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Microwave ablation of liver malignancies: comparison of effects and early outcomes of percutaneous and intraoperative approaches with different liver conditions

New advances in interventional oncology: state of the art

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Abstract

Liver thermal ablation is an alternative treatment for hepatocellular carcinoma (HCC) and secondary liver malignancies. Microwave ablation (MWA) produces large ablation zones (AZ) in short time; however, AZ prediction is based on preclinical ex vivo models, rising concerns about reproducibility and safety in humans. We aimed to investigate the effects produced by a new-generation MWA system on human liver in vivo with different approaches (percutaneous or intraoperative) and liver conditions (cirrhosis or previous chemotherapy treatment), in comparison with manufacturer-provided predictions based on ex vivo animal models. Complete tumor ablation (CA) and early clinical outcomes were also assessed. From October 2014, 60 consecutive patients (cirrhotic = 31; non-cirrhotic = 10; chemotherapy-treated = 19) with 81 liver nodules (HCC = 31; mets = 50) underwent MWA procedures (percutaneous = 30; laparotomic = 18; laparoscopic = 12), with a 2450 MHz/100 W generator with Thermosphere™ Technology (Emprint™, Medtronic). A contrast-enhanced CT or MR was performed after one month to assess CA and measure AZ. A linear correlation between AZ volumes and ablation times was observed in vivo, without differences from manufacturer-provided ex vivo predictions in all operative approaches and liver conditions. Other independent variables (sex, age, nodule location) showed no relationship when added to the model. Median (IQR) longitudinal and transverse roundness-indexes of the AZs were, respectively, 0.77(0.13) and 0.93(0.11). CA at 1 month was 93% for percutaneous and 100% for intraoperative procedures (p = 0.175). Thirty-day morbidity and mortality were 3% and 0%. MWA with Thermosphere™ Technology produces predictable AZs on human liver in vivo, according to manufacturer-provided ex vivo predictions. In our experience, this new-generation MWA system is effective and safe to treat liver malignancies in different operative and clinical settings.

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References

  1. Weis S, Franke A, Mossner J, Jakobsen JC, Schoppmeyer K. Radiofrequency (thermal) ablation versus no intervention or other interventions for hepatocellular carcinoma. Cochrane Database Systematic Rev. 2013;(12):CD003046. doi:10.1002/14651858.CD003046.pub3.

  2. Cirocchi R, Trastulli S, Boselli C, Montedori A, Cavaliere D, Parisi A, et al. Radiofrequency ablation in the treatment of liver metastases from colorectal cancer. Cochrane Database Systematic Rev. 2012;(6):CD006317. doi:10.1002/14651858.CD006317.pub3.

  3. Wong SL, Mangu PB, Choti MA, Crocenzi TS, Dodd GD 3rd, Dorfman GS, et al. American society of clinical oncology 2009 clinical evidence review on radiofrequency ablation of hepatic metastases from colorectal cancer. J Clin Oncol Off J Am Soc Clin Oncol. 2010;28(3):493–508. doi:10.1200/JCO.2009.23.4450.

    Article  Google Scholar 

  4. European Association for the Study of the L, European Organisation for R, Treatment of C. EASL-EORTC clinical practice guidelines: management of hepatocellular carcinoma. J Hepatol. 2012;56(4):908–43. doi:10.1016/j.jhep.2011.12.001.

    Article  Google Scholar 

  5. Ferlay J, Soerjomataram I, Dikshit R, Eser S, Mathers C, Rebelo M, et al. Cancer incidence and mortality worldwide: sources, methods and major patterns in GLOBOCAN 2012. Int J Cancer. 2015;136(5):E359–86. doi:10.1002/ijc.29210.

    Article  CAS  PubMed  Google Scholar 

  6. Lencioni R, Cioni D, Crocetti L, Franchini C, Pina CD, Lera J, et al. Early-stage hepatocellular carcinoma in patients with cirrhosis: long-term results of percutaneous image-guided radiofrequency ablation. Radiology. 2005;234(3):961–7. doi:10.1148/radiol.2343040350.

    Article  PubMed  Google Scholar 

  7. Liu PH, Hsu CY, Hsia CY, Lee YH, Huang YH, Chiou YY, et al. Surgical resection versus radiofrequency ablation for single hepatocellular carcinoma ≤ 2 cm in a propensity score model. Ann Surg. 2016;263(3):538–45. doi:10.1097/SLA.0000000000001178.

    Article  PubMed  Google Scholar 

  8. Yamakado K, Nakatsuka A, Takaki H, Yokoi H, Usui M, Sakurai H, et al. Early-stage hepatocellular carcinoma: radiofrequency ablation combined with chemoembolization versus hepatectomy. Radiology. 2008;247(1):260–6. doi:10.1148/radiol.2471070818.

