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C H A P T E R 4 8     oracic Spinal Stenosis
315
Prognosis after surgery depends on the extent of compression and neuro­logical deficit. Recurrent stenosis has been documented, making routine follow-up necessary.
20
For thoracic stenosis due to OPLL, multiple treatment options have been described, including laminectomy, laminoplasty, resection of the PLL, anterior decompression and fusion via thoracotomy, and posterior decom­pression and fusion. ported by a recent long-term study.
21,22
Anterior decompression with fusion has been sup-
23
Fujimura et al reviewed the data of 33 patients followed for more than 5 years after anterior decompression and fusion was performed for myelopathy in the thoracic spine due to ossifica­tion of the PLL. Their results suggested that anterior decompression with fusion can lead to favorable long-term results. They indicated, however, that patients with OPLL that affects multiple levels and those with concurrent OLF may not do as well in long-term follow-up.
Posterior surgical approaches provide an alternative treatment option for myelopathy due to OPLL, particularly when there is also OLF. It is sug­gested that, for OPLL, posterior decompression alone may not be sufficient due to draping of the spinal cord over the kyphotic thoracic spine. Some advocate a circumferential decompression through an isolated posterior approach.
24
High complication rates have been documented with this treat­ment, however, particularly when more than five levels are decompressed. In a study by Masahiko et al, as many as 33% of patients had deterioration in their neurological status following surgery. Both the relatively avascular nature of the thoracic spinal cord and adhesion of dural sac to the PLL are thought to contribute to these complications. Even higher rates of neurolog­ical deterioration have been seen with laminectomy alone, while lower rates have been reported with posterior decompression and fusion.
25
In theory, performing a laminectomy without fusion further destabilizes the spine and subjects the injured spinal cord to additional stresses that lead to a further decline in neurological function. Masashi et al suggested that in the neu­rologically intact patient, resection of the PLL is an acceptable treatment, but for patients with preoperative spinal cord injury, removal of the PLL increases the risk of paralysis.
26
Many patients with thoracic disc herniations are asymptomatic. When symptoms do exist, unlike patients with OPLL and OLF, conservative treat­ment and time can be sufficient to treat the majority of herniations. Modi­fication of activities, physical therapy, and the careful use of nonsteroidal antiinflammatory drugs are the mainstays of conservative care. The litera­ture suggests that less than 2% of thoracic discs require surgical treatment.
27
When conservative care fails to alleviate symptoms after 4 to 6 weeks, a neu­rological deficit progresses, or there is evidence of worsening myelopathy, surgical treatment is warranted.
Operative care of patients with thoracic disc herniations requires assess­ing several factors to determine operative risk and approach. Depending on the location and nature of the disc herniation, anterior, thoracoscopic, lateral, or posterior approaches may be used, the details of which are largely beyond the scope of this chapter. In general, anteriorlyoriented lesions require a direct ventral approach such as a transthoracic, thoracoscopic, or posterolateral (e.g., costotransversectomy, extracavitary) technique for safe resection that avoids cord manipulation, with bony reconstruction as necessary. Pulmonary function tests should be performed on patients with questionable pulmonary reserve if thoracotomy is considered. Discal calcifications, which are more common in the thoracic spine,
28
are associ­ated with a greater degree of dural adhesion or associated dural calcifica­tion. Such information is important for the treating surgeon in deciding how much disc to remove from the dura, and whether concomitant dural resection needs to be considered. Once in the operating room, it is essen­tial to identify the correct disc for resection. Sagittal CT reconstructions or MR images are essential to determine the appropriate level, and plain radiography or fluoroscopy in the operating room is standard practice for localization.
For most lateral soft disc herniations, the preferred approach is pos­terior and usually involves a pediculofacetectomy, typically perfomed by transpedicular or transfacet technique rather than laminectomy. Signifi­cant complications have been reported with posterior laminectomy alone,
29
including cord contusion and lack of improvement of symptoms. The need for fusion following thoracic disc removal remains controversial but generally depends on the assessed degree of stability of the region follow­ing decompression. It may be beneficial to resect a significant amount of
vertebral body in cases of multilevel disc disease, or when the disc is in the lower thoracic spine, which may render the spine unstable and require secondary fusion.

