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DOI:10.2214/AJR.05.1529
AJR 2006; 187:571-574
© American Roentgen Ray Society


Technical Innovation

Percutaneous MR-Guided Radiofrequency Ablation of Recurrent Sacrococcygeal Chordomas

Volker Teichgräber1,2, Christophe Aubé1, Diethard Schmidt1, Ekkehard Jehle3, Claudius König1, Claus D. Claussen1 and Philippe L. Pereira1

1 Department of Radiology, University of Tübingen, Hoppe-Seyler-Strasse 3, 70276 Tübingen, Germany.
2 Present address: Department of Medical Oncology/Tumor Research, West German Cancer Center, Essen, Germany.
3 Department of Surgery, University of Tübingen, Tübingen, Germany.

Received August 30, 2005; accepted after revision November 3, 2005.

 
Address correspondence to P. L. Pereira (philippe.pereira{at}med.uni-tuebingen.de).


Abstract
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Abstract
Introduction
Materials and Methods
Results
Discussion
References
 
OBJECTIVE. Radiofrequency ablation is emerging as a therapeutic technique for the treatment of an increasing variety of tumors. Exact visual guidance to the tumor and controlled delivery of energy is pivotal for ablation success.

CONCLUSION. Introducing MRI as a guidance technique ideally uses tumor-specific tissue characteristics, allows direct multiplanar reconstruction for precise needle positioning, and permits real-time monitoring and assessment of treatment-induced tissue signal changes to increase the safety of the procedure.

Keywords: ablation • dynamic MRI • interventional radiology • MRI • percutaneous • radiofrequency


Introduction
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Abstract
Introduction
Materials and Methods
Results
Discussion
References
 
Radiofrequency ablation is a minimally invasive technique used for the treatment of liver malignancies. Reports of approaches using radiofrequency ablation in the treatment of nonhepatic neoplasms have been published [1, 2]. For percutaneous radiofrequency ablations of liver tumors, sonography or CT is commonly used for guidance. Recent reports have already shown the successful coagulation of a chordoma using CT [3, 4]. We prefer to perform radiofrequency ablation of chordomas under MRI guidance because of tissue-specific characteristics, direct multiplanar reconstruction, and the near real-time monitoring of tissue changes. The latter feature represents our major argument in favor of MR guidance because precise ablation algorithms are missing [5]. Because of their high water content, chordomas may present with different electrical properties compared with liver tumors, and algorithms for extrahepatic tumor ablation are seldom reported in the literature [6]. We describe the successful ablation of two recurrent sacrococcygeal chordomas under MR guidance to show the potential of MR-guided radiofrequency ablation.


Materials and Methods
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Abstract
Introduction
Materials and Methods
Results
Discussion
References
 
A 66-year-old woman was diagnosed in 1998 with sacrococcygeal chordomas. From 1998 to 2001, she underwent four surgical resections, but several tumor foci were not completely resectable. The patient was suffering from mainly two tumor foci. First, the chordoma in the right pararectal space (Fig. 1A) caused severe local pain and a disturbing sensation of frequent urgent bowel movements. Second, the chordoma near the left ischiadic nerve aroused persisting sciatic neuralgia. In consensus with our surgeons, we suggested radiofrequency treatment under MR guidance. The patient agreed to the attempt of radiofrequency ablation.


Figure 1
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Fig. 1A 66-year-old woman with recurrent sacrococcygeal chordomas. A-C are T2-weighted transverse images. Follow-up images D-F are T1-weighted fat-saturated contrast-enhanced with high-field-strength MRI. For radiofrequency treatment, patient was placed in prone position on left side. (These images have been rotated to resemble regular supine scanning position.) Before procedure, location of paraanal sacrococcygeal chordoma was determined (arrow, A). Using multiplanar reconstruction in MRI, radiofrequency applicator (arrow, B) could be exactly placed in center of tumor (only transverse section is shown). After treatment, hyperintense signal of tumor is replaced by hypointense coagulated material (arrow, C).

 
Before ablation, localization of the tumor foci was obtained with T1-weighted spin-echo (TR/TE, 400/20) and T2-weighted turbo spin-echo (4,080/109) imaging on a 2-T open scanner (Magnetom Concerto, Siemens Medical Solutions), with and without application of 0.1 mmol/kg of body weight of gadopentetate dimeglumine (Magnevist, Schering). Radiofrequency ablation itself was performed using an MR-compatible radiofrequency system composed of a 480-kHz radiofrequency generator (CC, Valleylab) and an internally cooled MR-compatible applicator (CTM 1530, Valleylab). The length of the needle was 15 cm, including an active tip of 3 cm. Local anesthesia was achieved with lidocaine 1%. The MR-compatible applicator was placed using MR fluoroscopy (fast imaging with steady-state free precession [FISP], 50/18). For both ablations, exact needle position was confirmed before ablation after multiplanar reconstruction (Fig. 1B). Afterward, the treated regions were assessed using the same preinterventional MR settings (Fig. 1C). The total duration of the procedure, including applicator placement, was 90 minutes. Under CT guidance, the total time of the procedure would have been similar because of the required time-intense computed reconstructions of the intervention area.


