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Chapter25:Percutaneous ablation of bone metastases
Figure 25.6 Common anatomy to avoid.
Figure 25.7 Cryoablation in the proximity
of the obturator nerve.
Ideally, placement of the cryoprobes is based on the geom­etry of the target tumor so that the shape of the ice matches the shape of the target tumor. Typically, the cryoprobes are placed along the long axis of the tumor and at an angle to allow slow growth of the ice in the direction of adjacent critical structures.
Many bone and so-tissue metastases are adjacent to criti­cal structures. Understanding the path of major motor nerves and the artery of Adamkiewicz is helpful for the performance of safe ablation procedures.13 As illustrated in Figure25.6, these structures can be clearly identied and avoided at the time of the ablation procedure. An example of the use of cryoablation in the proximity of the obturator nerve is shown in Figure25.7. A so-tissue and bony metastasis involving the pubic bone
was treated with four cryoprobes placed through the tumor to generate ice that matched the shape of the complex tumor. e evolution of the ice ball showed complete coverage of the tumor while avoiding the adjacent obturatornerve.
Following completion of the second freeze cycle, the cryo­probes are warmed with active heating with helium gas until the temperature is >20°C. e cryoprobes can be withdrawn at this point, although continued warming of the probes over a period of approximately 10minutes may result in a reduced risk of hematoma formation. Immediate postprocedural pain is typically treated with intravenous fentanyl (Abbott Laboratories, Chicago, IL) and midazolam (Versed; American Pharmaceutical Partners, Los Angeles, CA). For patients with
249
Section VIII:Musculoskeletal
persistent pain, oral analgesics or a patient-controlled analge­sia unit can be used and the dose titrated to provide adequate pain relief.

