Abstract
A fast and reliable range monitoring method is required to take full advantage of the high linear energy transfer provided by therapeutic ion beams like carbon and oxygen while minimizing damage to healthy tissue due to range uncertainties. Quasi-real-time range monitoring using in-beam positron emission tomography (PET) with therapeutic beams of positron-emitters of carbon and oxygen is a promising approach. The number of implanted ions and the time required for an unambiguous range verification are decisive factors for choosing a candidate isotope. An experimental study was performed at the FRS fragment-separator of GSI Helmholtzzentrum für Schwerionenforschung GmbH, Germany, to investigate the evolution of positron annihilation activity profiles during the implantation of \(^{14}\)O and \(^{15}\)O ion beams in a PMMA phantom. The positron activity profile was imaged by a dual-panel version of a Siemens Biograph mCT PET scanner. Results from a similar experiment using ion beams of carbon positron-emitters \(^{11}\)C and \(^{10}\)C performed at the same experimental setup were used for comparison. Owing to their shorter half-lives, the number of implanted ions required for a precise positron annihilation activity peak determination is lower for \(^{10}\)C compared to \(^{11}\)C and likewise for \(^{14}\)O compared to \(^{15}\)O, but their lower production cross-sections make it difficult to produce them at therapeutically relevant intensities. With a similar production cross-section and a 10 times shorter half-life than \(^{11}\)C, \(^{15}\)O provides a faster conclusive positron annihilation activity peak position determination for a lower number of implanted ions compared to \(^{11}\)C. A figure of merit formulation was developed for the quantitative comparison of therapy-relevant positron-emitting beams in the context of quasi-real-time beam monitoring. In conclusion, this study demonstrates that among the positron emitters of carbon and oxygen, \(^{15}\)O is the most feasible candidate for quasi-real-time range monitoring by in-beam PET that can be produced at therapeutically relevant intensities. Additionally, this study demonstrated that the in-flight production and separation method can produce beams of therapeutic quality, in terms of purity, energy, and energy spread.
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Introduction
Proton therapy is currently the most widespread type of ion beam therapy. The rationale behind using ions heavier than protons for radiation therapy is the reduced lateral scattering with increasing ion mass and the higher relative biological effectiveness (RBE)1 in the tumor region. The facility for ions heavier than protons has a downside characterized by higher investment costs, typically ranging from 2 to 4 times more expensive and the cost per treatment of carbon ions is about 2–3 times higher than that of conventional therapy with X-rays2. Additionally, the heavy ions have the issue of unavoidable projectile fragmentation, which leads to an undesirable dose tail distal to the target. Carbon has been identified as an excellent compromise ion due to its favorable characteristics. It exhibits the best ratio of biologically effective dose in the tumor compared to the entrance channel for numerous indications. Consequently, carbon is presently the most widely utilized ion at all light ion beam therapy centers. Other light ions are also being considered, with oxygen being one of them3,4,5,6,7. The main rationale for using ions heavier than \(^{12}\)C is to further increase the particle’s linear energy transfer (LET), which can effectively target hypoxic tumors. Oxygen, despite having a linear energy transfer (LET) that is 80% higher than carbon, is often deemed too aggressive for most indications. However, it holds potential for application in multi-ion painting particle therapy. In this therapy approach, where multiple ion species are used to target different regions within a tumor, the higher LET of oxygen could potentially enhance the therapeutic outcomes7,8,9.
The dose and/or LET gradients induced in the volumes irradiated by light ions raise the need for precise beam range monitoring to ensure the compromise between the uniform target coverage and the sparing of the surrounding healthy tissue and critical structures. With no direct feedback on dose conformity during the treatment, ion beam therapy relies solely on the accuracy of treatment planning procedures and systems. Additionally, patient anatomical changes may occur during treatment. To address this, margins are typically added to the treated region, which unfortunately causes unnecessary dose deposition to healthy tissue, ultimately leading to increased toxicity10. Positron emission tomography (PET) is one of the most commonly employed methods to monitor dose delivery in ion beam therapy11. Here the positron-emitters are produced through fragmentation processes of the atomic nuclei in the beam and the tissue, and Monte Carlo codes are typically used to correlate the PET data with the actual dose profile. However, this process is typically performed as a post-irradiation procedure to validate treatment plans. In contrast to protons, the PET image of a \(^{12}\)C ion beam has an identifiable peak produced by the positron-emitting projectile fragments, but its mismatch with the primary beam range12, 13, the low statistics at typical fraction doses and the long half-life of the most abundantly produced positron-emitting projectile fragment (\(^{11}\)C) complicate fast in-beam PET range monitoring in clinical settings and limits the PET-based range verification accuracy to approximately 2–5 mm14, 15. The same challenges also apply to an \(^{16}\)O ion beam13, 16, 17.
