- Open Access
The dosimetric impact of implants on the spinal cord dose during stereotactic body radiotherapy
© The Author(s). 2016
- Received: 16 September 2015
- Accepted: 17 May 2016
- Published: 25 May 2016
The effects of spinal implants on dose distribution have been studied for conformal treatment plans. However, the dosimetric impact of spinal implants in stereotactic body radiotherapy (SBRT) treatments has not been studied in spatial orientation. In this study we evaluated the effect of spinal implants placed in sawbone vertebra models implanted as in vivo instrumentations.
Four different spinal implant reconstruction techniques were performed using the standard sawbone lumbar vertebrae model; 1. L2-L4 posterior instrumentation without anterior column reconstruction (PI); 2. L2-L4 anterior instrumentation, L3 corpectomy, and anterior column reconstruction with a titanium cage (AIAC); 3. L2-L4 posterior instrumentation, L3 corpectomy, and anterior column reconstruction with a titanium cage (PIAC); 4. L2-L4 anterior instrumentation, L3 corpectomy, and anterior column reconstruction with chest tubes filled with bone cement (AIABc). The target was defined as the spinous process and lamina of the lumbar (L) 3 vertebra. A thermoluminescent dosimeter (TLD, LiF:Mg,Ti) was located on the measurement point anterior to the spinal cord. The prescription dose was 8 Gy and the treatment was administered in a single fraction using a CyberKnife® (Accuray Inc., Sunnyvale, CA, USA). We performed two different treatment plans. In Plan A beam interaction with the rod was not limited. In plan B the rod was considered a structure of avoidance, and interaction between the rod and beam was prevented. TLD measurements were compared with the point dose calculated by the treatment planning system (TPS).
Results and discussion
In plan A, the difference between TLD measurement and the dose calculated by the TPS was 1.7 %, 2.8 %, and 2.7 % for the sawbone with no implant, PI, and PIAC models, respectively. For the AIAC model the TLD dose was 13.8 % higher than the TPS dose; the difference was 18.6 % for the AIABc model. In plan B for the AIAC and AIABc models, TLD measurement was 2.5 % and 0.9 % higher than the dose calculated by the TPS, respectively.
Spinal implants may be present in the treatment field in patients scheduled to undergo SBRT. For the types of implants studied herein anterior rod instrumentation resulted in an increase in the spinal cord dose, whereas use of a titanium cage had a minimal effect on dose distribution. While planning SBRT in patients with spinal reconstructions, avoidance of the rod and preventing interaction between the rod and beam might be the optimal solution for preventing unexpectedly high spinal cord doses.
- Stereotactic body radiotherapy
- Spinal implant
Bone is the third most common site of metastatic cancer, and bone metastasis occurs in approximately 70 % of patients with metastatic breast cancer and prostate cancer . The axial skeleton is the most frequently affected site [2–4]. Proper treatment of bone metastasis requires interdisciplinary care, and includes analgesics, corticosteroids (particularly in patients with spinal cord compression), hormonal therapy, bisphosphonates, surgery, chemotherapy, radiotherapy (RT), radiopharmaceuticals, or any combination of these.
Conventional external beam RT provides significant palliation of painful bone metastasis in 50–80 % of patients, but only 33 % of patients achieve complete pain relief at the treated site . Studies have shown equivalent pain relief for various RT protocols, such as 30 Gy in 10 fractions, 24 Gy in 6 fractions, 20 Gy in 5 fractions, and a single 8-Gy fraction [6, 7]; however, the need for re-irradiation because of recurrent pain was higher in the single fraction arm, as compared to the fractionated protocols (20 % vs. 8 %). Hartsell et al.  evaluated patients with spinal metastasis separately and only 61 % of patients experienced partial or complete pain relief at 1 month post-treatment. Such studies highlight the need for improved outcomes in patients with spinal metastasis. Increasing the RT dose to the target is a legitimate option for increasing control rate; however, spinal cord tolerance is the limiting factor for increasing the delivered dose using conventional RT techniques.
