Ori Barzilai1, Stefano Boriani2, Charles G Fisher3,4, Arjun Sahgal5, Jorrit Jan Verlaan5, Ziya L Gokaslan6,7,8, Aron Lazary9, Chetan Bettegowda10, Laurence D Rhines11, Ilya Laufer1. 1. Memorial Sloan-Kettering Cancer Center, New York, NY. 2. IRCCS Galeazzi Orthopedic Institute, Milan, Italy. 3. University of British Columbia, Vancouver, British Columbia, Canada. 4. Vancouver General Hospital, Vancouver, British Columbia, Canada. 5. University Medical Center Utrecht, Utrecht, the Netherlands. 6. The Warren Alpert Medical School of Brown University, Providence, RI, USA. 7. Rhode Island Hospital, Providence, RI, USA. 8. The Miriam Hospital, Providence, RI, USA. 9. National Center for Spinal Disorders and Buda Health Center, Budapest, Hungary. 10. Johns Hopkins University School of Medicine, Baltimore, MD, USA. 11. The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Abstract
STUDY DESIGN: Literature review. OBJECTIVE: To provide an overview of the recent advances in spinal oncology, emphasizing the key role of the surgeon in the treatment of patients with spinal metastatic tumors. METHODS: Literature review. RESULTS: Therapeutic advances led to longer survival times among cancer patients, placing significant emphasis on durable local control, optimization of quality of life, and daily function for patients with spinal metastatic tumors. Recent integration of modern diagnostic tools, precision oncologic treatment, and widespread use of new technologies has transformed the treatment of spinal metastases. Currently, multidisciplinary spinal oncology teams include spinal surgeons, radiation and medical oncologists, pain and rehabilitation specialists, and interventional radiologists. Consistent use of common language facilitates communication, definition of treatment indications and outcomes, alongside comparative clinical research. The main parameters used to characterize patients with spinal metastases include functional status and health-related quality of life, the spinal instability neoplastic score, the epidural spinal cord compression scale, tumor histology, and genomic profile. CONCLUSIONS: Stereotactic body radiotherapy revolutionized spinal oncology through delivery of durable local tumor control regardless of tumor histology. Currently, the major surgical indications include mechanical instability and high-grade spinal cord compression, when applicable, with surgery providing notable improvement in the quality of life and functional status for appropriately selected patients. Surgical trends include less invasive surgery with emphasis on durable local control and spinal stabilization.
STUDY DESIGN: Literature review. OBJECTIVE: To provide an overview of the recent advances in spinal oncology, emphasizing the key role of the surgeon in the treatment of patients with spinal metastatic tumors. METHODS: Literature review. RESULTS: Therapeutic advances led to longer survival times among cancer patients, placing significant emphasis on durable local control, optimization of quality of life, and daily function for patients with spinal metastatic tumors. Recent integration of modern diagnostic tools, precision oncologic treatment, and widespread use of new technologies has transformed the treatment of spinal metastases. Currently, multidisciplinary spinal oncology teams include spinal surgeons, radiation and medical oncologists, pain and rehabilitation specialists, and interventional radiologists. Consistent use of common language facilitates communication, definition of treatment indications and outcomes, alongside comparative clinical research. The main parameters used to characterize patients with spinal metastases include functional status and health-related quality of life, the spinal instability neoplastic score, the epidural spinal cord compression scale, tumor histology, and genomic profile. CONCLUSIONS: Stereotactic body radiotherapy revolutionized spinal oncology through delivery of durable local tumor control regardless of tumor histology. Currently, the major surgical indications include mechanical instability and high-grade spinal cord compression, when applicable, with surgery providing notable improvement in the quality of life and functional status for appropriately selected patients. Surgical trends include less invasive surgery with emphasis on durable local control and spinal stabilization.
