Skip to main content
Top
Published in: Abdominal Radiology 8/2021

01-08-2021 | Hepatocellular Carcinoma | Interventional Radiology

Radiofrequency versus microwave ablation for hepatocellular carcinoma within the Milan criteria in challenging locations: a retrospective controlled study

Authors: Xue Han, Jia-yan Ni, Shao-long Li, Han-xia Deng, Hui-ming Liang, Ying-ying Xu, Zhi-mei Huang, Tian-qi Zhang, Jin-hua Huang

Published in: Abdominal Radiology | Issue 8/2021

Login to get access

Abstract

Purpose

The aim of this study was to compare the safety and efficacy of radiofrequency ablation (RFA) with microwave ablation (MWA) for hepatocellular carcinoma (HCC) within the Milan criteria in challenging locations.

Methods

This study retrospectively investigated 201 consecutive patients with Milan criteria HCCs who underwent RFA (RFA group, n = 150) or MWA (MWA group, n = 51) between January 2012 and December 2016. Overall survival (OS), recurrence-free survival (RFS), local tumor control, and treatment-related complications were compared between the two groups. Prognostic factors were analyzed using the Cox proportional hazard regression model.

Results

Median follow-up duration was 36.7 months (range: 6.2–64.0 months). Cumulative 1-, 3-, and 5-year OS rates were 97.9%, 92.3%, and 80.6% in the MWA group and 96.4%, 87.4%, and 78.2% in the RFA group, respectively, (P = 0.450). Cumulative RFS rates at 1, 3, and 5 years were 93.2%, 74.4%, and 63.7% in the MWA group and 80.3%, 57.3%, and 49.6% in the RFA group, respectively, (P = 0.097). Multivariate analyses showed that variable categories “patient age above 65 years” (P = 0.004) and “more than one tumor” (P = 0.004) were associated with overall mortality, and “patient age above 65 years” (P = 0.048) and “tumor size greater than 3 cm” (P = 0.009) were associated with inferior RFS. The incidences of major complications were not significantly different between the two groups (3.3% vs 3.9%, P = 0.843).

