Thermal Ablation of Liver Tumours: How the Scenario Has Changed in the Last Decade - European Medical Journal

Thermal Ablation of Liver Tumours: How the Scenario Has Changed in the Last Decade

9 Mins
Hepatology
Download PDF
Authors:
Paola Tombesi, Francesca Di Vece, Lara Bianchi, *Sergio Sartori
Disclosure:

The authors have declared no conflicts of interest.

Received:
06.02.18
Accepted:
13.04.18
Citation:
EMJ Hepatol. ;6[1]:88-94. DOI/10.33590/emjhepatol/10314486. https://doi.org/10.33590/emjhepatol/10314486.
Keywords:
Hepatocellular carcinoma (HCC), laser ablation (LA), liver metastasis (LM), liver cancer, microwave ablation (MWA), percutaneous thermal ablation (PTA), radiofrequency ablation (RFS)

Each article is made available under the terms of the Creative Commons Attribution-Non Commercial 4.0 License.

Abstract

Surgical resection has long been considered the gold standard for the local treatment of primary and secondary liver tumours. Until recent years, percutaneous thermal ablation (PTA), in particular radiofrequency ablation (RFA), was not accepted as a first-line option for the treatment of liver tumours and was reserved for patients who were unsuitable for surgery. However, in the last decade the scenario has changed: interesting technical developments and innovations have improved the performance of RFA and broadened the availability of other ablative technologies, such as microwave ablation (MWA) and laser ablation (LA). The latest generation of MWA systems can achieve larger ablation areas than RFA and LA, with a multifibre technique that uses very thin needles, allowing physicians to treat nodules in at-risk locations with high flexibility and a very low risk ofcomplications. Nowadays, there is an increasingly accepted consensus on the role of PTA as a first-line option for the treatment of liver tumours <2 cm in size, as well as in patients potentially eligible for surgery, and it is likely that in the near future the 2 cm barrier could also be surpassed and extended to at least 3 cm. PTA is becoming more effective and important in the treatment of primary and secondary liver tumours, and, in the well-established scenario of a multimodal tailoredtreatment, it plays and will continue to play a central role. The aim of this paper is to examine the current role of PTA in such a scenario, focussing on advantages and limitations of the three available ablative techniques: RFA, MWA, and LA.

INTRODUCTION

Primary and secondary hepatic tumours are relatively common and significantly impact the overall survival (OS) of cancer patients. The incidence of hepatocellular carcinoma (HCC) is increasing worldwide; nowadays, HCC is the fifth most common cancer and the third most common cause of cancer-related mortality.1 Secondary involvement of the liver, particularly from colorectal carcinoma, is even more common.1,2 More than 50% of patients with gastrointestinal malignancies will develop liver metastases (LM), with significant morbidity and mortality.3,4

As a consequence, local treatments of liver tumours have gradually assumed a central role as part of multimodal cancer therapy. Liver transplantation represents the treatment of choice for selected patients with HCC, but it is only available to a restricted number of patients because of the high cost and shortage of donor livers.5 Surgical resection (SR) has widely been proven to improve OS in patients with either HCC or LM, particularly those with colorectal cancer liver metastases (CRLM), and for a long time it has been considered the gold standard for the local treatment of liver tumours.6-8 In the last two decades, percutaneous thermal ablation (PTA) has gained a key role in the treatment of patients who are not eligible for, poor candidates for, or refusing surgery, as well as being a bridge to liver transplantation.5 Although many studies have widely proven its effectiveness and safety, until very recently PTA was not accepted as a first-line option for the treatment of liver tumours and was reserved for patients unsuitable for surgery.5,9,10 However, compared with the first experiences, which were mostly based only on percutaneous ethanol injection and earlier devices for radiofrequency ablation (RFA), in the last decade the scenario has changed. Technical developments and innovations have improved the performance of RFA and broadened the availability of other ablative technologies, such as microwave ablation (MWA) and laser ablation (LA), allowing interventional radiologists and oncologists to offer an increasing number of tailored approaches for cancer patients, which have better outcomes. The aim of this narrative review is to examine the current role of PTA in the scenario of the multimodal tailored treatment of liver tumours, starting from the first and most widely used thermal ablation technique.

