The main challenge in treating malignant brain neoplasms lies in eradicating the tumor while minimizing treatment-related damage. Conventional radiation treatments are associated with considerable side effects. Synchrotron generated micro-beam radiation (SMBRT) has shown to preserve brain architecture while killing tumor cells, however physical characteristics and limited facility access restrict its use. We have created a new clinical device which produces mini beams on a linear accelerator, to provide a new type of treatment called mini-beam radiation therapy (MBRT). The objective of this study is to compare the treatment outcomes of linear accelerator based MBRT versus standard radiation treatment (SRT), to evaluate the tumor response and the treatment-related changes in the normal brain with respect to each treatment type. Pet dogs with de-novo brain tumors were accrued for treatment. Dogs were randomized between standard fractionated stereotactic (9 Gy in 3 fractions) radiation treatment vs. a single fraction of MBRT (26 Gy mean dose). Dogs were monitored after treatment for clinical assessment and imaging. When the dogs were euthanized, a veterinary pathologist assessed the radiation changes and tumor response. We accrued 16 dogs, 8 dogs in each treatment arm. In the MBRT arm, 71% dogs achieved complete pathological remission. The radiation-related changes were all confined to the target region. Structural damage was not observed in the beam path outside of the target region. In contrast, none of the dogs in control group achieved remission and the treatment related damage was more extensive. Therapeutic superiority was observed with MBRT, including both tumor control and the normal structural preservation. The MBRT findings are suggestive of an immune related mechanism which is absent in standard treatment. These findings together with the widespread availability of clinical linear accelerators make MBRT a promising research topic to explore further treatment and clinical trial opportunities.
The challenge in treating malignant brain neoplasms lies in eradicating the tumor while minimizing treatment-related damage to normal adjacent brain. Conventional radiation therapy of brain tumors relies on the radiobiological principle of temporal fractionation to exploit the differences in the ability of malignant cells and normal tissue cells to repair radiation damage. Conventional radiation therapy is administered in a series of 1.8–2.66 Gy daily doses or fractions, for a period of approximately 4 to 6 weeks (1–3). While this has dramatically increased physicians' ability to cure or provide long-term tumor control of many cancers, there are some tumors such as high-grade gliomas of the brain, for which the prognosis remains grim (3). Conventional radiation therapy is also associated with collateral damage to normal brain tissue (4). In long-term survivors, this may manifest as varying combinations of neurocognitive/neuropsychological problems and/or impaired bone growth. These clinical manifestations can be correlated to the imaging changes on follow up scans (5), and further explained on pathological examination of the brain adjacent or away from the targeted lesion. On necropsy studies, the treated regions show dose dependent changes ranging from minimal to complete avascular necrosis, extensive vacuolization in brain parenchyma along with rarefaction of the blood vessels (6–9). An elegant study elucidating long-term radiation effects on normal brain tissue as a function of dose and time showed the possibility of neuroinflammation as the basis for the long-term side effects of radiation (10). Most of the late radiation damage may be the consequence of ongoing radiation related changes in the vascular endothelial fabric network of the brain (11). However, irrespective of the underlying mechanism of action, mitigating the toxicity related to radiation treatment while eradicating the tumor is currently an unmet goal in the treatment of brain tumors. The dose of radiation to the brain during conventional radiation therapy for controlling or killing brain tumor cells has always been limited by the normal tissue tolerance and treatment-related long-term morbidities, underscoring the need for better or newer modalities of treatment (4).
Spatial fractionation radiation treatment using arrays of narrow, parallel micro-beams, has been explored extensively using synchrotron-generated X rays. With synchrotron-generated micro-beam radiation therapy (SMBRT), there are two main regions of dose distribution; the path of the micro-beam, or peak, and the tissue that is not directly traversed by the micro-beam, or valley. Beam width ranging from tens of microns up to 950 µm has been reported (12). Slatkin et al. demonstrated preservation of cellular integrity after SMBRT even at very large doses (13). Dilmanian et al. and Serduc et al. further showed the normal tissue-sparing effects of micro-beam radiation treatment on the brain (14, 15). When spatial fractionation is used, normal brain tissue has been shown to tolerate peak entrance doses of several hundred Gy with preservation of cognitive function clinically, and post-mortem neural architecture structurally (13–18).
