PET imaging has proven value in cancer diagnosis, follow-up, and patient management 1,2. It can also be used to design and adjust treatment plans in radiotherapy and chemotherapy 3.
The introduction of hybrid PET/computed tomography (CT) scanners over the last decade has improved the accuracy of attenuation correction and the ability to localize organs and tumors 4,5. However, a number of physical and physiological phenomena can affect the accuracy of PET and CT images. Indeed, it has been shown that the diaphragm can move by as much as 20 mm in the craniocaudal axis 6 and that the liver can move by an average of 11 mm 7 during quiet breathing in the supine position. It is also well known that breathing induces rotational and/or translation movements in thoracic and abdominal organs to a varying extent 8–10. For example, upper areas of the lungs are less subject to motion compared with the lower parts 6. Moreover, Rodarte et al.8 showed that even though the middle lobe of the canine lung and the lingula extend toward the diaphragm these structures are less subject to respiratory motion compared with the lower lobes.
CT images are acquired within a few seconds, whereas PET images are acquired over several minutes for each axial field of view. Even though the various CT slices in a free-breathing CT volume can be considered to be nonsynchronized ‘snapshots’, they will contain tissues from different respiratory states because the timeframe of a CT acquisition is roughly the same as that of the respiratory cycle (RC). Inversely, PET images of a moving uptake represent motion averaged over a few minutes. This difference in timeframe may induce registration errors, respiratory motion CT artifacts, and/or blurred PET images 11. Furthermore, PET smearing effects and the attenuation correction derived from CT may in turn induce erroneous quantification of the standardized uptake value in PET.
Several procedures and devices have been developed with a view to avoiding these problems. Here, we review current methods for dealing with respiratory motion in PET/CT.
Respiratory motion tracking
Tracking techniques rely on an external device to estimate respiratory motion during PET/CT examinations. There is a proven correlation between respiratory motion and the displacement of internal organs 12–14. Respiratory motion can be estimated by monitoring a physiological characteristic (such as the displacement of the thoracic cage or the volume of air exhaled) or a physical parameter (such as temperature or displacement of the skin surface). For analog sensors, the signal must be converted into a digital signal, which will be referred to as the respiratory signal (RS) throughout this review. Gated PET acquisition involves synchronization of the PET acquisition with the RS.
Several solutions have been implemented on commercial imaging systems by the PET/CT device manufacturers, whereas academic researchers have assessed a number of other techniques.
The AZ-733V (Anzai Medical Corp., Tokyo, Japan) is a pressure sensor integrated into an elastic chest belt (Fig. 1a). The pressure sensor can thus detect the displacement of the abdominal wall as a function of pressure variations during the RC (i.e. low pressure during expiration and high pressure during inspiration). An analog-to-digital converter yields a signal that is recorded as a text file and can be used for offline processing 16.
Another widely used method involves the Real-Time Position Management (RPM) system (Varian Medical Systems, Palo Alto, California, USA). Two infrared reflective markers are placed on a plastic box positioned on the patient’s thorax. A video camera placed at the end of the bed tracks the markers’ motion during the RC (Fig. 1b). The markers’ displacement is recorded by the video camera and yields an RS for further processing 16.
Otani et al.18 compared the AZ-733V and RPM external respiratory tracking devices and found that the respective RSs were well correlated.
Sensors measuring air temperature changes during respiration can also be used. Indeed, the air temperature in the upper airways during inspiration is lower than that during expiration because the air is warmed during its passage through the lungs. A high time resolution is needed for this type of sensor. In one embodiment of this system, a high-sensitivity thermistor can be mounted inside a conventional oxygen mask. In another variant, a probe is placed close to the patient’s nostrils (BioVet CT1 System; Spin Systems, Brisbane, Australia) (Fig. 1c) 16. Boucher et al. 19 have demonstrated the clinical feasibility of this type of device. However, this tracking device has not yet been implemented on commercial PET scanners and has not been greatly characterized in the literature.
A spirometer can be used to estimate the volume of air inhaled or exhaled during breathing. It can be placed close to the patient’s nostrils (PMM Spirometer; Siemens Medical Systems, Erlangen, Germany 16) or mouth (CPX Spirometer; Medgraphics, St Paul, Minnesota, USA 17) (Fig. 1d). However, use of this system with a clinical PET/CT gantry has not been investigated yet. The main drawbacks of this system are discomfort for the patient and the inability to provide simultaneous oxygen assistance. Similarly, Didierlaurent et al.20 connected a pneumotachograph (which measures the change in lung volume over time via the exhaled respiratory flow) to a PET/CT gantry.