RADIOFREQUENCY ABLATION: STATE-OF-THE-ART IN THE TREATMENT OF HEPATOCELLULAR CARCINOMA AND LIVER METASTASES

RFA is the best established and most used technique worldwide, and its effectiveness and safety have largely been proven over the last two decades.5,9-12

Radiofrequency Ablation and Hepatocellular Carcinoma

Although the role of RFA as a bridge to liver transplantation has widely been established, its efficacy in the treatment of HCC with curative intent is still influenced by tumour location and size. RFA of tumours located close to large vessels can achieve suboptimal results due to the well-known ‘heat sink’ effect, which causes the partial shunt of thermal energy by the cooler blood.13 Likewise, the treatment of large lesions can require multiple overlapping ablations to obtain an adequate safety margin, and results in tumours >5 cm in size are still poor.14-16 As a consequence, for a long time SR was considered the gold standard therapy in terms of OS and disease-free survival, and RFA was reserved for patients who were not eligible for surgery.

Nowadays, however, HCC is frequently diagnosed at an early stage. In 2001, the Barcelona Clinic Liver Cancer (BCLC) staging system and treatment strategy included RFA among curative treatments for very early (<2 cm) and early stage (<3 cm) HCC,17 and several more recent studies have suggested that RFA of very early stage HCC can achieve the same results as surgery in terms of OS.14,18-24 Moreover, hepatic resection is not an ideal treatment for very small sized cases of HCC because of the potential loss of liver function and the high risk of complications. Conversely, RFA is a minimally invasive, effective, and cost-effective technique, particularly in patients with poor liver function and related comorbidities. As a consequence, according to many authors, RFA could be considered the first-line option in the treatment of HCC <2 cm in size, as well as in patients potentially eligible for surgery.18-25

Radiofrequency Ablation and Liver Metastases

The locoregional treatment of LM must be included in a systemic and multimodal treatment plan because the long-term outcomes are mainly determined by the characteristics and natural history of the primary cancer. Most studies regarding the treatment of LM have been conducted on CRLM. SR is considered the procedure of choice, with 5-year survival rates of 51–58%.7,8 However, multiple or bilobar LM require major hepatic surgery, and the potential complications of this strategy may outweigh the theoretical benefits in terms of survival rates. Given that surgery is feasible in only 10–15% of patients with LM,26 nowadays many centres propose RFA as an alternative to surgery since RFA has been reported to improve survival and quality of life in selected patients, with very low risks of complications.27 Moreover, RFA can be indicated in patients with resectable lesions as an adjunct to resection, for inoperable lesions that demonstrate response after chemotherapy, or for recurrent or progressive lesions.28 In patients with a maximum of 5 or 6 LM with a diameter of 5–6 cm, RFA was reported to obtain 3-year and 5-year survival rates ranging 28–46%, with a median survival ranging 30–40 months.29-32

Although the efficacy of PTA of LM when compared to chemotherapy alone has, to the best of our knowledge, never been proven by randomised controlled trials (RCT), there are a large number of studies in the literature suggesting that combined multimodal treatments including PTA can achieve better outcomes than systemic chemotherapy alone in patients with CRLM.27-32 Among the several attempts to organise RCT comparing RFA plus systemic chemotherapy versus chemotherapy alone, just one trial, the CLOCC trial,33 planned by the European Organisation for Research and Treatment of Cancer (EORTC), was completed, but it was downscaled from a Phase III to a Phase II study because of difficulty recruiting participants. The preliminary results after a median follow-up of 4.4 years showed a significantly longer progression-free survival of the patients in the RFA plus chemotherapy cohort, but no difference in OS between the two cohorts.33 However, after a longer median follow-up (9.7 years), the OS results were significantly better in the combination cohort, with an observed median OS of 45.6 months (95% confidence interval: 30.3–67.8) for RFA plus chemotherapy versus 40.5 months (95% confidence interval: 27.5–47.7) for chemotherapy alone (p=0.01).34 To date, we can rationally conclude that the best available evidence points towards a benefit of the combination strategy using ablative treatments and chemotherapy in CRLM. Moreover, in recent years the role of RFA in combination with systemic chemotherapy has also been highlighted by several authors in the treatment of LM from breast cancer, gastrointestinal stromal tumours, and neuroendocrine tumours.35-37

