| INTRODUCTION |
Radiofrequency ablation (RFA) is currently recommended as an intended curative treatment for very early or early stage hepatocellular carcinoma (HCC) according to several of the most prominent guidelines for the management of HCC [1, 2, 3]. However, although RFA is widely accepted as an effective treatment option for small HCCs in nonsurgical candidates, it has a significantly higher rate of local tumor progression (LTP) compared to surgical resection, limiting its use in patients with resectable HCCs [4, 5, 6, 7]. Several studies have demonstrated that there are no significant differences in long-term therapeutic outcomes between RFA and surgery, albeit with high LTP in RFA [6, 8, 9]. However, in patients with LTP, the required number of interventional procedures for controlling recurrent tumors was significantly higher than that in patients without LTP to obtain a similar overall survival outcome [10]. Thus, it is clinically valuable to lower LTP rates with RFA, and for this purpose, the creation of a 5–10 mm ablative margin around the target tumor is necessary, which may not always be possible with RFA [11].
In 2016, Seror et al. [12] reported that no-touch RFA (NT-RFA) using multi-bipolar electrodes resulted in 94% 5-year LTP-free survival, an excellent therapeutic outcome for HCCs within the Milan criteria. Thereafter, several retrospective studies have also reported significantly better LTP rates of NT-RFA using multi-bipolar RF technology than conventional RFA using monopolar RF technology [13, 14, 15, 16]. However, a prospective cohort study by Hirooka et al. [17] reported that NT-RFA using multi-bipolar electrodes showed no differences in LTP rates, compared with conventional RFA using monopolar electrodes, despite having significantly better intrasubsegmental tumor recurrence-free survival [17]. Furthermore, in previous studies [12, 13, 14, 15, 16, 17], there were differences not only in RFA techniques but also in the number and types of RF electrodes and RF energy delivery modes (multipolar vs. monopolar). Thus, at present, it is not yet certain whether the better LTP rates of NT-RFA were due to the oncologically favorable features of NT-RFA, different efficacy of RF equipment, or differing background clinical characteristics [13, 14, 15, 17]. Therefore, to answer the question of whether NT-RFA can indeed provide better therapeutic efficacy, we conducted a randomized prospective study comparing NT-RFA with conventional RFA using the same RF ablation system and electrodes for the treatment of small HCCs.
| MATERIALS AND METHODS |
This single-center, two-arm, parallel-group, prospective randomized controlled study was approved by the Institutional Review Board of Seoul National University Hospital (IRB No.1604-136-758, NCT 02806076). All participants provided written informed consent for enrollment in the study. This study was financially supported by the RF Medical Co., Ltd. However, the authors had complete control of patient enrollment, data collection, and analysis at all times, without any input from the funding source.
Study Participants
From October 2016 to September 2018, we recruited participants who met the following eligibility criteria: 1) age 20 to 85 years, 2) Child-Pugh class A, 3) treatment-naive HCC or new HCC that developed more than 2 years after initial curative treatment for HCC, and 4) tumor size ≤ 2.5 cm. The 2.5 cm size limit was selected based on the results of a previous study, which showed that the ideal inter-electrode distance for the creation of a spherical ablation zone with bipolar electrodes was 3 cm [18].
The exclusion criteria were as follows: 1) > 2 HCCs or diffuse type, 2) tumors adjacent to the portal or hepatic veins with <5 mm proximity, 3) invisible tumor on ultrasonography (US)-MR/CT fusion technique, 4) presence of macrovascular invasion or extrahepatic metastasis (EM), or 5) severe coagulopathy or bleeding tendency (platelet count ≤ 50000/mm3 or international normalized ratio (INR) prolongation ≥ 50%). HCC was diagnosed based on its typical hallmarks on CT or the Korean guidelines for HCC management [19].