Synchronizing a respiratory signal with PET or computed tomography data
The RS can be synchronized with four-dimensional (4D) PET or CT data. In list-mode (LM) acquisitions, coincidence events and time tags are recorded in real time. As shown by Bruyant et al.21, a tag can be stored within the LM file whenever the user-defined RS threshold is reached. Given that the LM retains time data, PET synchronization and processing can be performed after the acquisition.
The respiratory gating methods based on motion tracking mostly use LM PET data to take advantage of the temporal component. There are two ways to process respiratory-gated PET data: dividing the RS into multiple phases (in multiphase or multibin methods) or considering only a single phase (in single-bin methods).
The RS can be processed as a function of time or amplitude. In both time-based and amplitude-based methods, the RC can be divided into equal-sized or different-sized bins. We shall detail each of these approaches in the following sections.
In the time-based approach, each RC (as delimited by two gating tags in the LM) is divided into several bins 22–27. Several different approaches have been suggested. Dawood et al.28 set a fixed time for all bins and for all RCs (Fig. 2a). However, depending on the RC length, some PET data may be lost. Manufacturers have offered time-based, respiratory-gated PET processing based on the division of each RC into the same number of bins (Fig. 2b) 29. In this method, users have to define a range of acceptable RC frequencies. Data from abnormally short or long RCs are excluded from the analysis.
The number of bins is an important determinant of image quality. In fact, there is a tradeoff between residual motion and counting statistics: the lower the number of bins, the weaker the blurring removal but the higher the signal-to-noise ratio in each bin. Conversely, a high number of bins translates into negligible residual motion and a marked decrease in the signal-to-noise ratio. On the basis of Monte Carlo methods, Vauclin et al.30 suggested that, although the accuracy in lesion volume estimation increases with the number of bins considered, there is a corresponding decrease in overall lesion detectability because the total count statistic was divided by the number of gated bins. Dawood et al.31 reported that six respiratory bins constituted the optimal tradeoff between residual motion in an individual bin on one hand and image quality on the other.
Furthermore, the degree of motion compensation differs from one bin to another. This is due to differences in tissue velocity in the different phases of the RC; some bins correspond to a very steep part of the RS, where the tissue velocity is high. Next, uptake restitution of the moving target is flawed by high residual motion. Moreover, respiratory amplitude varies significantly from one individual to another. Hence, events from different tissue positions may become mixed within a single bin, leading to a blurred image of the target. To minimize these differences and regularize the RC, some systems offer ‘vocal coaching’. This method is only partially effective, as ‘coached’ respiration is not always regular 15,32.
Many researchers have compared gated PET images with ungated PET images (i.e. those acquired in the absence of RC synchronization) 22–27. Table 1 summarizes the results associated with time-based methods 24–27. Depending on the lesion size, respiratory motion can lead to major errors in uptake detection. For motionless lesions, the detection limit is roughly two or three times the tomograph’s spatial resolution 33. The quantification bias increases as the lesion’s largest axis decreases 34. Adding a motion component raises the limit of detection and increases quantification bias.
The time-based approach has been implemented by all manufacturers because it does not require access to the RS. Indeed, the RS is generally obtained by third-party devices and is neither available nor processed on reconstruction workstations.
In this approach, the RS is divided into several bins as a function of its magnitude. Minimum and maximum thresholds define the range of motion (i.e. the range of amplitudes) to be processed. In one method, each bin contains equal ranges of amplitude 28,29. Use of an amplitude-based method means that the various bins are unlikely to contain the same number of coincidences (Fig. 2c). Indeed, the number of statistics in a steep part of the RS will be lower than that in the end-expiratory phase. To overcome this issue, variable bin processing has been suggested; each bin contains the same statistics but with variable remaining motion amplitude 28.
As for the time-based methods, the number of bins is an important determinant of image quality. Dawood et al.31 showed that the optimal configuration contained eight respiratory bins. However, Bettinardi et al.35 emphasized that the number of gates needed is related to a lesion’s size and displacement.