Stereotactic body radiotherapy (SBRT) is an innovative treatment option for spinal metastasis. SBRT facilitates the delivery of a higher dose of radiation precisely to the target while limiting the dose to the spinal cord with rapid dose fall-off. Clinical studies on SBRT reported that it is an efficacious technique for pain control, with a rapid onset of response (as early as within 24 h) [8–10]. Additional experience with SBRT for spinal metastasis suggests a dose-response relationship, with an increase in pain relief—particularly at doses ≥16 Gy . The major concern is the dose to the spinal cord, and the spinal dose constraint of 10 Gy to 10 % of the spinal cord defined in a maximum of 6 mm above and below the radiosurgery target is most commonly reported .
As SBRT is increasingly used in RT clinics for spinal metastases, patients with implants in the treatment field are often encountered. The spatial orientation of the implants in the vertebra is alike in patients with same implantation techniques. When a cage is used for vertebral column reconstruction the minimum distance between the cage and the spinal cord is 5 mm. The distance between the rods and the cord is more than 2 cm. The present study aimed to determine the dosimetric effect of spinal implants on the dose received by the spinal cord, in a sawbone model where the configuration of the implants could be simulated as in vivo.
TLD 100 chips were calibrated with 2 Gy to a field of 10 cm × 10 cm with Varian Clinac DHX High Performance linear accelerator (Varian Medical Systems, Inc., Palo Alto, CA) using 6 MV photons, as this process is not practical with a CyberKnife® . In total, 101 TLDs were placed in a specially designed water equivalent phantom (PMMA). Calibration factors were defined for each TLD.
where DoseTLD is the dose measured at each TLD in each model and DoseTPS is the dose calculated by the TPS.
TLD and TPS doses for each model
TPS dose (cGy)
1st measurement (cGy)
2nd measurement (cGy)
3rd measurement (cGy)
AIAC- Plan B
SBRT for the spine has been used at RT clinics in patients with spinal metastases with increasing frequency. The spinal cord dose constraint for SBRT is defined as 10 Gy in a single fraction, and because of the possible devastating results of a spinal cord overdose, this constraint is strictly followed. In the present study the effect of spinal implants on the spinal cord dose during SBRT for the treatment of spinal metastases was evaluated using morphologic replicas of vertebrae and implants that can be seen in patients in routine practice, and spinal cord doses ≤18.6 % higher than TPS doses were observed.
Patients with an impending fracture or a pathologic fracture, spinal instability, progressive spinal cord compression (SCC), progressive spinal deformity, or recurrent symptoms following RT require surgical intervention [16, 17]. Spinal cord compression is observed in approximately 20 % of patients with vertebral body metastases . In cases of collapsed vertebral bodies vertebroplasty is the treatment of choice. Several types of surgical techniques can be used for vertebral body stabilization. Instrumentation with a rod can be performed posteriorly or anteriorly with a cage—with or without anterior column reconstruction. Patchell et al.  compared surgery to RT alone in patients with SCC, and reported that surgery was superior to RT for all endpoints, such as fecal continence, overall survival, and the need for pain killers. The combination of surgery and RT resulted in a greater likelihood of walking in patients who were paraplegic prior to surgery. Even partial resection of spinal metastasis increased the effectiveness of RT . Ghogawala et al.  reported that wound complications occurred more frequently when surgery followed RT, as compared to when surgery was performed prior to RT (32 % vs. 12 %) ; therefore, surgery followed by RT is the recommended treatment for patients with SCC .
The most important problem with postoperative RT is radiation scatter due to implants. As implants are made of high atomic number materials, such as titanium, they cause dosimetric uncertainty due to beam attenuation and scatter . The dosimetric effect of hip implants in pelvic RT has been studied. Bahreyni Toossi et al.  studied electron and neutron contamination of 4 different hip prosthesis varying in composition, including cobalt-chromium-molybdenum, stainless steel, titanium-alloy, and titanium. They observed an increase in electron and neutron contamination in all 4 implants. On the other hand, Schneider et al. measured neutron doses owing to titanium-alloy prostheses during photon and proton therapy and found no impact of prostheses on neutron contamination . In another study based on 6 MV photons, dose inhomogeneity of 10 % was calculated in the vicinity of the implant, whereas in areas away from the implant dose homogeneity was within 5 % of the prescribed dose .