Cryoablation pain palliation outcomes

Multiple reports have found that percutaneous cryoablation is eective in treating painful primary and secondary bone neo­plasms. With excellent visibility of the ice ball with both CT and MRI, both imaging technologies have been employed for treatment of painful metastatic disease. MR monitoring of the cryoablation procedure oers the ability to visualize complex structures, such as important motor nerves, in multiple imag­ing planes, although the environment restricts devices that can be utilized. Sewell and colleagues reported the use of percu­taneous cryoablation for palliation of 16 painful tumors in 14 patients using MR guidance and monitoring.26 ey found the treatment provided a signicant reduction in patients’ pain in the immediate postoperative period. is pain relief continued over the long term with associated signicant improvement in patients’ quality of life. Tuncali and colleagues reported the use of MRI-guided and monitored cryoablation for treatment of patients with refractory or painful metastatic tumors in bone and so tissue adjacent to critical structures.27 Pain pal­liation was partially or completely achieved in 17/19 (89%) of patients, with complete pain relief in six of these patients. One patient experienced initial relief but subsequent recurrence of pain. With the visibility of the ice ball with MRI monitoring and with the use of additional measures to reduce the risk of injury, including warming urethral catheters, intramedullary rod placement, and skin warming, no immediate complica-
Table 25.2 Characteristics of patients treated with cryoablation in
a prospective multicenter trial
Number of patients
Female 22
Male 39
Age (years), mean (range) 61 (range 21–95)
Tumor type (number)
Lung 16 (31%)
Renal 10 (20%)
Colorectal 7 (14%)
Melanoma 4 (8%)
Prostate 4 (8%)
Squamous cell (non-lung) 3 (6%)
Transitional cell 2 (4%)
Paraganglioma 2 (4%)
Breast 2 (4%)
Other (one each) 11 (22%)
Tumor size (longest diameter; cm) 4.8 (range 1.0–11.0)
Tumor location
Rib/chest wall 33 (48%)
Iliac/ischium/pubic bones 20 (29%)
Scapula/clavicle/sternum 7 (10%)
Sacrum 5 (7%)
Extremity 2 (3%)
Vertebral body 1 (1%)
Mastoid 1 (1%)
tions were noted as a result of immediate thermal injury. One patient suered a femoral neck fracture 6weeks aer cryoabla­tion of a metastatic renal cell carcinoma in this location that was not treated with an intramedullaryrod.
Cryoablation is compatible with methods to monitor and avoid potential neural injury. Lessard and colleagues reported the use of somatosensory-evoked potentials to monitor the S1 nerve during ablation of a painful recurrent Ewing sarcoma in the mid and upper right hemisacrum. is treatment resulted in pain palliation and avoided nerve damage in this distribu­tion; however, the ablation caused incontinence of bowel and bladder, possibly due to ablation injury of the S2–S4 nerve roots bilaterally, compounded by prior extensive radiation therapy and baseline nerve dysfunction.
28
Although MRI oers excellent so-tissue resolution and tumor conspicuity, in most centers CT suites are more acces­sible for ablation procedures and have larger-bore diameters than those available with current MRI systems. Ullrick and colleagues reported the CT-guided and monitored use of cry­oablation for the treatment of three patients with painful meta­static disease involving the pelvis and ribs, with palliation in two out of three patients.
29
In a multicenter prospective clinical trial, 69 painful skel­etal metastases were treated with cryoablation in 61 patients.30 e patient cohort in the cryoablation trial is similar to the cohorts in the previous multicenter RFA trials for pain pallia­tion due to metastatic skeletal disease (Table25.2). Figure25.8
shows the cryoablation treatment of a painful metastatic para­ganglioma contained in a le rib with durable response to treatment throughout the follow-up period. Mean pain scores (worst pain in a 24-hour period using the BPI 10-point scale) signicantly decreased from 7.1 to 5.1, 4.0, 3.6, and 1.4 at 1, 4, 8, and 24 weeks aer treatment, respectively (Figure25.9). irty-nine of the 47 patients (83%) who reported opioid anal­gesic use prior to the procedure reported a reduction in their use. Asingle patient experienced a major complication (2%), with osteomyelitis occurring at the ablationsite.
A majority of patients received radiation to the treated site and had failed to achieve pain relief prior to entry into the trial. However, 23 of 61 patients (38%) patients had not received radiation prior to treatment and a total of 13 of 61 patients (21%) had received neither radiation treatment nor chemo­therapy prior to cryoablation treatment. Importantly, there was no signicant dierence in pain scores for patients who had or had not received radiation prior to cryoablation treatment and there was no signicant dierence in pain scores throughout the follow-up period. Postprocedure pain control was managed with patient-controlled intravenous opioid analgesia for 12 of 61 patients (20%) in the immediate posttreatment recovery period. No patients required placement of an epidural cath­eter in the immediate postprocedure recovery period or during their hospitalization. Hospitalization length of stay averaged
250
Chapter25:Percutaneous ablation of bone metastases
AC
BD
71
71
