To investigate mid- to long-term efficacy of MRgFUS in the treatment of accessible symptomatic osteoid osteomas
METHOD AND MATERIALSPatients were eligible if they had clinical and imaging diagnosis of Osteoid Osteoma. Lesions located in vertebral body were excluded; recurrences after RFA or surgery were included. Patients received focal therapy using MRgFUS (InSightec), delivered toward the nidus. Primary endpoints were pain relief assessed using questionnaires on Visual Analog Pain Score (VAS) and daily intake of Non-steroidal drugs (NSAIDs); secondary endpoints were need for further intervention and bone changes analyzed at imaging (CT and dynamic CE-MRI; Gd-BOPTA, Bracco). Patient’s follow-up, including clinical and imaging examinations, was established at 1 and 12 months
RESULTS36 patients (female 8; male, 28; mean age 26) were recruited for MRgFUS treatment; all patients completed the procedure without adverse events immediately after treatment or at follow-up. A mean number of 6 ± 1.5 sonications with mean energy of 991 ± 452 J was necessary to complete the treatment. Three patients underwent treatment as rescue (2 post-RFA, 1 post surgery). Complete clinical response was found in 32/36 (88.8%) patients (pain score=0 and NSAIDs discontinuation). There was a statistically significant difference (p=0.001) between baseline (7 ± 2) and follow-up values (0 ± 2) for pain severity, according to VAS. Two patients (5.1%) reported pain recurrence requiring both RFA and other two experienced pain decrease >2 points in the scale but did not reach 0, being classified as partial responders without requiring further interventions. Imaging evaluation with CE-MRI demonstrated marked reduction of nidus perfusion in all complete responders
CONCLUSIONMRgFUS can be effectively adopted for the treatment of Osteoid Osteoma. This application is totally non-invasive with robust pain relief
CLINICAL RELEVANCE/APPLICATIONMRgFUS can be performed safely with high rate of success for the noninvasive treatment of Osteoid Osteoma
To evaluate MRgFUS treatment efficacy in patients with painful bone metastases non responding to pain-killer drugs and radiation therapy.
METHOD AND MATERIALSOur study included 44 patients (14 female and 30 males; mean age 61,4 ± 9,5) suffering from metastatic bone disease. All patients were considered non responders to conventional therapies (radiation, analgesic drugs) and were preliminary analyzed by contrast-enhanced MR imaging and pain scale assessment (Quality of Life Questionnaire-BM22 and VAS scale). We treated 52 non-vertebral skeletal metastases with MRgFUS (ExAblate 2100, InSightec). Follow-up evaluation comprehended MR scan and pain scale scoring at 3 and 6 months after treatment.
RESULTSMRgFUS ablation was performed without adverse events. 26 out of 44 patients (60%) experienced a complete clinical response and suspended any other therapy. 13/44 patients (31%) reported an incomplete response (more than 2 points decrease in VAS pain scale). 5/44 patients (9%) have been classified as non-responders (less than 2 points decrease in VAS pain scale). Statistically significant differences between baseline, 3-month and 6-month follow-up have been demonstrated, in terms of VAS scale, analgesic drugs intake and pain interference on quality of life (QLQ- BM22).
CONCLUSIONMRgFUS treatment of bone metastases is effective and safe in pain palliation of selected patients.
CLINICAL RELEVANCE/APPLICATIONMRgFUS could be routinely introduced in treatment options for painful bone metastases non responding to conventional treatment.
Radiological percutaneous osteosynthesis and cementoplasty (RPOC) is a recent technique for interventional radiologists. It is a minimally invasive procedure and could be an alternative of surgery in patients with metastatic disease. We report our experience in the field of oncology.
METHOD AND MATERIALSWe retrospectively reviewed all cases of RPOC performed in our hospital in patients suffering from osteolytic metastases with or to prevent pathological fracture. An impending pathological fracture was defined by a Mirels' score > 8.
After institutional review board the patients were not candidates for surgery due to poor performans status, refusal or on-going chemotherapy. RPOC was performed with cannulated screws under computed tomography and scopic guidance with a CT-Navigation device.We retrospectively analyzed occurrence of post-procedural fractures, reduction in pain, technical feasibility, duration in the operating room, early complications and duration of hospitalization.