The American Association of Physicists in Medicine (AAPM) Task Group 63 published a report to inform the radiation oncology community of the problems associated with metal implants in the treatment field, and provide recommendations related to treatment planning and delivery in patients with hip prostheses . They proposed beam arrangements that completely or partially avoided prostheses; however, what was proposed had the potential to increase the dose to the OARs.
There are also dosimetric studies performed with spinal implants. Wang et al.  performed a dosimetric study based on small fields ranging from 2x2 to 5x5 cm, and used 5-mm thick titanium rods embedded in water. They reported that the dose was 6 % higher at the intersection point of the rod and water due to backscattered electrons, and was 7 % lower in the shadow of the rod because of photon attenuation. Liebross et al.  studied the dose perturbation of screws and rods used for spinal implants. They used a 20x20-cm field and observed a dose reduction behind the rods. Son et al.  measured doses in the space between 2 titanium screws and reported the dose was 1.9 % lower, as measured via an ionization chamber.
The spatial relationship that parts of implants have with each other and with the OARs was not taken into consideration in the studies mentioned above. To overcome this limitation Pekmezci et al. performed 4 spinal implant reconstructions in sawbone spine models to evaluate the effects of implants on dose distribution for a single field (postero-anterior) technique using a cobalt-60 unit and a 6-MV linear accelerator . Posterior instrumentation resulted in a 5 % lower dose, whereas the anterior instrumentation models did not have a significant effect on dose distribution.
The CyberKnife® is an image-guided stereotactic radiosurgery and SBRT device that facilitates tumor treatment by generating a large number of direction points (typically 1000-6000); however, use of a high number of beams at different angles causes complex interactions between each beam and the implants. We hypothesized that these complex interactions between beams and implants may cause an unpredictable and totally different dosimetric effect than the interactions between beams and implants that occur with conventional treatment plans. It has been shown that the TPS generally calculates wrong dose values in the vicinity of metal artifacts. This led to a standard procedure of setting the density to a value that would correspond to the soft tissue obscured by the artifacts during treatment planning . However, as both our planning CT and the TPS of CyberKnife® do not allow this option, we could not perform any compensation for the metal artifacts.
During stereotactic RT treatments in CyberKnife® patients are usually treated in supine position, and this device allows beam delivery from the anterior and lateral directions. Therefore, the anterior rod placement in this position results in an interaction between the rod and entering beams. However, in posterior instrumentations the rods are located in the path of exit beams. The present findings show that the interaction with the entering beams caused unacceptably high spinal doses. Furthermore, use of a titanium cage or chest tubes filled with cement placed anterior to the spinal cord did not have a significant dosimetric effect. This observation provides a guide in clinical practice because describing all implants as structure of avoidance according to the AAPM task group’s recommendation limits the angles that can be used with SBRT profoundly. Limiting the number of angles can result in unacceptably high doses in the adjacent organs. Based on the present findings, we suggest that only rods—when placed anterior to the spinal cord—should be considered structures of avoidance when using a TPS to calculate the absorbed dose.
Spinal implants may be present in the treatment field in patients scheduled to undergo SBRT. For the types of implants studied herein anterior rod instrumentation resulted in an increase in the spinal cord dose, whereas use of a titanium cage had a minimal effect on dose distribution. While planning SBRT in patients with spinal reconstructions, avoidance of the rod and preventing interaction between rod and entering beam might be the optimal solution for preventing unexpectedly high spinal cord doses.
This study was supported by a Hacettepe University research grant (1-05 A 101 009).