It has been theorized that normal brain tissue tolerance to SMBRT is related to the spatial fractionation of the radiation, which allows rapid repair of damage by neighboring endothelial and glial cells (19, 20). Micro-beams not only have potential for greater sparing of normal tissue, but are also more damaging to malignant tissues, with a superior therapeutic ratio (13, 14, 21, 22). However, the radiobiological mechanisms are not understood conclusively, with several competing theories concerning both immune response and chemical reaction pathways (13, 13, 13, 14, 13, 21,–13, 23). Nevertheless, it is clear from SMBRT studies that spatially fractionated micro-beams offer an advantage over conventional radiation therapy.
To extrapolate the knowledge learned from SMBRT studies and move towards human use, in 2009 a tungsten collimator was designed to produce a beam of 1,000 µm size that was named a “mini beam”, and could be used with an RT-250 superficial X-ray machine (24). This was the first step towards realizing the goal of using this new medical technology for the treatment of human cancers. Based on the findings from our bridging study done between the years, 2011 and 2013, with a view to transfer the therapeutic advantage of SMBRT to larger animals and possibly to human brain tumor treatment, a linear accelerator mounted mini-beam collimator for use at a nominal 6 MV beam energy was designed and characterized (25–27).
The mini beams generated on a linear accelerator (megavoltage mini beams) have potential advantages over kilovoltage beams generated on a synchrotron, with a comparatively higher energy that allows radiation to reach deeper targets within the patient while reducing the surface dose. Synchrotron beams generally cannot deliver radiation to targets at 6–10 cm depths without a significant surface dose. Nevertheless, synchrotron beams can have greater control of beam shape with a higher radiation intensity, but can be more limited in terms of availability for regular use compared to megavoltage radiation sources. Megavoltage mini beams also differ significantly from either kilovoltage beams or “classical” micro beams produced at synchrotron facilities in terms of beam geometry, peak-to-valley dose ratio (PVDR) and depth-dose characteristics. The megavoltage mini-beam collimator used in this work is the same physical device that has been described by Davis et al, and consists of 30 tungsten blades with 0.6 mm width and 10 cm length held in an aluminum frame and arranged to produce planar mini beams 1 mm thick with a maximum field size of 5 × 5 cm (27). The collimator assembly is mounted directly to the linac gantry head using a standard accessory mount. From ref. 29, using this collimator results in dose peaks with full width at half maximum (FWHM) of 1.0 mm at isocenter. The FWHM is relevant because megavoltage mini beams take a profile with a sharp peak widening towards the base, as opposed to synchrotron beams which are quasi-parallel. The PVDR of megavoltage beams is found to decrease with depth, but is still significant at a 10 cm depth while maintaining a low-surface dose. Both the FWHM and PVDR of megavoltage beams have a further dependence on the spot size of the initial electron beam, and are therefore dependent on the specific linac used. Due to these factors, the PVDR of the megavoltage mini-beam collimator in this work was found to be ∼1.47 at a 10 cm depth in water when averaging across results from 3 different machines (25, 27). This is significantly lower than the PVDR typically seen for synchrotron beams, which can be as high as 48 when 25 µm wide beams are used (19). It has been proposed that a higher PVDR results in lower normal tissue toxicity (15), but there is no known direct relationship between PVDR number and ultimate treatment efficacy.
With the megavoltage collimator available, this study aimed to examine animals larger than mice that are typically used in micro beam studies. Smaller laboratory animal studies have many pitfalls that were revealed in our initial study, including the disproportionate size of rapidly growing transplanted tumors compared to the actual small size of the brain, resulting in a short life span for these animals. This short follow-up time postirradiation precludes the gathering of information on tumor response or long-term side effects of radiation.
