J Korean Soc Magn Reson Med.  2011 Dec;15(3):200-207. 10.13104/jksmrm.2011.15.3.200.

Assessment of Therapeutic Response of Ablated Lesion after Radiofrequency Ablation in Patients with Unresectable Lung Malignancies by Multiphase Contrast-enhanced MRI

Affiliations
  • 1Department of Radiology, Chonbuk National University Medical School and Hospital, Research Institute of Clinical Medicine, Korea. gyjin@chonbuk.ac.kr
  • 2Department of Internal Medicine, Chonbuk National University Medical School and Hospital, Research Institute of Clinical Medicine, Korea.
  • 3Department of Preventive Medicine, Chonbuk National University Medical School and Hospital, Research Institute of Clinical Medicine, Korea.

Abstract

PURPOSE
We evaluated which phase was important to recognize local progression of an ablated zone after RFA on multiphase contrast-enhanced MRI (CE-MRI) in patients with unresectable lung malignancy.
MATERIALS AND METHODS
Twenty patients who had unresectable lung malignancy underwent multiphase CE-MRI examinations immediately after RFA. We evaluated the enhancement patterns of the ablated zone on multiphase CE-MRI: type I, no enhancement of the ablated zone; type II, enhancement of the ablated margin; type III, heterogeneous enhancement of the ablated zone. We evaluated the association enhancement type with local progression of the ablated zone on the follow up CT using Spearman's ranked test.
RESULTS
In complete ablation, the enhancement pattern was types I (11.1%) or II (88.9%). In unsuccessfully treated, type II (57.1%) or III (42.9%) pattern observed in the arterial phase. However, types II (21.4%) and III (78.6%) observed in the venous, and types II (7.1%) and III (92.9%) observed equilibrium phases. Local progression of the ablated zone was associated with the enhancement pattern in equilibrium phases (r=0.8, p < .05).
CONCLUSION
Equilibrium phases on multiphase CE-MRI might play a more important role in evaluating an ablated zone for predicting local recurrence after RFA.

Keyword

Lung neoplasms; Radiofrequency (RF) ablation; Magnetic resonance imaging (MRI)

MeSH Terms

Follow-Up Studies
Humans
Lung
Lung Neoplasms
Recurrence

Figure

  • Fig. 1 Diagrams of the enhancement patterns on the contrast-enhanced MRI performed immediately after RFA: The ablation zone was divided into the central region (central ablated zone except ablated margin) and the ablated margin (peripheral ablated zone within 10 mm of the outermost margin of the ablated zone). These enhancement patterns of ablated zone are classified into the following three types: Type I, absolutely no enhancement; Type II, only enhancement of the ablated margin; and Type III, heterogeneous enhancement of the ablated zone.

  • Fig. 2 46-year-old man with a complete response. He had undergone radiation therapy due to lung malignancy. (a) Chest CT scans (lung setting) before RFA shows a 1 cm, single metastatic nodule in the left lower lobe. (b) On the CE-MRI, the enhancement pattern of the ablated zone leads it to be categorized as type I in the arterial and venous phases. In the equilibrium phase, the enhancement pattern is type II. Enhancement of the hyperemic zone is observed on the equilibrium phases (arrow). (c) Eighteen months later, the previous single metastatic nodule had disappeared completely and a large uniloculated cavity is observed as a post-RFA complication on chest CT (lung setting).

  • Fig. 3 62-year-old man with progressive disease. (a) Contrast-enhance chest CT scans before RFA shows a 6 cm mass in the left lower lobe. (b) On CE-MRI, the enhancement pattern of the ablated zone leads it to be categorized as type II in the arterial and venous phase but the enhancement pattern in the equilibrium phase changes to type III. (c) Eight months later, the tumor size increase approximately 9 cm and completely obstructed the bronchus of the left lower lobe on contrast-enhanced CT.


