Differentiation of malignant tumours from granulomas by using dynamic [18F]-fluoro-L-α-methyltyrosine positron emission tomography
© Yamaguchi et al.; licensee Springer. 2015
Received: 24 February 2015
Accepted: 18 April 2015
Published: 30 April 2015
Previous clinical studies have revealed the potential of [18F]-fluoro-L-α-methyltyrosine (18F-FAMT) for the differential diagnosis of malignant tumours from sarcoidosis. However, one concern regarding the differential diagnosis with 18F-FAMT is the possibility of false negatives given the small absolute uptake of 18F-FAMT that has been observed in some malignant tumours. The aim of this study was to evaluate a usefulness of dynamic 18F-FAMT positron emission tomography (PET) for differentiating malignant tumours from granulomas.
Rats bearing both granulomas (Mycobacterium bovis bacillus Calmette-Guérin (BCG)-induced) and tumours (C6 glioma cell-induced) underwent dynamic 2-deoxy-2-[18F]-fluoro-D-glucose (18F-FDG) PET and 18F-FAMT PET for 120 min on consecutive days. Time-activity curves, static images, mean standardized uptake values (SUVs) and the SUV ratios (SUVRs; calculated by dividing SUV at each time point by that of 2 min after injection) were assessed.
In tumours, 18F-FAMT showed a shoulder peak immediately after the initial distribution followed by gradual clearance compared with granulomas. Although the mean SUV in the tumours (1.00 ± 0.10) was significantly higher than that in the granulomas (0.88 ± 0.12), a large overlap was observed. In contrast, the SUVR was markedly higher in tumours than in granulomas (50 min/2 min, 0.72 ± 0.06 and 0.56 ± 0.05, respectively) with no overlap. The dynamic patterns, SUVR, and mean SUV of 18F-FDG in the granulomas were comparable to those in the tumours.
Dynamic 18F-FAMT and SUVR analysis might compensate for the current limitations and help in improving the diagnostic accuracy of 18F-FAMT.
The differential diagnosis of benign from malignant lesions by using positron emission tomography (PET) is a problem that remains unsolved because 2-deoxy-2-[18F]-fluoro-D-glucose (18F-FDG) - the most frequently applied PET probe for tumour imaging - shows increased uptake in several benign pathologies such as inflammatory foci, sarcoidosis, and active tuberculosis [1,2]. To overcome this limitation, one promising approach is the use of 11C/18F-labelled amino acid PET tracers. In contrast to 18F-FDG, amino acid tracers show lower uptake in macrophages and other inflammatory cells  and thus have been evaluated for their potential to differentiate between benign and malignant lesions, both in animal models and in patients [4-6]. However, several studies have reported increased uptake of amino acid tracers in inflammatory lesions including radiation-induced necrosis  and lymphadenopathy in sarcoidosis . Therefore, the use of amino acid tracers for the differential diagnosis has yet to reach a consensus.
In contrast to other amino acid PET tracers, [18F]-fluoro-L-α-methyltyrosine (18F-FAMT) is selective for L-type amino acid transporter 1 (LAT-1) and interacts less with other transporters . In a previous study that evaluated sarcoidosis patients with suspected malignancy, 18F-FAMT showed significantly lower uptake in sarcoidosis lesions compared to tumour lesions, supporting the clinical utility of 18F-FAMT for the differential diagnosis . However, one concern regarding the differential diagnosis with 18F-FAMT is the possibility of false negative results, because 18F-FAMT shows relatively small absolute uptake, even in malignant tumours, which is occasionally lower than that in sarcoidosis. Therefore, an alternative parameter that can estimate differences in 18F-FAMT uptake between inflammation and tumours is needed.
Recently, Zhao et al.  reported the usefulness of dynamic PET imaging of L-11C-methionine (11C-MET; the most frequently used amino acid tracer) for the differential diagnosis of granulomas from malignant tumours, in rat models. This tracer exhibited a significantly different dynamic profile in granulomas compared to tumours. The success of dynamic PET using 11C-MET for the differential diagnosis raised the intriguing possibility that 18F-FAMT could be used as an alternative amino acid PET tracer. However, the dynamic profile of 18F-FAMT was unknown, and several characteristics of 18F-FAMT, such as the mechanism of transport and metabolism, could lead to a dynamic profile distinct from that of 11C-MET. Therefore, in this study, we evaluated the usefulness of dynamic 18F-FAMT PET for the differentiation of malignant tumours from granulomas in comparison with 18F-FDG in an experimental rat model.
The synthesis of 18F-FAMT was performed at the Gunma University Hospital (Cyclotron Facility) as previously described . The radiochemical yield and purity of 18F-FAMT were approximately 20% and 99%, respectively. The 18F-FDG was also produced in the Cyclotron Facility as previously described .