Entities:
Keywords:
metastases; oncology; stereotactic body therapy (SBRT); surgery; tumors
Recent advances in cancer therapy have dramatically improved overall survival times in
multiple cancer subtypes. Subsequently, the incidence of patients with metastatic spine
disease is on the rise and will likely continue to grow. The subjective and objective
outcomes of patients with spinal metastases have been shown to improve with proper
treatment. Goals of treatment for metastatic spine disease remain palliative and aside from
traditional goals such as local tumor control, strive toward symptom palliation and improved
health-related quality of life (HRQoL). The recent integration of modern diagnostic tools,
targeted and personalized treatments, and widespread use of new technologies have
revolutionized treatment of spinal metastases. Alongside the improvement in care for spinal
metastases, this wealth of knowledge and breadth of modern treatment tools has complicated
treatment paradigms tremendously. Spine cancer treatment requires a multidisciplinary team
effort, including surgeons, radiation and medical oncologists, pain and rehabilitation
specialists, and interventional radiologists. This review aims to highlight current concepts
to inform and help guide spine surgeons to undertake a leadership role in the modern
management of spinal cancer.
Patient Evaluation and Treatment Indications
The field of spinal oncology has made great progress in defining the key parameters
necessary for clear patient description. Consistent utilization of the requisite patient
descriptors facilitates communication, delineation of treatment indications and outcomes,
and comparative clinical research. The key parameters used to define the salient
characteristics of patients with spinal metastases include HRQoL, spinal mechanical
stability, neurologic examination and functional assessment, the extent of epidural tumor
extension, tumor histology, and genomic tumor profile.
Health Related Quality of Life
A main treatment goal for patients with spinal metastases is symptom palliation and
maintenance or improvement of HRQoL. Historically, clinical outcomes of metastatic spine
patients relied primarily on clinician-based measures such as gross measures of function.[1-3] In recent years, we have witnessed an increase in utilization of patient-reported
outcomes (PRO) since patient self-assessment tools express a direct measure of the value
of care as perceived by the recipient.[4] Several generic outcome measures have been widely used for PRO reporting in the
spinal oncology population, including EuroQol 5-D (EQ-5D), Oswestry Disability Index
(ODI), visual analogue scale (VAS), and Short Form 36 (SF-36)[5]; however, none of these instruments focus on cancer-specific symptoms that are
important to patients with spinal tumors. While the MD Anderson Symptom Inventory (MDASI)
has a spinal oncology–specific module, the majority of the questionnaire examines broad
cancer-associated symptoms and also lacks the specific focus on symptoms associated with
spinal tumors.[6]A systematic literature review conducted in 2009 revealed the absence of PRO instrument
specifically designed for assessment of HRQoL among patients with spinal oncologic disease.[1] The Spine Oncology Study Group Outcome Questionnaire (SOSGOQ) was designed to
address this need and represents the only PRO instrument fully focused on assessment of
patients with spinal tumors.[7,8] Psychometric evaluation and clinical validation of the SOSGOQ among an
international cohort of patients with spinal metastases who were treated with surgery
and/or radiotherapy confirmed the SOSGOQ as a reliable and valid PRO instrument with
strong correlation with SF-36 and ability to discriminate between clinically distinct
patient groups.[8] Additional testing confirmed that the SOSGOQ provides excellent quality of life
assessment among patients with spinal metastases and superior internal consistency and
coverage compared with EuroQol-5 Dimensions (EQ-5D).[9] Further component analysis indicated that Patient-Reported Outcomes Measurement
Information System (PROMIS) might perform better than the SOSGOQ in assessing pain
intensity and physical function and requires further investigation in large cohort analysis.[10] Currently, the extensive validity and reliability testing of the SOSGOQ positions
this survey as the best instrument for PRO assessment among patients with spinal
tumors.With growing interest in PRO data, the impact of surgical treatment of metastatic spine
disease on HRQoL has recently been the focus of investigation. Fehlings et al[11] analyzed prospectively collected data from the AOSpine North American Clinical
Research Network and demonstrated that surgery combined with radiation and systemic
therapies provides immediate and sustained improvement in pain, neurologic, and HRQoL
outcomes showing improvement in ODI, EQ-5D, pain interference, and SF-36 scores.[11] Additional prospective cohort studies demonstrated improvement in HrQOL following
open surgery,[2,12] as well as following minimally invasive surgery[13] for treatment of spinal metastases. In a recent analysis of the Epidemiology,
Process and Outcomes of Spine Oncology (EPOSO) data, significant improvement in HRQoL was
demonstrated using both SF-36 and the SOSGOQ in patients with oligometastatic and
widespread metastatic disease[14] demonstrating improvement in HRQoL for all surgically treated patients, regardless
of the extent of systemic disease. Furthermore, among patients with mechanically stable
metastatic tumors without compression of the spinal cord, treatment with SBRT resulted in
significant reduction in pain and symptom interference with daily life.[15] Hence, consistent attention and reporting of HRQoL provide high-quality data that
demonstrate the benefit of surgery and radiotherapy among appropriately selected patients
with spinal metastatic tumors.