To obtain more illuminating results using larger animals, this study compared megavoltage mini-beam radiation treatment (MBRT) to standard radiation treatment (SRT) of naturally occurring brain tumors in pet dogs. Primary nervous system tumors arise spontaneously in companion animals as in human patients, and radiation therapy is the standard treatment for most of these tumors. Client-owned dogs provide an excellent model for studying the response of normal brain and tumor to MBRT. Similar to humans, dogs have gyrencephalic brain whereas small animals like mice have lissencephalic brain. Dogs can present with naturally occurring tumors which mimic the biological behavior and complex tumor microenvironment of spontaneous human tumors. (28) Additionally, the response of canine brain tissue to radiation is similar to that of human brain tissue, and the physical dimensions of the dog brain and skull are closer to those of human patients than small rodents. Side effects in irradiated normal tissues can occur years after irradiation and limit the total dose that can be administered to a tumor. Pet dogs can be followed for long periods of time, up to their remaining lifespan, while having neurological and imaging examinations to assess for signs of tumor recurrence and long-term-side effects. Owners are generally able to give detailed information on the daily quality of life achieved after irradiation, as well as on subtle cognitive changes that may not be apparent upon a single examination by a veterinarian.
The objective of this study is to compare the treatment outcomes of linear accelerator based MBRT vs. SRT, to evaluate the tumor response and the treatment-related changes in normal brain tissue with respect to each treatment type.
MATERIALS AND METHODS
This study was approved by the local Animal Ethics Research Board of University of Saskatchewan, Canada, in accordance with best practices set by the Canadian Council on Animal Care. Pet dogs with spontaneously developed brain tumors were recruited for the study. These dogs were evaluated clinically using magnetic resonance imaging (MRI). Presumptive diagnosis was done based on the imaging study, with the results detailed in Table 2. None of the dogs underwent biopsy as per standard of practice. Upon completion of staging workup, the dogs were randomized to receive SRT vs. MBRT. All the dogs were anesthetized and immobilized using a vacuum-deformable body cushion. A thermoplastic neck cushion ventral to the head and cervical region was used along with a custom-made indexed maxillary plate, thermoplastic bite block and a thermoplastic head mask dorsal to the head region. Control dogs received standard radiation treatment of 9 Gy on 3 consecutive days for a total dose of 27 Gy (Fig. 1e–g and Table 1, SRT). The treatment was distributed using 5 entry ports delivered by rotating the linac gantry to fixed angles determined by the treatment planning system. Dogs in the investigational MBRT arm received a single 26 Gy fraction mean dose to the target (Fig. 2 g–i; Table 1, MBRT). In the case of MBRT the use of “mean dose” was adapted to refer to the whole target and is defined by the difference between the dose where the beamlet is traversing compared to where it is not. Due to this fact point doses are shown in Fig. 2g–i that are higher than 26 Gy due to the peak and valley dose distribution of the mini beams. The treatment type used can be defined as multiple port intersecting mini beams, and was delivered using 2 entry ports as shown in Fig. 2g. All dogs were maintained on steroid and anti-epileptic medications as needed. After the treatment, the dogs were followed at regular intervals by the referring veterinarian for clinical assessment. Dogs also had a follow-up MRI every 3 months. The images were evaluated by one neuroradiologist (SW). Depending on the decision of the owner of these pet animals, they were euthanized, and brains were obtained for centralized evaluation by a single veterinary neuropathologist (BP).