Between September 2013 and November 2015 RPOC was performed in 30 patients (10 women, 20 men, mean age of 59 y ± 11). The technical success was 96,7% with screwing a failed iliopubic branch too fragile. The average duration of the procedure was 92 minutes ± 19. All patients got up and walked on the day after the surgery. The average duration of hospital stay was 4 days ± 3 (range, 2-10).Twenty patients had RPOC for impending malignant pathological fracture, 14 of the proximal femur and 6 of the acetabulum roof. The average Mirels' score was 9.8 ± 1.1 (range, 8-12).For the proximal femur, no fracture occurred, with a median follow-up of 242 days (range, 11-600).For the acetabulum roof, 2 pathological fractures occurred (fracture rate=33,3%, mean follow-up of 245 days).Ten patients had RPOC for 10 painful pathologic fractures.For symptomatic patients (n = 17), visual analog scale (VAS) decreased from 6.8 ± 1.2 (range, 5-9) before treatment, to 2.3 ± 1.1 (range, 1-4) one month later.
CONCLUSIONRadiological Percutaneous Osteosynthesis and Cementoplasty for osteolytic metastasis is a safe and feasible technique.For fragile patients that are not candidates for surgical stabilization, RPOC can be a good alternative in pain relief of pathologic fractures or consolidation of lytic metastasis with a high fracture risk.
CLINICAL RELEVANCE/APPLICATIONAlternative at surgical stabilization for fragile metastatic patients
To use an elastomeric polymer material rather than traditional polymethymethacrylate ("PMMA") or acrylic bone cement in vertebroplasty could theoretically lower the number of secondary fractures. Primary endpoint of the present study was to assess safety of image-guided vertebroplasty using a novel silicone based elastomeric polymer material (elastoplasty). Secondary endpoint was the effectiveness in pain relief.
METHOD AND MATERIALS19 patients (13 females, mean age 72±10 y) underwent elastoplasty between 2010 and 2016. 14 patients had osteoporotic fractures, 2 patients traumatic fractures, 1 patient a painful myeloma localization, and 1 patient a painful vertebral angioma. 15 patients were using a brace and all were consuming drugs for pain relief. A total of 33 vertebrae were treated (range L1-T6). Patients were treated under local anesthesia and fluoroscopic guidance, using transpedicular approach and 2-6 ml of silicone based elastomeric polymer material (VK100) was injected by an interventional radiologist with more than 20 years’ experience in vertebroplasty. Chest x-ray was performed after the procedure in order to detect pulmonary embolism. Immediate and late complications, if any, were recorded, and VAS and Oswestry before and after the procedure evaluated.
RESULTSIt was always possible to complete the procedure. In 6/19 (31.5%) asymptomatic leakage of the material was observed. Minimal asymptomatic pulmonary embolism was seen in 4/19 (21%) patients, with no alteration of the saturation parameters. After two days no evidence of pulmonary emboli existed. In 18/19 (94%) patients had a recovery from pain symptoms. One patient with painful angioma did not experienced any change in symptoms. VAS and Oswestry scores were significantly reduced after the procedure, from 7.9±1.1 to 0.7±1.4 (p<0.001) and from 79.6±12% to 9.9±14% (p<0.001) respectively. 14/15 (93%) of the patients no longer required a brace after the procedure (p<0.001) and 16/19 (84%) completely stopped using any drugs for pain relief after treatment (p<0.001). At a mean follow-up of 2.1±2.4 years, no new treatment for symptomatic vertebral fractures were needed.
CONCLUSIONImage-guided elastoplasty is a safe and effective procedure when performed by experienced operator.
CLINICAL RELEVANCE/APPLICATIONelastopasty is a novel procedure that can be safely performed by experienced operators, and holds the potential of lowering the number of secondary fractures.
To evaluate the technical feasibility and safety of CT and fluoroscopy guided percutaneous vertebroplasty in the treatment of tumoral vertebral fractures with epidural involvement.