OTHER CAUSES FOR THORACIC SPINAL STENOSIS

Neoplasms
Both intramedullary and extramedullary spinal cord tumors can lead to thoracic myelopathy and must be considered as a possible etiology in every older patient with thoracic spinal stenosis. In their experience treating 78 patients with intramedullary spinal cord tumors, Sandalcioglu et al found that 32% of the tumors were located in the thoracic spine. Low-grade neu­roepithelial tumors, ependymomas, astrocytomas, vascular tumors, and metastatic lesions were identified. The most important predictor of post­operative neurological status was a patient’s preoperative neurological func-
30
tion.
Compared to patients with intramedullary tumors in the cervical or lumbar spine, these authors found that those with thoracic lesions had a higher surgical morbidity. This most likely reflects the regional vulner­ability of the thoracic cord due to tenuous blood supply, constricted canal anatomy, and kyphosis. When intramedullary spinal cord tumors are identi­fied, decompression and tumor removal can be performed by laminectomy or laminoplasty.
Metastatic disease to the thoracic spine is more common than metasta­sis to the cervical or lumbar spine, due to the greater relative size and bony blood supply of the thoracic region. Lesions from lung, breast, prostate, and gastrointestinal carcinomas, as well as other tumor types, are known to metastasize to the thoracic spine. Until recently, many authors could not define the best mode of treatment for extramedullary spinal cord tumors with cord compression causing neurological symptoms. Earlier studies looking at laminectomy alone or laminectomy in combination with radio­therapy did not show surgery to be beneficial.
31-33
The importance of surgi­cal decompression, however, was shown in a randomized multicenter trial by Patchell et al, who compared the outcomes of 101 patients treated with either radiotherapy alone or a combination of radiotherapy and decom­pressive surgery.
34
All but 13 of the patients had tumors in the thoracic spine. The median age of their study group was 60. The authors found that patients treated with a combination of postoperative radiotherapy and decompressive surgery were significantly better in terms of ambulatory sta­tus, functionality, maintenance of urinary continence, strength, and overall survival than those treated with radiation alone. Their data also suggested that laminectomy may not always be the best mode of treatment. Rather, approaching the lesion directly: anterior tumors anteriorly, posterior tumors posteriorly, and lateral tumors laterally may offer the best results for decom­pression (see Figure 48-6).
Synovial Cysts
Rare cases of synovial cysts leading to thoracic myelopathy have been reported. Graham et al outlined a case in which a 54-year-old woman developed right lower extremity weakness secondary to a cyst at T11-12.35 The cyst was successfully excised via a laminectomy and the patient had a full recovery. Aspiration has been used as a treatment for synovial cysts in the lumbar spine and might prove to be a useful treatment option in the thoracic spine.

PROGNOSIS

An understanding of the long-term results of surgical treatment of thoracic spinal stenosis due to OLF is limited due to the lack of sufficient study. The literature suggests that a number of factors may make surgical outcomes less favorable. These include a longer duration of symptoms prior to decom-
36
pression, of stenosis. between preoperative symptom duration and results of surgery, although only 24 patients were evaluated. of symptoms, the data are also not clear on how preoperative neurological status affects surgical outcome. A meta-analysis by J. Anamasu et al suggests that the larger, more recent studies indicate a positive association between
the presence of a proximal stenotic lesion,37 and a greater degree
38
Another study looking at OLF did not show an association
39
As with the importance of the duration
316
P A R T V I Other Surgical Treatment Modalities: Thoracic Spine
preoperative neurological function and surgical outcomes.40 Other studies have highlighted some of the long-term complications of thoracic decom­pressive surgery, including the development of late kyphotic deformities and spondylosis.
41,42
Treatment of thoracic stenosis due to disc herniation has poorer out­comes for those patients with advanced age, extended preoperative duration of the condition, and greater degrees of myelopathy. Studies of patients with nonligamentous causes of thoracic stenosis have questioned the long-term prognosis following surgical decompression. Palumbo et al reviewed 12 patients with thoracic stenosis.
43
In 11 of the patients, stenosis was due to spondylosis. Their results showed that 5 of 12 patients had initial improve­ment that later declined. They suggested that deterioration was due to development of delayed stenosis, instability, or deformity.

CONCLUSIONS

Although thoracic spinal stenosis is a relatively rare condition as compared
to stenosis of the cervical or lumbar spine, the treating physician must con­sider it in the differential diagnosis of the older patient with thoracic back pain or symptoms or signs of myelopathy. This awareness may prevent delay in the diagnosis of this condition due to its similarity to the presentation of lumbar stenosis. Most patients with a discogenic etiology for their pain can be treated conservatively. Both CT and MRI aid in defining the pathol­ogy and determining the most appropriate treatment. CT myelography should be avoided when possible in patients with OLF, as it can exacerbate myelopathy. When surgery is indicated, the approach should be dictated by the location of the disc. Patients with OLF or posterior longitudinal ligament or neoplasm will most likely require both surgical decompression and fusion.
Circumferential decompression carries a high risk of neurological dete­rioration. Patients with neurological complications due to metastatic lesions in the thoracic spine benefit from surgical decompression in addition to radiation. Larger, longer-term studies need to be performed to better define the importance of preoperative duration of symptoms, neurological status, and mode of decompression to overall prognosis. This task is made difficult by the relative rarity of thoracic spinal stenosis.