Neoplastic Spinal (In)Stability
Loss of structural integrity of the spinal column represents one of the most debilitating
sequelae of spinal metastases. In 2010, the Spine Oncology Study Group (SOSG) defined
cancer-related spinal instability as “loss of spinal integrity as a result of a neoplastic
process that is associated with movement-related pain, symptomatic or progressive
deformity, and/or neural compromise under physiologic loads.”[16] The Spinal Instability Neoplastic Score (SINS)[16] was developed to facilitate diagnosis and classification of spinal instability and
provide a common language across clinical disciplines and among spine surgeons. This score
assesses the degree of spinal instability in a standardized and reproducible manner and
can be used by nonspine specialists. The introduction of SINS has improved the uniform
reporting of spinal instability in the published literature and lead to improved
communication among treating and referring physicians.[17]Patients with spinal mechanical instability typically require surgical stabilization.[18] Since radiation or systemic treatment do not treat spinal instability, an unstable
spine should be surgically stabilized to allow pain palliation and to prevent neurologic
compromise and spinal deformity progression. Increasing SINS correlates with increasing
severity of pain and functional disability.[19] Patients with low SINS typically experience resolution of pain after radiotherapy
treatment, while patients with higher SINS have a higher risk of radiotherapy failure.[20,21] On the other hand, patients with indeterminate (7-12) and high (13-18) SINS
experience significant benefit from surgical stabilization leading to pain relief and
functional improvement.[19] These data support the treatment of mechanically stable patients with radiotherapy
and illustrate the need for surgical stabilization among mechanically unstable
patients.
Epidural Spinal Cord Compression
Epidural spinal cord compression (ESCC) places patients at risk for the development of
neurologic deficits and, if not detected early and treated expeditiously, results in
significant functional disability. Therefore, assessment of patients with spinal tumors
must involve a thorough discussion of ambulation changes, timing of symptom onset, careful
neurologic examination, and magnetic resonance imaging (MRI) of the spine.Loss of ambulation and bowel and bladder dysfunction represent the most severe and
debilitating sequelae of MESCC. The severity of neurologic deficits due to MESCC is
associated with the severity of HRQoL impairment among cancer patients and subtle
neurologic deficits may lead to significant quality of life impairment (unpublished data).
Furthermore, the functional status of cancer patients correlates with survival, with
ambulatory patients surviving longer than patients who have lost the ability to ambulate.[2,22,23] Multiple clinical studies demonstrate neurological improvement after surgery for
patients experiencing neurologic deficits due to MESCC, as measured by American Spinal
Injury Association (ASIA) Impairment Scale (AIS) and ambulation. However, the true
functional benefit of surgery represented by clearly defined useful ambulation,
restoration of activities of daily living and return to work requires further study.A prospective randomized trial demonstrated that surgery followed by radiotherapy
provides superior outcomes when compared with radiotherapy alone for the treatment of
symptomatic MESCC.[22] Surgery resulted in superior functional outcomes such as preservation and
restoration of ambulation and bowel and bladder function, pain control, and survival.