METHOD AND MATERIALSInstitutional review board approval and informed consent were obtained for this study. Sixty-three consecutive adult patients (35 women, 28 men; mean age +/- standard deviation: 69 years +/- 14) with tumoral spinal fractures that compromised the posterior vertebral column with epidural involvement were prospectively treated by means of percutaneous vertebroplasty with CT and fluoroscopy guidance. Only local anesthesia was used during these procedures. Postoperative outcome was assessed using the Kostuik index.
RESULTSSixty-three vertebroplasties were performed on thirty-four thoracic (54%), twenty-six lumbar (41%), and three (5%) cervical vertebrae. The etiologies of the fractures were metastasis in twenty-eight (44%), myeloma in twenty-five (40%) and hemangioma in ten (16%). Almost all fractures (94%) were consolidated after vertebroplasty (score of Kostuik <3) (p < 0.001). No major complications were reported in our series of cases.
CONCLUSIONThis study suggests that tumoral spinal fractures with posterior vertebral wall involvement can be successfully and safely treated by CT and fluoroscopy-guided percutaneous vertebroplasty.
CLINICAL RELEVANCE/APPLICATIONPercutaneous vertebroplasty in tumoral fractures with posterior vertebral wall involvement is feasible, efficient and safe. Its use by the physicians in charge is recommended to benefit the patient.
AwardsTrainee Research Prize - Medical Student
We aim to establish an effective and novel nomogram for intradiscal cement leakage (ICL) following percutaneous vertebroplasty (PVP) in patients with osteoporosis vertebral compression fractures (OVCFs).
METHOD AND MATERIALSPatients with OVCFs who underwent their first PVP in our department between January 2007 and December 2013 were included in this study. Univariate and multivariate analysis were used to predict the independent risk factors. The Nomogram was then created based on the identified independent risk factors.
RESULTSA total of 241 patients and 330 vertebrae were included. The mean age of the patients was 73.5 (SD 7.9) years old, and the mean number of treated vertebrae was 1.4 per person. ICL was observed in 93 (28.2%) of the treated vertebrae. Greater fracture severity (P=0.016), cortical disruption of the endplate (P<0.0001), absence of Kummell’s disease (P=0.010), and higher CT values (P=0.050) are the independent risk factors for ICL.
CONCLUSIONGreater fracture severity, cortical disruption of the endplate, absence of Kummell’s disease, and higher CT values are the independent risk factors for ICL. The novel nomogram gives accurate prediction of ICL.
CLINICAL RELEVANCE/APPLICATIONThis predictive nomogram can guide physicians do something to prevent ICL
evaluate the feasibility and effectiveness of CT-guided percutaneous screw fixation plus cementoplasty (PSFPC) in patients with painful vertebral metastases with fractures or to prevent pathological fracture.
METHOD AND MATERIALSTwenty patients (7 men and 13 women, median age 52 years) with 24 vertebral metastases (7 NSCLC, 7 multiple myeloma, 6 breast carcinoma) underwent CT–guided PSFPC. The procedure was performed in a single vertebra in 16 patients and in two vertebrae in 4 patients. The vertebral approach was unilateral with a single screw in thirteen patients and bilateral with two screws in the remaining 7. We analyzed the feasibility and complications of the procedure, the decrease in pain using a visual analogue scale (VAS) and the functional outcome assessed according to the evolution of their walking ability.
RESULTSThere were no complications related to infections or incorrect positioning of the screws or leakage of cement. VAS score decreased from 7.4 (range, 4- 9) to 1.2 (range, 0-3). All patients were able to walk within 6 hours after the procedure and have improved their walking capacity at six months. No new bone fracture occurred during a median follow up of 10 months.
CONCLUSIONour results suggest that PSFPC is a safe and effective procedure which allows us to stabilize the fracture and prevent pathological fractures with a significant pain relief and good recovery of walking ability. PSFPC seems to be a promising alternative for patients who are not candidates for surgery. Further studies are required to confirm this preliminary experience.
CLINICAL RELEVANCE/APPLICATIONThese results may introduce a new method of palliative treatment in patients with painful vetebral metastatic lesion with fracture or at high risk of fracture.
The objectives of this study were to determine the accuracy of percutaneous image-guided spinal biopsy of osseous spinal lesions in patients with known or suspected underlying malignancy in reference to the imaging appearance of the biopsied lesion and to analyze factors affecting the higher biopsy yield.