All experimental protocols were approved by the Laboratory Animal Care and Use Committee of Gunma University. Seven-week-old male Wistar King Aptekman/hok rats (weight, 240 to 290 g; Japan SLC, Inc., Shizuoka, Japan) were used in all experiments. We adopted the Mycobacterium bovis bacillus Calmette-Guérin (BCG)-induced intramuscular granuloma model that has a similar histological feature as sarcoidosis . The BCG strain of Japan (1 × 107 colony-forming unit (CFU); Japan BCG Laboratory, Tokyo, Japan) was suspended in 0.2 ml of phosphate-buffered saline , or allogenic rat glioma cells (C6, 2 × 106 cells/0.2 ml) were inoculated into the left and right calf muscles of the animals to generate a rat model bearing both granulomas and tumours. The C6 glioma cell line (RCB2854) was provided by the RIKEN BRC through the National BioResource Project of the MEXT, Japan.
Dynamic PET study
At 20 days after the inoculation of BCG and 10 days after the inoculation of the glioma cells, rats (n = 6) were kept fasting overnight, anaesthetized with isoflurane, and injected intravenously with 18F-FDG (11.7 ± 2.57 MBq). Dynamic PET (list mode acquisition) was performed for 120 min with the hind leg region in the field of view by using an Inveon PET scanner dedicated to small animal imaging (Siemens Medical Solutions USA Inc., Knoxville, TN, USA). The next day, 18F-FAMT (19.4 ± 1.91 MBq) was injected intravenously, and dynamic PET was performed according to a similar protocol. The injection doses of 18F-FDG and 18F-FAMT were determined based on the half-life of 18F (110 min)  and the tumour accumulation levels of 18F-FDG and 18F-FAMT.
The data were reconstructed and corrected for attenuation and scatter by using two-dimensional filtered backprojection. The image matrix was 128 × 128 × 159, which resulted in a voxel size of 0.77 × 0.77 × 0.796 mm. The individual time sequence was the following: 4 scans × 1 min, 3 scans × 2 min, 4 scans × 5 min and 9 scans × 10 min. For quantitative analysis, images were analysed by manually drawing volumes of interest (VOIs) in order to trace the contours of the granulomas and tumours without correction for partial volume effects. The time-activity curves, static images (50 to 60 min for 18F-FAMT and 18F-FDG) and the mean SUVs in the lesions were calculated. The SUV was determined by using the following equation: SUV = activity in a VOI (MBq/cc)/[injected dose (MBq)/body weight (g)].
To further evaluate the dynamic pattern of 18F-FAMT uptake, the SUV ratio (SUVR) was determined. The ratio of SUVs of 18F-FAMT at each time point to that at 2 min post injection (p.i.) was calculated. The SUVRs of 18F-FDG were also calculated from the SUVs at 120 min p.i. relative to that of 2 min p.i.
Paraformaldehyde-fixed (4%), paraffin-embedded, 3-μm-thick tumour and granuloma tissue sections were stained with haematoxylin and eosin (H&E). Immunofluorescent staining of the adjacent tissue sections was also performed according to a standard protocol. Glucose transporter 1 (GLUT-1) was detected by using an anti-GLUT-1 polyclonal antibody (rabbit IgG, synthetic peptide, Abcam, Cambridge, UK). LAT-1 was stained by using an anti-LAT-1 mAb (rabbit IgG, synthetic peptide, Abcam). The primary antibodies were detected with the corresponding isotype-specific goat anti-rabbit IgG H&L (DyLight 488, Abcam). Adjacent tissue sections incubated with rabbit IgG instead of the primary antibodies were used as negative controls.
Repeated measures analysis of variance was used to assess the significance of differences in the dynamic patterns of 18F-FAMT and 18F-FDG uptake between granulomas and tumours. A paired t-test was performed to evaluate the significance of differences in SUVs and SUVRs. A two-tailed value of p < 0.05 was considered significant.
Dynamic PET study
We found that dynamic 18F-FAMT PET is useful for differentiating granulomas from malignant tumours in a rat model. The moderate shoulder peak (6 to 15 min p.i.) and prolonged clearance in the time-activity curves of 18F-FAMT in tumours may reflect the high expression levels of LAT-1 in malignant lesions as compared to granulomatous lesions. The high expression levels of LAT-1 were confirmed by immunohistochemical staining. These results are consistent with previous clinical studies that showed a correlation between 18F-FAMT uptake and the expression levels of LAT-1 [16-18].