    Article  PubMed  Google Scholar 

  9. Chen MS, Li JQ, Zheng Y, Guo RP, Liang HH, Zhang YQ, et al. A prospective randomized trial comparing percutaneous local ablative therapy and partial hepatectomy for small hepatocellular carcinoma. Ann Surg. 2006;243(3):321–8. doi:10.1097/01.sla.0000201480.65519.b8.

    Article  PubMed  PubMed Central  Google Scholar 

  10. Hou YF, Wei YG, Yang JY, Wen TF, Xu MQ, Yan LN, et al. Combined hepatectomy and radiofrequency ablation versus TACE in improving survival of patients with unresectable BCLC stage B HCC. Hepatobiliary Pancreat Dis Int HBPD INT. 2016;15(4):378–85.

    Article  PubMed  Google Scholar 

  11. Choi D, Lim HK, Joh JW, Kim SJ, Kim MJ, Rhim H, et al. Combined hepatectomy and radiofrequency ablation for multifocal hepatocellular carcinomas: long-term follow-up results and prognostic factors. Ann Surg Oncol. 2007;14(12):3510–8. doi:10.1245/s10434-007-9492-7.

    Article  PubMed  Google Scholar 

  12. van Amerongen MJ, van der Stok EP, Futterer JJ, Jenniskens SF, Moelker A, Grunhagen DJ, et al. Short term and long term results of patients with colorectal liver metastases undergoing surgery with or without radiofrequency ablation. Eur J Surg Oncol J Eur Soc Surg Oncol Br Assoc Surg Oncol. 2016;42(4):523–30. doi:10.1016/j.ejso.2016.01.013.

    Google Scholar 

  13. Philips P, Groeschl RT, Hanna EM, Swan RZ, Turaga KK, Martinie JB, et al. Single-stage resection and microwave ablation for bilobar colorectal liver metastases. Br J Surg. 2016;103(8):1048–54. doi:10.1002/bjs.10159.

    Article  CAS  PubMed  Google Scholar 

  14. Wada Y, Takami Y, Tateishi M, Ryu T, Mikagi K, Saitsu H. Efficacy of surgical treatment using microwave coagulo-necrotic therapy for unresectable multiple colorectal liver metastases. OncoTargets Ther. 2016;9:937–43. doi:10.2147/OTT.S97824.

    Article  Google Scholar 

  15. Yang PC, Lin BR, Chen YC, Lin YL, Lai HS, Huang KW, et al. Local control by radiofrequency thermal ablation increased overall survival in patients with refractory liver metastases of colorectal cancer. Medicine. 2016;95(14):e3338. doi:10.1097/MD.0000000000003338.

    Article  PubMed  PubMed Central  Google Scholar 

  16. Nielsen K, Scheffer HJ, Volders JH, van der Vorst MJ, van Tilborg AA, Comans EF, et al. Radiofrequency ablation to improve survival after conversion chemotherapy for colorectal liver metastases. World J Surg. 2016;40(8):1951–8. doi:10.1007/s00268-016-3554-6.

    Article  PubMed  Google Scholar 

  17. Solbiati L, Ahmed M, Cova L, Ierace T, Brioschi M, Goldberg SN. Small liver colorectal metastases treated with percutaneous radiofrequency ablation: local response rate and long-term survival with up to 10-year follow-up. Radiology. 2012;265(3):958–68. doi:10.1148/radiol.12111851.

    Article  PubMed  Google Scholar 

  18. Weng M, Zhang Y, Zhou D, Yang Y, Tang Z, Zhao M, et al. Radiofrequency ablation versus resection for colorectal cancer liver metastases: a meta-analysis. PLoS ONE. 2012;7(9):e45493. doi:10.1371/journal.pone.0045493.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  19. Gillams A, Goldberg N, Ahmed M, Bale R, Breen D, Callstrom M, et al. Thermal ablation of colorectal liver metastases: a position paper by an international panel of ablation experts, the Interventional Oncology Sans Frontieres meeting 2013. Eur Radiol. 2015;25(12):3438–54. doi:10.1007/s00330-015-3779-z.

    Article  PubMed  PubMed Central  Google Scholar 

  20. Wells SA, Hinshaw JL, Lubner MG, Ziemlewicz TJ, Brace CL, Lee FT Jr. Liver ablation: best practice. Radiol Clin North Am. 2015;53(5):933–71. doi:10.1016/j.rcl.2015.05.012.

    Article  PubMed  Google Scholar 

  21. Barral M, Auperin A, Hakime A, Cartier V, Tacher V, Otmezguine Y, et al. Percutaneous thermal ablation of breast cancer metastases in oligometastatic patients. Cardiovasc Interv Radiol. 2016;39(6):885–93. doi:10.1007/s00270-016-1301-x.