Several additional studies focused on the functional and neurologic outcomes after surgery
for MESCC. The duration of ambulation loss, bladder dysfunction and Medical Research
Council (MRC) muscle strength 30] Surgeons should aim to shorten the duration of neurologic deficit and prevent
further neurologic deterioration.Physicians commonly administer steroids at the time of MESCC diagnosis. The data to
support steroid utilization as part of the treatment of MESCC largely rest on animal
studies and limited clinical evidence in the setting of radiotherapy.[31-33] The role of dexamethasone administration in patients undergoing surgery for the
treatment of MESCC has not been examined to date and is the focus of a prospective cohort
study incorporated into the Metastatic Tumor Research and Outcomes Network (MTRON).
Currently, utilization of low-dose dexamethasone protocol (16 mg daily) is recommended for
patients with MESCC, since the potential neuroprotective benefit may outweigh the
dexamethasone toxicity risk.[34]The radiographic degree of epidural spinal cord compression is an important component of
the MESCC assessment. Fortunately, the ready availability of MRI leads to early diagnosis
of MESCC among cancer patients, with most spinal metastases diagnosed at the time of early
symptoms, usually starting with pain. Clear description and communication of epidural
tumor extension has been facilitated through the development of the ESCC scale (also known
as the Bilsky scale).[4] Grades 0 and 1 represent tumor confined to bone or impinging on the thecal sac
without compression or displacement of the spinal cord. Grades 2 and 3 are considered
high-grade spinal cord compression with displacement and/or compression of the spinal cord
and obliteration of the surrounding cerebral spinal fluid (CSF) space. Utilization of
T2-weighted and T1-weighted gadolinium-enhanced axial MR images in order to assess the
ESCC grades showed good inter- and intrarater reliability in validation studies of the scale.[4] Clear description of ESCC severity is required in order to determine whether the
patient can safely undergo SBRT and whether they require surgical decompression. Spinal
metastases confined to bone or with minor epidural extension (ESCC 0 and 1) can be
definitively treated with SBRT without requiring decompressive or excisional surgery.
However, patients with spinal cord compression (ESCC 2 and 3) generally require surgical
decompression prior to SBRT to optimize the radiation dose delivered to the entire tumor
volume without delivering excessive radiation dose to the spinal cord. Hybrid therapy with
surgical decompression and postoperative SBRT results in durable local control and
improvement in HRQoL.[12,35]
Precision Medicine
Oncology has made great strides in the understanding of genetic basis of disease,
deciphering the molecular drivers of tumor proliferation and development of drugs that
specifically target the aberrant molecular pathways. Giant technological advances in
sequencing lead to the development of next-generation sequencing, which can be readily
performed at the point of care and already serves as one of the standard techniques for
clinical classification of tumors. Genomic profiling currently guides clinical management
of tumors such as melanoma, sarcomas, and carcinomas of the lung, breast, thyroid, ovary,
and colon.[36] Clinical trials support treating several mutations with targeted therapy, with a
continuously growing list of potential targets undergoing clinical testing. Epidermal
growth factor receptor (EGFR) mutation in lung cancer serves as one of the most notable
examples of targeted therapy success, with tyrosine kinase inhibition of the EGFR pathway
resulting in the extension of survival from 8-11 months to 24-36 months among patients
with metastatic non–small lung carcinoma (NSCLC) with targetable EGFR mutations.[37] Evaluation of literature specifically reporting survival among patients with NSCLC
metastatic to the spine showed that while the overall survival of patients with lung
cancer metastases to the spine was 3.6 to 9 months, the median reported survival of NSCLC
patients with targetable EGFR mutations was 18 months.[38] Thus, while previously, patients with NSCLC metastases were considered poor
surgical candidates due to very short expected survival, current therapy provides extended
survival among subgroups of NSCLC patients making them realistic surgical candidates.