Conclusions

RFA and MWA were associated with comparable safety and efficacy for HCC within the Milan criteria in challenging locations. Further study in a large, multi-center patient cohort is necessary to validate the results.
Literature
1.
go back to reference 1. Forner A, Llovet JM, Bruix J. Hepatocellular carcinoma. Lancet. 2012;379:1245-1255.CrossRef 1. Forner A, Llovet JM, Bruix J. Hepatocellular carcinoma. Lancet. 2012;379:1245-1255.CrossRef
2.
go back to reference 2. Jemal A, Bray F, Center MM, et al. Global cancer statistics. CA Cancer J Clin. 2011;61:69-90.CrossRef 2. Jemal A, Bray F, Center MM, et al. Global cancer statistics. CA Cancer J Clin. 2011;61:69-90.CrossRef
3.
go back to reference 3. European Association for Study of Liver; European Organisation for Research and Treatment of Cancer. EASL-EORTC clinical practice guidelines: management of hepatocellular carcinoma. Eur J Cancer. 2012;48:599-641.CrossRef 3. European Association for Study of Liver; European Organisation for Research and Treatment of Cancer. EASL-EORTC clinical practice guidelines: management of hepatocellular carcinoma. Eur J Cancer. 2012;48:599-641.CrossRef
4.
go back to reference 4. Bruix J, Sherman M. Management of hepatocellular carcinoma: An update. Hepatology. 2011;53:1020-1022.CrossRef 4. Bruix J, Sherman M. Management of hepatocellular carcinoma: An update. Hepatology. 2011;53:1020-1022.CrossRef
5.
go back to reference 5. Himoto T, Kurokohchi K, Watanabe S, et al. Recent advances in radiofrequency ablation for the management of hepatocellular carcinoma. Hepat Mon. 2012; 12: e5945.CrossRef 5. Himoto T, Kurokohchi K, Watanabe S, et al. Recent advances in radiofrequency ablation for the management of hepatocellular carcinoma. Hepat Mon. 2012; 12: e5945.CrossRef
6.
go back to reference 6. Liang P, Yu J, Yu XL, et al. Percutaneous cooled-tip microwave ablation under ultrasound guidance for primary liver cancer: a multicentre analysis of 1363 treatment-naive lesions in 1007 patients in China. Gut. 2012; 61: 1100-1101.CrossRef 6. Liang P, Yu J, Yu XL, et al. Percutaneous cooled-tip microwave ablation under ultrasound guidance for primary liver cancer: a multicentre analysis of 1363 treatment-naive lesions in 1007 patients in China. Gut. 2012; 61: 1100-1101.CrossRef
7.
go back to reference 7. Bruix J, Reig M, Sherman M. Evidence-Based Diagnosis, Staging, and Treatment of Patients With Hepatocellular Carcinoma. Gastroenterology. 2016; 150: 835-853.CrossRef 7. Bruix J, Reig M, Sherman M. Evidence-Based Diagnosis, Staging, and Treatment of Patients With Hepatocellular Carcinoma. Gastroenterology. 2016; 150: 835-853.CrossRef
8.
go back to reference 8. Feng K, Yan J, Li X, et al. A randomized controlled trial of radiofrequency ablation and surgical resection in the treatment of small hepatocellular carcinoma. J Hepatol. 2012; 57:794-802.CrossRef 8. Feng K, Yan J, Li X, et al. A randomized controlled trial of radiofrequency ablation and surgical resection in the treatment of small hepatocellular carcinoma. J Hepatol. 2012; 57:794-802.CrossRef
9.
go back to reference 9. Chen MS, Li JQ, Zheng Y, et al. A prospective randomized trial comparing percutaneous local ablative therapy and partial hepatectomy for small hepatocellular carcinoma. Ann Surg. 2006;243:321-328.CrossRef 9. Chen MS, Li JQ, Zheng Y, et al. A prospective randomized trial comparing percutaneous local ablative therapy and partial hepatectomy for small hepatocellular carcinoma. Ann Surg. 2006;243:321-328.CrossRef
10.
go back to reference 10. Andreano A, Huang Y, Meloni MF, et al. Microwaves create larger ablations than radiofrequency when controlled for power in ex vivo tissue. Medical physics. 2010; 37: 2967-2973.CrossRef 10. Andreano A, Huang Y, Meloni MF, et al. Microwaves create larger ablations than radiofrequency when controlled for power in ex vivo tissue. Medical physics. 2010; 37: 2967-2973.CrossRef
11.
go back to reference 11. Shady W, Petre EN, Gonen M, et al. Percutaneous Microwave versus Radiofrequency Ablation of Colon Cancer Liver Metastases: Ablation with clear margins (A0) provides the best local tumor control. J Vasc Interv Radiol. 2018; 29: 268-275.CrossRef 11. Shady W, Petre EN, Gonen M, et al. Percutaneous Microwave versus Radiofrequency Ablation of Colon Cancer Liver Metastases: Ablation with clear margins (A0) provides the best local tumor control. J Vasc Interv Radiol. 2018; 29: 268-275.CrossRef
12.
go back to reference 12. Mulier S, Ni Y, Jamart J, et al. Local recurrence after hepatic radiofrequency coagulation: multivariate meta-analysis and review of contributing factors. Ann Surg. 2005; 242: 158-171.CrossRef 12. Mulier S, Ni Y, Jamart J, et al. Local recurrence after hepatic radiofrequency coagulation: multivariate meta-analysis and review of contributing factors. Ann Surg. 2005; 242: 158-171.CrossRef