MICROWAVE ABLATION: ADVANTAGES OVER RADIOFREQUENCY ABLATION OF THE LATEST GENERATION SYSTEMS

Despite the introduction of more effective devices, such as cluster, expandable, and multitined electrodes, the main limit of RFA remains tumour size. Local control rates >90% have been reported for nodules up to 3 cm, but only rates of 6–10% for tumours >5 cm.14-16 The capability of microwaves to propagate through tissues with low electrical conductivity, high impedance, or low thermal conductivity, like charred tissues, allows the MWA device to generate very high temperatures inside the lesion in a very short time. Moreover, microwave energy radiates into the tissue through an interstitial antenna, which determines direct heating of the lesion regardless of the closeness to the large vessels.38 As a consequence, MWA can improve PTA efficacy by obtaining larger ablation volumes and broader safety margins. Several studies have demonstrated that early-generation MWA had comparable effectiveness and safety than RFA, with a shorter ablation time.38-40 However, in recent years, technical advances in MWA technology have allowed the development of safer and more slender MWA antennas with a similar gauge with respect to RFA electrodes, minimising the drawback of the back heating effect and enabling physicians to achieve larger ablation areas than with RFA.41,42 The introduction of these latest generation MWA systems could surpass the 2 cm barrier in the treatment of HCC, and extend it to at least 3 cm.43 Surgery remains the gold standard for nodules >3 cm and MWA could be considered the first-line choice for nodules up to 3 cm, particularly if they are central or deeply located or close to large vessels. Reported 3-year and 5-year survival rates in HCC patients range from 72–73% and 51–57%, respectively, with single HCC <5 cm in diameter or up to three HCC <3 cm in diameter.44

Given the typical infiltrative growth and lack of clear margins of LM, the capability of MWA to achieve larger ablation areas and obtain adequate safety margins can play a crucial role in the treatment of LM. Studies on the outcomes of MWA are less numerous and generally involve smaller patient numbers than studies of RFA. Moreover, most studies investigating the effectiveness of MWA were conducted before the introduction of the most recent advances in MWA technology, so at present the best available evidence suggests similar outcomes for RFA and MWA. MWA of LM has been reported to achieve 3-year and 5-year survival rates ranging 46–51% and 17–32%, respectively, with a median survival ranging 20–48 months.45-47 However, in the near future we can expect better outcomes from studies based on the use of the latest generation of MWA systems.22

LASER ABLATION: ITS ROLE IN THE TREATMENT OF TUMOURS IN AT-RISK LOCATIONS AND MULTIPLE TUMOURS OF DIFFERENT SIZES

LA uses laser optical fibres to deliver high-energy laser radiation to the tissue. As a result of light absorption, temperatures of up to 150°C are reached, leading to coagulative necrosis.28 Neodymium-doped yttrium aluminum garnet (Nd:YAG [wavelength: 1,064 nm]) and diode (wavelength: 800–1,064 nm) lasers are most commonly used because penetration of light is optimal in the near infrared spectrum. Although it is less frequently investigated than RFA and MWA, LA is currently used in several centres for the treatment of HCC and LM, and the available data on its effectiveness and safety are good and comparable to those of RFA and MWA.28,48-50 The multifibre technique49,50 enables clinicians to simultaneously use from one to four 300 μm bare-tip optical fibres to treat the tumour according to its size. Usually, one or two fibres are used to treat nodules up to 1.5 cm, three fibres to treat nodules 1.5–2.5 cm, and four fibres to treat nodules >2.5 cm.51-53 The main advantage of LA is its feasibility because LA needs very fine needles (21 gauge) to introduce the fibres into the tumour, allowing nodules to be treated in at-risk locations with a very low risk of complications. Moreover, the possibility of using one to four fibres at once allows physicians to achieve different ablation areas according to the tumour size and makes LA the most flexible ablation technique to treat multiple lesions of different sizes in the same session, sparing the noncancerous parenchyma as much as possible.

Most studies on LA are focussed on the treatment of HCC. Complete response rates ranging from 82–97% and cumulative 3-year survival rates up to 73% were reported in Child–Pugh Class A patients with single HCC <5 cm, or up to three nodules <3 cm, treated with multiple bare-tip fibres.52-55 Moreover, a complete response rate of 95.5% was reported in tumours with high-risk locations.50 Likewise, good results have also been achieved in the treatment of CRLM with a diameter up to 5 cm, with 3-year and 5-year survival rates ranging from 28.0–72.4% and 10.0–37.0%, respectively.56-58 Due to its novel features, LA has been proposed as the technique of choice in cases of multiple, bilobar, small, and variably sized LM (for instance, from neuroendocrine tumours), because it provides the ability to better modulate the volume of necrosis and more effectively avoid the liver parenchyma than RFA, achieving similar results.58-60