Figure 25.8 Cryoablation treatment
of a painful metastatic paraganglioma contained in a left rib.
10
8
6
4
Mean Worst Pain
2
0
0
246810 12 14 16 18 20 22 24
N =615754474735323126222118171649
10
8
6
4
10
8
6
4
Mean Average Pain
2
0
0
246810 12 14 16 18 20 22 24
N =6156534746343231262221181
100
80
60
40
Mean Pain Relief
2
Mean Pain Interference
20
649
0
0
246810 12 14 16 18 20 22 24
N =625653474734323125222118171748
Weeks Weeks
0
246810 12 14 16 18 20 22 24
0
N =6056534647343231262221181
649
Figure 25.9 Mean pain scores.
251
Section VIII:Musculoskeletal
1.5days, with a range from 0 to 6days. No patients suered an injury to a major motor nerve or reported neuropathic pain following the procedure. Although the complication rate using RFA for treatment of painful metastases is low, two of 55 (4%) of patients suered neurologic injuries in a clinical trial.
16
Comparison of outcomes from RFA and cryoablation for palliation of painful bone metastases is dicult, despite similar cohorts of patients in clinical trials that were conducted with consistent tools for measuring patient response. In general, the clinical response rates and magnitude of pain palliation are similar. Even though clinical outcomes may be similar follow­ing RFA, cryoablation can be performed on tumors more con­dently in close proximity to critical structures due to visibility of the ice ball with non-contrast CT imaging. In the recent cry­oablation study,30 the major complication rate was 2% (one of 61 patients), with the one complication due to an infection in the treatment area. No patients suered an injury to a major motor nerve or reported neuropathic pain following the proce­dure, as has been observed with RFA treatment. Although the overall complication rate using RFA for treatment of painful metastases is low, two of 55 (4%) of patients suered neurologic injuries in a clinical trial.16 In addition, pain management fol­lowing RFA can be dicult, oen requiring regional anesthetic blocks or epidural catheters when possible, while postproce­dural pain with cryoablation is readily managed with intrave­nous or oral opioid analgesia when necessary.
31
Comparison of patient response scores following percu­taneous cryoablation to data reported from the treatment of patients with radiotherapy is dicult, as the methods that have been used in radiotherapy trials for measuring patient pain response do not correspond directly with the BPI used in the cryoablation study and the number of patients in the prospec­tive cryoablation trial is small. However, some comparisons are possible, as cryoablation results in signicant pain reduction, with a 43% mean reduction in worst pain in 4 weeks, which is considered to be clinically signicant.32 Patients also reported that pain relief 4weeks following cryoablation ranged from
heat into the targeted tumor. acoustic pathway to the target tumor is needed, as bowel or neurologic structures intervening between the skin and skel­etal tumor are at potential risk of injury.
Most recently, a prospective randomized clinical trial of the use of MRgFUS for palliation of painful skeletal metastases was conducted that included a measure of the placebo eect.38 is study involved a 3:1 randomization to treatment for 112 patients and a sham arm of 35 patients. MRgFUS was superior to the placebo, with a drop in average worst pain from 7/10 at presentation to 3.4/10 for the treatment arm versus a drop to
6.1/10 for the placebo arm at the 3-month time point. e most common side eect of treatment was pain related to sonication during the procedure (32.1% of patients), which ranged from mild, to moderate, to severe in 6.2%, 10.7%, and 15.2%, respec­tively. Severity of adverse events was not reported, although two fractures (one likely unrelated to the procedure), one instance of neuropathy, and one third-degree skin burn werenoted.
Several additional thermal and non-thermal ablative tech­nologies are available beyond RFA, cryoablation, and MRgFUS to treat painful tumors and have been applied to skeletal metas­tases in limited series. Reports of the use of ethanol, laser abla­tion (or laser interstitial thermal therapy), and microwave ablation have all shown that these focal therapies are eective for palliation of painful metastases. a heat-based technique similar to RFA, using percutaneously placed antennae to transmit microwave spectrum of energy (915MHz or 2.45GHz). Oscillation of water molecules within tissue about the antennae leads to localized heating, which reaches cytotoxic temperatures faster than RFA and should also theoretically penetrate intact bone more eectively.42 Laser ablation utilizes small-caliber, exible, Nd-YAG or diode laser bers placed coaxially through a thin access needle. An advan­tage of laser ablation systems is MRI compatibility. e abla­tion size obtained with each laser activation is small and most experience with laser ablation in bone has been in the treat­ment of osteoid osteomas.
36,37
However, a direct ultrasound
39,40,41
Microwave ablation is
43
50% to100%, which compares favorably to reported radiother­apy responses. Further conclusions about the relative benet of ablation treatments and radiotherapy are not possible and a randomized prospective trial comparing cryoablation and radiotherapy would be necessary to determine the relative response of patients’ pain to these treatments.

