Skip to main content

Advertisement

Log in

Extracranial radiosurgery—applications in the management of benign intradural spinal neoplasms

  • Review
  • Published:
Neurosurgical Review Aims and scope Submit manuscript

Abstract

Stereotactic radiosurgery has enabled the delivery of higher doses of radiation and decreased fractionation due to improved accuracy. Spinal radiosurgery has been increasingly utilized for the management of metastatic extradural spinal disease. However, surgical resection remains the primary treatment strategy for intradural spinal tumors. Preliminary evidence suggests that radiosurgical ablation with stereotactic radiation for intradural spinal lesions may be efficacious in certain clinical scenarios. Local tumor control, pain relief, and improvement in neurologic function with minimal morbidity have been reported in short-term follow-up. However, long-term efficacy of radiosurgery in the management of intradural spinal neoplasms necessitates further validation. As extracranial radiosurgery is a newly evolving modality, a continuative review of the current literature is appropriate. Until a standardized therapeutic window of safety and efficacy can be determined, the recommendation of radiosurgical applications for benign spinal tumors should be reserved for carefully selected cases.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Lo SS, Chang EL, Yamada Y, Sloan AE et al (2007) Stereotactic radiosurgery and radiation therapy for spinal tumors. Expert Rev Neurother 7(1):85–93

    Article  PubMed  Google Scholar 

  2. Takacs I, Hamilton AJ (1999) Extracranial stereotactic radiosurgery. Applications for the spine and beyond. Neurosurg Clin N Am 10(2):257–270

    PubMed  CAS  Google Scholar 

  3. Niranjan A, Maitz AH, Lunsford A, Gerszten PC et al (2007) Radiosurgery techniques and current devices. Prog Neurol Surg 20:50–76

    Article  PubMed  Google Scholar 

  4. Dodd RL, Ryu M, Kamnerdsupaphon P, Gibbs IC et al (2006) Cyberknife radiosurgery for benign intradural extramedullary spinal tumors. Neurosurgery 58(4):674–685

    Article  PubMed  Google Scholar 

  5. Rock JP, Ryu S, Yin FF, Schreiber F et al (2004) The evolving role of stereotactic radiosurgery and stereotactic radiation therapy for patients with spine tumors. J Neuro-Oncol 69:319–334

    Article  Google Scholar 

  6. Yamada Y, Lovelock DM, Bilsky MH (2007) A review of image-guided intensity-modulated radiotherapy for spinal tumors. Neurosurgery 61(2):226–235

    Article  PubMed  Google Scholar 

  7. Gerszten PC, Ozhasoglu C, Burton SA, Vogel WJ et al (2004) CyberKnife frameless stereotactic radiosurgery for spinal lesions: clinical experience in 125 cases. Neurosurgery 55(1):89–99

    PubMed  Google Scholar 

  8. Ryu SI, Chang SD, Kim DH, Murphy MJ et al (2001) Image-guided hypo-fractionated stereotactic radiosurgery to spinal lesions. Neurosurgery 49:838–846

    Article  PubMed  CAS  Google Scholar 

  9. Chang SD, Main W, Martin DP et al (2003) An analysis of the accuracy of the CyberKnife: a robotic frameless stereotactic radiosurgical system. Neurosurgery 52:140–147

    Article  PubMed  Google Scholar 

  10. Hamilton AJ, Lulu BA, Fosmire H, Gossett L (1996) LINAC-based spinal stereotactic radiosurgery. Stereotact Funct Neurosurg 66:1–9

    Article  PubMed  CAS  Google Scholar 

  11. Ho AK, Fu D, Cotrutz C, Hancock SL et al (2007) A study of the accuracy of cyberknife spinal radiosurgery using skeletal structure tracking. Neurosurgery 1(60):147–156

    Google Scholar 

  12. Lovelock DM, Hua C, Wang P, Hunt M et al (2005) Accurate setup of paraspinal patients using a noninvasive patient immobilization cradle and portal imaging. Med Phys 32:2606–2614

    Article  PubMed  Google Scholar 

  13. Benzil DL, Saboori M, Mogilner AY, Rocchio R et al (2004) Safety and efficacy of stereotactic radiosurgery for tumors of the spine. J Neurosurg 101(Suppl 3):413–418

    PubMed  Google Scholar 

  14. Degen JW, Gagnon GJ, Voyadzis JM, McRae DA et al (2005) CyberKnife stereotactic radiosurgical treatment of spinal tumors for pain control and quality of life. J Neurosurg: Spine 2:540–549