FINAL CONSIDERATIONS AND PROPOSALS

The high incidence worldwide of HCC and LM makes it crucial to plan the best strategy of multimodal treatment.1-4 Concerning HCC, liver transplantation remains the gold standard in selected patients, and for a long time SR has represented the first-line therapy when patients cannot undergo liver transplantation.5-8 Until very recently, PTA was restricted to patients unsuitable for surgery or used as a bridge to liver transplantation.5,9,10 Nowadays, the scenario has changed and the role of PTA as the first-line treatment of very early and early HCC with curative intent is widely accepted. The inclusion of PTA among the curative therapies for single HCC <2 cm or for up to three HCC <3 cm in patients with comorbidities dates back to the early 2000s,17 and its relevance has got progressively stronger.6,9 PTA of very early HCC has widely been demonstrated to achieve the same results as SR with lower morbidity and mortality,15,18-23 and its capability to spare the noncancerous liver parenchyma makes its role even more central in the tailored approach to patients with HCC. Therefore, at present, PTA can be considered the first-line therapy for very early and early HCC.61,62 The vast majority of studies on PTA of HCC refer to RFA. Despite its efficacy and safety, and the technical developments that have improved the performance of the more recent RFA devices, the main limitation of RFA remains tumour size, and at present the outcome of nodules >3 cm is still poor. Latest generation MWA systems produce larger ablation volumes than RFA,41,42 enabling HCC up to 3 cm to be treated with the same efficacy as SR and the same safety as RFA.62 Moreover, some authors have reported local tumour control rates of nodules up to 5 cm, nearly identical to those achieved for tumours up to 3 cm.43 However, the question of whether the time has come to increase the 2 cm tumour size barrier to 3 cm is still open for discussion and further randomised studies with longer follow-up are needed. In any case, MWA should be preferred for the treatment of HCC >2 cm, particularly when located close to large vessels. The role of LA is less investigated, but the results reported by several authors are quite similar to those of RFA.48-55 The multifibre technique makes LA particularly interesting in the treatment of HCC at difficult or high-risk locations, and in the treatment of multiple and very small HCC in order to spare the noncancerous parenchyma as much as possible.

With regard to LM, SR in association with systemic chemotherapy represents the best choice in resectable patients with CRLM.7,9 However, SR can be offered to a small number of patients and the high risk of complications in major liver surgery makes it inappropriate for use in frail patients and in the treatment of multiple or bilobar LM. In nonsurgical-selected patients, PTA has been demonstrated to improve survival with a very low risk of complications,27,61 particularly when an aggressive approach is adopted to obtain an adequate safety margin.63 The efficacy of PTA in CRLM compared with chemotherapy alone, as well as the superiority of chemotherapy alone over PTA, have not been proven by RCT.64 To date, just one prospective RCT comparing RFA plus systemic chemotherapy versus systemic chemotherapy alone has been published.33 After an adequate follow-up, the trial reported a significantly improved OS in the combination cohort.34 Likewise, numerous studies reported that combined therapeutic strategies including PTA provide better results than chemotherapy alone.27-31 PTA can also be considered for patients with potentially resectable lesions as an adjunct to resection, with nonsurgical lesions that demonstrate response after chemotherapy, or with recurrent or progressive lesions.28 Moreover, when ablation was applied as the first-line therapy to resectable patients, the 5-year survival rates resulted in very similar results to surgical studies.65,66

In this regard, a position paper on PTA of CRLM has recently been published by an international panel of ablation experts.26 A strong consensus level was achieved for the treatment of nodules up to 5 cm when well located (with easy access), and for up to five nodules. Likewise, a strong level of consensus was achieved for combination strategies with respect to systemic treatments alone. The panel also agreed in considering PTA as potentially curative in resectable patients when used as a first-line treatment. Indeed, although most surgical studies have reported higher local tumour progression following ablation than after SR, the OS was comparable.67 Of course, it is mandatory that PTA is performed by skilled operators and that adequate safety margins are obtained. The authors’ experiences are consistent with those of this position paper, as well as with the assumption regarding the convenience of exploiting the advantages and minimising the limits of all three ablation techniques. In this regard, an algorithm aimed at tailoring PTA to the patient’s and tumour’s characteristics to obtain the best outcome has recently been proposed.59 As a consequence of these considerations on the technical characteristics, advantages, and limitations of the three available ablation techniques, the possibility to always select the most suitable option for each single case allows clinicians to optimise the potential of PTA and its expected outcome.