Summary

Treatment of patients with pain due to metastatic disease involving bone or so tissue with focal therapies has proven to be eective at palliation of pain and can be performed safely. ese focal therapies are eective for patients who have refused

Emerging technologies

Recently, several reports have appeared describing the use of MR-focused ultrasound (MRgFUS) for the palliation of pain­ful skeletal metastases.
33,34,35
Focused ultrasound energy is
radiation therapy and for those who have failed to derive pain relief or developed recurrent pain following radiation treat­ment. e quality of life for patients treated with these focal therapies is also improved. Importantly, the pain reduction that is achieved is durable over many months of observation.
directed at the target, using MRI guidance, that leads to focal tissue heating and tissue destruction. is technique combines excellent tumor delineation with MRI for targeting and ther­mal feedback for treatment monitoring, and has the advantage of being a non-invasive tumor ablation treatment. Typically the procedure is performed with conscious sedation, although pain with sonication is best managed with the use of region blocks or epidural catheter analgesia, where appropriate.35 e high acoustic absorption of bone results in ecient transfer of

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15. Callstrom MR, Charboneau JW, Goetz MP, Rubin J, Atwell TD, Farrell MA, etal. Image-guided ablation of painful metastatic bone tumors:a new and eective approach to a dicult problem. Skeletal Radiol 2006; 35 (1):1–15.
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17. Callstrom MR, Atwell TD, Charboneau JW, Farrell MA, Goetz MP, Rubin J, etal. Painful metastases involving bone:percutaneous image-guided cryoablation–prospective trial interim analysis. Radiology 2006; 241 (2):572–580.
18. Grieco CA, Simon CJ, Mayo-Smith WW, DiPetrillo TA, Ready NE, Dupuy DE. Image-guided percutaneous thermal ablation for the palliative treatment of chest wall masses. Am J Clin Oncol Cancer Clin Trials 2007; 30 (4):361–367.
19. Sabharwal T, Katsanos K, Buy X, Gangi A. Image-guided ablation therapy of bone tumors. Semin Ultrasound CT MR 2009; 30 (2):78–90.
20. Sabharwal T, Salter R, Adam A, Gangi A. Image-guided therapies in orthopedic oncology. Orthoped Clin North Am 2006; 37 (1):105.
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29. Ullrick SR, Hebert JJ, Davis KW. Cryoablation in the musculoskeletal system. Curr Probl Diagn Radiol 2008; 37 (1):39–48.
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31. Thacker PG, Callstrom MR, Curry TB, Mandrekar JN, Atwell TD, Goetz MP, etal. Palliation of painful metastatic disease involving bone with image-guided treatment:comparison of patients immediate response to radiofrequency ablation and cryoablation. AJR Am J Roentgenol. 2011; 197 (2): 510–515.
32. Farrar JT, Young JP, Jr., LaMoreaux L, Werth JL, Poole RM. Clinical importance of changes in chronic pain intensity measured on an 11-point numerical pain rating scale. Pain 2001; 94:149–158.
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34. Napoli A, Anzidei M, Marincola BC, Brachetti G, Ciolina F, Cartocci G, etal. Primary pain palliation and local tumor control in bone metastases treated with magnetic resonance-guided focused ultrasound. Invest Radiol 2013; 48 (6):351–358.
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38. Hurwitz MD, Ghanouni P, Kanaev SV, Ioze D, Gianfelice D, Fennessy FM, etal. Magnetic resonance-guided focused ultrasound for patients with painful bone metastases:Phase III trial results. J Natl Cancer Inst 2014; 106(5).
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40. Pusceddu C, Sotgia B, Fele RM, Melis L. Treatment of bone metastases with microwave thermal ablation. J Vasc Interv
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42. Brace CL. Radiofrequency and microwave ablation of the liver, lung, kidney, and bone:what are the dierences? Curr Probl Diagn Radiol 2009; 38 (3):135–143.
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254
Chapter