Although the amplitude-based approach is superior to the time-based approach 28,29, the workstations require access to the RS during data processing. Multibin approaches can describe a lesion’s displacement during the RC, which can be of value for radiotherapy planning 36. However, these two approaches do not provide adequate attenuation correction. Indeed, CT images, usually acquired in free-breathing mode in a single volume, show a number of respiratory artifacts and, furthermore, do not correspond to a defined respiratory state. These two phenomena introduce errors into the attenuation correction and quantification of the uptake 29.
The deep-inspiration breath-hold method
Nehmeh et al.37 and Meirelles et al.38 developed the deep-inspiration breath-hold (DIBH) method. A device is used to track RS and deliver voice instructions (e.g. ‘breathe in’, ‘hold’, and ‘relax’). A 15-s CT scan chest is acquired while the patient holds his/her breath in deep end-inspiration. The PET stage consists of nine independent, 20-s breath-hold acquisitions (again during deep end-inspiration). The patient is allowed to relax for 20 s between each acquisition. Finally, these acquisitions are summed, corrected for attenuation (using the CT data), and reconstructed with a conventional algorithm (Fig. 3).
With the DIBH method, both PET and CT data are acquired at the same tissue position during a deep end-inspiration breath-hold; this guarantees accurate attenuation correction. However, repeated 20-s acquisitions may be stressful and tiring in dyspneic patients. Even when breathing is coached and monitored, there is no guarantee that the patient will hold his/her breath at the same point in all the acquisitions. To avoid the need for repeated breath-hold acquisition, two groups have shown that it is feasible to acquire PET data during a single DIBH 39–41. Kawano et al.39 and Torizuka et al.41 respectively considered that a breath-hold of 30 or 20 s is sufficient. However, the body phantom studies used in these two studies do not fully model clinical reality because of high concentration of activity in the spheres and the absence of noise in the thoracic cavity.
The DIBH method has been assessed in routine clinical practice (mainly for lung imaging) 38–43. Indeed, the method allows the fully expanded lungs to be imaged and small tumors can be detected easily. Other researchers have evaluated this method for imaging the abdomen 43,44. The main findings of these DIBH studies are summarized in Table 2.
The computed tomography-based method
Daouk et al.45 and Fin et al.46 have described a CT-based method, in which a 10-min LM PET acquisition is performed. The patients then hold their breath at the normal end-expiration point for 6 s, during which a breath-hold CT (BH-CT) scan is performed. The RS is recorded throughout the two sessions. The researchers chose this normal end-expiration because it is the most reproducible phase of the RC 47. Given that end-expiration lasts longer than any other phase, selecting the events recorded during this phase improves counting statistics and provides the best image quality. In end-expiration, a plateau on the RS corresponds to a specific tissue position. An event selection range (ESR) is defined around this plateau. The portions of the RS falling within this ESR thus define the portions of the LM that should be conserved. The selected PET data are attenuation-corrected with the BH-CT data during reconstruction. Placing the ESR around the breath-hold position defined by BH-CT acquisition provides accurate matching between anatomical and functional images and yields accurate attenuation correction (Fig. 4).
The drawback of using end-expiration is the low lung volume in this phase of the RC, which may make it more difficult to detect small tumors. Furthermore, the CT-based method rejects a large proportion of the acquired PET data. Hence, a 10-min acquisition is needed to achieve the same quality as a standard 3-min acquisition 48.
When applied to the lungs 46,49 and the liver 50,51, the CT-based method was found to be more sensitive than ungated imaging. Table 3 summarizes the differences in maximum standardized uptake values in these studies.
Chang et al.52 have proposed a solution in which respiratory motion amplitude is captured during a whole-body CT acquisition. The RS amplitude is picked up at the entry and exit of the bed step where the lesion is localized in order to define an amplitude range (AR). Unlike the previously mentioned method, a gated, triggered LM acquisition then gathers only PET events corresponding to the defined AR. These PET data are used to generate a single motion-free volume. The drawback of this solution relates to its dependence on the patient’s breathing pattern; if the patient breathes quickly, the influence of respiratory motion cannot be fully excluded. Moreover, the patient may not breathe in the same way for the CT and PET acquisitions. In such an event, the AR determined in the CT scan will not correspond to the respiratory amplitudes at the lesion’s site according to the PET acquisition.