GY made contributions to conception, design, and analysis of the study and revised the manuscript. SYS drafted the manuscript and performed the statistical analysis. FYY participated in the design of the study, irradiation of the spine models, calculating the physical measurements and acquisition of data. SDB, AY, GD, MG and PH participated in the design of the study, irradiation of the spine models, drafting the manuscript and performing the statistical analysis. MY, GO and MC helped to draft the manuscript, revised it critically for important intellectual content, and gave the final approval of the version to be published. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
- Hage WD, Aboulafia AJ, Aboulafia DM. Incidence, location, and diagnostic evaluation of metastatic bone disease. Orthop Clin North Am. 2000;31:515–28.View ArticlePubMedGoogle Scholar
- Asdourian PL, Weidenbaum M, DeWald RL, Hammerberg KW, Ramsey RG. The pattern of vertebral involvement in metastatic vertebral breast cancer. Clin Orthop Relat Res. 1990;250:164–70.PubMedGoogle Scholar
- Steinmetz MP, Mekhail A, Benzel EC. Management of metastatic tumors of the spine: strategies and operative indications. Neurosurg Focus. 2001;11:e2.View ArticlePubMedGoogle Scholar
- Wong DA, Fornasier VL, MacNab I. Spinal metastases: the obvious, the occult, and the impostors. Spine (Phila Pa 1976). 1990;15:1–4.View ArticleGoogle Scholar
- Chow E, Harris K, Fan G, Tsao M, Sze WM. Palliative radiotherapy trials for bone metastases: a systematic review. J Clin Oncol. 2007;25:1423–36.View ArticlePubMedGoogle Scholar
- Steenland E, Leer JW, van Houwelingen H, Post WJ, van den Hout WB, Kievit J, et al. The effect of a single fraction compared to multiple fractions on painful bone metastases: a global analysis of the Dutch Bone Metastasis Study. Radiother Oncol. 1999;52:101–9.View ArticlePubMedGoogle Scholar
- Hartsell WF, Scott CB, Bruner DW, Scarantino CW, Ivker RA, Roach 3rd M, et al. Randomized trial of short- versus long-course radiotherapy for palliation of painful bone metastases. J Natl Cancer Inst. 2005;97:798–804.View ArticlePubMedGoogle Scholar
- Gerszten PC, Burton SA, Welch WC, Brufsky AM, Lembersky BC, Ozhasoglu C, et al. Single-fraction radiosurgery for the treatment of spinal breast metastases. Cancer. 2005;104:2244–54.View ArticlePubMedGoogle Scholar
- Degen JW, Gagnon GJ, Voyadzis JM, McRae DA, Lunsden M, Dieterich S, et al. CyberKnife stereotactic radiosurgical treatment of spinal tumors for pain control and quality of life. J Neurosurg Spine. 2005;2:540–9.View ArticlePubMedGoogle Scholar
- Ryu S, Jin R, Jin JY, Chen Q, Rock J, Anderson J, et al. Pain control by image-guided radiosurgery for solitary spinal metastasis. J Pain Symptom Manage. 2008;35:292–8.View ArticlePubMedGoogle Scholar
- Sahgal A, Larson DA, Chang EL. Stereotactic body radiosurgery for spinal metastases: a critical review. Int J Radiat Oncol, Biol, Phys. 2008;71:652–65.View ArticleGoogle Scholar
- Ryu SPG, Gerzten P, Fang-Fang Y, Timmerman RD, Dicker A, Movsas B, et al. RTOG 0631 Protocol Information. In Ryu S (ed) RTOG 0631 Protocol Information. NRG Oncology 2011. https://www.rtog.org/clinicaltrials/protocoltable/studydetails.aspx?action=openFile&FileID=12804.