References

1. R. Van Oostenbrugge, Spinal cord compression caused by unusual location and extension
of ossified ligamenta flava in a Caucasian male: a case report and literature review, Spine 24
(1999) 486–488.
2. J. Kruse, Ossification of the ligamentum flavum as a cause of myelopathy in North America:
report of three cases, J. Spinal Disord. 13 (1) (2009) 22-25.
3. T. Shiraishi, Thoracic myelopathy due to isolated ossification of the ligamentum flavum,
J. Bone Joint Surg. Br. 77 (1995) 131–133.
4. T. Aizawa: Thoracic myelopathy in Japan: epidemiological retrospective study in Miyagi pre-
fecture during 15 years, Tohoku J Exp Med., 210 (3) (2006) 199-208.
5. P.S.P. Ho, Ligamentum flavum: appearance on sagittal and coronal MR images, Radiology
168 (1988) 469–472.
6. M. Payer, Thoracic myelopathy due to enlarged ossified yellow ligaments, J. Neurosurg. Spine
92 (1) (2000) 105-108.
7. N.E. Epstein, Ossification of the yellow ligament and spondylosis and/or ossification of the
posterior longitudinal ligament of the thoracic and lumbar spine, J. Spinal Disord. 12 (1999)
250–256.
8. C.L. Vera, Paraplegia due to ossification of the ligamenta flava in x-linked hypophosphate-
mia: a case report, Spine 22 (1997) 710–715.
9. D. Resnick, Calcification and ossification of the posterior spinal ligaments and tissues, in:
D. Resnick, D. Niwayama (Eds.), Diagnosis of bone and joint disorders, ed 2, WB Saunders,
Philadelphia, 1988.
10. K. Yonenobu et al: Thoracic myelopathy secondary to ossification of the spinal ligament,
J. Neurosurg. 66 (1987) 511-518.
11. T. Aizawa, Thoracic myelopathy in Japan: epidemiological retrospective study in Miyagi pre­fecture during 15 years.
12. M. A. Rogers, Surgical treatment of the symptomatic herniated thoracic disc, Clin. Orthop. 300 (1994) 70–78.
13. K.B. Wood, Magnetic resonance imaging of the thoracic spine: evaluation of asymptomatic individuals, J. Bone Joint Surg. Am. 77 (1995) 1631–1638.
14. K.B. Wood, The natural history of asymptomatic thoracic disc herniations, Spine 22 (1997) 525–530.
15. M. Takahata, Clinical results and complications of circumferential spinal cord decompres­sion through a single posterior approach for thoracic myelopathy caused by ossification of posterior longitudinal ligament, Spine 33 (11 ) (2008) 1199–1208.
16. Xiong, et al., CT and MRI characteristics of ossification of the ligamenta flava in the thoracic spine, Eur. Radiol. 11 (2001) 1798–1802.
17. M. A. Rogers, Surgical treatment of the symptomatic herniated thoracic disc, Clin. Orthop. 300 (1994) 70–78.
18. Xiong, et al., CT and MRI characteristics of ossification of the ligamenta flava in the thoracic spine, Eur. Radiol. 11 (2001) 1798–1802.
19. O.S. Okadak, Thoracic myelopathy caused by ossification of the ligamentum flavum: clinico­pathologic study and surgical treatment, Spine 16 (1991) 280–287.
20. K. Yonenobu, Thoracic myelopathy secondary to ossification of the spinal ligament, J. Neurosurg. 66 (1987) 511–518.
21. Y. Fujimura, Long-term follow-up study of anterior decompression and fusion for thoracic myelopathy resulting from ossification of the posterior longitudinal ligament, Spine 22 (3) (1997) 305–311.
22. M. Yamazaki, Clinical results of surgery for thoracic myelopathy caused by ossification of the posterior longitudinal ligament: operative indication of posterior decompression with instrumented fusion, Spine 31 (13) (2006) 1452–1460.
23. M. Takahata, Clinical results and complications of circumfrential spinal cord decompression through a single posterior approach for thoracic myelopathy caused by ossification of poste­rior longitudinal ligament, Spine 33 (11): 1199–1208
24. M. Yamazaki, Clinical results of surgery for thoracic myelopathy caused by ossification of the posterior longitudinal ligament: operative indication of posterior decompression with instrumented fusion, Spine 31 (13) (2006) 1452–1460.
25. Masashi, Clinical results of surgery for thoracic myelopathy caused by ossification of the posterior longitudinal ligament, operative indication of posterior decompression with instru­mented fusion, Spine 31 (13) (2006) 1452–1460.
26. C.B. Stillman, Management of thoracic disc disease, Clin. Neurosurg. 38 (1992) 325–352.
27. P. Severi, Multiple calcified thoracic disc herniations: a case report, Spine 17 (4) (1992) 449–451.
28. C.A. Arce, Thoracic disc herniation: improved diagnosis with computed tomographic scan­ning and a review of the literature, Surg. Neurol. 23 (1985) 356–361.
29. I.E. Sandalcioglu, T. Gasser, S. Asgari, Functional outcome after surgical treatment of intra­medullary spinal cord tumors. Experience with 78 patients. Spinal Cord 43 (2005) 34-41.
30. P.S. Sorensen, Metastatic epidural spinal cord compression: results of treatment and survival, Cancer 65 (1990) 1502–1508.
31. R .F. Young, Treatment of spinal epidural metastases: randomized prospective comparison of laminectomy and radiotherapy, J. Neurosurg. 53 (1980) 741–748.
32. G.F.G. Findley, Adverse effects of the management of malignant spinal cord compression, J. Neurol. Neurosurg. Psych. 47 (1984) 761–768.
33. R .A. Patchell, Direct decompressive surgical resection in the treatment of spinal cord com­pression caused by metastatic cancer: a randomized trial, Lancet 366 (2005) 643–648.
34. E. Graham, Myelopathy induced by a thoracic intraspinal synovial cyst: case report and review of the literature, Spine 26(17): E392–394.
35. N. Miyakoshi, Factors related to long-term outcome after decompressive surgery for ossifica­tion of the ligamentum flavum of the thoracic spine, J. Neurosurg. Spine 99 (2003) 251–256.
36. C.J. Chen, Intramedullary high signal intensity on T2-weighted MR images in cervical spondylitic myelopathy: prediction of prognosis with type of intensity, Radiology 221 (2001) 789–794.
37. K. Shiokawa, Clinical analysis and prognostic study of ossified ligamentum flavum of the thoracic spine, J. Neurosurg. Spine 94 (2001) 221–226.
38. L. Cheng-Chin, Surgical experience with symptomatic thoracic ossification of the ligamen­tum flavum, J. Neurosurg. Spine 2 (2005) 34–39.
39. J. Inamasu, A review of factors predictive of surgical outcome for ossification of the ligamen­tum flavum of the thoracic spine, J. Neurosurg. Spine 5 (2006) 133–139.
40. L. Cheng-Chin, Surgical experience with symptomatic thoracic ossification of the ligamen­tum flavum, J. Neurosurg. Spine 2 (2005) 34–39.
41. M. A. Palumbo, Surgical treatment of thoracic spinal stenosis: a 2- to 9- year follow-up. Spine 26 (5) (2001) 558–566.
42. M. A. Palumbo, Surgical treatment of thoracic spinal stenosis: a 2- to 9- year follow-up. Spine 5 26 (2001) 558–566.
Stereotactic Radiosurgery for Spine Tumors
Carmina F. Angeles, Robert E. Lieberson, and Jon Park
49
k e y p o i n t s
e CyberKnife system is a frameless stereotactic radiosurgery (SRS)
instrument that consists of a six megavolt linear accelerator (LINAC) mounted on an industrial robot, a repositionable treatment couch, orthogonally placed digital x-ray cameras, and a computerized targeting system, used to treat spine tumors.
e overall accuracy of image-guided spinal SRS is ± 0.5 to 1.0 mm.Lesions amenable to spinal SRS mainly include metastatic tumors,
intradural extramedullary tumors, select intramedullary tumors, and vascular malformations.
Spinal instability and severe or progressive neurological deficits from mass
effect are contraindications for SRS unless decompression and stabilization have been performed first.
Radiation-induced myelopathy is the most feared complication of SRS, but
is uncommon.