X-Ray Fluorescence Imaging
Synchrotron-based X-ray fluorescence imaging (XFI) was performed at the Stanford Synchrotron Radiation Light source on beamline 10-2, with the SPEAR3 storage ring operating in top-up mode at 3 GeV and 500 mA, following established methods (29). Beamline 10-2 was equipped with a 33-pole 1.45-Tesla wiggler, using a Si(111) double-crystal monochromator (φ = 90° orientation) and a Rh-coated mirror for focusing. A micro-focussed beam, approximately 35 × 35 µm, was achieved using an aperture downstream of the I0 ion chamber. Samples were mounted at 45° to the incident beam and raster scanned using Newport IMS Series stages (Irvine, CA) in 30 µm steps, providing an oversampling pixel size of 30 µm, using a dwell time of 200 ms per point. An incident energy of 13,450 eV was employed, and X-ray fluorescence was detected with a silicon-drift Vortex detector positioned 45° to the sample normal (90° to the incident beam). Multichannel array spectra for each pixel in the XFI map were processed using the Micro Analysis Toolkit SMAK (30).
A total of 16 dogs were treated in the study, 8 animals per group between the years 2013 and 2017. The initial diagnosis and lesion characteristics for each dog based on the MRI are shown in Table 1, as determined prior to radiation treatment. The lesions were denoted as “well defined” if the lesion borders could be clearly visualized. They are labelled “ill defined,” if the borders could not be clearly visualized on the MRI. By location of the tumors both groups were having equal proportion (50%) of tumors located on either side of the tentorium. Among the standard radiation treatment group only 2 out of 8 dogs showed features suggesting an aggressive nature tumor (dogs 2 and 5) with brain parenchymal invasion compared to 7 out of 8 dogs in MBRT group (dogs 10 to 16) showing aggressive features including brain parenchymal invasion or invasion into the canal in the base of skull.
Two dogs treated in the standard radiation treatment arm had to be euthanized a short time after the treatment, 1 within 48 h and 1 at day 45. Similarly, 1 dog in the MBRT arm had to be euthanized within 48 h (Table 2). The autopsy study of these 3 dogs showed aspiration pneumonia and sepsis as the cause for death. Following assessment, these were all deemed unrelated to the treatment, and therefore these 3 dogs were not included in the final analysis. The remaining dogs in the study in both arms were euthanized during follow-up at the discretion of their owners depending on their symptoms and how they were thriving.
Clinical Evaluation During Follow-up
The overall survival ranged from 45 to 1,500 days for the standard radiation treatment group, 150 days to 1,080 days for the MBRT group. The median and mean survival was 710 days and 652 days, respectively, for standard radiation treatment group. The median and mean survival for MBRT group was 210 days and 384 days, respectively. Full results for all dogs individually are reported in Table 2. During the first 2 months of follow-up there was no significant difference observed between the two treatment arms, in terms of their symptoms or the medications required. However, clinical evaluation beyond 2 months showed seizure was the more predominant symptom among the MBRT dogs compared to the standard radiation treatment group, while progressively worsening of existing neurological deficits or new neurological symptoms were more predominant in control arm (standard radiation treatment) dogs compared to MBRT group.
Follow-up Imaging analysis
Follow-up images showed tumor response at varying time intervals in the MBRT group, including complete response in 2 dogs. There was treatment-related edema noted in 2/7 dogs. One dog that received MBRT showed changes suggestive of tumor necrosis versus recurrence on followup imaging. This has been confirmed upon necropsy study as radiation necrosis was present with no visible tumor. Among the standard radiation treatment group, 2 dogs did not have follow-up imaging as the owners declined follow up imaging. By comparison, tumors persisted in all standard radiation treatment dogs (4/4) with minimal shrinkage noted in only 2 dogs. Treatment-related brain edema changes in the standard radiation treatment arm were noted in 2 of the 4 dogs.
Synchrotron X-ray fluorescence imaging on the MBRT dog brain showed preservation of normal structural anatomy at in the brain immediately adjacent to the target area as well as along the path of the beam.