13.
go back to reference 13. Kamal A, Elmoety AAA, Rostom YAM, et al. Percutaneous radiofrequency versus microwave ablation for management of hepatocellular carcinoma: a randomized controlled trial. J Gastrointest Oncol. 2019;10:562-571.CrossRef 13. Kamal A, Elmoety AAA, Rostom YAM, et al. Percutaneous radiofrequency versus microwave ablation for management of hepatocellular carcinoma: a randomized controlled trial. J Gastrointest Oncol. 2019;10:562-571.CrossRef
14.
go back to reference 14. Xu Y, Shen Q, Wang N, et al. Microwave ablation is as effective as radiofrequency ablation for very-early-stage hepatocellular carcinoma. Chin J Cancer. 2017; 36:14.CrossRef 14. Xu Y, Shen Q, Wang N, et al. Microwave ablation is as effective as radiofrequency ablation for very-early-stage hepatocellular carcinoma. Chin J Cancer. 2017; 36:14.CrossRef
15.
go back to reference 15. Facciorusso A, Di Maso M, Muscatiello N. Microwave ablation versus radiofrequency ablation for the treatment of hepatocellular carcinoma: A systematic review and meta-analysis. Int J Hyperthermia. 2016;32:339-344.CrossRef 15. Facciorusso A, Di Maso M, Muscatiello N. Microwave ablation versus radiofrequency ablation for the treatment of hepatocellular carcinoma: A systematic review and meta-analysis. Int J Hyperthermia. 2016;32:339-344.CrossRef
16.
go back to reference 16. Poulou LS, Botsa E, Thanou I, et al. Percutaneous microwave ablation vs radiofrequency ablation in the treatment of hepatocellular carcinoma. World J Hepatol. 2015;7:1054-1063.CrossRef 16. Poulou LS, Botsa E, Thanou I, et al. Percutaneous microwave ablation vs radiofrequency ablation in the treatment of hepatocellular carcinoma. World J Hepatol. 2015;7:1054-1063.CrossRef
17.
go back to reference 17. Abdelaziz A, Elbaz T, Shousha HI, et al. Efficacy and survival analysis of percutaneous radiofrequency versus microwave ablation for hepatocellular carcinoma: an Egyptian multidisciplinary clinic experience. Surg Endosc. 2014; 28:3429-3434.CrossRef 17. Abdelaziz A, Elbaz T, Shousha HI, et al. Efficacy and survival analysis of percutaneous radiofrequency versus microwave ablation for hepatocellular carcinoma: an Egyptian multidisciplinary clinic experience. Surg Endosc. 2014; 28:3429-3434.CrossRef
18.
go back to reference 18. Teratani T, Yoshida H, Shiina S, et al. Radiofrequency ablation for hepatocellular carcinoma in so-called high-risk locations. Hepatology. 2006;43:1101-1108.CrossRef 18. Teratani T, Yoshida H, Shiina S, et al. Radiofrequency ablation for hepatocellular carcinoma in so-called high-risk locations. Hepatology. 2006;43:1101-1108.CrossRef
19.
go back to reference 19. Francica G, Meloni M F, De Sio I, et al. Radiofrequency and microwave ablation of subcapsular hepatocellular carcinoma accessed by direct puncture: Safety and efficacy. Eur J Radiol. 2016; 85:739-743.CrossRef 19. Francica G, Meloni M F, De Sio I, et al. Radiofrequency and microwave ablation of subcapsular hepatocellular carcinoma accessed by direct puncture: Safety and efficacy. Eur J Radiol. 2016; 85:739-743.CrossRef
20.
go back to reference 20. Filippiadis D K, Spiliopoulos S, Konstantos C, et al. Computed tomography-guided percutaneous microwave ablation of hepatocellular carcinoma in challenging locations: safety and efficacy of high-power microwave platforms. Int J Hyperthermia. 2017;34:1-29. 20. Filippiadis D K, Spiliopoulos S, Konstantos C, et al. Computed tomography-guided percutaneous microwave ablation of hepatocellular carcinoma in challenging locations: safety and efficacy of high-power microwave platforms. Int J Hyperthermia. 2017;34:1-29.
21.
go back to reference 21. Nha A , Aa A , Rnu A , et al. CT-Guided Percutaneous Microwave Ablation of Tumors in the Hepatic Dome: Assessment of Efficacy and Safety. J Vasc Interv Radiol. 2016;27:496-502.CrossRef 21. Nha A , Aa A , Rnu A , et al. CT-Guided Percutaneous Microwave Ablation of Tumors in the Hepatic Dome: Assessment of Efficacy and Safety. J Vasc Interv Radiol. 2016;27:496-502.CrossRef
22.
go back to reference 23. S Nahum Goldberg , Clement J Grassi, John F Cardella, et al. Image-guided Tumor Ablation: Standardization of Terminology and Reporting Criteria—A 10-Year Update[J]. J Vasc Interv Radiol. 2014;25:1691-1705.CrossRef 23. S Nahum Goldberg , Clement J Grassi, John F Cardella, et al. Image-guided Tumor Ablation: Standardization of Terminology and Reporting Criteria—A 10-Year Update[J]. J Vasc Interv Radiol. 2014;25:1691-1705.CrossRef
23.