Group Assignment
Participants underwent a 1:1 random assignment to the NT-RFA or conventional-RFA group by stratified randomization and block randomization (Fig. 1). Randomization was stratified by the size of the tumor (<2 cm or 2–2.5 cm), number of tumors (single or two), and type of HCC (treatment-naive or recurrent). The randomization process was performed using a web-based randomization service managed by our institution's medical research collaboration center. Study participants and those assessing outcomes were blinded to group assignments.
|
RFA Procedure
One radiologist with 20 years of experience in percutaneous RFA performed all RFA procedures with assistance from one radiology fellow or resident, on an inpatient basis, under conscious sedation. For RFA procedure planning, pre-procedural CT or MRI studies were reviewed, followed by real-time US-CT/MR fusion imaging (Easy fusion, Samsung Medison) for localization of the target lesion and evaluation of technical feasibility [20]. The detailed RFA procedure of conventional RFA with tumor puncture using twin internally cooled wet (TICW) electrodes (CWTN-T, RF Medical) is described in Supplement.
NT-RFA : bipolar RFA was performed using TICW electrodes and the same generator unit used in the conventional RFA group. For the NT-RFA technique, the two tines of TICW electrodes were inserted into the perimeter of the index tumor (generally 3–5 mm from the margin of the target tumor) at an inter-electrode distance of 2–3 cm, depending on tumor size, under the guidance of real-time US-CT/MR fusion imaging [14, 15, 17, 21]. An example case is shown in Figure 2. However, if there was no safe route for insertion of electrodes into the target tumor using the NT technique under multimodality fusion imaging, we converted patients from the NT-RFA group to the conventional RFA group. Furthermore, if the electrode incidentally passed through the tumor, it was recorded and regarded as an unintentional protocol change into conventional RFA, and the conversion rates of NT-RFA to conventional RFA were calculated. An example of a converted case is shown in Figure 3.
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Evaluation of Procedure and Follow-Up
After the completion of RFA procedures, multiphasic contrast-enhanced CT studies were immediately conducted to assess ablation size, post-procedural complications, and technical success based on the reporting criteria suggested by the International Working Group on Image-guided Tumor Ablation [22]. Technical success of RFA was defined as complete coverage of the target tumor by the ablation zone on immediate follow-up CT or MRI [22] (Fig. 2). Post-procedural complications were also evaluated according to the guidelines of the Society of Interventional Radiology [23]. A detailed evaluation of the ablation zone and sufficiency of the margin (> 5 mm) is described in Supplement. Any residual enhancement at the ablation margin was considered to be an unablated residual tumor [24], and patients underwent additional ablation on the same day.
After RFA, contrast-enhanced CT or MRI was performed one month after RFA, and every 3 months to detect LTP, intrahepatic distant recurrence (IDR), and EM during the initial 2 years, after which the interval for CT or MRI was adjusted according to the clinician's decision in the range of 3–6 months [22]. Technical efficacy was defined as complete coverage of the target tumor by the ablation zone, assessed by imaging at one-month follow up. LTP was defined as newly appearing tumor foci at the margin of the ablation zone after achieving treatment success in a follow-up study with contrast-enhanced CT or MRI [22].
Outcomes
The primary endpoint was to compare the cumulative incidence of LTP between the NT-RFA and conventional RFA groups. In addition, we determined the NT-RFA to conventional RFA conversion rates and evaluated the cumulative incidence of LTP in study patients according to the received RFA techniques (as-treated analysis). As secondary endpoints, we also compared IDR, EM, and the following procedural characteristics between the two groups: technical parameters, technical success, technical efficacy, and rates of complications.