Neuropathological analysis revealed that all the dogs in the control group treated with standard radiation treatment displayed residual brain tumor during examination under microscope at any magnification (Table 2), a situation which was labeled as “partial response” (PR). A situation in which no residual tumor was visualized under any magnification was denoted as “pathological complete response” (pCR). None of the dogs treated with standard radiation treatment showed pCR, i.e., 0% pCR. There were extensive mitotic figures seen, and macrophage infiltration was noted in the residual tumor as seen in Fig. 1a. Widespread vacuolar edema, in the form of vacuolations, was seen in both white matter and gray matter (Fig. 1b and c). Radiation treatment-related changes outside the targeted area can also be seen. Encephalomalacia was noted even in regions of the brain that received lower doses than 50% (Fig. 1d). There was rarefication of vessel density along with few perivascular or parenchymal inflammatory cell infiltrations (Fig. 1c).
By comparison, the MBRT dogs showed excellent response, excluding the dog that was euthanized within 48 h of treatment, with 71% (5/7) of dogs showing no residual tumor, indicating pCR. Even the dog that was euthanized early within 48 h of treatment, had also shown tumor necrosis and reduction in tumor size. The remaining 2 dogs (2/7) that achieved partial remission, showed few residual tumor cells. One dog showed hemorrhagic necrosis in the tumor bed (Fig. 2a) similar to what has been reported by Tiller-Borcich et al. (31).
Among the dogs designated with pCR, the tumor bed region showed only karyorrhectic debris (Fig. 2b), with lymphocyte and macrophage infiltration (Fig. 2d and e). The microvasculature in this region also showed fibrinoid necrosis in the vascular walls along with lymphocyte infiltration. The density of lymphocyte infiltration was more florid in perivascular regions (Fig. 2c and d). Lymphocyte infiltration was also seen in the meninges and in the brain parenchyma.
Among the MBRT dogs, white matter vacuolation was noted in close proximity to the target area (Fig. 2b and c). However, there were features of gliofibrillary activation/ repair in the area. Similarly, there were intact neural cells in the targeted area, months after the treatment, suggestive of neuropil recovery (Fig. 2c). All the radiation-induced changes were confined to the area that received >50% dose, closer to the area that was targeted with MBRT. The rest of the brain traversed by MBRT, though in close proximity to the target, remained anatomically intact and did not show treatment-related changes (Fig. 2f). There were no tracks of megavoltage mini beam present in the region of the brain traversed by the beam (the dose given through each beamlet was approximately 50% of the prescription dose to the target, i.e., 13 Gy). Specific immunostaining showed infiltration by T lymphocytes and plasma cells in the MBRT group while this was nearly absent in the control group (Fig. 3).
In this study, all dogs treated with MBRT showed a response. Among this group 71% achieved complete pCR, with no residual tumor on postmortem study, in comparison to control group (standard radiation treatment) where dogs showed only partial response at best. The persistence of tumors after the treatment noted in the standard radiation treatment group, was similar to the tumor responses observed in the studies done in the past (6–8). The long-term treatment related changes seen in the standard radiation treatment group such as extensive vacuolization in brain parenchyma, encephalomalacia and rarefaction of vessels were similar to the findings reported in the literature (6–9).
In the MBRT group, the late-radiation-induced changes were mostly confined to areas that received >50% of the dose. There was no cellular or anatomical architectural damage related to treatment noted in the path of the MBRT beam. The findings from XFI provide insight into the distribution and concentration of elements, providing a measure of the metabolic state (including ion concentrations) in the tissue and demonstrate if there is any detectable damage to healthy brain. XFI results confirm that there is no detectable damage to healthy brain even in both entry and exiting paths of the mini beams. On neuropathological evaluation, the lethal treatment effects were seen only in the areas where spatially fractionated arrays of beams were intersected to overlap each other, which was planned with the intention of achieving more treatment effect in the target region. Despite the tissue destruction in the form of pan-necrosis (necrosis of cells and neuropil), it was confined mostly to the targeted area, and there were findings suggestive of cellular regeneration and recovery close to the area outside the targeted region. Neuropil recovery was noted within millimeters from the ablated target. By contrast in the control dogs, the late radiation changes in the brain, including microvacuolation and encephalomalacia, were noted in the areas that received doses <50% of the target area dose.