Although SUV assessment of 18F-FAMT showed significant differences between granulomas and tumours, the SUV value alone could not reliably provide the differential diagnosis in all cases, because the individual SUV values of tumours and granulomas overlapped substantially. It should be noted that unlike a clinical study of sarcoidosis patients , in our granuloma model, 18F-FAMT accumulated in the granulomas at 60 min p.i. Because the kinetics of 18F-FAMT depends on both increased local blood flow and LAT-1, one possible explanation for this difference is the effect of the concentration of radioactivity in the blood. However, even in the clinical study, the SUVs of 18F-FAMT in lung cancer lesions showed a substantial overlap with sarcoidosis lesions and background . Because of the lower maximal SUVs, even in malignant lesions, the sensitivity of 18F-FAMT is lower than that of 18F-FDG [18,19]. Thus, a more definitive indicator that can improve the accuracy of the differential diagnosis is needed.
To address this issue, we evaluated the SUVR of 18F-FAMT relative to the SUV of 2 min p.i. and found that the overlap in SUVRs diminished and showed a significant difference in most of acquisition times (3 min p.i. to 120 min p.i.) because of prolonged retention of 18F-FAMT in the tumours. The SUVR appeared to depend on the existence of specific uptake, because there were no significant differences in the SUVRs between granulomas and muscle tissue where specific uptake was absent. These data suggested that the dynamic profile of 18F-FAMT in malignant lesions could reflect LAT-1-dependent specific uptake, regardless of the maximal SUV. Therefore, we believe that SUVR will be useful for differential diagnosis even if the maximal SUV is low. However, the calculation points should be optimized for each lesion, because differences between species or types of cancer might affect the absolute uptake or clearance rate of 18F-FAMT. Therefore, it is worth performing a clinical study to investigate whether SUVR measurement can improve the sensitivity of 18F-FAMT.
As predicted, 18F-FDG showed comparable time-activity curve patterns, SUVs and expression levels of GLUT-1 in tumours and granulomas. Although the SUVRs of 18F-FDG in the tumours were slightly higher than those in the granulomas, there was a considerable overlap. Therefore, 18F-FDG may provide less reliable information for the differential diagnosis, even if dynamic imaging is performed. These data support that BCG-induced granulomas could serve as a proper model for the differential diagnosis of tumours from inflammation, as was used in a study of 11C-MET .
However, unlike 11C-MET, which tended to be retained in both lesions after the initial distribution, 18F-FAMT showed slow, exponential clearance from both lesions. This difference might be attributed to the transport mechanism and metabolic pathway of the tracers. Indeed, 11C-MET can be a substrate for various transporters such as system L, A, ASC and y + L [20,21]. Additionally, following incorporation, 11C-MET is rapidly metabolized and trapped inside the cells . These properties of 11C-MET may result in the retention of the tracer, both in tumours and in normal tissues. In contrast, 18F-FAMT is incorporated into cancer cells solely via LAT-1, which functions as a bi-directional transporter with an obligatory exchange mechanism [5,23]. The transport activity depends on the availability of intracellular exchange substrates with similar influx and efflux selectivity. Once incorporated, 18F-FAMT remained intact in cells for up to 60 min, and it was metabolized to protein to only a small extent . These characteristics might cause a gentle decrease in 18F-FAMT in tumour cells along with a decrease in the concentration of 18F-FAMT in plasma. However, regardless of these properties, 18F-FAMT also showed distinct dynamic profiles in tumours and granulomas as 11C-MET did. Thus our results implicate potential wide applicability of dynamic PET for the differential diagnosis, even for the other amino acid tracers that show slow exponential clearance from the tumours.
Taken together, dynamic 18F-FAMT could be a more reliable imaging method for distinguishing tumours from granulomas, compared to conventional static images. Thus, dynamic 18F-FAMT PET in addition to standard 18F-FDG-PET would increase the accuracy of the differential diagnosis of malignant tumours from sarcoidosis, radiation-induced necrosis and tuberculosis. As dynamic 18F-FAMT showed comparable results to 11C-MET, clinical studies evaluating the applicability of dynamic amino acid PET for the differential diagnosis will be the objective of future research.
The dynamic profile of 18F-FAMT showed significant differences between tumours and granulomas. Additionally, SUVR of 18F-FAMT diminished the overlap between tumours and granulomas, which has been observed in SUV analysis. These results indicate that dynamic 18F-FAMT and SUVR analysis might compensate for current imaging limitations and help with improving the diagnostic accuracy of 18F-FAMT.
We are grateful to Dr. Koji Kishimoto (Department of Biochemistry, Gunma University Graduate School of Medicine) for kindly providing BCG and to Mr. Shuji Senokuchi, Ms. Saki Inamoto (Faculty of Pharmaceutical Sciences, Suzuka University of Medical Science) for excellent technical assistance.
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