Statistical Analysis
The sample size was approximated to be 55 patients in each group, but based on interim analysis, the study was terminated early in 78 patients (details in Supplement). Statistical evaluation was performed for the intention-to-treat analysis according to the initially assigned group and the as-treated analysis according to the actual treatment method [25]. Demographic factors and technical parameters were analyzed using the chi-squared test or Fisher's exact test for categorical variables and the independent t test for continuous variables. Technical success, technique efficacy, and LTP rates were analyzed using per-nodule data, based on the as-treated analysis. The Kaplan-Meier method and log-rank test were used for survival analysis between the two groups. Cox proportional hazards regression analysis was performed to evaluate predictors of LTP (details in Supplement). Variables with a p value <0.2, on univariable analysis, were included in the multivariable analysis. Statistical significance was set at p <0.05. All statistical analyses were conducted using IBM SPSS Statistics for Windows, Version 25.0 (IBM Corp.) and R Statistical Software (version 4.0.3, R Foundation for Statistical Computing). Our institutional Medical Research Collaborating Center supported us in carrying out the statistical methodology.
| RESULTS |
Participant Enrollment
Between July 2016 and September 2018, we screened 78 potentially eligible patients who were referred for RFA for study enrollment. Five patients were excluded for the following reasons: poor visibility despite fusion imaging (n = 1), refusal to submit informed consent (n = 2), and poor liver function (n = 2). Seventy-three participants with 76 HCCs were enrolled and randomly assigned to the two groups. Four participants in the NT-RFA group were converted to conventional RFA. Therefore, the intention-to-treat analysis involved 36 conventional RFA participants with 38 HCCs vs. 37 NT-RFA participants with 38 HCCs, and the as-treated analysis comprised 40 conventional RFA participants with 42 HCCs vs. 33 NT-RFA participants with 34 HCCs (Fig. 1). There were no statistically significant differences in demographic factors and tumor characteristics between the groups (Tables 1, 2).
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Procedure Characteristics
Procedure-related technical parameters according to intention-to-treat analysis are presented in Table 3. There were no significant differences in ablation size (Dmax, Dmin, Dv), ablation volume, effective ablation volume, and technical parameters, including procedure time, ablation time, and total energy in both groups (Table 3).
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Among the NT-RFA group, conversion to conventional RFA was performed in four patients (10.8%, 4/37). The main reasons for conversion in these four patients were the lack of a safe access route and subcapsular location with insufficient peritumoral parenchyma (<5 mm) (Fig. 3). According to the as-treated analysis, 76.1% (32/42) of patients achieved sufficient ablation margin (> 5 mm) in the conventional RFA group, while NT-RFA group patients achieved a higher rate of sufficient ablation margin (88.2%, 30/34), albeit without statistical significance (p = 0.178). Technical success was achieved in all cases. The technique efficacy rates of the conventional and NT-RFA groups at the 1-month follow-up were 100% (42/42) and 94.1% (32/34), respectively (p = 0.111). The mean follow-up period was 30.9 ± 12.3 months (median: 33.2 months).
Procedure-Related Complications
In the NT-RFA group, there were no procedure-related deaths or major complications. There was only one major complication of bleeding during the immediate follow-up CT in the conventional RFA group, which had spontaneously stopped on follow-up hepatic angiogram. There were also no significant differences between the two groups in minor complications, based on the as-treated analysis (n = 1, NT-RFA group; n = 2, conventional RFA group; p = 0.673). Minor thermal injuries were reported in three of the cases in post-procedure CT: two cases in the gallbladder (one in each group) and one case in the stomach (conventional RFA group). None of the patients required additional medical treatment.
Outcome-LTP, IDR, and EM
In the intention-to-treat analysis, the estimated 1-year and 3-year cumulative incidences of LTP were both 5.6% in the NT-RFA group, and 11.8% and 21.3%, respectively, in the conventional RFA group. The two groups did not differ significantly in LTP rates (log-rank test, p = 0.073) (Fig. 4A). In the as-treated analysis, the estimated 1-year and 3-year cumulative incidences of LTP were both 0% in the NT-RFA group, and 15.6% and 24.5%, respectively, in the conventional RFA group. The two groups differed significantly in LTP rates (log-rank test, p = 0.004) (Fig. 4B).
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On multivariable Cox regression analysis in the as-treated analysis, RFA type was the only predictive factor for LTP (hazard ratio = 0.061, 95% confidence interval = 0.000–0.497 with conventional RFA as the reference; p = 0.004). Other predictable factors did not show statistical significance at the 5% level (Table 4). As for IDR and EM, there was no significant difference between the two groups in both analyses. The cumulative incidences of these analyses are summarized in Table 5.