- Shaw E, Kline R, Gillin M, Souhami L, Hirschfeld A, Dinapoli R, et al. Radiation Therapy Oncology Group: radiosurgery quality assurance guidelines. Int J Radiat Oncol, Biol, Phys. 1993;27:1231–9.View ArticleGoogle Scholar
- Zorlu F, Dugel G, Ozyigit G, Hurmuz P, Cengiz M, Yildiz F, et al. Determination of gonad doses during robotic stereotactic radiosurgery for various tumor sites. Med Phys. 2013;40:041703.View ArticlePubMedGoogle Scholar
- Kutcher GJ, Coia L, Gillin M, Hanson WF, Leibel S, Morton RJ, et al. Comprehensive QA for radiation oncology: report of AAPM Radiation Therapy Committee Task Group 40. Med Phys. 1994;21:581–618.View ArticlePubMedGoogle Scholar
- Loblaw DA, Laperriere NJ. Emergency treatment of malignant extradural spinal cord compression: an evidence-based guideline. J Clin Oncol. 1998;16(4):1613–24.PubMedGoogle Scholar
- Okunieff P MTM, Porter AT, and David M. Metastatic Disease: Bone, Spinal Cord, Brain, Liver, and Lung. In Gunderson LL, Tepper, J. E. (ed) Clinical Radiation Oncology, Third Edition. Philadelphia: Elsevier Saunders; 2012;421-438.Google Scholar
- Siegal T, Siegal T. Current considerations in the management of neoplastic spinal cord compression. Spine (Phila Pa 1976). 1989;14:223–8.View ArticleGoogle Scholar
- Patchell RA, Tibbs PA, Regine WF, Payne R, Saris S, Kryscio RJ, et al. Direct decompressive surgical resection in the treatment of spinal cord compression caused by metastatic cancer: a randomised trial. Lancet. 2005;366:643–8.View ArticlePubMedGoogle Scholar
- Ghogawala Z, Mansfield FL, Borges LF. Spinal radiation before surgical decompression adversely affects outcomes of surgery for symptomatic metastatic spinal cord compression. Spine (Phila Pa 1976). 2001;26:818–24.View ArticleGoogle Scholar
- Reft C, Alecu R, Das IJ, Gerbi BJ, Keall P, Lief E, et al. Dosimetric considerations for patients with HIP prostheses undergoing pelvic irradiation. Report of the AAPM Radiation Therapy Committee Task Group 63. Med Phys. 2003;30:1162–82.View ArticlePubMedGoogle Scholar
- Bahreyni Toossi MT, Behmadi M, Ghorbani M, Gholamhosseinian H. A Monte Carlo study on electron and neutron contamination caused by the presence of hip prosthesis in photon mode of a 15 MV Siemens PRIMUS linac. J Appl Clin Med Phys. 2013;14(5):52–67.PubMedGoogle Scholar
- Schneider U, Fiechtner A, Besserer J, Lomax A. Neutron dose from prostheses material during radiotherapy with protons and photons. Phys Med Biol. 2004;49(9):N119–24.View ArticlePubMedGoogle Scholar
- Nielsen MS, Carl J, Nielsen J. A phantom study of dose compensation behind hip prosthesis using portal dosimetry and dynamic MLC. Radiother Oncol. 2008;88:277–84.View ArticlePubMedGoogle Scholar
- Wang X, Yang JN, Li X, Tailor R, Vassilliev O, Brown P, et al. Effect of spine hardware on small spinal stereotactic radiosurgery dosimetry. Phys Med Biol. 2013;58:6733–47.View ArticlePubMedGoogle Scholar
- Liebross RH, Starkschall G, Wong PF, Horton J, Gokaslan ZL, Komaki R. The effect of titanium stabilization rods on spinal cord radiation dose. Med Dosim. 2002;27:21–4.View ArticlePubMedGoogle Scholar
- Son SH, Kang YN, Ryu MR. The effect of metallic implants on radiation therapy in spinal tumor patients with metallic spinal implants. Med Dosim. 2012;37:98–107.View ArticlePubMedGoogle Scholar
- Pekmezci M, Dirican B, Yapici B, Yazici M, Alanay A, Gürdalli S. Spinal implants and radiation therapy: the effect of various configurations of titanium implant systems in a single-level vertebral metastasis model. J Bone Joint Surg Am. 2006;88:1093–100.View ArticlePubMedGoogle Scholar
- Maerz M, Koelbl O, Dobler B. Influence of metallic dental implants and metal artefacts on dose calculation accuracy. Strahlenther Onkol. 2015;191:234–41.View ArticlePubMedGoogle Scholar