Several ideas for a feedback system are being explored to mitigate this problem. Among these, image-guided ion beam therapy with positron-emitting radioactive beams in combination with PET is one of the most promising ones. The general idea behind utilizing positron emitters as therapy beams is to achieve sub-millimeter precision for range verification through PET. This idea was pursued early on during the pilot project on heavy ion beam therapy at the Lawrence Berkeley Laboratory (LBNL)18. The merits of ion beam therapy using positron emitters have been extensively reviewed by multiple authors19, 20. The Heavy Ion Medical Accelerator in Chiba (HIMAC), Japan, investigated the feasibility of using secondary beams of \(^{11}\)C and \(^{15}\)O positron emitters, produced by projectile fragmentation, for both therapy and in-beam PET range verification21,22,23.
To fully realize the benefits of positron-emitting therapy beams, it is crucial to have quasi-real-time feedback on any potential deviations from the treatment plan with minimal exposure to healthy tissue. Since the quasi-real-time approach requires in-beam PET, it avoids the relocation of the patient, which pose a challenge to accurate patient positioning. Additionally, since the patient relocation process itself typically takes at least five minutes, the imaging quality can be negatively affected by biological washout24,25,26,27. It must be noted that a fast image reconstruction algorithm and an adequate computational infrastructure are equally important in exploiting the benefits of quasi-real-time range verification offered by short-lived positron-emitting therapy beams. In this sense, relying on 2D feedback is a more pragmatic approach.
The BARB (Biomedical Applications of Radioactive Beams) project at GSI, aims at pre-clinical validation of in vivo beam visualization in heavy ion beam therapy with positron emitting carbon and oxygen isotopes28,29,30,31. The project also conducts related basic studies. As a part of this project, experiments were performed with the fragment separator FRS studying the evolution of the PET image during irradiation with positron emitters of carbon (\(^{10}\)C and \(^{11}\)C) and oxygen (\(^{14}\)O and \(^{15}\)O). The properties of these isotopes are shown in Table 1.
The positron emitters were produced and separated in-flight by the FRS and implanted in a polymethyl methacrylate (PMMA) phantom for PET imaging studies using an in-beam dual panel PET scanner. The primary goal of the experiments was to establish a relationship between the minimum amount of detected decays required to achieve a range verification precision better than the typical systematic uncertainty of the patient positioning systems. The results from the carbon experiment, which provide a detailed description of the experimental setup and methodology, have already been published30. This article reports on an experiment with positron emitters of oxygen, \(^{14}\)O and \(^{15}\)O, and the results are compared to the data obtained for \(^{10}\)C and \(^{11}\)C within the context of quasi-real-time in-beam range monitoring30.
Materials and methods
Positron emitting beams
The FRS at GSI, where this experiment was conducted, is an in-flight secondary-beam facility33. Secondary beams of positron emitters of oxygen were produced by projectile fragmentation of the \(^{16}\)O ion beams accelerated by the SIS18 synchrotron and impinging on an 8 g/cm\(^2\) thick beryllium production target at the entrance of the FRS. Two different primary beam energies were used: 370 MeV/u (low-energy run) and 465 MeV/u (high-energy run). The secondary beams of interest were separated in-flight using the FRS with the well-established \(B\rho\)-\(\Delta E\)-\(B\rho\) technique34. The FRS was operated in its standard ion-optical mode, characterized by being overall-achromatic with an acceptance of 20 \(\pi\) mm mrad and momentum spread \(\Delta p/p\) of 2\(\%\) (FWHM). The angle of the wedge-shaped degrader was chosen such that the overall achromatism was preserved. The thickness of the wedge degrader was adjusted to have the same mean range during the implantation of different isotopes in an individual run. The definition of the “mean range” used in the following is the depth at which half of the particles are stopped. The estimated water equivalent mean range of low- and high-energy runs are 53 and 124 mm, respectively, according to the calculations with ATIMA 1.2 code using LISE++ program35. These values are chosen to represent typical values used in heavy ion beam therapy. Prior to irradiating the phantoms at high intensity for imaging purposes, the purity of the beam was evaluated through event-by-event particle identification at low intensity. For more details on the beam properties, see Table 2. During the imaging runs, a dedicated gas-filled parallel-plate ionization chamber (IC)36 was used to record the beam intensity.