Nehmeh et al.53 developed a gating method using a single tissue position. The tissue position is determined with respect to an external 18F-FDG point source that appears on each image of a dynamic PET acquisition. On the first reconstructed frame, the point source’s position is defined as the reference, and a region of interest (ROI) is drawn around it. The ROI is then carried over onto all frames but only those in which the point source falls within the ROI are considered. Finally, the corresponding PET raw data are summed and reconstructed.
To avoid increasing the duration of PET acquisitions (due to the loss of statistics related to compensation techniques), some researchers have developed techniques to correct for respiratory motion. To the best of our knowledge, these techniques have not yet been used in routine clinical practice. Motion correction is usually performed by introducing a deformation field before, during, or after the tomographic reconstruction. Determination of the deformation field is beyond the scope of this paper but we shall detail these three approaches (before, during, or after reconstruction) in the following sections.
Prereconstruction correction methods: data-driven approaches
Prereconstruction correction involves changing the position of lines of response (LORs) 54–57 as a function of a precomputed deformation field. However, the LORs are displaced by means of affine transformations only; this means that the technique is well suited to the correction of head motion 58,59 but not to the correction of the nonrigid motion typically seen during breathing. The loss of some LORs may occur during repositioning (e.g. outside the gantry or between the detectors in 3D acquisitions) 57. Moreover, the exact projection of the deformation field in raw space data may require a rounding step in LOR repositioning, which introduced noise into the final raw data 56.
Motion correction during reconstruction
With the availability of fast computers, PET images are usually obtained by applying expectation maximization algorithms 60–63. Continuous-object reconstructions are generally based on discrete-data formulations through parallelepiped functions (i.e. voxels) and a system matrix, which links acquired data and the object’s basis functions.
To correct for respiration motion, several groups have suggested the computation of a system matrix for each respiratory state 64–67. The main drawback of these approaches relates to the rigid nature of the basis function commonly used. Indeed, voxels do not deform along with the motion correction, which generates discontinuities between voxels. The solution presented by Reyes and colleagues 68,69 uses spherical basis functions inscribed in voxels. Basis functions could be approximated by deformable ellipsoids, which avoid the discontinuities caused by tissue deformation.
Another way of correcting for respiratory motion is to take account of a-priori knowledge about an object (edges, anatomical features, etc.) by incorporating spatiotemporal regularization into the reconstruction algorithm 70–74. Grotus et al.75 integrated temporal regularization with a temporally adaptive basis function. However, one drawback of these solutions relates to the determination of scalar weighting parameters, which can be performed empirically on phantoms but is not necessarily suited to clinical situations.
Postreconstruction motion correction
This method relies on summing gated images (obtained with a multibin approach) after a registration step 76–81. In principle, this is an attractive approach, although PET image registration is complicated by the spatial resolution and by partial volume effects. In addition, this method suffers from the limitations described above in the section on multibin compensation. Moreover, the summed image is affected by the sum of the noise levels in each image. Nevertheless, registration of the gated PET images enables the determination of the deformation field required by the above-mentioned motion correction methods.
Future trends and conclusion
At the outset, respiratory motion compensation and correction techniques were aimed at improving diagnosis and follow-up during nuclear medicine examinations of the thorax and abdomen. However, recent advances in radiotherapy mean that metabolic images are taken into account in treatment planning 82. Moreover, intensity-modulated radiotherapy planning and dose painting require information on the respiratory motion of lesions. In this context, multibin compensation techniques are the only methods capable of describing the lesion’s path during the RC. Nevertheless, specific attenuation maps for each phase are required to describe intrinsic heterogeneities within lesions. One solution is provided by 4D CT, albeit at the cost of a substantial increase in the radiation dose and acquisition time. Now that combined PET/MRI scanners are becoming more widely available, a few reports have emphasized the value of MRI for correct PET images for respiratory motion 83–85. In MRI, the patient is not exposed to ionizing radiation. Moreover, the fact that most recent gantries perform PET and MRI acquisitions simultaneously (rather than sequentially, as in PET/CT scanners) improves the quality of registration.
This work was funded by the Canceropôle Nord Ouest France.
The authors thank Dr David Fraser (Biotech Communication, Damery, France) for his helpful advice on the English language in this paper.
Conflicts of interest
There are no conflicts of interest.
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