    Google Scholar 

  15. Gerszten PC, Burton SA, Ozhasoglu C (2007) CyberKnife radiosurgery for spinal neoplasms. Prog Neurol Surg 20:340–358

    Article  PubMed  Google Scholar 

  16. Ryu S, Jin JY, Jin R, Rock J et al (2007) Partial volume tolerance of the spinal cord and complications of single-dose radiosurgery. Cancer 109(3):628–636

    Article  PubMed  Google Scholar 

  17. Ryu S, Rock J, Rosenblum M, Kim JH (2004) Patterns of failure after single-dose radiosurgery for spinal metastasis. J Neurosurg 101(Suppl 3):402–405

    PubMed  Google Scholar 

  18. Gerszten PC, Ozhasoglu C, Burton SA, Vogel WJ et al (2003) CyberKnife frameless single-fraction stereotactic radiosurgery for benign tumors of the spine. Neurosurg Focus 14(5):1–5

    Article  Google Scholar 

  19. Yin FF, Ryu S, Ajlouni M, Yan H et al (2004) Image-guided procedures for intensity-modulated spinal radiosurgery. J Neurosurg 101(3):419–424

    PubMed  Google Scholar 

  20. Kim B, Soisson ET, Duma C, Chen P, Hafer R et al (2008) Image-guided helical tomotherapy for treatment of spine tumors. Clin Neurol Neurosurg 110:357–362

    Article  PubMed  Google Scholar 

  21. Yin FF, Ryu S, Ajiouni M, Zhu J et al (2002) A technique of intensity-modulated radiosurgery (IMRS) for spinal tumors. Med Phys 29(12):2815–2822

    Article  PubMed  Google Scholar 

  22. Teh BS, Paulino AC, Lu HH, Chiu JK et al (2007) Versatility of the Novalis system to deliver image-guided stereotactic body radiation therapy (SBRT) for various anatomical sites. Technol Cancer Res Treat 6(4):347–354

    PubMed  Google Scholar 

  23. Bhatnagar AK, Gerszten PC, Ozhasaglu C, Vogel WJ et al (2005) CyberKnife frameless radiosurgery for the treatment of extracranial benign tumors. Technol Cancer Res Treat 4(5):571–576

    PubMed  Google Scholar 

  24. Gerszten PC, Ozhasoglu C, Burton SA, Vogel W et al (2003) Evaluation of CyberKnife frameless real-time image-guided stereotactic radiosurgery for spinal lesions. Stereotact Funct Neurosurg 81:84–89

    Article  PubMed  Google Scholar 

  25. Murphy MJ, Chang SD, Gibbs IC, Le QT et al (2003) Patterns of patient movement during frameless image-guided radiosurgery. Int J Radiat Oncol Biol Phys 55(5):1400–1408

    PubMed  Google Scholar 

  26. Gerszten PC (2007) The role of minimally invasive techniques in the management of spine tumors: percutaneous bone cement augmentation, radiosurgery, and micro-endoscopic approaches. Orthop Clin North Am 38:441–450

    Article  PubMed  Google Scholar 

  27. Muacevic A, Staehler M, Drexler C, Wowra B et al (2006) Technical description, phantom accuracy, and clinical feasibility for fiducial-free frameless real-time image-guided spinal radiosurgery. J Neurosurg Spine 5:303–312

    Article  PubMed  Google Scholar 

  28. Adler JR, Chang SD, Murphy MJ, Doty J et al (1997) The CyberKnife: a frameless robotic system for radiosurgery. Stereotact Funct Neurosurg 69:124–128

    Article  PubMed  Google Scholar 

  29. Welch WC, Gerszten PC (2005) Accuracy cyberknife image-guided radiosurgical system. Expert Rev Med Devices 2(2):141–147

    Article  PubMed  Google Scholar 

  30. Shrieve DC, Klish M, Wendland MM, Watson GA (2004) Basic principles of radiobiology, radiotherapy, and radiosurgery. Neurosurg Clin N Am 15:467–479

    Article  PubMed  Google Scholar 

  31. Leber KA, Bergloff J, Pendl G (1998) Dose-response tolerance of the visual pathways and cranial nerves of the cavernous sinus to stereotactic radiosurgery. J Neurosurg 88:43–50

    Article  PubMed  CAS  Google Scholar 

  32. Schultheiss TE, Kun LE, Ang KK et al (1995) Radiation response of the central nervous system. Int J Radiat Oncol Biol Phys 31:1093–1112

    PubMed  CAS  Google Scholar 

  33. Ryu S, Yin FF, Rock J et al (2003) Image-guided intensity-modulated radiosurgery for spinal metastasis. Cancer 97:2013–2018