Imaging
Isotopically pure beams of \(^{14}\)O, \(^{15}\)O and \(^{16}\)O (see Table 2) were delivered to the PET imaging setup at the final focal plane of the symmetric branch of the FRS (see Fig. 1). Ions were implanted in a homogeneous polymethyl methacrylate (PMMA) phantom for PET imaging studies using One-sixth of a modified version of a Siemens Biograph mCT clinical scanner, configured as a dual-panel scanner37. Each panel is composed of a 4\(\times\)4 array of Siemens Biograph mCT block detectors that cover a total area of 225\(\times\)220 mm\(^2\). Each block detector consists of a 13\(\times\)13 array of 4\(\times\)4\(\times\)20 mm\(^3\) LSO (lutetium oxyorthosilicate doped with cerium) scintillation crystals read out by a 2\(\times\)2 array of PhotoMultiplier Tubes (PMTs). The panels were placed 35 cm apart with the positioning structure for the PMMA phantom in between. The panels are curved around the beam axis with a radius of curvature of 42.1 cm. The geometrical efficiency of the scanner is estimated to be about 32% for a central point source38. The PMMA phantom has a size of 120\(\times\)250\(\times\)350 mm\(^3\) and was placed in-between the two PET scanner panels with its long side in the beam direction and its short side in the vertical direction, see Fig. 1. After each measurement, the phantom was exchanged in order to avoid the influence of the previous activation. A system with sliding rails and positioning pins was employed to allow easy exchange and precise positioning of the phantom. Positioning of the phantom relative to the scanner’s field of view (FoV) along the beam axis was possible in steps of 35 mm with a precision ±0.25 mm. During the irradiation, the phantom positions were chosen such that the implantation depth of the beam was as close to the center of the FoV of the scanner as possible. The ion beam range in the phantom was calculated prior to the experiment with the ATIMA 1.2 code with the LISE++ program35.
Positron activity profiles and time structure of the implanted beams
Secondary beams produced by the FRS are inherently pulsed since the driver accelerator is a synchrotron. The nominal extraction time was chosen to be 1.0 s followed by a 1.3 or 1.5 s beam-off time, during which the next ion bunch was accelerated. A beam cycle is defined as a time period comprising both beam-on and beam-off times. The beam cycle time for high energy runs of \(^{14}\)O and \(^{15}\)O was 2.5 s, while for all other cases, it was 2.3 s, see Table 2.
The time structure of the beam is clearly visible in the intensity measurement by the large area parallel plate ionization chamber (IC) installed in front of the phantom. As an example, the time evolution of the intensity of the \(^{15}\)O beam as derived from the IC data and the number of coincidence events from the PET data are shown in Fig. 2. The time structure of the beam is also manifested in the PET data as a higher count rate during beam-on times compared to the beam-off time. The rate increase during beam-ON time can be attributed to the fast-decaying positron-emitting projectile fragments (e.g.\(^{9}\)C, \(^{12}\)N, \(^{13}\)O with half-lives in the millisecond range) produced within the phantom during the stopping process as well as to prompt \(\gamma\)-emission from excited nuclear levels39. These fast-decaying positron-emitters have positrons with high endpoint energies, which broaden the spatial distribution of the positron-emitters and are therefore excluded from the data analysis, see e.g. 40, 41.
Two detector events, one in each panel, were registered as a coincidence event in event list mode if they occurred within a time window of 4.1 ns and had an energy between 435 and 650 keV. Each coincidence event included a time stamp with 1 ms resolution. The time stamp enabled the monitoring of the time evolution of the positron activity profile during irradiation. The reconstruction procedure used to create 2D PET images of the positron activity profiles is described in detail by Ozoemelam et al.42. The 2D image reconstruction of coincidence events was performed using a 2\(\times\)2 mm\(^{2}\) pixel size. Further, the corrections for the attenuation of gamma rays in the phantom and the scanner’s sensitivity must also be taken into account for the accurate quantification of the images. These corrections are specific to the geometrical configuration of the imaging setup. Systematic offline measurements using a \(^{22}\)Na source were performed to map the sensitivity and attenuation corrections for the two different phantom positions used during the irradiation. A detailed description of the procedure can be found in Kostyleva et al.30 Figures 3 and 4 display the in-beam 2D PET images of \(^{14,15,16}\)O ions implanted into the PMMA phantom during both the high-energy run and the low-energy run, following various implantation cycles.