Similar extended survival groups were identified among patients with metastatic melanoma
harboring BRAF mutation and tumors responsive to immunotherapy.[36,39] While the effect of systemic therapy on osseous metastases has been limited, a
recent clinical trial showed favorable response of osseous renal cell carcinoma metastases
treated with cabozantinib, which is a small molecule tyrosine kinase inhibitor, indicating
that new systemic therapy agents may offer local tumor control for osseous metastases.[40] With the popularization of precision medicine through patient education, research,
and clinical implementation, surgeons treating cancer patients will need to increasingly
gain familiarity with the clinical genomic and molecular oncology landscape in order to
make informed decisions in patient care.The NOMS framework facilitates treatment decisions for patients with spinal metastatic
tumors through incorporation of the key parameters discussed above into 4 patient
evaluation categories: Neurologic, Oncologic, Mechanical, and Systemic.[41] The combination of the neurologic evaluation, ESCC grade and tumor histology guide
the selection of radiotherapy modality and the need for surgical decompression. The
mechanical evaluation of the spine determines the need for spinal stabilization. The
systemic component considers the medical comorbidities, the extent of systemic tumor
burden and the genomic profile of the tumors to determine the patient’s ability to
tolerate treatment and the desired durability of therapy.
Treatment Techniques
Radiotherapy
Conventional Radiotherapy
Conventional external beam radiotherapy (cEBRT) has been used as the primary and
adjuvant treatment of spinal metastatic tumors for decades. cEBRT generally delivers
wide-field radiation in small additive doses, such as 30 Gy in 10 fractions, with the
dose delivered to the tumor limited by the dose that can be tolerated by the surrounding
organs at risk, such as the spinal cord.[42] Tumors exhibit a wide range of response duration and recurrence after cEBRT
treatment. Examination of cEBRT treatment outcomes among patients with spinal metastases
resulted in classification of tumors as radiosensitive and radioresistant based on the
primary tumor histology.[43,44] Tumors that respond well to cEBRT include most hematologic malignancies (ie,
lymphoma, multiple myeloma, and plasmacytoma), as well as selected solid tumors (ie,
breast, prostate, ovarian, and seminoma).[45,46] However, most solid tumors respond poorly to cEBRT (ie, radioresistant),
including renal cell carcinoma (RCC), colon, NSCLC, thyroid carcinoma, hepatocellular
carcinoma, melanoma, and sarcoma.[44-47]
Stereotactic Body Radiation Therapy
The incorporation of stereotactic body radiation therapy (SBRT) into the metastatic
spine tumor realm has revolutionized treatment paradigms and changed surgical
indications along with the type and extent of surgery currently performed. Radiosurgery
overcomes tumor radioresistance through safe delivery of high doses of radiation to the
tumor while minimizing radiation dose to the surrounding organs at risk, such as the
spinal cord.[48,49] The basis of overcoming radioresistance lies in the recruitment of additional
tumoricidal pathways when delivering a high dose per fraction radiation treatment
compared to the known mechanisms of cell death secondary to cEBRT.[50-53] Since the introduction of spinal SBRT, an abundance of data has established the
safety and efficacy of SBRT. In a single institution experience, Yamada et al[54] analyzed 811 spine radiosurgery targets and showed local control rates of up to
98% over 4 years, noting that response rates were irrespective of tumor histology or
volume but rather dose-dependent. Other series with single-fraction or hypofractionated
SBRT report comparable rates of local control.[54-56] Recent interest focuses on evaluation of dosing and fractionation regimens as
optimal dosing and fractionation remain controversial and various treatment regimens are
currently utilized. For example, Tseng et al[57] recently described a single-institution experience using 24 Gy in 2 fractions,
showing this regimen to be safe and effective, leading to 1-year and 2-year local
failure rates of 9.7% and 17.6%, respectively. SBRT has been shown to not only affect
local control but also shown to result in significant reduction in patient-reported pain
and symptom interference among mechanically stable patients.[15] Currently, SBRT is used not only in the de novo setting but also for patients who
were previously irradiated. For example, a prospective study of 59 patients, using doses
of 30 Gy in 5 fractions or 27 Gy in 3 fractions, showed 1-year local control rate of
76%, and significant improvements in pain control.[58]The currently accepted dose constraints limit utilization of SBRT in the setting of