go back to reference 24. Filippiadis DK, Binkert C, Pellerin O, et al. CIRSE quality assurance document and standards for classification of complications: the CIRSE classification system. Cardiovasc Intervent Radiol. 2017;40: 1141-1146.CrossRef 24. Filippiadis DK, Binkert C, Pellerin O, et al. CIRSE quality assurance document and standards for classification of complications: the CIRSE classification system. Cardiovasc Intervent Radiol. 2017;40: 1141-1146.CrossRef
24.
go back to reference 25. Liu W, Zheng Y, He W, et al. Microwave vs radiofrequency ablation for hepatocellular carcinoma within the Milan criteria: a propensity score analysis. Aliment Pharmacol Ther. 2018; 48:671-681.CrossRef 25. Liu W, Zheng Y, He W, et al. Microwave vs radiofrequency ablation for hepatocellular carcinoma within the Milan criteria: a propensity score analysis. Aliment Pharmacol Ther. 2018; 48:671-681.CrossRef
25.
go back to reference 26. Izzo F, Granata V, Grassi R, et al. Radiofrequency Ablation and Microwave Ablation in Liver Tumors: An Update. Oncologist. 2019;19. pii: theoncologist.2018-0337.CrossRefPubMedPubMedCentral 26. Izzo F, Granata V, Grassi R, et al. Radiofrequency Ablation and Microwave Ablation in Liver Tumors: An Update. Oncologist. 2019;19. pii: theoncologist.2018-0337.CrossRefPubMedPubMedCentral
26.
go back to reference 27. Lu MD, Xu HX, Xie XY, et al. Percutaneous microwave and radiofrequency ablation for hepatocellular carcinoma: a retrospective comparative study. J Gastroenterol. 2005; 40:1054-1060.CrossRef 27. Lu MD, Xu HX, Xie XY, et al. Percutaneous microwave and radiofrequency ablation for hepatocellular carcinoma: a retrospective comparative study. J Gastroenterol. 2005; 40:1054-1060.CrossRef
27.
go back to reference 28. Shibata T, Iimuro Y, Yamamoto Y, et al. Small hepatocellular carcinoma: comparison of radiofrequency ablation and percutaneous microwave coagulation therapy. Radiology. 2002; 223: 331-337.CrossRef 28. Shibata T, Iimuro Y, Yamamoto Y, et al. Small hepatocellular carcinoma: comparison of radiofrequency ablation and percutaneous microwave coagulation therapy. Radiology. 2002; 223: 331-337.CrossRef
28.
go back to reference 29. Tan W, Deng Q, Lin S, et al. Comparison of microwave ablation and radiofrequency ablation for hepatocellular carcinoma: a systematic review and meta-analysis. Int J Hyperthermia. 2019;36:264-272.PubMed 29. Tan W, Deng Q, Lin S, et al. Comparison of microwave ablation and radiofrequency ablation for hepatocellular carcinoma: a systematic review and meta-analysis. Int J Hyperthermia. 2019;36:264-272.PubMed
29.
go back to reference 22. Vo Chieu VD, Werncke T, Hensen B, et al. CT-Guided Microwave Ablation of Liver Tumors in Anatomically Challenging Locations. Cardiovasc Intervent Radiol. 2018; 41:1520-1529.CrossRef 22. Vo Chieu VD, Werncke T, Hensen B, et al. CT-Guided Microwave Ablation of Liver Tumors in Anatomically Challenging Locations. Cardiovasc Intervent Radiol. 2018; 41:1520-1529.CrossRef
30.
go back to reference 30. Lee KF, Hui JW, Cheung YS, et al. Surgical ablation of hepatocellular carcinoma with 2.45-GHz microwave: a critical appraisal of treatment outcomes. Hong Kong Med J. 2012; 18: 85-91.PubMed 30. Lee KF, Hui JW, Cheung YS, et al. Surgical ablation of hepatocellular carcinoma with 2.45-GHz microwave: a critical appraisal of treatment outcomes. Hong Kong Med J. 2012; 18: 85-91.PubMed
31.
go back to reference 31. Liang P, Wang Y. Microwave ablation of hepatocellular carcinoma. Oncology 2007; 72: Suppl 1: 124-131.CrossRef 31. Liang P, Wang Y. Microwave ablation of hepatocellular carcinoma. Oncology 2007; 72: Suppl 1: 124-131.CrossRef
32.
go back to reference 32. van Tilborg AA, Scheffer HJ, de Jong MC, et al. MWA Versus RFA for Perivascular and Peribiliary CRLM: A Retrospective Patient- and Lesion-Based Analysis of Two Historical Cohorts. Cardiovasc Intervent Radiol. 2016; 39:1438-1446.CrossRef 32. van Tilborg AA, Scheffer HJ, de Jong MC, et al. MWA Versus RFA for Perivascular and Peribiliary CRLM: A Retrospective Patient- and Lesion-Based Analysis of Two Historical Cohorts. Cardiovasc Intervent Radiol. 2016; 39:1438-1446.CrossRef
Metadata
Title
Radiofrequency versus microwave ablation for hepatocellular carcinoma within the Milan criteria in challenging locations: a retrospective controlled study
Authors
Xue Han
Jia-yan Ni
Shao-long Li
Han-xia Deng
Hui-ming Liang
Ying-ying Xu
Zhi-mei Huang
Tian-qi Zhang
Jin-hua Huang
Publication date
01-08-2021
Publisher
Springer US
Published in
Abdominal Radiology / Issue 8/2021
Print ISSN: 2366-004X
Electronic ISSN: 2366-0058
DOI
https://doi.org/10.1007/s00261-021-03105-9

Other articles of this Issue 8/2021

Abdominal Radiology 8/2021 Go to the issue