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| DISCUSSION |
In this prospective randomized controlled trial, NT-RFA using TICW electrodes demonstrated better LTP than conventional RFA using tumor puncture. According to the as-treated analysis, the estimated 1- and 3-year cumulative incidences of LTP were 0% in the NT-RFA group, which was significantly lower than the 15.6% and 24.5% in the conventional RFA group (p = 0.004). In addition, the complication rate of NT-RFA (3.3%, 1/33) was shown to be similar to that of conventional tumor puncture RFA (7.5%, 3/40). Indeed, our study results are in good agreement with several previous retrospective studies [13, 14, 16, 26] and a prospective cohort study [17] reporting lower LTP rates of NT-RFA with bipolar electrodes compared to conventional RFA with a monopolar electrode. However, while previous studies utilized different numbers and types of RF electrodes, as well as different RF energy delivery modes on both NT-RFA and conventional RFA groups, our study used the same RF equipment and RF delivery mode for both groups, suggesting that the better LTP rates of NT-RFA were due to the oncologically favorable features of the NT-RFA technique. Based on our study results, NT-RFA may be preferentially used for the treatment of small HCCs ≤ 2.5 cm compared to conventional RFA with tumor puncture.
Of note, although NT-RFA showed better LTP rates than conventional RFA, there was no significant difference in ablation zone size between the two groups. These results regarding ablation size could be attributed to the fact that if necessary to acquire optimal ablation margin, additional cycles of RFA were performed after repositioning of the electrode(s) in both groups. Therefore, the better LTP results of NT-RFA could be explained by several factors. First, the higher energy deposition in the peritumoral ablative margin, related to the geometry between the tumor and electrodes, in the NT-RFA group, might be an important contributing factor. According to a previous multicenter study [27], NT-RFA showed better LTP than standard monopolar RFA for HCCs located near large vessels, because more homogenous and extensive tissue necrosis and ablation zones were achieved beyond the macroscopic tumor boundary by placing the needles away from the tumor periphery. Second, blockage of drainage vessels from the target tumor may have been achieved in the early period of the ablation procedure, which may have blocked the dispersal of tumor cells into the drainage portal bloodstream, and may also be less susceptible to the heat sink effect [17, 28]. Third, the centripetal thermal conduction from the periphery to the center of the index tumor may provide a theoretical advantage of less elevation of intratumoral pressure compared to conventional RFA [13, 17]. Tanaka et al. [29] and Ueki et al. [26] also reported that intrahepatic metastasis of HCC occurred more frequently when intratumoral pressure increased after ethanol injection, resulting in a lower risk of track seeding along the electrode [30].
In our study, four patients (10.8%, 4/37) were converted from the NT-RFA technique to the conventional RFA technique. This represents the technical difficulty of NT-RFA compared to conventional tumor puncture RFA, as NT-RFA necessitates the insertion of multiple electrodes outside the target tumor with ideal geometry to create an ablative margin around the tumor [13, 31]. The insertion of two electrodes around the tumor, at equidistance, while avoiding vital structures, can be technically challenging under the guidance of the US. In that regard, real-time fusion guidance or CT guidance might be more advantageous than US guidance. We found that real-time US-CT/MR fusion guidance was very useful for placing electrodes in an ideal peritumoral position as it can provide better conspicuity of the target tumor as well as adjacent vascular structures or organs compared with B-mode US guidance [20, 32, 33]. Thus, to lower the technical difficulty of NT-RFA, additional modifications of RF energy delivery modes, such as combined bipolar and monopolar modes, could be used for NT-RFA. In this regard, further studies on the ideal RF delivery mode for NT-RFA, especially for larger tumors (≥ 3 cm), are warranted. Moreover, NT-RFA had great difficulty in placing the electrodes in the surrounding peritumoral liver parenchyma for subcapsular located tumors, especially near the hepatic angle or hepatic dome portion, and this was the main cause of conversion of NT-RFA to conventional RFA.