high-grade epidural disease. However, with technological improvement and better
understanding of spinal cord radiation tolerance, SBRT may become a viable approach in
select cases of high-grade MESCC. Ryu et al[59] performed single-session radiosurgery on 85 lesions (from 62 patients), showing
mean epidural tumor volume reduction was 65% 2 months postradiosurgery. However, several
patients experienced neurologic deterioration and currently utilization of SBRT for the
treatment of high-grade MESCC is limited to experimental protocols.Dose constraints and the toxicity risks have been established for all major organs at
risk, including para- and intraspinal structures.[60,61] Fortunately, high-grade toxicity after SBRT seldom occurs and most complications
are mild.[62] Long-term data is becoming more readily available and a series of patients who
were followed for at least 5 years after SBRT exhibited a 17% rate of grade ≥2 toxicity;
yet, many of these patients underwent SBRT as salvage treatment after failed cEBRT.[63] Vertebral compression fractures (VCFs) are one complication that require
assessment of spine surgeons. VCFs following SSRS have been described in up to 40% of
treatments compared with a less than 5% risk following cEBRT.[64-66] The majority of post-SBRT VCF are asymptomatic radiographic findings, with
interventions such as kyphoplasty required for a small proportion of these fractures.[67]The International Spine Radiosurgery Consortium developed contouring and planning
guidelines for spinal radiosurgery planning[68,69] and recent consensus guidelines have also been created for postoperative target contouring.[70] It is recommended that spine surgeons familiarize with these guidelines and
actively participate in the treatment planning.In summary, SBRT provides safe and durable local control for patients with spinal
metastases and serves as one of the integral treatment modalities in modern spinal
oncology. While the availability and utilization of SBRT for the treatment of spinal
tumors has been steadily growing and has become the standard treatment modality in many
spinal oncology centers, many regions and medical centers throughout the world do not
have SBRT readily available. In places with limited SBRT availability, cEBRT remains the
major radiation modality for spinal tumors, requiring greater utilization of excisional
tumor surgery to optimize local tumor control. Surgeons should work closely with their
radiation oncology colleagues to select the optimal treatment modality for their
patients and to tailor their surgical indications according to the expected response to
the available radiotherapy.
Surgery
Surgical stabilization and decompression is strongly recommended for patients with
radioresistant tumors in the setting of high-grade spinal cord compression.[71] The primary evidence for this recommendation was provided by Patchell et al,[22] who conducted a prospective randomized trial that illustrated improved ambulation
outcomes after direct surgical decompression compared with radiotherapy for patients with
solid tumor metastases causing symptomatic ESCC. Furthermore, stabilization surgery is
recommended for patients with mechanical instability of the spinal column, even in the
absence of high-grade spinal cord compression. A wide range of surgical decompression and
stabilization techniques has been described. Corpectomy, laminectomy, and transpedicular
decompression represent the most commonly used decompression techniques.Prior to popularization of SBRT, gross total surgical excision of radioresistant tumors
was required for local control. The excision can be carried out using intralesional and en
bloc techniques. The excellent local tumor control that can be achieved with excisional
surgery in appropriately selected patients and the surgical approaches and techniques
required for such surgeries have been thoroughly described.[72-75] Integration of SBRT into the treatment of spinal tumors, lead to the development of
less invasive surgical options, since significant tumor excision is no longer required to
achieve durable local control, except in select cases of recurrent tumors. Methods for
spinal stabilization vary and may entail open surgery, percutaneous stabilization or, in
select cases of isolated anterior column compromise, kyphoplasty/vertebroplasty.[13] Separation surgery and minimal access surgery represent some of the most recent
advances in decompression and stabilization techniques for spinal tumor surgery and may
well be changing the conventional surgical indications for this patient population. In
places with limited access to SBRT, surgeons and oncologists must continue to rely on the
more aggressive excisional surgical techniques to improve HRQoL and local control for
patients with spinal tumors.