Figure 2
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Fig. 1B 66-year-old woman with recurrent sacrococcygeal chordomas. A-C are T2-weighted transverse images. Follow-up images D-F are T1-weighted fat-saturated contrast-enhanced with high-field-strength MRI. For radiofrequency treatment, patient was placed in prone position on left side. (These images have been rotated to resemble regular supine scanning position.) Before procedure, location of paraanal sacrococcygeal chordoma was determined (arrow, A). Using multiplanar reconstruction in MRI, radiofrequency applicator (arrow, B) could be exactly placed in center of tumor (only transverse section is shown). After treatment, hyperintense signal of tumor is replaced by hypointense coagulated material (arrow, C).

 

Figure 3
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Fig. 1C 66-year-old woman with recurrent sacrococcygeal chordomas. A-C are T2-weighted transverse images. Follow-up images D-F are T1-weighted fat-saturated contrast-enhanced with high-field-strength MRI. For radiofrequency treatment, patient was placed in prone position on left side. (These images have been rotated to resemble regular supine scanning position.) Before procedure, location of paraanal sacrococcygeal chordoma was determined (arrow, A). Using multiplanar reconstruction in MRI, radiofrequency applicator (arrow, B) could be exactly placed in center of tumor (only transverse section is shown). After treatment, hyperintense signal of tumor is replaced by hypointense coagulated material (arrow, C).

 

Results
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Abstract
Introduction
Materials and Methods
Results
Discussion
References
 
Results of previous studies suggest that radiofrequency-treated lesions have a characteristic appearance on contrast-enhanced T1- and T2-weighted MR images [7]. On T2-weighted cross sections, an inner hypointense zone corresponds to necrotic tissue, and a hyperintense outer zone corresponds to edema or hemorrhage surrounding the ablation area. Therefore, the first radiofrequency ablation was stopped after 2 minutes to acquire T2-weighted images for the assessment of signal changes in the treated area. In accordance with these observations, viable chordoma presented with hyperintensity on T2-weighted images, and coagulated tissue became hypointense (Figs. 1B and 1C). For radiofrequency ablation of the paraischiadic chordoma, we delivered 39.9 kJ heat energy to this area (130 W for 2 minutes [electric current1 = 1.3 A] and 135 W for 3 minutes [electric current2 = 1.35 A]), with intermittent MRI (T2-weighted) after 2 minutes and 3 minutes, respectively. Subsequently, 49.2 kJ was applied to the paraanal tumor (164 W for 2 minutes [electric current1 = 1.6 A] and 164 W for 3 minutes [electric current2 = 1.64 A]), and intermittent MRI control was also obtained after the first 2 minutes. Ablation areas showed clear loss of signal intensity at T2-weighted imaging, corresponding to structural changes within the tumors. Immediately after the radiofrequency session, the patient experienced a complete regression of her symptoms. Two hours after postinterventional monitoring, the patient refused the previously scheduled admission because her complaints had become nonexistent, and she was discharged.


Figure 4
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Fig. 1D 66-year-old woman with recurrent sacrococcygeal chordomas. A-C are T2-weighted transverse images. Follow-up images D-F are T1-weighted fat-saturated contrast-enhanced with high-field-strength MRI. In longitudinal study 4 weeks after thermal ablation therapy, pararectal ablation area (arrow) shows thermal-induced necrosis and peripheral inflammation. Surrounding muscular structures show slight alterations, but no damages such as abscesses can be observed.

 


Figure 5
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Fig. 1E 66-year-old woman with recurrent sacrococcygeal chordomas. A-C are T2-weighted transverse images. Follow-up images D-F are T1-weighted fat-saturated contrast-enhanced with high-field-strength MRI. In second control 4 months after ablation, region shows scarring and residual edema (arrow). Necrotic areas are no longer detectable in pararectal region. Alterations of surrounding structures are regressive in obturator muscle.

 


Figure 6
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Fig. 1F 66-year-old woman with recurrent sacrococcygeal chordomas. A-C are T2-weighted transverse images. Follow-up images D-F are T1-weighted fat-saturated contrast-enhanced with high-field-strength MRI. Regeneration (arrow) continues after 10 months. No signs of tumor relapse and complete regression of clinical symptoms are indicators of successful ablation.

 
In follow-up examinations, the pararectal ablation area presented with increasing tissue scarring (Figs. 1D, 1E, and 1F). The lesion in the vicinity of the ischiadic nerve showed the preceding signs of tissue reorganization without edema, and the size of the coagulative area was shrinking as well. In summary, both radiofrequency-ablated sacrococcygeal chordomas showed signs of progressive scarring and size reduction.


Discussion
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Abstract
Introduction
Materials and Methods
Results
Discussion
References
 
Sacrococcygeal chordoma is the most common primary malignant tumor of the spine in adults excluding lymphoproliferative neoplasms [8]. The therapy of choice is surgical resection, but prognosis remains poor because sacrococcygeal chordomas have an almost 100% recurrence rate, resulting in a 10-year average survival.