Fitting of the 1D-positron activity profiles
The 1D-positron activity profiles in the direction of the beam were obtained by laterally integrating the reconstructed 2D images over a region whose width is equal to plus or minus two times the standard deviation of the positron activity distribution.
To perform further analysis of the 1D-positron activity distributions shown in Fig. 5, an asymmetric peak shape was used to describe the data. Due to its simplicity and the small number of parameters necessary, the so-called GE function, which is a central Gaussian smoothly connected to exponential functions at both or one of the peak edges, was chosen43. The capability of the GE function to model the positron activity profiles produced by the implantation of carbon isotopes in a PMMA phantom was successfully demonstrated in the preceding work by Kostyleva et al.30 The maximum of the GE peak coincides with the mean of the central Gaussian and the maximum of the positron activity profile is defined by this parameter. It will be referred to as peak position in the following. The data were fitted with the GE function using the curve-fitting routine of the commercial software program Igor Pro. The reduced chi-square (\(\chi ^{2}_{red}\)) test was used to determine the goodness-of-fit. For the \(^{14}\)O and \(^{15}\)O data sets, the GE function represents 90% of the proximal and distal fall-off regions of the positron activity peak. In the case of \(^{16}\)O, the fit region covers 70% of the proximal and distal fall-off regions. A typical example of a peak analysis procedure to extract the evolution of the peak position over the course of irradiation is demonstrated in Fig. 5 using the high-energy run of \(^{14}\)O as an example. The precision of range determination is quantified as the standard deviation of the peak position parameter of the GE fitting function. The peak position parameter with the smallest uncertainty is the most precise. It is also considered to be the most accurate value, and it is used as the reference value for the data points with lower statistics. The top panel of Fig. 5 shows the evaluation of the positron activity peak position and its uncertainty over the course of the implantation. Already after the second implantation cycle, the peak position approaches the asymptotic value within the uncertainty and after the third implantation cycle, its uncertainty drops below 1 mm.
Results
The main focus of this paper is to explore the possibility of fast positron activity range monitoring by quasi-real-time in-beam PET using therapy beams of positron-emitting isotopes of oxygen, \(^{15}\)O and \(^{14}\)O. For this purpose, the evaluation of the peak position and its uncertainty during the course of implantation is studied in detail as explained in the previous section.
Positron activity profiles of \(^{14}\)O, \(^{15}\)O and \(^{16}\)O beams
Figure 6 shows the 1D positron activity profiles obtained after 100 implantation cycles of \(^{14}\)O, \(^{15}\)O and \(^{16}\)O. The activity profiles are normalized to the total implanted ions. The energy of all three isotopes was adjusted to have the same implantation depth in the phantom. The image peak positions of \(^{14}\)O, \(^{15}\)O coincide with each other and their estimated mean range is within the positioning tolerance of the PMMA phantom (±0.25 mm), whereas the positron activity peak of the \(^{16}\)O has a position proximal to the mean range and is about two orders of magnitude smaller in height.
The positron activity profiles (within the vicinity of the fit region) of \(^{16}\)O, \(^{15}\)O, and \(^{14}\)O over the first few implantation cycles are illustrated in Fig. 7. During this stage, the production cross-sections, half-lives, and ranges of positron-emitting projectile fragments, especially the fast decaying ones like \(^{8}\)B and \(^{10}\)C, significantly influence the development of positron activity profiles. As a result, the temporal effect, combined with low statistics, results in significant uncertainty in the fit parameters until the most abundant positron emitter becomes the dominant contributor. For \(^{14}\)O, the low-energy run yielded no identifiable peak before the fourth implantation cycle. The high-energy run yielded an identifiable peak already on the first implantation cycle due to the fivefold higher intensity (see Table 2). The most significant time-dependent effect on the positron activity profile and peak position is observed in the case of \(^{16}\)O. Since the primary beam is not a positron-emitter, the positron activity profile is composed of contributions from the positron-emitting projectile fragment peaks superimposed on a plateau formed by the positron-emitting target fragments. In contrast to \(^{16}\)O, the positron activity peaks resulting from the implantation of \(^{15}\)O and \(^{14}\)O are expected to match closely the corresponding ion-beam range. Although significantly less compared to the case of \(^{16}\)O, the short-lived positron-emitting projectile fragments influence the peak shape until the decays from the projectiles themselves take prominence. In the first few cycles of both the low- and high-energy runs of \(^{14}\)O and \(^{15}\)O, the presence of short-lived positron-emitting projectile fragments has a slight but discernible impact on the peak shape. The factor 1.7 shorter half-life of \(^{14}\)O results in a higher yield of coincidence events compared to that of \(^{15}\)O for the same number of implanted ions.