Radiation produces both neuropil injury and vascular injury. Encephalomalacia, or necrotic brain, can be seen with many causal origins which can be due to either vascular etiology and/or direct neuropil effect of high-energy photons. Evidence of both can be found in standard radiation treatment dogs in this study. In addition, tumor response to the radiation might be adduced from the lymphocyte infiltration. Supporting this idea was our finding of differential lymphocytes infiltration seen between MBRT and standard radiation treatment groups. The macrophage infiltration by contrast was more causally related to the necrosis.
Lymphocyte infiltration confined to the area of treatment after a single large dose open beam treatment has been reported (10) and presumed to be part of neuroinflammation response. The long standing neuroinflammation noted in this study shows that there is a possibility of long-term memory for immune system surveillance against tumor recurrence. Eloquent studies by Bouchet et al., showed the possibility that the tumoricidal effect of spatially fractionated doses may be mediated through immune modulation involving a complex network of mediators (32, 33). Interestingly, our study has shown more diffuse lymphocyte infiltration in the targeted region for MBRT patients, both perivascularly as well in the parenchyma outside the targeted area, which was not seen in the control group. This raises the possibility of immune modulation as a possible mechanism for the impressive results noticed with MBRT, however these results cannot conclusively determine the mechanism(s) responsible for pCR in MBRT patients. Immune modulation also possibly explains the exceedingly early response noted in the dog that was euthanized within 48 hours after treatment in the MBRT group. There are currently multiple hypothesis regarding the precise mechanism of action that leads to improved outcomes from synchrotron based micro or mini-beam treatments, none of which have been able to fully explain the outcomes (13, 14, 21–23). Similarly regarding MBRT generated on a linear accelerator, the immune modulation may play a role as one of the main mechanistic effects of MBRT that results in improved tumor cell destruction and related long-term effects noticed on normal brain tissue. However, a full explanation of the immune effects occurring during MBRT is beyond the scope of this work.
Results similar to those reported here have been shown for SMBRT where a study comparing SMBRT to synchrotron-generated open beam treatment for brain tumor has shown better tumor response with micro-beams (34). Despite this, MBRT clearly shows superior tumoricidal effects compared to standard radiation treatment with a significant sparing of damage to normal tissue.
Beam width of micro-beams may have significant impact on the tissue-sparing ability. A study comparing spatially fractionated beams with widths ranging between 200–800 µm, showed more uniform cellular necrosis including mature vasculature compared to beams with width <100 µm, where cellular necrosis involved specifically immature vasculature in zebrafish (35). However, another study (36) showed vascular normalization irrespective of beam width or dose, presumably from pericyte activation. In our study the beam width was kept to 1,000 µm in size, and no cellular damage noted in the beam path (both entrance and exit path). Our study finding is also contrary to a study using deuteron micro-beams, which showed destruction of normal tissue with 1,000 µm beams (37). The differences between synchrotron beam and megavoltage beam shape also results in a different dose to the interface between heavily irradiated peaks and nominally unirradiated valley tissues. Regenerative and reparative mechanisms possibly persist at this interface, as observed on microscopic examination as well as XFI, showing the regeneration of glial fabric and neural cell preservation very close to the targeted region just outside the intersected mini beams (Fig. 2c and f). Therefore, it can be speculated that the efficacy of these mechanisms may be different for megavoltage beams compared to synchrotron beams. Tissues irradiated with megavoltage mini beams will have a larger peak-to-valley interface region that receives a partial dose compared to tissues irradiated with SMBRT which has a sharper interface between peak and valley. This work shows delivering radiation in a spatially fractionated array of beamlets in a fashion similar to SMBRT, unlike the uniform dose delivery with standard conventional radiation treatment, would achieve superior tumor cell kill while preserving normal anatomy resulting in less tissue damage or side effects.