METHOD AND MATERIALSWe retrospectively reviewed 247 consecutive percutaneous spinal biopsies. Size (< 2 cm and ≥ 2 cm), location (C-, T-, L-spine, and sacrum), and CT density (osteoblastic, osteolytic, mixed, and isodense) of the lesion, guiding modality (CT and fluoroscopy), years of biopsy attending experience (< 2 years and ≥ 2 years), number of approach (one and ≥ 2), pathologic report of the biopsy, and final diagnosis of the lesion were recorded. A biopsy was considered as diagnostic if it provided a confident pathologic result or non-diagnostic if the pathology could not suggest a specific diagnosis. All variables were compared using Pearson’s chi square test or Fisher’s exact test.
RESULTSIn all, 197 of 247 (79.8%) biopsies were diagnostic. On multivariate analysis, size, CT density, and final diagnosis of the lesion were statistically significant factors on affecting biopsy yield. Biopsy in larger lesions (≥ 2 cm) showed significantly higher diagnostic yield than smaller lesion (p = 0.006). The osteolytic lesions had highest diagnostic rate (87.6%), followed by mixed (84.4%), osteoblastic (66.7%) and isodense lesions (61.1%). There was statistically significant difference in the diagnostic biopsy rates of osteolytic versus osteoblastic lesions (p=0.004) and of osteolytic versus isodense lesions (p=0.031). Metastasis had highest diagnostic rate (97.2%), followed by primary malignancy (84.2%) and benign lesion (39.4%) with statistical significance.
CONCLUSIONIn the percutaneous image-guided biopsy for the spinal lesion, size, CT density, and final diagnosis of the lesion can affect the higher biopsy yield. Osteolytic lesions have higher diagnostic biopsy rate than osteoblastic or isodense lesions. Metastatic lesions have highest diagnostic biopsy rate followed by primary malignant and benign lesions.
CLINICAL RELEVANCE/APPLICATIONPercutaneous biopsies for osteolytic or mixed spinal lesions have a higher diagnostic yield than for osteoblastic or isodense lesions.
AwardsStudent Travel Stipend Award
We aim to compare the short- and long-term effects of cryoablation (Cryo) versus radiofrequency ablation (RFA) on nontarget articular cartilage tissue during CT-guided periarticular bone ablation in an in vivo porcine model.
METHOD AND MATERIALSFollowing Institutional Animal Care and Use Committe approval, 3 juvenile female miniature pigs underwent a 2-arm study using the animals as their own control. Pigs #1 and #2 underwent CT-guided periarticular bone ablations (pig#1-Cryo; pig#2-RFA) at 4 different sites each, and all limbs (including 1 control site) were removed from both pigs immediately following the procedures. Pig #3 underwent periarticular bone Cryo or RFA at 3 different sites each, and all limbs (including 1 control site) were removed 7 weeks following the procedure. For all ablations, an 11-gauge coaxial introducer was percutaneously advanced into the target epiphyseal site followed by placement of single RFA or Cryo probe 1cm from the articular surface under general anesthesia. RFA was performed for a total of 6 minutes at a target temperature of 90 degrees Celsius using 17G cooled-tip electrodes. Cryo was performed using 17G probes for two 10-5-minute freeze-thaw cycles. All bone and articular cartilage specimens were examined histologically with H&E staining.
RESULTSIn vivo Cryo and RFA both resulted in acute osteonecrosis at the ablation sites without associated histologic articular cartilage disruption immediately following the procedure. Cryo and RFA resulted in focal osteonecrosis and inflammatory reaction with bone remodeling at the ablation sites without associated histological cartilage disruption 7 weeks following the percutaneous ablation therapy.
CONCLUSIONIn vivo Cryo and RFA of periarticular bone in a porcine model did not result in short- or long-term histological articular cartilage disruption. These findings suggest that both Cryo and RFA may not cause significant damage to the adjacent articular cartilage tissue during percutaneous periarticular osseous ablation therapies.
CLINICAL RELEVANCE/APPLICATIONNontarget articular cartilage disruption is a potential risk associated with periarticular thermal bone ablation, and there is paucity of data on the long-term effects.