Typical uncertainties assumed in robust treatment planning for \(^{12}\)C ion therapy are a setup uncertainty of ±3 mm and a range uncertainty of ±3.5% of the range44. Recent advancements in dual-energy CT technology will allow further reduction of range uncertainty. Regions with greater density changes, such as head and neck tumors, experience higher uncertainties of 2%, whereas, in more homogeneous regions like the liver, uncertainties may be reduced to 1.7%45. Range verification should thus have a precision of better than about ±1 mm to have a positive impact on patient treatment.
In the context of quasi-real-time in-beam PET, the number of implanted ions (which translates to the dose deposition) and the time required for adequate range verification from the start of the implantation are the decisive factors for choosing a candidate. The important questions to be addressed here are:
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What is the minimum number of ions needed to be implanted to determine the positron activity range with a precision that will bring clinical benefit to patients (±1 mm or better)?
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How much time is needed to reach the required precision?
To achieve unambiguous range verification by PET in light ion therapy, the detected positron activity distribution must show a distinct peak, and its position and associated uncertainty should be within the expected range of technical (e.g. patient positioning) and biological (i.e., anatomical changes) factors. The conditions for data points to satisfy these criteria are as follows:
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The data point should have an identifiable peak.
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The deviation of the peak position from the asymptotic value (the one obtained from the highest statistics case) should be within \(\le \pm\)0.75 mm.
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The statistical uncertainty in peak position should be within \(\le \pm\)0.75 mm.
The value of 0.75 mm is chosen somewhat arbitrarily, but such that it is well within the estimated minimum requirement of ±1 mm. Figures 8 and 9 display the changes in peak position and their uncertainty during the implantation of high- and low-energy \(^{15}\)O and \(^{14}\)O ions. These changes are depicted as a function of two variables: accumulated number of implanted ions (Fig. 8) and elapsed measurement/implantation time (Fig. 9). Data from our prior study on positron emitters of carbon, \(^{11}\)C and \(^{10}\)C, are included in both figures for comparison 30. Compared to Fig. 8, the Fig. 9 provides a clearer picture of the practical aspects of in-beam PET, including the efficiency of producing different isotopes using the in-flight method. The values presented here are specific to the experimental setup’s geometric configuration and reconstruction algorithms used in this experiment, as detailed in Kostyleva et al.’s work30. It should be noted that the results can be easily scaled to other PET systems.
Discussion
PET scanners can determine the range of positron activity with a certain precision by collecting a certain minimum number of counts. The actual number of counts required depends on the geometry and sensitivity of the scanners. From an instrumental perspective, the slower decay rate of long-lived positron emitters compared to short-lived ones can be compensated by higher intensity. However, for therapeutic applications, the required dose, and consequently, the number of ions implanted is defined by medical requirements. Therefore, it is advantageous to achieve range verification as quickly as possible with the smallest possible dose.