    Article  PubMed  Google Scholar 

  34. Merchant TE, Boop FA, Kun LE, Sanford RA (2008) A retrospective study of surgery and reirradiation for recurrent ependymoma. Int J Radiat Oncol Biol Phys 71(1):87–97

    PubMed  Google Scholar 

  35. Gerszten PC, Burton SA, Ozhasoglu C, Welch WC (2007) Radiosurgery for spinal metastases. Spine 32(2):193–199

    Article  PubMed  Google Scholar 

  36. Solero CL, Fornari M, Giombini S, Lasio G et al (1989) Spinal meningiomas: review of 174 operated cases. Neurosurgery 25(2):153–160

    Article  PubMed  CAS  Google Scholar 

  37. Roux FX, Nataf F, Pinaudeau M, Borne G et al (1996) Intraspinal meningiomas: review of 54 cases with discussion of poor prognosis factors and modern therapeutic management. Surg Neurol 46:458–464

    Article  PubMed  CAS  Google Scholar 

  38. Schick U, Marquardt G, Lorenz R (2001) Recurrence of benign spinal neoplasms. Neurosurg Rev 24:20–25

    Article  PubMed  CAS  Google Scholar 

  39. Hamilton AJ, Lulu BA, Fosmire H, Baldassarre S et al (1995) Preliminary clinical experience with linear accelerator-based spinal stereotactic radiosurgery. Neurosurgery 36(2):311–319

    Article  PubMed  CAS  Google Scholar 

  40. Gerszten PC, Burton SA, Ozhasoglu C, McCue KJ et al (2008) Radiosurgery for benign intradural spinal tumors. Neurosurgery 62(4):887–896

    Article  PubMed  Google Scholar 

  41. Sahgal A, Dhou D, Ames C, Ma L et al (2007) Image-guided robotic stereotactic body radiotherapy for benign spinal tumors: the University of California San Francisco preliminary experience. Technol Cancer Res Treat 6(6):595–603

    PubMed  CAS  Google Scholar 

  42. Gerszten PC, Burton SA (2008) Clinical assessment of stereotactic IGRT: spinal radiosurgery. Med Dosim 33(2):107–116

    Article  PubMed  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to James S. Harrop.

Additional information

Comments

Stephanie E. Combs, Jürgen Debus, Heidelberg, Germany

Saraceni and colleagues report on the use of extracranial radiosurgery for the treatment of benign intradural spinal neoplasms. The authors summarize the different technical approaches possible for radiosurgery, including the Cyberknife® Robotic Technique and stereotactic radiosurgery using a linear accelerator (LINAC).

The authors summarize and discuss the clinical results on radiosurgery of benign spinal tumors and conclude that radiosurgery can be applied safely in patients with benign spinal neoplasms not amenable to a complete surgical resection. However, timely surgical resection should be performed as the first treatment of choice in cases with tumors leading to extensive spinal cord compression, if mechanical destabilization is present or for highly radioresistant tumors. We would like to congratulate the authors on this nice work that reports not only high tumor control rates, but also discusses the risk attributed to high-dose single fraction radiosurgery with respect to radiation tolerance of the adjacent normal tissue, i.e., mainly the spinal chord.

When treating patients with benign spinal tumors, this risk for treatment toxicity must be considered diligently, keeping in mind the unimpaired life expectancy of the patients with non-malignant diseases. Most data on radiosurgery treatment have been gathered from patients with fast growing, malignant tumors. However, long-term radiation injury, especially high-grade toxicity, might develop not within months after treatment, but over years of follow-up.

The most important factors associated with long-term sequelae, which in the case of spinal tumors is mainly radiation-induced myelopathy, include the total dose applied, fraction size, the length of the treatment volume or the spinal volume receiving radiation dose, as well as the duration of treatment. The tolerance dose of the spinal chord to conventional fractionated external beam radiation therapy lies somewhere between 45 and 50 Gy delivered in conventional fractionation of 1.8 to 2 Gy (1–3). However, most volumes treated included much larger volumes than exposed in most cases of radiosurgery or in fractionated stereotactic radiotherapy (FSRT). Therefore, concluding from the published literature, a risk of 5% for myelopathy can be estimated after 57 to 61 Gy applied in fractions of 2 Gy.

Until now, the threshold for spinal cord toxicity after single-dose treatment of spinal tumors has not been determined; however, the existing literature has shown distinct differences between radiation sensitivity of different regions of the spinal cord. Moreover, preceding surgical interventions may also sensitize the spinal cord to subsequent radiation (3).

Therefore, the treatment volume must influence the indication for spinal radiosurgery, since the risk for side effects certainly increases with growing treatment volumes.