INTRODUCTION

Stereotactic radiosurgery (SRS) for the spine is a noninvasive technique that accurately delivers large doses of radiation to small targets, through the use of numerous highly collimated cross-fired beams. Spinal SRS has proved effective in treating most metastases, many benign intradural tumors, some intramedullary tumors, and compact intramedullary arteriovenous malfor­mations. It can be used for the older patient or in patients with widely meta­static disease, when open surgery might be contraindicated.
Radiosurgery was developed in 1949 by Lars Leksell and Bjorn Lars­son at the Karolinska Institute in Stockholm. Their first system used ortho­voltage x-rays, and a subsequent variant used a proton beam generated by a cyclotron. Leksell’s Gamma Knife was introduced in 1967, as a lower cost and more efficient system. Gamma Knife treatments provided a steeper dose gradient outside the target region. Embedded in a cast-iron enclosure, the device contained 201 radioactive cobalt sources focused at a single point or
isocenter. During treatment, the patient’s head was secured to a rigid frame with pins and then inserted into the cast-iron device with the lesion posi­tioned at the isocenter. In the mid-1980s, to make radiosurgery more acces­sible and less costly, Betti and Colombo modified conventional radiotherapy linear accelerator-based (LINAC) systems to deliver frame-based radiosur­gery. Although both the Gamma Knife and LINAC systems were powerful tools for intracranial disease, they could not be easily adapted for extracranial cases, primarily because of the necessity for frame-based target localization.
In 1991, the frameless CyberKnife system was developed by Adler at Stanford University. From its inception, this device was intended to treat both cranial and extracranial lesions with sub-millimeter accuracy. Since the installation of the first clinical unit in 1994, over 8000 spinal lesions have been treated at more than 180 worldwide CyberKnife sites. As in cranial radiosurgery, spinal SRS delivers large but precise doses of radiation to a target while sparing adjacent healthy tissues. In comparison, conventional radiotherapy doses are limited by the sensitivity of the spinal cord.