Our study has several limitations that warrant mention. First, the small number of study patients was a major limitation. Becuase we had found a significant difference in LTP rates between NT-RFA and conventional RFA, we chose to terminate our clinical trial earlier than originally planned. Further studies with larger populations are warranted. Second, our short-term follow-up duration after RFA (mean of 36 months) was not sufficient to assess overall survival, and there were no significant differences between the two groups in IDM and EM. However, since the main purpose of our study was to evaluate the efficacy of the two RFA techniques in LTP, three years of follow-up should be sufficient to evaluate LTP after RFA. Third, the number of patients who had received RFA as the first treatment for de novo HCC was limited. Therefore, we could not perform a fair comparison of NT-RFA and conventional RFA in terms of the overall survival of the two groups after RFA. Finally, our study results were achieved by an experienced operator during percutaneous tumor ablation. Therefore, considering the technical difficulty and complexity of the NT-RFA procedure, it is not clear whether the favorable results of NT-RFA in the current study could be reproducible with less experienced operators. However, with the technical development of real-time US fusion imaging, NT-RFA for small HCCs (<2.5 cm) with favorable locations can be applied to less experienced operators. Despite these limitations, we believe that this study is meaningful, as it is a randomized prospective study comparing NT-RFA and conventional RFA using the same RF equipment and RF methodology, which demonstrated that NT-RFA provided lower LTP at similar safety levels.
In conclusion, NT-RFA using TIWC electrodes in bipolar mode demonstrated significantly lower cumulative LTP rates than conventional RFA for small HCCs, which warrants a larger study for further confirmation.
Notes
This study was supported by a research grant from RF Medical Co., Ltd. (Seoul, Korea, No. 06-2016-2370).
Conflicts of Interest: Jeong Min Lee received a research grant from RF Medical Co., Ltd. Other authors have no potential conflicts of interest to disclose.
Author Contributions:
1. European Association for the Study of the Liver. EASL clinical practice guidelines: management of hepatocellular carcinoma. J Hepatol 2018;69:182–236.
2. Korean Liver Cancer Association (KLCA); National Cancer Center (NCC). 2018 Korean Liver Cancer Association-National Cancer Center Korea practice guidelines for the management of hepatocellular carcinoma. Korean J Radiol 2019;20:1042–1111.
3. Heimbach JK, Kulik LM, Finn RS, Sirlin CB, Abecassis MM, Roberts LR, et al. AASLD guidelines for the treatment of hepatocellular carcinoma. Hepatology 2018;67:358–380.
4. Ng KKC, Chok KSH, Chan ACY, Cheung TT, Wong TCL, Fung JYY, et al. Randomized clinical trial of hepatic resection versus radiofrequency ablation for early-stage hepatocellular carcinoma. Br J Surg 2017;104:1775–1784.
5. 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;243:321–328.
6. Feng K, Yan J, Li X, Xia F, Ma K, Wang S, 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.
7. Xu XL, Liu XD, Liang M, Luo BM. Radiofrequency ablation versus hepatic resection for small hepatocellular carcinoma: systematic review of randomized controlled trials with meta-analysis and trial sequential analysis. Radiology 2018;287:461–472.
8. Lee DH, Kim JW, Lee JM, Kim JM, Lee MW, Rhim H, et al. Laparoscopic liver resection versus percutaneous radiofrequency ablation for small single nodular hepatocellular carcinoma: comparison of treatment outcomes. Liver Cancer 2021;10:25–37.
9. Kang TW, Kim JM, Rhim H, Lee MW, Kim YS, Lim HK, et al. Small hepatocellular carcinoma: radiofrequency ablation versus nonanatomic resection—propensity score analyses of long-term outcomes. Radiology 2015;275:908–919.
10. Lee DH, Lee JM, Lee JY, Kim SH, Yoon JH, Kim YJ, et al. Radiofrequency ablation of hepatocellular carcinoma as first-line treatment: long-term results and prognostic factors in 162 patients with cirrhosis. Radiology 2014;270:900–909.