Figure 9 compares positron emitters in quasi-real-time in-beam PET, illustrating the impact of half-life and intensity on image quality. It also helps to infer the influence of implantation cycle time structure on coincidence events per cycle. For instance, in the high-energy run, \(^{10}\)C shows better precision than \(^{15}\)O by the end of the first beam cycle, despite its 20 times lower beam intensity. This result is due to \(^{10}\)C’s shorter half-life, 6 times less than \(^{15}\)O, with two-fold longer implantation (2.0 seconds beam-ON) and decay (2.8 s beam-OFF) times. A quantitative comparison is challenging due to coupled factors like half-life, beam intensity, and different cycle time structures used for oxygen and carbon experiments. To facilitate comparison, a formulation considering these factors is essential. In this experiment, positron-emitting secondary beams were generated via projectile fragmentation of primary beams (\(^{12}\)C and \(^{16}\)O ions). The secondary beam intensity (\(I_{s}\)) in ions/pulse is given by:
where \(\eta\) is the conversion factor (see Table 3), representing the ratio of positron-emitting ions delivered to the imaging phantom (\(I_{s}\)) to primary ions accelerated in the synchrotron (\(I_{0}\)). \(\eta\) is given by:
where \(\sigma _{cs}\) is the production cross-section (see Table 3), and \(\rho _{A}\) is the areal density of the production target (in number of atoms/cm\(^{2}\)). \(\epsilon\) is an efficiency factor defined as the ratio of the isotope beam intensity available for imaging to the intensity of the reaction products produced in the primary reaction. Irradiation is performed in a pulsed mode with a beam-ON time \(t_p\) and a subsequent beam-OFF time \(t_r\). The beam cycle time T is defined as \(t_p+t_r\). The number of positron emitters \(N_{0}\) accumulated by the end of a beam-ON time is given by:
where \(\lambda =\ln (2)/t_{1/2}\) is the decay constant. The number of decays during the subsequent beam-OFF time \(t_r\), \(N_{D}\), is given by:
Equation 4 represents the number of decays, and therefore also the number of coincidence events recorded during the beam-OFF time. This is because only these coincidence events are used for image reconstruction and further analysis, see Fig. 2. This equation is applicable for the first beam cycle. For subsequent pulses, it becomes essential to consider the contribution of decay from positron emitters deposited in preceding implantation cycles. The total number of decays accumulated after after n implantation cycles is thus given by:
The calculated relative yield of coincidence events, as depicted in Fig. 10a, suggests that the model presented in Eq. 5 effectively captures the data showcased in Fig. 9. Notably, the 13% higher coincidence yield of \(^{10}\)C compared to \(^{15}\)O can be attributed to the favorable beam cycle time structure of the carbon experiment. To facilitate a fair comparison of the performance among different positron emitters it is crucial to eliminate the influence of the difference in the beam cycle time between the oxygen and carbon experiments. To achieve this, the relative yield of coincidence events for various positron emitters is calculated under the assumption that they share the same beam cycle time structure, and is presented in Fig. 10b. The beam cycle time structure from the oxygen experiment was employed for these calculations. This analysis reveals that if the beam cycle time structure is standardized across all isotopes presented here, \(^{15}\)O emerges as the superior candidate.
In Eq. 5, the primary beam intensity \(I_{0}\) and the components of the conversion factor \(\eta\), namely the areal density of the target \(\rho _{A}\) and the efficiency of beam transport \(\epsilon\), are system-dependent parameters (see Eqs. 1 and 2). To extend the results of this work to a system-independent context, it is advantageous to introduce a Figure of Merit (FOM) that is based on two decisive fundamental quantities: the half-life and the production cross-section. The production cross-section addresses the availability of therapy-relevant intensities, while the half-life of the positron-emitter, along with the beam cycle structure, addresses the quasi-real-time PET feedback aspects of the positron emitters under consideration.
To construct the FOM, it is assumed that all system-dependent factors, \(I_{0}\), \(\rho _{A}\), and \(\epsilon\), are approximately the same for all isotopes, and their values are set to unity; i.e., \(I_{0}\) is equal to 1 ion/pulse, \(\rho _{A}\) is equal to 1 atom/cm\(^{2}\), and \(\epsilon\) is equal to 1. The resulting FOM is a dimensionless value that is proportional to N(n) (see Eq. 5).
To illustrate the application of the Figure of Merit (FOM), results for \(^{15}\)O, \(^{14}\)O, \(^{11}\)C, and \(^{10}\)C are presented in Fig. 11 for the first beam cycle for the same cycle time T but three different beam-ON times \(t_p\). These examples show that, regardless of the beam cycle time structure, \(^{15}\)O consistently emerges as the superior candidate, confirming the experimental results obtained in this work.
In terms of the half-live, \(^{10}\)C is the best candidate for quasi-real-time range monitoring. However, the production cross-section of \(^{10}\)C is an order of magnitude lower than that of \(^{11}\)C and \(^{15}\)O. This is also true for \(^{14}\)O. This implies that the production of \(^{10}\)C and \(^{14}\)O requires an order of magnitude higher intensity from the driver accelerator to reach therapeutical intensities. In the case of \(^{11}\)C, the half-life of 1221.8 s makes it not optimal for quasi-real-time range monitoring using in-beam PET. For the therapy-relevant positron emitter \(^{13}\)N, the same holds true47. From measurements (see Figs. 9 and 10b) \(^{15}\)O comes out as a clear favorite among all considered isotopes for quasi-real-time range monitoring by in-beam PET during therapy as quantified in the figure of merit analysis. It must be noted that the characteristic fragmentation tail of heavy ions is higher for oxygen compared to carbon. This issue is unavoidable but relevant in the choice of therapeutic isotope. A comprehensive discussion of this matter is beyond the scope of this work.