In an interdisciplinary approach to the treatment of sacrococcygeal chordomas, percutaneous radiofrequency ablation is an alternative to surgery, which could be considered a new first choice in the treatment of recurring mesenchymal tumors.

Our patient reported immediate relief of symptoms after the thermal ablation. Radiofrequency treatment of the paraanal lesion has saved her from proctectomy and diverting colostomy. But radiofrequency ablation in sensitive locations like the paraproctium or in the vicinity of important vessels and nerves can be accompanied by severe complications. In our case, perforation of the rectum, lesion of the anal sphincter with anal incontinence, and definite destruction of the ischiadic nerve were obvious risks. In the vicinity of nerves, nerve conduction studies could help monitor the integrity of the structure. But our patient was not sedated and thus was able to provide verbal feedback.

Although the field of radiofrequency is constantly growing with regard to the types of tumors that are potentially treatable with this method, algorithms to monitor the course of the ablation do not exist for treatment of tumors other than hepatic malignancies. MRI has some advantages over CT and sonography for guidance of radiofrequency ablation of chordomas. First, the nucleus pulposus-like tissue features of the mesenchymal sacrococcygeal chordoma make MRI the technique of choice. T2-weighted imaging clearly delineates chordoma from the surrounding tissue, allowing an excellent assessment of the tumor. Second, MRI allows multiplanar reconstruction for optimal spatial and temporal needle positioning into the tumor. Third, interventional MR monitoring allowed us to assess immediately the extent of thermally induced tissue alterations. The loss of protons in coagulated tissue corresponds to a readily detectable and sensitive signal change in T2-weighted imaging. Because no protocols are available for the radiofrequency ablation of chordomas and many other tumors (in terms of power, current, time, and resistance), the quick loss of signal intensity in T2-weighted imaging makes controlled empirical procedures possible and safer. In our case, the intraprocedural monitoring precisely directed us to interrupt the intervention after a total ablation time of 5 minutes. In contrast, specific findings on CT after radiofrequency of neoplasms are air bubbles and lack of signal enhancement after the administration of contrast material. Unfortunately, the amount of contrast material is limited because of its nephrotoxicity, and after repeated injections of contrast material an equilibrium is established; that is, further discrimination of the focus is not possible because of residues of dye in the organ and in the lesion. Moreover, the guided probing of the chordomas using CT fluoroscopy delivers high doses of radiation. At the same time, the MR technique disqualifies standard metal radiofrequency ablation probes for the intervention. Therefore, commercially available MR-compatible probes were used and worked reliably.

In conclusion, despite lacking long-term data, this study shows that MR-guided radiofrequency ablation is effective and safe and should be considered for the treatment of malignancies located in the pelvis. Major progress in the field of radiofrequency ablation depends on the development of a noninvasive online monitoring of the induced thermal effects in patients. Especially in areas with delicate anatomic structures, MRI of small regions of interest may render radiofrequency ablation safer.


References
Top
Abstract
Introduction
Materials and Methods
Results
Discussion
References
 

  1. Dupuy DE, Zagoria RJ, Akerley W, Mayo-Smith WW, Kavanagh PV, Safran H. Percutaneous radiofrequency ablation of malignancies in the lung. AJR 2000; 174:57 -59[Free Full Text]
  2. Callstrom MR, Charboneau JW, Goetz MP, et al. Painful metastases involving bone: feasibility of percutaneous CT- and US-guided radio-frequency ablation. Radiology 2002;224 : 87-97[Abstract/Free Full Text]
  3. Neeman Z, Patti JW, Wood BJ. Percutaneous radiofrequency ablation of chordoma. AJR 2002;179 : 1330-1332[Free Full Text]
  4. Anis N, Chawki N, Antoine K. Use of radio-frequency ablation for the palliative treatment of sacral chordoma. AJNR2004; 25:1589 -1591[Abstract/Free Full Text]
  5. McDannold NJ, King RL, Jolesz FA, Hynynen KH. Usefulness of MR imaging-derived thermometry and dosimetry in determining the threshold for tissue damage induced by thermal surgery in rabbits. Radiology 2000;216 : 517-523[Abstract/Free Full Text]
  6. Lewin JS, Nour SG, Connell CF, et al. Phase II clinical trial of interactive MR imaging-guided interstitial radiofrequency thermal ablation of primary kidney tumors: initial experience. Radiology2004; 232:835 -845[Abstract/Free Full Text]
  7. Aschoff AJ, Rafie N, Jesberger JA, Duerk JL, Lewin JS. Thermal lesion conspicuity following interstitial radiofrequency thermal tumor ablation in humans: a comparison of STIR, turbo spin-echo T2-weighted, and contrast-enhanced T1-weighted MR images at 0.2 T. J Magn Reson Imaging 2000; 12:584 -589[CrossRef][Medline]
  8. Resnick DR, Greenway GD. Tumors and tumor-like lesions of bone: imaging and pathology of specific lesions. In: Resnick DR, ed. Bone and joint imaging. Philadelphia, PA: Saunders, 1996:1046 -1048

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