Studies have alluded (38, 39) to the feasibility of 2 interlacing micro-beams to deliver a large ablative dose to the target while exploiting the use of the tissue-tolerating effect of micro-beams in their path, before and after the intersection. One such study (39) hypothesized that the interlacing of the beams might allow for dose reduction, while achieving the same biological effect on the tumors. The positive effects of intersecting mini beams were achieved in this study where pan-necrosis was noticed in the area where 2 MBRT beams were intersected in the tumor-bearing targeted region. Just 26 Gy mean dose was applied in a single fraction to completely ablate the tumor (pCR 71%).
Use of more than one intersecting, non-parallel opposed MBRT beams would help encompass the target with a near-total prescribed dose, with relatively lower entry and exit doses. The main goal of this approach is to ablate the tumor in its entirety, while attempting to preserve normal structures. Two or more non-parallel MBRT beams, used to intersect over the target region appear to achieve this aim, as the entrance and exit beam paths will still have the peak-to-valley dose ratio maintained (from 50% to 30% i.e., from 0 cm to 10 cm depth) (25). The postmortem analysis of the brains of MBRT dogs show minimal to no radiation-induced damage in both the beam entrance and exit path, unlike the control dogs treated with a more uniform dose.
This new therapeutic modality does have few caveats including, limited use of gantry angles (degrees of freedom), the collimator itself needs to be manually attached to linear accelerator head, and requires a large number of monitor units to deliver the desired dose as the collimator output factor is low. However, these issues may not translate to major disadvantage for MBRT pending further development of the technology.
This is the first randomized study using MBRT generated on a linear accelerator with 1,000 µm size beams to treat de novo brain tumors in larger animals with a gyrencephalic brain. Findings in larger gyrencephalic brains with de novo tumors may be more closely applicable to the human brain, compared to findings from the lissencephalic brains of rodent animals such as rats or mice with transplanted tumors in their brain. The findings in this study reflect the long-term treatment outcome including both tumor control and late treatment-related effects on brain. The findings of MBRT have been discussed considering the published SMBRT work found in the literature.
This study using pet dogs which unlike human patients, are not cared for medically from the point of disease progression to death. Instead, they were euthanized at the discretion of their owners depending on social and emotional factors. This makes the survival or progression-free interval assessment impossible to discern. Nevertheless, this study showed an impressive 71% pCR in the study arm with 0% pCR in control arm, indicating clear therapeutic superiority of MBRT. In addition, the study also showed sparing of normal tissue in the study arm, compared to the control arm, highlighting the superior therapeutic ratio. The superior therapeutic results noted with MBRT including both tumor control, and normal structural preservation in the presence of neuroinflammation suggests the possibility of an immune-related mechanism in both therapy and toxicity. This justifies a potential scope for using immune modulatory agents, along with MBRT in the treatment of brain tumors. MBRT produced on a linear accelerator offers greater equipment accessibility to explore further treatment/ clinical trial opportunities.
We thank Dr Barbara E Powers, DVM, PhD, DACVP. (Veterinary Pathologist) for her invaluable support and time reporting on all the brain specimens of the dogs treated on this study. We thank Dr. Viktor Zherebitskiy, MD, FRCPC, ABP9NP/AP), FACP, FASCP (Neuropathologist) for his invaluable administrative support for this work. Synchrotron-based X-ray fluorescence imaging (XFI) was performed at the Stanford Synchrotron Radiation Lightsource (SSRL). The Stanford Synchrotron Radiation Lightsource, SLAC National Accelerator Laboratory, is supported by the U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences under Contract No. DE-AC02-76SF00515. The SSRL Structural Molecular Biology Program is supported by the DOE Office of Biological and Environmental Research, and by the National Institutes of Health, National Institute of General Medical Sciences (P30GM133894). This work was supported by a grant from Saskatchewan Cancer Agency (OGF 414311). Neuropathology evaluation was supported by Mrs. J. Olszewska Neuropathology Fund.