A systematic investigation was conducted on the production of \(^{11}\)C and \(^{15}\)O using the in-flight method at HIMAC, Japan. The study demonstrated the feasibility of producing \(^{15}\)O beams suitable for medical treatment, with a reported production yield of 0.43(2)% and 97.2% purity, achieved through projectile fragmentation of a 430 MeV/u \(^{16}\)O beam. Similarly, a production yield of 0.76% with 99% purity was reported for \(^{11}\)C by projectile fragmentation of a 430 MeV/u \(^{12}\)C beam at HIMAC, the maximum primary beam intensities available for \(^{16}\)O and \(^{12}\)C are 1.1\(\times\)10\(^{9}\) ions/s and 1.9\(\times\)10\(^{9}\) ions/s, respectively19, 21. The present study also demonstrates the feasibility of producing \(^{15}\)O beams suitable for medical treatment using an in-flight method, achieving, purity, and energies required for the purpose (see Table 2).
With the method and parameters used in this work (including the intensity of the primary beam, energy of the primary and secondary beam, production target material and thickness, phase space acceptance of the separator, choice of degrader material and thickness), the beam intensity of \(^{15}\)O exceeds that of \(^{14}\)O by a factor of 10 to 20. The conversion factors for the high-energy runs of \(^{15}\)O and \(^{14}\)O are provided in Table 3, while for the low-energy runs, they are 8\(\times\)10\(^{-5}\) for \(^{14}\)O and 1\(\times\)10\(^{-4}\) for \(^{15}\)O. The higher conversion factor of \(^{15}\)O compared to \(^{14}\)O results primarily from its greater production cross-section, while the disparity between low and high energy primarily arises from differences in transmission through the separator48. The conversion factors for analogous studies conducted with carbon isotopes are presented in Table 3. These beams have a similar implantation depth as the high-energy run of oxygen. The two times higher conversion factor for \(^{15}\)O compared to \(^{11}\)C is because the smaller emittance of the former leads to a higher transmission through the FRS spectrometer.
It should be noted that the maximum intensity achieved for \(^{16}\)O in the SIS18 is 10\(^{11}\) ions/cycle49. Therefore, there is potential to increase the intensity of \(^{15}\)O at the symmetric branch of FRS by an order of magnitude. This would make it comparable to the typical intensity of about 5\(\times\)10\(^{8}\) ions/s available at a \(^{12}\)C treatment facility50.
ISotope On-Line (ISOL) is a method alternative to in-flight for RIB production. CRC Louvain-la-Neuve in Belgium has produced a low-energy beam ISOL beam of \(^{15}\)O with an intensity of 6\(\times\)10\(^{7}\) ions/s, and LBNL has produced a \(^{14}\)O beam with an intensity of 3\(\times\)10\(^{7}\) ions/s51,52,53. The highest intensity achieved for an ISOL beam of \(^{11}\)C is 1\(\times\)10\(^{8}\) ions/s by LBNL54. Although the ISOL technique produces highly pure and intense Radioactive Ion Beams (RIB), the production of a RIB with sufficient energy for ion beam therapy using the ISOL technique has not yet been demonstrated. A recent Technical Design Report (TDR)50 published by the MEDICIS-Promed network55 provides a comprehensive exploration of implementing ISOL-produced post-accelerated \(^{11}\)C radioisotopes in particle therapy centers. The TDR presents findings from a thorough review of clinical applicability, utilizing a combination of experimental data and Monte Carlo simulations. This in-depth study covers various technical solutions, including production, ionization, acceleration, and transport, with a specific emphasis on upgrading existing \(^{12}\)C particle therapy centers. These findings can be easily extended to therapy beams involving \(^{15}\)O.