RADIOSURGERY

Ionizing radiation damages DNA, protein, and lipids by creating free radicals and causing either mitotic or apoptotic cell death. Larger doses, while more effective in killing neoplastic tissues, endanger normal structures. Conven­tional radiotherapy, which uses small numbers of broad and relatively inac­curate beams, addresses the problem by dividing the dose over many daily treatments. In contrast, SRS instruments can deliver scores of small, precisely collimated beams. As a consequence, large radiation doses can be directed at irregularly shaped lesions while avoiding adjacent radiosensitive tissue. The target’s location and shape are delineated using computed tomography (CT) or magnetic resonance (MR) images, and processed using dedicated treat­ment-planning software. Current radiosurgery systems capable of treating spinal lesions include the CyberKnife, the Tomoscan (a CT-like device) and various modified linear accelerators (LINACs). The Gamma Knife is cur­rently able to treat only select upper cervical lesions.
The CyberKnife system is a completely frameless, image-guided, robotic radiosurgery system which consists, in part, of a lightweight, six megavolt
Clinical Case Examples
CASE 1
MC, a 66-year-old woman with medical contraindications to open surgery, was treated with SRS for a spinal schwannoma. She initially presented with a chronic cough and generalized weakness. Routine laboratory studies showed pancytopenia, and flow cytometry was consistent with acute lym­phocytic leukemia. e diagnosis was confirmed by bone marrow biopsy. While undergoing chemotherapy in December 2008, she developed lower back pain with subjective right leg weakness. A 10-by 7-mm epidural lesion,
compressing the S1 nerve root, was seen on MRI (Figure 49-1). A CT­guided biopsy was consistent with schwannoma, but definitive treatment was postponed because of her leukemia. By July 2009, the pain became intolerable. She had 4/5 gastrocnemius weakness, numbness in the S1 dis­tribution, and loss of the ankle reflex. A repeat MRI confirmed an increase in the size of the schwannoma. Open surgery remained high risk, so in Sep­tember 2009, the patient underwent CyberKnife treatment. She received 16 Gray (Gy) in a single session. Pain complaints improved, and all examina­tion findings resolved over 2 months.
317
318
P A R T V I Other Surgical Treatment Modalitites: Thoracic Spine
F IG UR E 49 - 1  Gadolinium-enhanced T1-weighted axial image  demon-
strating a 10- by 7-mm intradural extramedullary lesion compressing the S1 nerve  root. A CT-guided biopsy was consistent with schwannoma.
CASE 2
WF is a 68-year-old man with melanoma who received SRS treatment for a recurrent spinal metastasis in a previously irradiated field. e patient was initially seen with a melanoma of the back in 1999 and another of the neck in 2003. Following local resections, he remained disease-free until March 2007, when, after complaining of low back pain, he was found to have a 4 × 3 cm lesion of the L3 vertebral body. ere was significant compres­sion of the cauda equina due to epidural extension. A PET-CT showed hypermetabolic areas in the lung, bone, and brain. He received conventional
F IG UR E 4 9 -2   Sagittal  T1-weighted  image  with  contrast,  demonstrating  enlarge-
ment of the previously treated L3 vertebral body metastasis with epidural extension causing  central canal stenosis.
radiotherapy of 37.5 Gy to the brain and 37.5 Gy to the lumbar spine. In September 2009, the patient returned with increasing back pain, associated with weakness. His strength was 4/5 in the right leg but his sensation was intact. A follow-up PET-CT and MRI showed multiple new lesions and enlargement of the previously treated L3 mass (Figure 49-2). Additional conventional radiotherapy was not an option and a surgical decompression was contraindicated based on his other medical problems. e L3 lesion was treated with CyberKnife SRS, 24 Gy in three sessions. His symptoms improved.
C H A P T E R 4 9     Stereotactic Radiosurgery for Spine Tumors
319
C
A
B
D
F IG UR E 4 9- 3  CyberKnife frameless stereotactic radiosurgery suite. A 
modified 6-MV X-band LINAC designed specifically for radiosurgery is mounted  on  a  highlymaneuverable  robotic  manipulator  (KUKA  Roboter  GmbH,  Augs­burg, Germany) (A). Two high-resolution x-ray cameras are  mounted  orthogo­nally to the headrest (B). One of the two x-ray sources is mounted in the ceiling  projecting onto the  camera  (C).  The  treatment  couch  is  mobile, allowing the  x-ray sources to image targets at any point along the neuraxis (D).
linear accelerator attached to an industrial robot (Figure 49-3). The robotic arm is unconstrained, using six degrees of freedom to deliver beams to vir­tually any part of the body from a wide range of angles. During treatment, real-time orthogonal images of the patient are obtained frequently, enabling the system to identify and automatically correct for small changes in patient position.
Several conventional radiation therapy systems have been modified to provide spinal SRS. The BrainLab Novalis and TX systems both use floor­and ceiling-mounted x-ray cameras to verify patient position during therapy. In contrast, the Varian Trilogy and Elektra Synergy systems utilize cone­beam CT scanners mounted on the gantry of the LINAC. The cone CT scanners acquire images before treatment, but do not do so regularly during each session, and cannot always accommodate for changes in patient move­ment during therapy.