11. Ahmed M, Brace CL, Lee FT Jr, Goldberg SN. Principles of and advances in percutaneous ablation. Radiology 2011;258:351–369.
12. Seror O, N’Kontchou G, Nault JC, Rabahi Y, Nahon P, Ganne-Carrié N, et al. Hepatocellular carcinoma within milan criteria: no-touch multibipolar radiofrequency ablation for treatment—Long-term results. Radiology 2016;280:611–621.
13. Hocquelet A, Aubé C, Rode A, Cartier V, Sutter O, Manichon AF, et al. Comparison of no-touch multi-bipolar vs. monopolar radiofrequency ablation for small HCC. J Hepatol 2017;66:67–74.
14. Kawamura Y, Ikeda K, Fujiyama S, Hosaka T, Kobayashi M, Saitoh S, et al. Potential of a no-touch pincer ablation procedure that uses a multipolar radiofrequency ablation system to prevent intrasubsegmental recurrence of small and single hepatocellular carcinomas. Hepatol Res 2017;47:1008–1020.
15. Seror O, N’Kontchou G, Van Nhieu JT, Rabahi Y, Nahon P, Laurent A, et al. Histopathologic comparison of monopolar versus no-touch multipolar radiofrequency ablation to treat hepatocellular carcinoma within Milan criteria. J Vasc Interv Radiol 2014;25:599–607.
16. Chai Y, Li K, Zhang C, Chen S, Ma K. The short-term efficacy of no-touch radiofrequency ablation in treating cirrhosis-based small hepatocellular carcinoma. BMC Cancer 2019;19:497.
17. Hirooka M, Hiraoka A, Ochi H, Koizumi Y, Michitaka K, Joko K, et al. Prospective cohort trial to confirm the efficacy of no-touch radio frequency ablation. J Gastroenterol Hepatol 2019;34:567–574.
18. Lee JM, Han JK, Kim SH, Lee JY, Shin KS, Choi BI. An ex-vivo experimental study on optimization of bipolar radiofrequency liver ablation using perfusion-cooled electrodes. Acta Radiol 2005;46:443–451.
19. Korean Liver Cancer Study Group (KLCSG); National Cancer Center, Korea (NCC). 2014 Korean Liver Cancer Study Group-National Cancer Center Korea practice guideline for the management of hepatocellular carcinoma. Korean J Radiol 2015;16:465–522.
20. Ahn SJ, Lee JM, Lee DH, Lee SM, Yoon JH, Kim YJ, et al. Real-time US-CT/MR fusion imaging for percutaneous radiofrequency ablation of hepatocellular carcinoma. J Hepatol 2017;66:347–354.
21. Kim TH, Choi HI, Kim BR, Kang JH, Nam JG, Park SJ, et al. No-touch radiofrequency ablation of VX2 hepatic tumors in vivo in rabbits: a proof of concept study. Korean J Radiol 2018;19:1099–1109.
22. Ahmed M, Solbiati L, Brace CL, Breen DJ, Callstrom MR, Charboneau JW, et al. Image-guided tumor ablation: standardization of terminology and reporting criteria--a 10-year update. Radiology 2014;273:241–260.
23. Sacks D, McClenny TE, Cardella JF, Lewis CA. Society of Interventional Radiology clinical practice guidelines. J Vasc Interv Radiol 2003;14:S199–S202.
24. Shropshire EL, Chaudhry M, Miller CM, Allen BC, Bozdogan E, Cardona DM, et al. LI-RADS treatment response algorithm: performance and diagnostic accuracy. Radiology 2019;292:226–234.
25. Ten Have TR, Normand SL, Marcus SM, Brown CH, Lavori P, Duan N. Intent-to-treat vs. non-intent-to-treat analyses under treatment non-adherence in mental health randomized trials. Psychiatr Ann 2008;38:772–778.