The emergence of high-LET FLASH radiotherapy56 as a potential breakthrough in cancer treatment has sparked interest in optimizing its delivery since it is characterized by the delivery of an ultra-high dose of radiation in a single pulse. By incorporating in-beam quasi-real-time range verification offered by the \(^{15}\)O beam, the precision and safety of high-LET FLASH therapy can be significantly enhanced. An ion beam therapy center equipped with a \(^{15}\)O beam presents a unique and promising opportunity to perform in-beam range verification using a low-intensity probe pulse prior to the FLASH.
Conclusions
This study provides a comprehensive quantitative and qualitative comparison of the therapy-relevant beams of positron-emitting isotopes of carbon and oxygen within the context of quasi-real-time range verification capability. \(^{11}\)C is currently the most researched candidate for therapeutic RIB due to its enhanced imaging potential without dosimetric drawbacks, but its half-life is too long to be considered for fast range monitoring using in-beam PET. The lower production cross-section of \(^{10}\)C and \(^{14}\)O makes it challenging to produce them with intensities of therapeutical needs. The results also demonstrate that, from the perspective of an in-flight production and separation method, \(^{15}\)O is the better choice in terms of achievable intensity. In conclusion, \(^{15}\)O is the most technically feasible choice for a therapeutic beam that allows quasi-real-time range monitoring by in-beam PET due to its faster response at a lower dose. This study also demonstrates the feasibility of producing \(^{15}\)O beams with an intensity, purity, and energy suitable for ion-beam therapy using the method of \(^{16}\)O-projectile fragmentation and separation in-flight.
Further research and development in this field have the potential to significantly advance ion beam therapy techniques and improve treatment outcomes for cancer patients. For example, by incorporating in-beam quasi-real-time range verification and utilizing the positron-emitting oxygen beam, the precision and safety of high-LET FLASH therapy can be substantially enhanced.
Data availability
The datasets used and/or analysed during the current study can be made available under a collaboration agreement with the GSI Helmholtzzentrum für Schwerionenforschung GmbH, Darmstadt, Germany. Please contact the corresponding authors for more information.
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Acknowledgements
The work is supported by European Research Council (ERC) Advanced Grant 883425 (BARB) to Marco Durante. Additional funding came from the Justus-Liebig-Universität (JLU), Gießen, Germany, and GSI under the JLU-GSI strategic Helmholtz partnership agreement. The measurements were performed within the Super-FRS Experiment Collaboration (Experiment No. S533 by S. Purushothaman et al.) at GSI in the framework of the FAIR Phase-0 experimental program. Authors would like to thank Dr. I. Ozoemelam, Dr. M. Kapusta, and Dr. H. Törnqvist for data acquisition support, Dr. O. Sokol for discussions on medical aspects of the ion beam therapy, and careful reading and insightful comments on the manuscript, K.-H. Behr, T. Blatz, J. Hellmund, P. Kewes, F. Koch, P. Schwarz, B. Szczepanczyk, T. Weber, M. Will, and B. Zapien Campos for the engineering, technical and organizational help during experiment preparation and colleagues from Deutsches Krebsforschungszentrum (DKFZ), Heidelberg for providing the calibration sources.
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S.P. conceptualized the experimental proposal and the PET imaging experimental setup, contributed to defining the experimental procedure, coordinated and performed the experiment, conducted 1D-positron activity analysis and interpretation, prepared figures, and wrote the manuscript. D.K. contributed to PET data acquisition, developed analysis code, performed the experiment, processed data, reconstructed images, and produced the 1D and 2D positron activity data. P.D. conceptualized the experimental proposal, contributed to PET data acquisition, provided guidance with PET data processing, analysis, and interpretation, and contributed to manuscript preparation. E.H. and H.G. conceptualized the experimental proposal, contributed to defining the experimental procedure, performed the experiment, and contributed to the manuscript preparation. U.W., C.S., and D.B. contributed to beam intensity monitoring and characterization. T.D., C.G., C.H., E.K., N.K.F., I.M., S.P., H.R., C.S., Y.K.T., and J.Z. performed experiments. M.D., K.P., and C.S.provided overall leadership of the project and contributed to the editorial review of the manuscript. M.D. conceived the original idea of the BARB project, secured the ERC Grant, and organized the project. All authors participated in the review of the manuscript.
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Purushothaman, S., Kostyleva, D., Dendooven, P. et al. Quasi-real-time range monitoring by in-beam PET: a case for 15O. Sci Rep 13, 18788 (2023). https://doi.org/10.1038/s41598-023-45122-2
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DOI: https://doi.org/10.1038/s41598-023-45122-2
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