CONCLUSION

In conclusion, PTA has become increasingly more effective in the treatment of primary and secondary liver tumours; for example, in the well-established scenario of a multimodal tailored treatment, PTA now plays a central role. The careful characterisation and selection of patients and nodules, according to size, number, and location, will offer the best chance of treatment for liver cancer patients.

References
World Health Organization. Health Statistics and Health Information Systems. WHO Mortality Database. Available at: http://www.who.int/healthinfo/statistics/mortality_rawdata/en/. Last accessed: 18 March 2018. Jemal A et al. Cancer statistics, 2009. CA Cancer J Clin. 2009;59(4):225-49. Greenlee RT et al. Cancer statistics, 2001. CA Cancer J Clin. 2001;51(1):15-36. Erratum in: CA Cancer J Clin. 2001;51(2):144. Landis SH et al. Cancer statistics, 1999. CA Cancer J Clin. 1999;49(1):8-31. Bruix J, Sherman M; American Association for the study of Liver Diseases. Management of hepatocellular carcinoma: An update. Hepatology. 2011;53(3):1020-2. Llovet JM et al. Intention-to-treat analysis of surgical treatment for early hepatocellular carcinoma: Resection versus transplantation. Hepatology. 1999;30(6):1434-40. de Haas RJ et al. Long-term outcomes after hepatic resection for colorectal metastases in young patients. Cancer. 2010;116(3):647-58. de Haas RJ et al. Impact of expanding criteria for resectability of colorectal metastases on short- and long-term outcomes after hepatic resection. Ann Surg. 2011;253(6):1069-79. Gervais DA et al. Society of Interventional Radiology position statement on percutaneous radiofrequency ablation for the treatment of liver tumors. J Vasc Interv Radiol. 2009;20(1):3-8. European Association For The Study Of The Liver; European Organisation For Research And Treatment Of Cancer. EASL–EORTC clinical practice guidelines: Management of hepatocellular carcinoma. J Hepatol. 2012;56(4):908-43. Poon RT et al. Locoregional therapies for hepatocellular carcinoma: A critical review from the surgeon’s perspective. Ann Surg. 2002;235(4):466-86. Buscarini E et al. Radiofrequency thermal ablation of liver tumors. Eur Radiol. 2005;15(5):884-94. Lu DS et al. Influence of large peritumoral vessels on outcome of radiofrequency ablation of liver tumors. J Vasc Interv Radiol. 2003;14(10):1267-74. Chen MS 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. Lencioni R, Crocetti L. Image-guided thermal ablation of hepatocellular carcinoma. Crit Rev Oncol Hematol. 2008;66(3):200-7. Kudo M. Local ablation therapy for hepatocellular carcinoma: Current status and future perspectives. J Gastroenterol. 2004;39(3):205-14. Bruix J et al.; EASL Panel of Experts on HCC. Clinical management of hepatocellular carcinoma. Conclusions of the Barcelona-2000 EASL Conference. European Association for the Study of the Liver. J Hepatol. 2001;35(3):421-30. Poon D et al.; Asian Oncology Summit. Management of hepatocellular carcinoma in Asia: Consensus statement from the Asian Oncology Summit 2009. Lancet Oncol. 2009;10(11):1111-8. Choi D et al. Percutaneous radiofrequency ablation for early-stage hepatocellular carcinoma as a first-line treatment: Long-term results and prognostic factors in a large single institution series. Eur Radiol. 2007;17(3):684-92. Livraghi T et al. Sustained complete response and complications rates after radiofrequency ablation of very early hepatocellular carcinoma in cirrhosis: Is resection still the treatment of choice? Hepatology. 2008;47(1):82-9. Lü MD et al. [Surgical resection versus percutaneous thermal ablation for early-stage hepatocellular carcinoma carcinoma: A randomized clinical trial.] Zhonghua Yi Xue Za Zhi. 2006;86(12):801-5. (In Chinese). Tombesi P et al. Resection vs thermal ablation of small hepatocellular carcinoma: What’s the first choice? World J Radiol. 2013;5(1):1-4. Xu XL et al. Radiofrequency ablation versus hepatic resection for small hepatocellular carcinoma: Systematic review of randomized controlled trials with meta-analysis and trial sequential analysis. Radiology. 