Separation Surgery
While SBRT provides effective and durable local control for spinal metastases
regardless of tumor histology, volume, and prior radiation history, SBRT is less
effective when delivered to tumors causing spinal cord compression. Avoiding
radiation-induced spinal cord injury while maximizing treatment dose requires sufficient
distance between the radiation target and the spinal cord. Hence, patients with
high-grade epidural spinal cord compression are not considered candidates for “up-front”
radiation treatment. Separation surgery was first described in 2000 as decompression
surgery that provides the foundation for concomitant SBRT.[76] The goal of separation surgery is to create distance (typically 1-2 mm) between
the tumor and spinal cord providing an optimal target for SBRT while also
circumferentially decompressing the spinal cord and stabilizing the spinal column.[77] Generally, this is performed though a single-stage posterolateral transpedicular
approach. Through this approach, circumferential epidural decompression is achieved,
without the need for significant cytoreduction or gross tumor removal. Resection of the
posterior longitudinal ligament allows ventral tumor separation, and cement augmentation
can aid in ventral column reconstruction[78] without need for cage placement or more extensive reconstruction. It is important
to realize that although this is a posterior-only approach, a simple laminectomy may not
provide adequate ventral separation. Among patients with adequate separation between the
tumor and the spinal cord, more than 90% local control at 1-year follow-up has been reported.[79] However, patients with persistent high-grade epidural tumor extension after
separation surgery remain at significant risk of postoperative tumor recurrence.[80] Ultrasonography can be used intraoperatively to ensure adequate tumor separation.[81]
Minimal Access Surgery
Decompression, stabilization, and tumor control can be accomplished through smaller
corridors that minimize iatrogenic pain and surgical morbidity.[82] Minimal access spine techniques for the treatment of spinal tumors are gaining
acceptance as they have limited perioperative morbidity, allow for quick recovery and
rapid return to radiation or systemic treatment.[13] For spinal tumor surgery, MAS techniques include percutaneous instrumentation,
mini-open approaches for decompression, and tumor removal with or without
tubular/expandable retractors and thoracoscopy/endoscopy.[83] Studies have shown decreased blood loss, transfusion rates, and hospitalization
length with minimal access surgery (MAS) stabilization techniques.[84-87] Recent reports continue exploring these innovative strategies describing MAS
stabilization with additional techniques for spinal cord and nerve root decompression.[88] Notably, a systematic literature review found that although some studies have
shown superiority of outcomes using MAS techniques, especially using “mini-open”
decompression, the available data is still of low quality and strong recommendations
cannot be made.[89] MAS stabilization permits utilization of concomitant SBRT, which can be
administered before or after surgery.[90] As technology continues to improve, surgical adjuncts such as the use of spinal
laser interstitial thermotherapy (SLITT) for MESCC[91] and radiofrequency ablation[92] may become more widely used.Experience gained in degenerative, deformity, and trauma spine surgery has streamlined
integration of spinal navigation for cancer.[93] Data supporting improved hardware placement accuracy, reduced screw placement
time, and a decreased risk of reoperation.[94-96] A variety of intraoperative navigational tools are available, including
fluoroscopic- and computed tomography–based devices. Apart from screw placement, these
tools can facilitate the intraoperative assessment of tumor resection extent and allow
integration of ablation therapies. Robot-assisted spine surgery is currently under
investigation and aims to reduce human error and further improve the accuracy of spinal
instrumentation along with reducing potential complications. Initial experience with
such techniques in spine tumor surgery demonstrate its feasibility,[97] yet larger experience is required to determine its efficacy and necessity.
Stabilization Techniques
Cancer patients frequently have poor bone quality secondary to osteolytic disease,
chemotherapy, radiation therapy, steroid use, and osteoporosis. Low probability of
arthrodesis in the setting of radiation and chemotherapy along with the poor bone
quality provide a challenging substrate for spinal stabilization. Furthermore, the
increasing duration of postoperative survival due to advances in systemic therapy,
requires durable stabilization constructs. A systematic literature review and expert
survey support the use of prefabricated prosthetic and/or polymethylmethacrylate bone cement[98] among patients requiring anterior column reconstruction. The posterior column
should be stabilized using bilateral pedicle screw fixation above and below the level of
the tumor.[98] Fenestrated screws facilitate screw cement augmentation and may be used in order
to improve osseous purchase in osteoporotic patients with cancer.[99]Implant material selection must take into consideration postoperative radiation plans.