INDICATIONS FOR SPINAL RADIOSURGERY

Indications for spinal SRS continue to evolve (Tables 49-1 and 49-2). The most commonly treated spinal lesions are metastatic (Table 49-3). A biopsy may not be necessary prior to treatment if the diagnosis is clear from the clinical history and imaging. Ideally, lesions should be less than 5 cm in maximal diameter, well demarcated, and clearly seen on CT and/ or MRI. For most tumors, local control rates are equivalent or superior to conventional radiation and complications are generally lower than with open surgery. In some particular cases, spinal SRS may be useful for ablating the more radioresistant tumors. irradiated patients where the adjacent spinal cord has already received the maximum tolerated radiation dosage, the efficacy of spinal radiosur­gery may be compromised because of the need to lower the radiosurgical dose.
Spinal SRS is contraindicated in several situations. When there is sig­nificant cord or nerve root compression resulting in severe or progressive neurological deficits, surgery may yield the best outcome. This is especially true for bony or benign lesions, which involute slowly following treatment. In the presence of spinal instability, SRS should only be performed as an adjuvant therapy after decompression and stabilization or vertebroplasty has been performed first. In cases in which there is no known systemic disease and pathology cannot be reasonably ascertained by radiographic studies, radiosurgery is contraindicated without first establishing a diag­nosis. Some large tumors are best treated with a debulking procedure fol­lowed by SRS.
1
However, in those previously
TA BL E 49 -1 In dications for Spina l SRS
Tumors that are highly radiosensitive.
Post-resection cavity
Post-radiation therapy local irradiation
Recurrent disease post surgery and/or irradiation
Inoperable lesion
High-risk location of lesion
Slowly progressive but minimal neurological deficits
Patient with medical comorbidities that preclude surgery
Patient declines surgery.
TA BL E 49 -2 Contr aind icat ions for S pina l SRS
Spinal instability
Neurological deficit due to physical spinal cord or nerve root compression
Adjacent cord previously irradiated to the maximum dosage
Generalized metastatic involvement of the axial skeleton
Epidural carcinomatosis
TA BL E 49 -3 Le sion s Treata ble with Cybe rKni fe Radi osur gery
Tumors
Benign
Neurofibroma, schwannoma, meningioma, hemangioblastoma, chordoma, paraganglioma, ependymoma, epidermoid
Malignant/metastatic
Breast, renal, non-small cell lung, colon, gastric and prostate metastases; squamous cell (laryngeal, esophageal, and lung) tumors; osteosarcoma; carcinoid; multiple myeloma; clear cell carcinoma; adenoid cystic carcinoma; malignant nerve sheath tumor; endometrial carcinoma; malignant neuroen­docrine tumor
Vascular Malformations
Arteriovenous malformation (types 2 and 3)

TREATMENT DETAILS

Image-guided systems do not require rigid immobilization or invasive frames. Instead, noninvasive custom masks or cradles are made for each patient and used during image acquisition and radiosurgery. These devices improve comfort, expedite alignment, and limit movement. For upper cervi­cal lesions, a thermoplastic mask is made for each patient (Aquaplast, WFR Corp., Wyckoff, NJ; Figure 49-4A). For thoracic and lumbar lesions a cus­tom vacuum-molded body cradle is used (AlphaCradle, Smithers Medi­cal Products, Inc., Akron, OH; Figure 49-4B). For some cervicothoracic lesions, both devices are utilized.
Bony landmarks of the spine are used to target cervical, thoracic, and lumbar lesions, as well as some pelvic lesions, scapular and rib head masses, and paravertebral soft tissue tumors. The presence of spinal sta­bilization hardware does not interfere with target localization. Digitally­reconstructed radiographs (DRRs) are created as part of the treatment plan and are used to establish the relationship of the target to regional bony landmarks. The accuracy of CyberKnife using bony landmarks approaches ±0.5 mm
2
.
320
Synthetic image A
P A R T V I Other Surgical Treatment Modalitites: Thoracic Spine
A
F IG UR E 4 9 -4   The Aquaplast mask is used as an immobilization device in cervical spine patients during CyberKnife treatment (A). AlphaCradle custom body 
mold is used in thoracic, lumbar, and sacral lesions during CyberKnife treatment (B).
Camera image A Overlay of images A
Synthetic image B Camera image B Overlay of images B
B
F IG UR E 4 9 -5   Implanted gold seeds (fiducials). Left: CT-based DRRs from the perspective of the two orthogonal CyberKnife mounted x-ray cameras (A and
B). Center: Real time x-ray images from the two x-ray cameras. Right: Superimposed DRRs and actual radiographic images.
C H A P T E R 4 9     Stereotactic Radiosurgery for Spine Tumors
321
F IG UR E 4 9- 6   Fine-cut CT is used in delineating the lesion to be treated. Contour of L3 metastasis in axial, sagittal, and coronal projections is drawn. The 
epidural metastasis is in red.
For lesions not associated with bony landmarks, or where there is severe osteoporosis, localization may be based on implanted fiducials. Stain­less steel screws in adjacent bone, or “gold seeds” adjacent to or within the lesion, can be inserted prior to imaging (Figure 49-5). A minimum of three clearly visible, non-collinear fiducials is needed. Ideally, they are placed in bone or firm tissue, surround the target lesion, and do not overlap in 45° oblique images. Prior to treatment delivery, the tumor location relative to the implants or bony landmarks is established based on DRRs. The accu­racy using implanted fiducials may be lower than with bony landmarks and depends on the number and location of the implants.
2
Most patients are imaged and treated supine. Treatment planning begins with a fine cut CT scan, (1.25-mm slices). The CT has the special resolu­tion of available technologies and is required to delineate the lesion (Figure
Physical parameters are adjusted and refined iteratively until an optimal plan is obtained. Ideally, the beams are evenly distributed over the surface of the target, the target receives at least the prescribed dose, and the dose to adjacent structures is minimized.
Spinal SRS is an outpatient procedure. At the time of treatment, patients are positioned so that the lesion is near the center of an imaginary 80 cm diameter sphere. Orthogonal images are obtained by the digital x-ray cameras and compared with precalculated DRRs. The couch position is adjusted and the location of the target is confirmed. The robotic arm then moves the LINAC to each of the individual beam positions, and each beam’s dose is delivered. During treatment, images are repeated frequently and the couch position is adjusted to preserve accuracy. The process is automatic, but is monitored closely by a radiation therapist.
49-6) and create the DRRs used for localization (Figure 49-7). MRIs, posi-
tron emission tomography (PET) scans, or three-dimensional (3-D) angio­grams are commonly used in addition. Treatment plans for CyberKnife are designed using the Accuray Multiplan System (Figure 49-8). The various stereotactic image sets needed for target definition are transferred to the planning computer and aligned to one another using a semi-automatic pro­cess. Utilizing a graphic interface, the surgeon outlines the target lesion and adjacent radiation-sensitive structures, such as the spinal cord, esophagus, or kidneys, creating a 3-D representation of relevant anatomy (Figure 49-9). A dose and treatment schedule is specified by the surgeon and the radia­tion oncologist. A radiation physicist computes treatment plans, seeking an optimal dose conformation and a corresponding array of treatment beams.