    Article  CAS  Google Scholar 

  22. Meloni MF, Andreano A, Laeseke PF, Livraghi T, Sironi S, Lee FT Jr. Breast cancer liver metastases: US-guided percutaneous radiofrequency ablation—intermediate and long-term survival rates. Radiology. 2009;253(3):861–9. doi:10.1148/radiol.2533081968.

    Article  PubMed  PubMed Central  Google Scholar 

  23. Guner A, Son T, Cho I, Kwon IG, An JY, Kim HI, et al. Liver-directed treatments for liver metastasis from gastric adenocarcinoma: comparison between liver resection and radiofrequency ablation. Gastric Cancer Off J Int Gastric Cancer Assoc Jpn Gastric Cancer Assoc. 2016;19(3):951–60. doi:10.1007/s10120-015-0522-z.

    CAS  Google Scholar 

  24. Velez E, Goldberg SN, Kumar G, Wang Y, Gourevitch S, Sosna J, et al. Hepatic thermal ablation: effect of device and heating parameters on local tissue reactions and distant tumor growth. Radiology. 2016;281(3):782–92. doi:10.1148/radiol.2016152241.

    Article  PubMed  Google Scholar 

  25. Tannous BA, Teng J. Secreted blood reporters: insights and applications. Biotechnol Adv. 2011;29(6):997–1003. doi:10.1016/j.biotechadv.2011.08.021.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  26. Kim KR, Thomas S. Complications of image-guided thermal ablation of liver and kidney neoplasms. Semin Interv Radiol. 2014;31(2):138–48. doi:10.1055/s-0034-1373789.

    Article  Google Scholar 

  27. Lee KF, Wong J, Hui JW, Cheung YS, Chong CC, Fong AK, et al. Long-term outcomes of microwave versus radiofrequency ablation for hepatocellular carcinoma by surgical approach: a retrospective comparative study. Asian J Surg. 2016;. doi:10.1016/j.asjsur.2016.01.001.

    Google Scholar 

  28. Poulou LS, Botsa E, Thanou I, Ziakas PD, Thanos L. Percutaneous microwave ablation vs radiofrequency ablation in the treatment of hepatocellular carcinoma. World J Hepatol. 2015;7(8):1054–63. doi:10.4254/wjh.v7.i8.1054.

    Article  PubMed  PubMed Central  Google Scholar 

  29. Ierardi AM, Mangano A, Floridi C, Dionigi G, Biondi A, Duka E, et al. A new system of microwave ablation at 2450 MHz: preliminary experience. Updates Surg. 2015;67(1):39–45. doi:10.1007/s13304-015-0288-1.

    Article  PubMed  Google Scholar 

  30. Ierardi AM, Giorlando F, Piacentino F, Fontana F, Novario R, Angileri SA, Duka E, Carrafiello G. Factors predicting outcomes of microwave ablation of small hepatocellular carcinoma. Radiol Med. 2016. doi:10.1007/s11547-016-0694-6.

    Google Scholar 

  31. Ierardi AM, Floridi C, Fontana F, Chini C, Giorlando F, Piacentino F, Brunese L, Pinotti G, Bacuzzi A, Carrafiello G. Microwave ablation of liver metastases to overcome the limitation of radiofrequency ablation. Radiol Med. 2013;118(6):949–61. doi:10.1007/s11547-013-0968-1.

    Article  PubMed  Google Scholar 

  32. Yun D, Kim S, Song I, Chun K. Comparative analysis of Laparoscopic versus open surgical radiofrequency ablation for malignant liver tumors. Korean J Hepato-Biliary-Pancreat Surg. 2014;18(4):122–8. doi:10.14701/kjhbps.2014.18.4.122.

    Article  Google Scholar 

  33. Casaccia M, Andorno E, Nardi I, Troilo B, Barabino G, Santori G, et al. Laparoscopic US-guided radiofrequency ablation of unresectable hepatocellular carcinoma in liver cirrhosis: feasibility and clinical outcome. J Laparoendosc Adv Surg Techn Part A. 2008;18(6):797–801. doi:10.1089/lap.2008.0039.

    Article  Google Scholar 

  34. Chiang J, Wang P, Brace CL. Computational modelling of microwave tumour ablations. Int J Hyperth Off J Eur Soc Hyperth Oncol N Am Hyperthe Group. 2013;29(4):308–17. doi:10.3109/02656736.2013.799295.

    Article  Google Scholar 

  35. Shyn PB, Bird JR, Koch RM, Tatli S, Levesque VM, Catalano PJ, et al. Hepatic microwave ablation zone size: correlation with total energy, net energy, and manufacturer-provided chart predictions. J Vasc Interv Radiol JVIR. 2016;27(9):1389–96. doi:10.1016/j.jvir.2016.05.009.