2017. [Epub ahead of print]. Mironov O et al. Thermal ablation versus surgical resection for the treatment of Stage T1 hepatocellular carcinoma in the surveillance, epidemiology, and end results database population. J Vasc Interv Radiol. 2017;28(3):325-33. Salati U et al. State of the ablation nation: A review of ablative therapies for cure in the treatment of hepatocellular carcinoma. Future Oncol. 2017;13(16):1437-48. Gilliams A et al. Thermal ablation of colorectal liver metastases: A position paper by an international panel of ablation experts, the interventional oncology sans frontières meeting 2013. Eur Radiol. 2015;25(12):3438-54. Dodd GD et al. Minimally invasive treatment of malignant hepatic tumors: At the threshold of a major breakthrough. Radiographics. 2000;20(1):9-27. Vogl TJ et al. Thermal ablation of liver metastases from colorectal cancer: Radiofrequency, microwave and laser ablation therapies. Radiol Med. 2014;119(7):451-61. Solbiati L et al. Radiofrequency thermal ablation of hepatic metastases. Eur J Ultrasound. 2001;13(2):149-58. Gilliam AR, Lees WR. Radiofrequency ablation of colorectal liver metastases. Abdom Imaging. 2005;30(4):419-26. Hildebrand P et al. Influence of operator experience in radiofrequency ablation of malignant liver tumors on treatment outcome. Eur J Surg Oncol. 2006;32(4):430-4. Lee WS et al. Clinical outcomes of hepatic resection and radiofrequency ablation in patients with solitary colorectal liver metastasis. J Clin Gastroenterol. 2008;42(8):945-9. Ruers T et al. Radiofrequency ablation combined with systemic treatment versus systemic treatment alone in patients with non-resectable liver metastases: A randomized EORTC Intergroup Phase II study (EORTC 40004). Ann Oncol. 2012;23(10):2619-26. Ruers T et al. Radiofrequency ablation (RFA) combined with chemotherapy for unresectable colorectal liver metastases: Long-term survival results of a randomized phase II study of the EORTC-NRCI CCSG-ALM Intergroup 40004 (CLOCC). Abstract 3501. American Society of Clinical Oncology (ASCO) Annual Meeting, 29 May-2 June, 2015. Vogl TJ et al. Thermal ablation therapies in patients with breast cancer liver metastases: A review. Eur Radiol. 2013;23(3):797-804. Hakimé A et al. A role for adjuvant RFA in managing hepatic metastases from gastrointestinal stromal tumors (GIST) after treatment with targeted systemic therapy using kinase inhibitors. Cardiovasc Intervent Radiol. 2014;37(1):132-9. Elias D et al. Combined liver surgery and RFA for patients with gastroenteropancreatic endocrine tumors presenting with more than 15 metastases to the liver. Eur J Surg Oncol. 2009;35(10):1092-7. Schramm W et al. Contribution of direct heating, thermal conduction and perfusion during radiofrequency and microwave ablation. Conf Proc IEEE Eng Med Biol Soc. 2006;1:5013-6. Livraghi T et al.; Collaborative Italian Group using AMICA system. Complications of microwave ablation for liver tumors: Results of a multicenter study. Cardiovasc Intervent Radiol. 2012;35(4):868-74. Quian GJ et al. Efficacy of microwave versus radiofrequency ablation for treatment of small hepatocellular carcinoma: Experimental and clinical studies. Eur Radiol. 2012;22(9):1983-90. Cavagnaro M et al. A minimally invasive antenna for microwave ablation therapies: Design, performances, and experimental assessment. IEEE Trans Biomed Eng. 2011;58(4):949-59. Di Vece F et al. Coagulation areas producted by cool-tip radiofrequency ablation and microwave ablation using a device to decrease back-heating effects: A prospective pilot study. Cardiovasc Intervent Radiol. 2014;37(3):723-9. Thamtorawat S et al. Preliminary outcome of microwave ablation of hepatocellular carcinoma: Breaking the 3-cm barrier? J Vasc Interv Radiol. 2016;27(5):623-30. Dong B et al. Percutaneous sonographically guided microwave coagulation therapy for hepatocellular carcinoma: Results in 234 patients. AJR Am J Roentgenol. 2003;180(6):1547-55. Liang P et al. Prognostic factors for percutaneous microwave coagulation therapy of hepatic metastases. AJR Am J Roentgenol. 