Cobalt chrome causes significant beam scatter thus altering the dose delivered to the
tumor and organs at risk whereas titanium has been shown to cause minimal radiation beam scatter.[100,101] Carbon fiber implants may provide a superior stabilization option for patients
with planned postoperative proton beam therapy treatment, since the presence of metallic
implants has been shown to have a detrimental effect on local tumor control after proton therapy.[102,103] Implants based on from carbon fiber also offer superior MR image quality, which
may be beneficial for long-term surveillance/monitoring of local tumor control.
Stabilization with polymethylmethacrylate does not appear to alter radiation dosimetry.[104]
Conclusions
Great strides in systemic therapy, radiotherapy, and surgical techniques have vastly
improved the outcomes for patients with spinal metastases. Standardization of patient
population description and outcome reporting results in clear delineation of treatment
indications, care team communication and comparative research. SBRT provides durable local
control for the majority of patients with spinal metastases. Surgical indications include
mechanical instability and high-grade spinal cord compression. Surgical trends include less
invasive surgery with emphasis on durable local control and spinal stabilization. Extensive
evidence supports current radiotherapy and surgical indications with clear evidence of
patient benefit.
Authors: Roy A Patchell; Phillip A Tibbs; William F Regine; Richard Payne; Stephen Saris; Richard J Kryscio; Mohammed Mohiuddin; Byron Young Journal: Lancet Date: 2005 Aug 20-26 Impact factor: 79.321
Authors: Alexis Falicov; Charles G Fisher; Joe Sparkes; Michael C Boyd; Peter C Wing; Marcel F Dvorak Journal: Spine (Phila Pa 1976) Date: 2006-11-15 Impact factor: 3.468
Authors: Dirk Rades; Fabian Fehlauer; Lukas J A Stalpers; Ingeborg Wildfang; Oliver Zschenker; Steven E Schild; Hans J Schmoll; Johann H Karstens; Winfried Alberti Journal: Cancer Date: 2004-12-01 Impact factor: 6.860
Authors: Eugene K Wai; Joel A Finkelstein; Ronald P Tangente; Lori Holden; Edward Chow; Michael Ford; Albert Yee Journal: Spine (Phila Pa 1976) Date: 2003-03-01 Impact factor: 3.468
Authors: Mark H Bilsky; Yoshiya Yamada; Kamil M Yenice; Michael Lovelock; Margie Hunt; Philip H Gutin; Steven A Leibel Journal: Neurosurgery Date: 2004-04 Impact factor: 4.654
Authors: C Bouthors; S Prost; C Court; B Blondel; Y P Charles; S Fuentes; H P Mousselard; C Mazel; C H Flouzat-Lachaniette; P Bonnevialle; F Saihlan Journal: Support Care Cancer Date: 2019-08-09 Impact factor: 3.603
Authors: P James Jensen; Jordan A Torok; C Rory Goodwin; Scott R Floyd; Qiuwen Wu; Q Jackie Wu; John P Kirkpatrick Journal: J Radiosurg SBRT Date: 2022
Authors: Joyce H Keyak; Mando L Eijansantos; Katherine G Rosecrance; Daniel Wong; Sayeh Feizi; Aleen L Meldosian; Pranav Peddinti; Clifford M Les; Harry B Skinner; Varun Sehgal Journal: Phys Med Biol Date: 2022-04-01 Impact factor: 4.174
Authors: Giuseppe Di Perna; Fabio Cofano; Cristina Mantovani; Serena Badellino; Nicola Marengo; Marco Ajello; Ludovico Maria Comite; Giuseppe Palmieri; Fulvio Tartara; Francesco Zenga; Umberto Ricardi; Diego Garbossa Journal: J Bone Oncol Date: 2020-09-26 Impact factor: 4.072
Authors: Julio C Furlan; Jefferson R Wilson; Eric M Massicotte; Arjun Sahgal; Michael G Fehlings Journal: Neuro Oncol Date: 2022-01-05 Impact factor: 13.029