    Article  PubMed  Google Scholar 

  36. Siriwardana PN, Singh S, Johnston EW, Watkins J, Bandula S, Illing RO, et al. Effect of hepatic perfusion on microwave ablation zones in an ex vivo porcine liver model. J Vasc Interv Radiol JVIR. 2016;. doi:10.1016/j.jvir.2016.03.006.

    PubMed  Google Scholar 

  37. Amabile C, Ahmed M, Solbiati L, Meloni MF, Solbiati M, Cassarino S, et al. Microwave ablation of primary and secondary liver tumours: ex vivo, in vivo, and clinical characterisation. Int J Hyperth Off J Eur Soc Hyperth Oncol N Am Hyperthe Group. 2016;. doi:10.1080/02656736.2016.1196830.

    Google Scholar 

  38. Wang LG, Jiang WJ, Fan WJ, Zheng YB, Song XP, Liu S, et al. Microwave ablation: the differences between biliary cirrhosis and normal porcine liver using a cooled-tip electrode. Anticancer Res. 2016;36(3):1221–6.

    CAS  PubMed  Google Scholar 

  39. Wang X, Sofocleous CT, Erinjeri JP, Petre EN, Gonen M, Do KG, et al. Margin size is an independent predictor of local tumor progression after ablation of colon cancer liver metastases. Cardiovasc Interv Radiol. 2013;36(1):166–75. doi:10.1007/s00270-012-0377-1.

    Article  CAS  Google Scholar 

  40. Shady W, Petre EN, Gonen M, Erinjeri JP, Brown KT, Covey AM, et al. Percutaneous radiofrequency ablation of colorectal cancer liver metastases: factors affecting outcomes—a 10-year experience at a single center. Radiology. 2016;278(2):601–11. doi:10.1148/radiol.2015142489.

    Article  PubMed  Google Scholar 

  41. Common Terminology Criteria for Adverse Events (CTCAE) Version 4.0. The National Cancer Institute, Bethesda Approved after October 1, 2009; 2010.

  42. Liu D, Brace CL. CT imaging during microwave ablation: analysis of spatial and temporal tissue contraction. Med Phys. 2014;41(11):113303. doi:10.1118/1.4897381.

    Article  PubMed  PubMed Central  Google Scholar 

  43. Bouda D, Lagadec M, Alba CG, Barrau V, Burgio MD, Moussa N, et al. Imaging review of hepatocellular carcinoma after thermal ablation: the good, the bad, and the ugly. J Magn Reson Imaging JMRI. 2016;44(5):1070–90. doi:10.1002/jmri.25369.

    Article  PubMed  Google Scholar 

  44. Lencioni R, de Baere T, Martin RC, Nutting CW, Narayanan G. Image-guided ablation of malignant liver tumors: recommendations for clinical validation of novel thermal and non-thermal technologies—a western perspective. Liver Cancer. 2015;4(4):208–14. doi:10.1159/000367747.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  45. Sotirchos VS, Petrovic LM, Gonen M, Klimstra DS, Do RK, Petre EN, et al. Colorectal cancer liver metastases: biopsy of the ablation zone and margins can be used to predict oncologic outcome. Radiology. 2016;280(3):949–59. doi:10.1148/radiol.2016151005.

    Article  PubMed  Google Scholar 

  46. Poggi G, Tosoratti N, Montagna B, Picchi C. Microwave ablation of hepatocellular carcinoma. World J Hepatol. 2015;7(25):2578–89. doi:10.4254/wjh.v7.i25.2578.

    Article  PubMed  PubMed Central  Google Scholar 

  47. Nafidi O, Desy D, Letourneau R, Cote J, Plasse M, Vandenbroucke F, et al. Hypertrophy of the non-embolized liver after chemotherapy. HPB Off J Int Hepato Pancreato Biliary Assoc. 2009;11(2):103–7. doi:10.1111/j.1477-2574.2009.00004.x.

    Article  Google Scholar 

  48. Rubbia-Brandt L, Audard V, Sartoretti P, Roth AD, Brezault C, Le Charpentier M, et al. Severe hepatic sinusoidal obstruction associated with oxaliplatin-based chemotherapy in patients with metastatic colorectal cancer. Ann Oncol Off J Eur Soc Med Oncol. 2004;15(3):460–6.

    Article  CAS  Google Scholar 

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Correspondence to Paolo Marra.

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De Cobelli, F., Marra, P., Ratti, F. et al. Microwave ablation of liver malignancies: comparison of effects and early outcomes of percutaneous and intraoperative approaches with different liver conditions. Med Oncol 34, 49 (2017). https://doi.org/10.1007/s12032-017-0903-8

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