TREATMENT OF SPINAL METASTASES

In older populations, the majority of spinal tumors are metastatic (see Case
2). Forty percent of cancer patients develop at least one spinal metastasis. SRS is perhaps the least invasive of available treatments, and can deliver much higher doses than conventional radiotherapy while limiting cord expo­sure. SRS generally takes 1 to 3 days, while conventional radiotherapy may require 4 to 6 weeks. Multiple lesions can be treated safely and, because of the shorter treatment schedules, the treatment of asynchronous metastases is more convenient. SRS is appropriate as an adjuvant following a debulking procedure or in conjunction with a stabilization procedure such as fusion or
322
P A R T V I Other Surgical Treatment Modalitites: Thoracic Spine
F IG UR E 4 9 -7   Contour of L3 metastasis and spinal roots with superimposed isodose lines from the treatment plan, in axial, sagittal, and coronal projections. 
The epidural metastasis is in red, the spinal roots are blue, and the 80% isodose line is the smaller green line.
vertebroplasty. SRS can be a good treatment modality for those with limited life expectancies, or those undergoing other concurrent treatments. Spinal radiosurgery can be highly effective in controlling pain, such as in Case 1, with up to 100% of patients reporting relief in some series.
3
Debate continues regarding the most appropriate treatment margins. Some centers radiate only tumor seen on MRI, while others recommend treating the entire affected vertebral body including pedicles. Up to 18% of local failures are due to recurrences in the pedicles.
4
Amdur et al5 advo­cate treating visible tumor plus a 1-cm margin in bone or a 2-mm volume beyond the cortex. We typically treat only the volume of tumor seen on CT or MRI. There are no studies that clearly demonstrate a benefit of one approach over the other. Dose recommendations are variable, with single session prescriptions ranging from 8 to 24 Gy in the published literature. We use 16 to 25 Gy in one to three fractions, depending on tumor type. Local control is achieved in 77% to 100% of cases, and control rates are
histology have been shown to respond well to SRS. SRS for these benign spinal lesions is appropriate for inaccessible tumors, syndromic lesions that are multiple, for patients with significant medical comorbidities, or for those who decline open surgery. In older patients, the risks associated with open surgery are greater, so SRS may be appropriate for most intradural extra­medullary lesions in this population.
In our institution, we have treated 110 patients with 117 lesions (unpublished data). Fifty-six percent of schwannomas (see Case 1) and meningiomas have stabilized after SRS and 44% have regressed radiograph­ically. Neurofibromas did less well, with 11% enlarging, and up to 80% of patients reporting progressive neurological deficits. We have observed that most myelopathies and radiculopathies improve after SRS treatment. Two
5
of our SRS-treated patients required open resection for tumor enlargement. Three needed surgery for persistent or progressing symptoms. One patient developed a radiation-induced myelopathy.
independent of histopathology (Table 49-4).