Reference

1. Fry WA, Phillips JL, Menck HR. Ten-year survey of lung cancer treatment and survival in hospitals in the United States: a national cancer data base report. Cancer. 1999. 86:1867–1876.
2. Hsu CP, Hsu NY, Chen CY. Surgical experience in treating T4 lung cancer: its resectability, morbidity, mortality and prognosis. Eur J Surg Oncol. 1996. 22:171–176.
3. Lee JM, Jin GY, Goldberg SN, et al. Percutaneous radiofrequency ablation for inoperable non-small cell lung cancer and metastases: preliminary report. Radiology. 2004. 230:125–134.
4. Suh RD, Wallace AB, Sheehan RE, Heinze SB, Goldin JG. Unresectable pulmonary malignancies: CT-guided percutaneous radiofrequency ablation--preliminary results. Radiology. 2003. 229:821–829.
5. Ketchedjian A, Daly B, Luketich J, Fernando HC. Minimally invasive techniques for managing pulmonary metastases: video-assisted thoracic surgery and radiofrequency ablation. Thorac Surg Clin. 2006. 16:157–165.
6. Dupuy DE, Zagoria RJ, Akerley W, Mayo-Smith WW, Kavanagh PV, Safran H. Percutaneous radiofrequency ablation of malignancies in the lung. AJR Am J Roentgenol. 2000. 174:57–59.
7. Steinke K, Glenn D, King J, et al. Percutaneous imaging-guided radiofrequency ablation in patients with colorectal pulmonary metastases: 1-year follow-up. Ann Surg Oncol. 2004. 11:207–212.
8. Bojarski JD, Duppy DE, Mayo-Smith WW. CT imaging findings of pulmonary neoplasmas after treatment with radiofrequency ablation: results in 32 tumors. AJR Am J Roentgenol. 2005. 185:466–471.
9. Jin GY, Lee JM, Lee YC, Han YM, Lim YS. Primary and secondary lung malignancies treated with percutaneous radiofrequency ablation: evaluation with follow-up helical CT. AJR Am J Roentgenol. 2004. 183:1013–1020.
10. Okuma T, Matsuoka T, Yamamoto A, et al. Assessment of early treatment response after CT-guided radiofrequency ablation of unresectable lung tumours by diffusion-weighted MRI: a pilot study. Br J Radiol. 2009. 82:989–994.
11. Oyama Y, Nakamura K, Matsuoka T, et al. Radiofrequency ablated lesion in the normal porcine lung: long-term follow-up with MRI and pathology. Cardiovasc Intervent Radiol. 2005. 28:346–353.
12. Rofsky NM, Lee VS, Laub G, et al. Abdominal MR imaging with a volumetric interpolated breath-hold examination. Radiology. 1999. 212:876–884.
13. Karabulut N, Martin DR, Yang M, Tallaksen RJ. MR imaging of the chest using a contrast-enhanced breath-hold modified three-dimensional gradient-echo technique: comparison with two-dimensional gradient-echo technique and multidetector CT. AJR Am J Roentgenol. 2002. 179:1225–1233.
14. Goldberg SN, Grassi CJ, Cardella JF, et al. Image-guided tumor ablation: standardization of terminology and reporting criteria. Radiology. 2005. 235:728–739.
15. Vogl TJ, Straub R, Lehnert T, et al. Percutaneous thermoablation of pulmonary metastases. Experience with the application of laser-induced thermotherapy(LITT) and radiofrequency ablation(RFA), and a literature review. Rofo. 2004. 176:1658–1666.
16. Liao WJ, Luo RC, Kang SJ, et al. Investigation of short-term therapy results for radiofrequency ablation by positron emission tomography. Di Yi Jun Yi Da Xue Xue Bao. 2002. 22:376–377.
17. Miao Y, Ni Y, Bosmans H, et al. Radiofrequency ablation for eradication of pulmonary tumor in rabbits. J Surg Res. 2001. 99:265–271.
18. Lencioni R, Crocetti L, Cioni R, et al. Radiofrequency ablation of lung malignancies: where do we stand. Cardiovasc Intervent Radiol. 2004. 27:581–590.
19. Smith S, Gillams A. Imaging appearances following thermal ablation. Clinical Radiology. 2008. 63:1–11.
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