2003;181(5):1319-25. Tanaka K et al. Outcome after hepatic resection versus combined resection and microwave ablation for multiple bilobar colorectal metastases to the liver. Surgery. 2006;139(2):263-73. Ogata Y et al. Intraoperative thermal ablation therapy for small colorectal metastases to the liver. Hepatogastroenterology. 2008;55(82-83):550-6. Francica G et al. Factors predicting complete necrosis rate after ultrasound-guided percutaneous laser thermoablation of small hepatocellular carcinoma tumors in cirrhotic patients: A multivariate analysis. Acta Radiol. 2007;48(5):514-9. Pacella CM et al. Percutaneous laser ablation in the treatment of hepatocellular carcinoma with small tumors: Analysis of factors affecting the achievement of tumor necrosis. J Vasc Interv Radiol. 2005;16(11):1447-57. Di Costanzo GG et al. A novel needle guide system to perform percutaneous laser ablation of liver tumors using the multifiber technique. Acta Radiol. 2013;54(8):876-81. Francica G et al. Effectiveness, safety, and local progression after percutaneous laser ablation of hepatocellular carcinoma nodules up to 4 cm are not affected by tumor location. AJR Am J Roentgenol. 2012;199(6):1393-401. Francica G et al. Influence of ablative margin on local tumor progression and survival in patients with HCC ≤4 cm after laser ablation. Acta Radiol. 2012;53(4):384-400. Di Costanzo GG et al. Laser ablation of small hepatocellular caricoma: State of the art and future perspectives. World J Hepatol. 2014;6(10):704-15. Pacella CM et al. Long-term outcome of cirrhotic patients with early hepatocellular carcinoma treated with ultrasound-guided percutaneous laser ablation: A retrospective analysis. J Clin Oncol. 2009;27(16):2615-21. Eichler K et al. Magnetic resonance-guided laser-induced thermotherapy in patients with oligonodular hepatocellular carcinoma: Long-term results over a 15-years period. J Clin Gastroenterol. 2012;46(9):796-801. Vogl TJ et al. MR-guided laser-induced thermotherapy (LITT) of liver tumours: Experimental and clinical data. Int J Hyperthermia. 2004;20(7):713-24. Puls R et al. Laser ablation of liver metastases from colorectal cancer with MR thermometry: 5-year survival. J Vasc Interv Radiol. 2009;20(2):225-34. Vogl TJ et al. Colorectal cancer liver metastases: Long-term survival and progression-free survival after thermal ablation using magnetic resonance-guided laser-induced interstitial thermotherapy in 594 patients: Analysis of prognostic factors. Invest Radiol. 2014;49(1):48-56. Tombesi P et al. Radiofrequency, microwave, and laser ablation of liver tumors: Time to move toward a tailored ablation technique? Hepatoma Research. 2015;1:52-7. Sartori S et al. Laser ablation of liver tumors: An ancillary technique, or an alternative technique to radiofrequency and microwave? World J Radiol. 2017;9(3):91-6. Wells SA et al. Liver ablation: Best practice. Radiol Clin North Am. 2015;53(5):933-71. Shi Y, Zhai B. A recent advance in image-guided locoregional therapy for hepatocellular carcinoma. Gastrointest Tumors. 2016;3(2):90-102. Liu M et al. Percutaneous thermal ablation for the treatment of colorectal liver metastases and hepatocellular carcinoma: A comparison of local therapeutic efficacy. Int J Hyperthermia. 2017;22:1-11. Sartori S et al. Thermal ablation in colorectal liver metastases: Lack of evidence or lack of capability to prove the evidence? World J Gastroenterol. 2016;22(13):3511-5. Hammill CW et al. Outcome after laparoscopic radiofrequency ablation of technically respectable colorectal liver metastases. Ann Surg Oncol. 2011;18(7):1947-54. Otto G et al. Radiofrequency ablation as first-line treatment in patients with early colorectal liver metastases amenable to surgery. Ann Surg. 2010;251(5):796-803. Reuter NP et al. Radiofrequency ablation vs. resection for hepatic colorectal metastasis: Therapeutically equivalent? J Gastrointest Surg. 2009;13(3):486-91.

Rate this content's potential impact on patient outcomes

Average rating / 5. Vote count:

No votes so far! Be the first to rate this content.