M. Fully 3D scatter estimation in axially long FOV PETCT scanners: residual estimation approach. 2021 IEEE Nuclear Science Symposium and Medical Imaging Conference (NSS/MIC); 2021. p. 1–4.
METAS FIoM. Ordinance about measuring equipment for ionizing radiation. METAS; 2012.
Yushkevich PA, Piven J, Hazlett HC, Smith RG, Ho S, Gee JC, et al. User-guided 3D active contour segmentation of anatomical structures: significantly improved efficiency and reliability. Neuroimage. 2006;31:1116–28. https://doi.org/10.1016/j.neuroimage.2006.01.015.
NEMA standards publication NU 2-2012: performance measurements of positron emission tomographs (PET). Rosslyn: National Electrical Manufacturers Association; 2013.
Boellaard R, O'Doherty MJ, Weber WA, Mottaghy FM, Lonsdale MN, Stroobants SG, et al. FDG PET and PET/CT: EANM procedure guidelines for tumour PET imaging: version 1.0. European journal of nuclear medicine and molecular imaging. 2010;37:181–200. https://doi.org/10.1007/s00259-009-1297-4.
Jakoby BW, Bercier Y, Conti M, Casey ME, Bendriem B, Townsend DW. Physical and clinical performance of the mCT time-of-flight PET/CT scanner. Phys Med Biol. 2011;56:2375–89. https://doi.org/10.1088/0031-9155/56/8/004.
Soderlund AT, Chaal J, Tjio G, Totman JJ, Conti M, Townsend DW. Beyond 18F-FDG: characterization of PET/CT and PET/MR scanners for a comprehensive set of positron emitters of growing application–18F, 11C, 89Zr, 124I, 68Ga, and 90Y. Journal of nuclear medicine: official publication, Society of Nuclear Medicine. 2015;56:1285–91. https://doi.org/10.2967/jnumed.115.156711.
Delso G, Furst S, Jakoby B, Ladebeck R, Ganter C, Nekolla SG, et al. Performance measurements of the Siemens mMR integrated whole-body PET/MR scanner. Journal of nuclear medicine: official publication, Society of Nuclear Medicine. 2011;52:1914–22. https://doi.org/10.2967/jnumed.111.092726.
Maughan NM, Eldib M, Faul D, Conti M, Elschot M, Knesaurek K, et al. Multi institutional quantitative phantom study of yttrium-90 PET in PET/MRI: the MR-QUEST study. EJNMMI physics. 2018;5:7. https://doi.org/10.1186/s40658-018-0206-y.
Kunnen B, Beijst C, Lam M, Viergever MA, de Jong H. Comparison of the Biograph Vision and Biograph mCT for quantitative (90)Y PET/CT imaging for radioembolisation. EJNMMI physics. 2020;7:14. https://doi.org/10.1186/s40658-020-0283-6.
van Sluis J, Boellaard R, Somasundaram A, van Snick PH, Borra RJH, Dierckx R, et al. Image quality and semiquantitative measurements on the biograph vision PET/CT system: initial experiences and comparison with the biograph mCT. Journal of nuclear medicine : official publication, Society of Nuclear Medicine. 2020;61:129–35. https://doi.org/10.2967/jnumed.119.227801.
Vandendriessche D, Uribe J, Bertin H, De Geeter F. Performance characteristics of silicon photomultiplier based 15-cm AFOV TOF PET/CT. EJNMMI physics. 2019;6:8. https://doi.org/10.1186/s40658-019-0244-0.
Scott NP, McGowan DR. Optimising quantitative (90)Y PET imaging: an investigation into the effects of scan length and Bayesian penalised likelihood reconstruction. EJNMMI Res. 2019;9:40. https://doi.org/10.1186/s13550-019-0512-y.
Caribe P, Koole M, D’Asseler Y, Deller TW, Van Laere K, Vandenberghe S. NEMA NU 2–2007 performance characteristics of GE Signa integrated PET/MR for different PET isotopes. EJNMMI physics. 2019;6:11. https://doi.org/10.1186/s40658-019-0247-x.
Seo Y, Khalighi MM, Wangerin KA, Deller TW, Wang YH, Jivan S, et al. Quantitative and qualitative improvement of low-count [(68)Ga]citrate and [(90)Y]microspheres PET image reconstructions using block sequential regularized expectation maximization algorithm. Mol Imaging Biol. 2020;22:208–16. https://doi.org/10.1007/s11307-019-01347-0.
Labour J, Boissard P, Baudier T, Khayi F, Kryza D, Durebex PV, et al. Yttrium-90 quantitative phantom study using digital photon counting PET. EJNMMI physics. 2021;8:56. https://doi.org/10.1186/s40658-021-00402-6.
Siman W, Mikell JK, Mawlawi OR, Mourtada F, Kappadath SC. Dose volume histogram-based optimization of image reconstruction parameters for quantitative (90) Y-PET imaging. Med Phys. 2019;46:229–37. https://doi.org/10.1002/mp.13269.
Levillain H, Burghelea M, Derijckere ID, Guiot T, Gulyban A, Vanderlinden B, et al. Combined quality and dose-volume histograms for assessing the predictive value of (99m)Tc-MAA SPECT/CT simulation for personalizing radioembolization treatment in liver metastatic colorectal cancer. EJNMMI physics. 2020;7:75. https://doi.org/10.1186/s40658-020-00345-4.
Funding
Open access funding provided by University of Bern
Author information
Authors and Affiliations
Corresponding author
Ethics declarations
Ethics approval
All procedures performed in studies involving human participants were in accordance with the ethical standard of the institutional and/or national research committee and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards.
Consent to participate
Informed consent was obtained from all individual participants included in the study.
Competing interests
Maurizio Conti is a full-time employee of Siemens Healthineers, Knoxville, TN, USA. Hasan Sari is a full-time employee of Siemens Healthcare AG, Lausanne, Switzerland. No other potential conflicts of interest relevant to this article including employment, royalties, stock options, or patents.
Additional information
Publisher's note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
This article is part of the Topical Collection on Oncology - General.
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
About this article
Cite this article
Zeimpekis, K.G., Mercolli, L., Conti, M. et al. Phantom-based evaluation of yttrium-90 datasets using biograph vision quadra. Eur J Nucl Med Mol Imaging 50, 1168–1182 (2023). https://doi.org/10.1007/s00259-022-06074-3
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s00259-022-06074-3