Cementoplasty and musculoskeletal interventions

26
Dimitri Filippiadis, Sean Tutton and Alexis Kelekis

Introduction

Nearly 60% of oncologic patients will eventually develop osse­ous metastasis with bone pain, potential fracture, and impaired mobility. While the rst-line therapy for these patients is oen medical, including narcotic analgesics, according to the World Health Organization recommendations, and bisphosphonate therapy such as zoledronic acid infusions, a signicant portion of patients have intractable pain. Similarly, those patients who are treated with palliative external-beam radiotherapy may have incomplete pain relief that is not always durable.
1,2
Furthermore, pain relief from radiotherapy can take up to 4weeks and can be complicated by osteonecrosis or neural damage.
1,2
e high per­centage of oncologic patients suering from painful metastatic bone lesions and their fractures, compounded with suboptimal results of conservative medical and radiotherapy, have been the drivers for development of minimally invasive local treatments, including embolization, ablation, and cement augmentation (also known as cementoplasty or osteoplasty).
Percutaneous cementoplasty is a term referring to the injec­tion of poly methylmethacrylate (PMMA), a polymer (similar in certain ways to orthopedic cement) inside an osseous struc­ture through a trocar under imaging guidance. When the tech­nique is applied in the spine, the term used is vertebroplasty. Alternatives to standard vertebroplasty include balloon kyphop­lasty, augmented vertebroplasty by means of stents, nitinol cages, and polyether ether ketone (PEEK) polymer cages, and radiofrequency-mediated vertebroplasty or kyphoplasty.
2,3,4,5,6
When one of these techniques is applied to the sacrum the term used is sacroplasty. described by the term osteoplasty.
7,8
Cement injection in peripheral bones is
2,9,10
e rst ever description of imaging-guided cement injection was performed by Galibert etal. for the treatment of an aggressive cervical hemangioma.11 Awider term now used to include all these percutaneous approaches of material injection inside bone is bone augmentation.

Indications

When considering oncologic patients a strict denition of the treatment goal is necessary for best practice and outcomes. Palliative goals include cement injection for pain reduction
in patients with multiple metastases, some of which are pain-
12,13
ful.
Currently, new technologies and material allow us to consider curative treatment, which can be performed in oligo­metastatic patients, aiming at both local control and necrosis of the tumor as well as pain reduction and mobility improvement. In the latter case, cementoplasty must be combined with other therapies. such as radiotherapy, ablation, embolization, or sur­gical resection and/or xation.
12,13,14,15
Primary indications for cementoplasty in oncologic patients include the presence of symptomatic metastatic lesions in an osseous structure located anywhere from the spine to the periph­eral skeleton. Denition of the treatment goal will determine not only the technique, but also any potential combination ther­apies in addition to sequencing of the various techniques. Symptomatic hematopoietic neoplasms (such as leukemia and multiple myeloma) or symptomatic vascular tumors (heman­gioma) respond well to percutaneous cementoplasty alone or in combination with xation techniques, discussed later.
17,18,19

Contraindications

Absolute contraindications to bone injection in oncologic patients include the presence of concomitant systemic or local infection, uncorrectable bleeding diathesis, allergy to cement, and insucient cardiopulmonary status to tolerate sedation. Any kind of anticoagulation must be interrupted; duration of interruption is according to the international guidelines for each medication. In the presence of infection, bone augmenta­tion must be postponed until the patient undergoes a full anti­biotic course and becomes afebrile with normal white blood cell values and negative blood cultures.
Relative contraindications include factors which techni­cally increase the diculty of the procedure without rendering it impossible. ese factors include posterior wall disruption with or without tumor extension in the epidural space, myelop­athy or radiculopathy secondary to tumor extension in the spi­nal canal or neural foramen, signicant loss of vertebral height (vertebra plana), and inability to image the target lesion either with uoroscopy or computed tomography (CT) guidance due to various factors.
2,4,6,20
14,15,16
2,4,6
Interventional Oncology, Second Edition, ed. Jean-François H.Geschwind and Michael C.Soulen. Published by Cambridge University Press. ©Cambridge University Press2016
255
Section VIII:Musculoskeletal
Preproceduralcare
When evaluating the cancer patient, prior to performing bone augmentation the interventional oncologist should be aware of the tumor histology (benign or malignant), the patient’s gen­eral condition, and the degree of bone destruction. ese fac­tors, along with the strictly dened treatment goal, will direct a nal decision, which should be obtained at multidisciplinary oncologic boards.
orough medical record examination is necessary in order to exclude anticoagulation, evidence of infection, or comorbidities that increase the mortality and morbidity rate of the session. Laboratory workup should include complete blood cell count, coagulation study, and screening of basic metabolic panel. Electrocardiography, chest X-ray, and anes­thesia evaluation are performed according to local practice guidelines.
Physical examination is critical for proper patient selection. e majority of oncologic patients will have more than one metastasis; however, only symptomatic levels should be treated. Point tenderness at the spinous process of the pathologic ver­tebrae assists in localizing and targeting treatment in patients with multiple lesions. Localization can be precise, by placing metallic markers at the level of point tenderness on the skin and having a lateral uoroscopy image or a lateral radiograph of the spine. Neurologic examination should be performed in all patients. In the case of a patient with pre-existing neuro­logic decits, a baseline neurologic exam, repeated on the day of procedure, is required to assess the patient’s neurologic func­tion prior to any procedure. Achanging neurologic exam is reason to consult a spine surgeon for possible decompression.
Radiographs can serve as initial imaging evaluation; how­ever, they provide limited information in oncologic patients. Magnetic resonance imaging (MRI) is the study of choice since it best illustrates the presence of a lesion, bone edema, extra­osseous tumor extension, and potential pressure upon nerve structures. Total body diusion-weighted sequences illustrate the extent of malignancy. If MRI is contraindicated (e.g., pace­maker or cochlear implant), CT scans combined with bone scintigraphy can be performed.21 CT is superior in illustrating the sclerotic/blastic character of the lesion and the integrity of osseous cortex or vertebral body’s posteriorwall.