TREATMENT OF INTRAMEDULLARY LESIONS

TREATMENT OF INTRADURAL EXTRAMEDULLARY LESIONS

Most intradural extramedullary lesions are benign. Surgical resection is most commonly recommended since it provides immediate decompression, yields a tissue diagnosis, and is usually curative. Intracranial lesions of similar
Sixteen of the 92 hemangioblastomas treated in our institution were spi­nal intramedullary tumors. These were treated with a median radiosurgi­cal dose of 23 Gy. After a median follow-up of 34 months, 15 of the 16 spinal hemangioblastomas either decreased or remained the same in size. Intramedullary hemangioblastomas associated with significant edema or
6
C H A P T E R 4 9     Stereotactic Radiosurgery for Spine Tumors
323
F IG UR E 4 9- 8  Treatment plan for L3 metastasis is designed using the Accuray Multiplan System.
cysts might do less well, based on our experience with similar intracranial lesions.
Although the data for ependymomas are limited, a few published stud-
ies have shown SRS to be efficacious.
7
We know less about SRS for spinal astrocytomas, but for those which are well circumscribed, spinal SRS may be an appropriate alternative to surgery.
Intramedullary spinal cord metastases are rarely seen. They constitute only 8.5% of central nervous system metastases, likely increase with longer patient survival and as the population ages. Wowra et al
9
reported that 96% of spinal metastases were well controlled
8
but their frequency will
with spinal SRS and that the risk of radiation myelopathy was less than 1%.

COMPLICATIONS

SRS treatment failures can be categorized as “in-field failures” and “marginal failures.” “In-field failures” involve tumor regrowth within the treated vol­ume and may be related to inadequate dosing. “Marginal failures” involve regrowth at the edges of the treated volume and may be related to poor imaging, an underestimation of the tumor volume, or inaccuracies in the position or set-up. “Distant failures,” which involve new lesions in untreated portions of the spine, occur in 5% of patients, and are due to the underlying disease and not to a failure of technique.
Neurological complications of SRS are categorized by their time of onset. Acute complications occur within a month and are usually
transient. They are related to edema and can be treated with steroids. Subacute complications occur 3 to 6 months after treatment and are usually secondary to demyelination. The prognosis for recovery is good. Radiation-induced myelopathy, the most feared side effect of SRS, is a late effect, occurs after 6 months, and is usually irreversible. In 1000 patients treated with CyberKnife for spinal lesions, six developed myelopathy (0.6%).
10
To prevent radiation-induced myelopathy, we avoid exposing more than one cubic centimeter of spinal cord to more than 8Gy in single session plans.
Other less severe side effects of spinal SRS include local skin reac­tions, which are occasionally seen when the posterior elements are treated, and gastrointestinal complaints such as nausea, pharyngitis, esophagi­tis, or diarrhea. Renal complications are rare even after thoracolumbar treatments.

CONCLUSION

The successes of intracranial radiosurgery inspired the development of spi­nal SRS. Many spinal lesions may not be amenable to complete surgical resection. SRS is both safe and effective treatment for metastatic lesions of the spine and for some intradural extramedullary tumors. Early results in treating intramedullary lesions are encouraging. Spinal SRS, a completely noninvasive treatment, is particularly suited for older patients and those with significant concomitant medical problems.
324
P A R T V I Other Surgical Treatment Modalitites: Thoracic Spine
F IG UR E 4 9 -9   Outlines of the target lesion and adjacent radiation-sensitive structures, such as the spinal nerves and kidneys, with dose lines as specified by 
the surgeon and the radiation oncologist.
TA BL E 49 -4 SRS for Spinal Vert ebral Metastas es
Site
Amdur, et al., 2009
Wowra, et al., 2009
Yamada, et al., 2008
Gibbs, et al., 2007
Chang, et al., 2007
Ryu, et al., 2007
Gerszten, et al.,
17
2005
Milker-Zabel,
18
2003
16
et al.,
Lesions / Patients
11
25 / 21 Various LINAC / IMRT 15 Gy / 1 Lesion with
15
134 / 102 Various CyberKnife 15 to 24
14
103 / 93 Various LINAC / IMRT 18 to 24
6
102 / 74 Various CyberKnife 14 to 25 Gy /
7
74 / 63 Various LINAC / IMRT 27 to 30 Gy /
230 / 177 Various LINAC / IMRT 8 to 18
68 / 50 Breast CyberKnife 12.5 to 22.5
19 / 18 Various LINAC / IMRT
Tumor Type Modality
or FCRT
Dose / Fractions Contouring Complications
No neurological
margin
toxicity
Not specified No SRS-related
Gy/ 1
neurological deficits
Gy/ 1
Entire verte­bral body
No neurological toxicity
Lesion only ree cases
1 to 5
3 to 5
Gy / 1
Gy / 1
24 to 45 / variable
Entire verte­bral body
Entire body with pedicles
Entire verte­bral body
Entire verte­bral body
myelopathy
No neurological toxicity
1% risk of myelopathy
No neurological toxicity
No neurological toxicity
Pain Reduced
Local Control
Overall Survival
43% 95% 25% at
1 year
86% 88% Median
survival
1.4 years
Not reported
84% No symptom
90% 36% at
3 years
46% at
progression
1 year
60% 77% 70% at
1 year
85% 96% 49% at
1 year
96% 100% Not
reported
81% 95% 65% at
1 year