Optimal delineation of the target volume, including modern imaging modalities such as advanced MR imaging or PET scanning using tumor-specific markers can help delineate the optimal target volume. Additionally, it must be kept in mind that potential microscopic spread should be considered when defining target volumes, and that the goal of applying high-dose techniques to spinal tumors with low morbidity should not counteract optimal oncological treatment.

Additionally, precise patient positioning and pre-treatment verification are essential when applying millimeter-precise treatment plans. Therefore, optimal and precise target definition and image-guided treatment inevitably complement each other.

Modern radiosurgery techniques are an essential part of the present-day radiation oncology arsenal and can be used as a safe and effective treatment alternative for a subgroup of patients. Alternative treatment opportunities, however, such as modern fractionated regimens should be considered when making management decisions. Alternative beam qualities, such as particle therapy, when available should also be taken into account due to the distinct physical characteristics potentially improving dose distribution, especially with respect to the integral dose to normal tissue. For radioresistant spinal tumors, such as chordomas and chondrosarcomas, high-LET particles, such as carbon ions, might also be beneficial due to their characteristic biological effects.

In conclusion, during the task of treating spinal tumors independently of histology, we are faced with dose- and treatment-limiting factors, and sophisticated techniques such as radiosurgery can help to overcome some of the limitations when applied cautiously to selected patients.

(1) Rampling R, Symonds P (1998) Radiation myelopathy. Curr Opin Neurol 11:627–632

(2) Marcus RB Jr, Million R (1990) The incidence of myelitis after irradiation of the cervical spinal cord. Int J Radiat Oncol Biol Phys 19:3–8

(3) Debus J, Hug EB, Liebsch NJ, O'Farrel D, Finkelstein D, Efird J, Munzenrider JE (1999) Dose-volume tolerance of the brainstem after high-dose radiotherapy. Front Radiat Ther Oncol 33:305–314

Comments

Ralf A. Schneider, Villigen, Switzerland

In the present issue, C. Saraceni, J. B. Ashman, and J. S. Harrop review equipment, techniques, and published clinical outcomes on extracranial, spinal radiosurgery of benign intradural neoplasms. This is an excellent manuscript, showing the currently available radiosurgery and stereotactic body radiotherapy (SBRT) equipment, as well as discussing the available update and literature on the subject.

Except for some missing photographs demonstrating dose distributions of the compared radiosurgical techniques, e.g., for a typical intradural spinal tumor, C. Saraceni, J. B. Ashman, and J. S. Harrop describe in detail the different radiosurgical techniques and their results.

The authors report on improvements in tumor control as well as long-term side effects after innovative non-invasive radiosurgical techniques compared to conventional photon irradiation. Indications for surgery and/or radiosurgery of benign intradural spinal neoplasms are very well explained by the authors. Especially, the discussion about dose constraints of organs at risks doing radiosurgery demonstrates impressively the difficulties in defining adequate dose limits to lower serious long-term toxicity.

The present issue shows impressively the technological progress in radiosurgery in the past 10–15 years. Today, radiosurgery is an excellent treatment option in the management of benign intradural spinal neoplasms. The availability and the frequency of radiosurgical treatments will be enhanced by the more precise and efficient application in the future.

Even with the best photon treatment technique, the ultimate goal of any high-dose radiotherapy is complete target coverage with minimum dose to critical organs at risk. Limitation of photon-based spinal radiosurgery is the physical characteristic of dose falloff from high to low isodoses. The higher the dose to the tumor, e.g., for atypical and anaplastic meningiomas, the more problematic could be the dose to organs at risk. Especially in younger patients with a long expectancy of life even low-dose areas in the thorax or abdomen may cause serious long-term side effects as for example second malignancies. This requires long periods of follow-up outcomes for those patients.

Worldwide, a significant number of modern proton radiation therapy units are under construction or already fully operational. Maybe particle therapy will improve further on toxicities because of a decreased integral dose surrounding the target volumes. It will be interesting to study the long-term results after proton irradiation in comparison to modern radiosurgical photon therapy in the next few decades. Depending on the developments of costs of particle therapy in the future, it might replace photon therapy because of the possibility to lower the irradiated volume significantly without compromising the target volume.

In summary, today, photon-based radiosurgery represents a tremendous technological advancement and has created promising opportunities in addition or in place of neurosurgical intervention. The present issue may help surgeons and radiation oncologists to decide in daily practice whether a patient may profit from radiosurgery or not.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Saraceni, C., Ashman, J.B. & Harrop, J.S. Extracranial radiosurgery—applications in the management of benign intradural spinal neoplasms. Neurosurg Rev 32, 133–141 (2009). https://doi.org/10.1007/s10143-008-0183-z

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10143-008-0183-z

Keywords

Navigation