Technique

All cementoplasty techniques are performed under imag­ing guidance, antibiotic prophylaxis, and strict sterility. Fluoroscopy is the imaging modality in most of the cases. When high precision is necessary, multidetector CT or cone-beam CT can be used as modality of choice.
In the spine, a posterolateral transpedicular approach is more commonly used in the lumbar and thoracic spine. In the upper cervical spine a transoral approach is preferred (Figures
26.1 and 26.2). In the mid and lower cervical levels an antero-
lateral approach through the vertebral body is performed in the majority of the cases. Occasionally variations of the aforemen­tioned approaches or alternative ones are performed depend­ing on the location of the lesion to be treated and the treatment
goal. Since neoplastic lesions tend to be located in the poste­rior vertebral elements, occasionally the needle may need to be placed within the pedicle for cement injection (pediculo­plasty).22 For sacroplasty the two more common approaches include passage through the sacroiliac joint targeting the S1 corridor or posterior approach parallel to and medial to the sacroiliac joint. Approaches for peripheral osteoplasty vary according to the location of the lesion to be treated and the treatmentgoal.
Following needle placement, its position is veried, with some operators choosing to inject contrast medium prior to cementation. Despite the fact that cement and contrast medium have dierent viscosities, it seems that contrast injection prior to cementation provides valuable information for the poten­tial distribution patterns of the cement and illustrates potential leakagesites.
Cement injection can be likened to embolization with direct communication to the vasculature and should there­fore be performed under continuous uoroscopy.
2,4,6
In onco­logic patients, the cement of choice is PMMA, which sets and hardens via a polymerization reaction during which there is exothermic release of heat sucient to cause a temperature increase in the treated tissue.
Balloon kyphoplasty is a variant of vertebroplasty during which a cavity is created by rst drilling followed by ination of a balloon tamp in order to achieve height restoration and reduce rates of cement leakage.
2,3,4,5,6
Currently, augmented vertebroplasty by means of intravertebral nitinol cages, stents, or PEEK polymer coils/cages is performed, aiming to enhance safety and ecacy rates
2,3,4,5,6
(Figure26.3). ese techniques are particularly useful in cancer-related pathologic fractures when there is extensive osteolysis causing destruc­tion of the posterior or anterior cortices as they can aord additional protection by cement containment. Further, these implant-based vertebral augmentation techniques rely on the implant for structural stability and allow for employment of biologically active tumoricidal cements currently in develop­ment. Early studies are promising, but additional studies of these techniques in oncologic patients are necessary for their superiority to be proven.
3
Oncologic patients typically suer from multiple lesions requiring treatment. Ideally these lesions should be treated within a single procedure and anesthetic session. Factors to be considered for such treatments include PMMA or local anes­thetic toxicity, fat pulmonary embolism (during cement injec­tion marrow droplets are pushed into the circulation), and duration of the procedure in the context of performance status. Comparison of procedures up to and more than three treated vertebral levels favors the latter for cost-eectiveness without any expense of safety or ecacy.
23
In the setting of oligometastatic disease the goal of treat­ment can be curative. e question of when to oer ablation alone, cementoplasty alone, or combination therapy has not been adequately answered. Cementoplasty provides stabiliza­tion and pain reduction. e question whether PMMA alone can provide enough cytotoxicity to destroy the lesion is still under debate. In the non-surgical patient, ablation is steadily
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Chapter26:Cementoplasty and musculoskeletal interventions
Figure 26.1 Breast Ca metastatic lesion in T7. (A) P-A fluoroscopic view illustrating bilateral transpedicular access. (B) Lateral fluoroscopic view illustrating bilateral
transpedicular access with the needles beyond the posterior vertebral wall. (C) Coaxially a bone biopsy needle was introduced for lesion sampling. (D) Lateral fluoroscopic view illustrating bilateral transpedicular access with the needles in anterior third of the vertebral body. (E) P-A fluoroscopic view illustrating bilateral transpedicular access with the needles towards the midline of the vertebral body. (F) Lateral fluoroscopic view illustrating vertebroplasty needles and cement injection. (G) Lateral fluoroscopic view illustrating satisfactory filling of the vertebral body with the polymer extending from top to bottom and beyond the midline.
Figure 26.2 71-year-old patient post left nephrectomy with new L1 lesion. (A) CT scan, axial reconstruction illustrating lesion at L1 vertebral body.
(B, C) CT scan, axial reconstruction during RFA and vertebroplasty of the biopsy proven RCC metastasis in the L1 vertebral body. (D) Six month follow-up contrast CT scan (coronal recostruction) showing local control of disease. (E) Six month follow-up contrast CT scan (axial recostruction) showing local control of disease.
gaining ground as a treatment of choice. Ablation is discussed in the previous chapter.
When performed in weight-bearing bones, unexpected fractures can occur secondary to access holes in the cortex or due to osteonecrosis induced by the ablation zone.24 In this
setting, cementoplasty with or without screw xation may be combined to strengthen the underlying bone when there is con­cern about collapse or fracture. Cementoplasty should follow ablation and enough time should be allowed between the two techniques for internal bone temperature to return to normal
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Section VIII:Musculoskeletal
Figure 26.3 Multiple myeloma – lytic lesion in L4 vertebral body. (A) Lateral fluoroscopic view illustrating vertebroplasty needle in anterior third of the vertebral
body. (B) Lateral fluoroscopic view illustrating satisfactory filling of the vertebral body with the polymer extending from top to bottom and beyond the midline. (C) P-A fluoroscopic view illustrating satisfactory filling of the vertebral body with the polymer extending from top to bottom and beyond the midline.
Figure 26.4 44-year-old patient with metastatic melanoma resulting in pain with ambulation. (A) CT scan, coronal reconstruction illustrating impending
acetabular fracture. (B) CT scan, axial reconstruction during RFA of acetabular lesion with articulating RF probe. (C) CT scan, axial reconstruction post PMMA augmentation of the acetabular defect (D) CT scan, coronal reconstruction illustrating 8 mm cannulated screw fixation of acetabular defect with augmentation. (E) CT scan, sagittal reconstruction of augmented screw fixation.
so as not to accelerate cement polymerization in the case of heat-based ablation or have unpredictable cement ll due to residual ice ball in setting of cryoablation. Cementoplasty has been combined with multiple therapies, including radiother­apy, ablation, embolization, or surgery
12,13,14,15
(Figure26.4).
Injection of PMMA is a recognized augmentation strategy, but also has been utilized as an embolic agent in malignant vascular bone lesions. Specically for vertebral hemangiomas, cementoplasty is both an embolic and an augmentation agent whenever the lesion is contained within the vertebral body and cement lls the whole lesion or at least its largest part; in case of
epidural extension direct puncture or microcatheter emboliza­tion should precede cementoplasty. In this setting digital sub­traction angiography for localization of anterior spinal artery (Adamkiewicz’s artery) provides critical information.
Ecacy and complications
e success rate of cementoplasty ranges from 60% to 85% with respect to pain reduction and mobility improvement. overall complication rate in oncologic patients is 5–10%. Potential complications include cement leakage, pulmonary embolism, hematoma/hemorrhage, infection, hypotension,
2,4,6
e
2,4,6
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