26. Ueki T, Sakaguchi S, Miyajima Y, Hatono N, Tohara K, Nakabayashi S, et al. Usefulness of tumor pressure as a prognostic factor in cases of hepatocellular carcinoma where the diameter of the tumor is 3 cm or less. Cancer 2002;95:596–604.
27. Mohkam K, Dumont PN, Manichon AF, Jouvet JC, Boussel L, Merle P, et al. No-touch multibipolar radiofrequency ablation vs. surgical resection for solitary hepatocellular carcinoma ranging from 2 to 5 cm. J Hepatol 2018;68:1172–1180.
28. Mohkam K, Rode A, Mabrut JY. Influence of ablation technique on treatment failure for perivascular hepatocellular carcinoma. J Hepatol 2018;69:750–751.
29. Tanaka T, Yamanaka N, Oriyama T, Furukawa K, Okamoto E. Factors regulating tumor pressure in hepatocellular carcinoma and implications for tumor spread. Hepatology 1997;26:283–287.
30. Otsuka Y, Kaneko H. Laparoscopic liver resection in the treatment of HCC with liver cirrhosis: would it provide superiority to conventional open hepatectomy? Hepatobiliary Surg Nutr 2017;6:356–358.
31. Yoon JH, Lee JM, Woo S, Hwang EJ, Hwang I, Choi W, et al. Switching bipolar hepatic radiofrequency ablation using internally cooled wet electrodes: comparison with consecutive monopolar and switching monopolar modes. Br J Radiol 2015;88:20140468
32. Lee MW. Fusion imaging of real-time ultrasonography with CT or MRI for hepatic intervention. Ultrasonography 2014;33:227–239.
33. Lee DH, Lee JM. Recent advances in the image-guided tumor ablation of liver malignancies: radiofrequency ablation with multiple electrodes, real-time multimodality fusion imaging, and new energy sources. Korean J Radiol 2018;19:545–559.
34. Kang TW, Lim HK, Lee MW, Kim YS, Rhim H, Lee WJ, et al. Long-term therapeutic outcomes of radiofrequency ablation for subcapsular versus nonsubcapsular hepatocellular carcinoma: a propensity score matched study. Radiology 2016;280:300–312.
Yun Seok Suh
Department of Radiology, Seoul National University Hospital, Seoul
Jae Won Choi
Department of Radiology, Seoul National University Hospital, Seoul
Jeong Hee Yoon
Department of Radiology, Seoul National University Hospital, Seoul
Dong Ho Lee
Department of Radiology, Seoul National University Hospital, Seoul
Yoon Jun Kim
Department of Internal Medicine, Seoul National University Hospital, Seoul
Jeong Hoon Lee
Department of Internal Medicine, Seoul National University Hospital, Seoul
Su Jong Yu
Department of Internal Medicine, Seoul National University Hospital, Seoul
Eun Ju Cho
Department of Internal Medicine, Seoul National University Hospital, Seoul
Jung Hwan Yoon
Department of Internal Medicine, Seoul National University Hospital, Seoul
Jeong Min Lee
Department of Radiology, Seoul National University Hospital, Seoul
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Abstract
Objective
This study aimed to compare the efficacy between no-touch (NT) radiofrequency ablation (RFA) and conventional RFA using twin internally cooled wet (TICW) electrodes in the bipolar mode for the treatment of small hepatocellular carcinomas (HCC).
Materials and Methods
In this single-center, two-arm, parallel-group, prospective randomized controlled study, we performed a 1:1 random allocation of eligible patients with HCCs to receive NT-RFA or conventional RFA between October 2016 and September 2018. The primary endpoint was the cumulative local tumor progression (LTP) rate after RFA. Secondary endpoints included technical conversion rates of NT-RFA, intrahepatic distance recurrence, extrahepatic metastasis, technical parameters, technical efficacy, and rates of complications. Cumulative LTP rates were analyzed using Kaplan-Meier analysis and the Cox proportional hazard regression model. Considering conversion cases from NT-RFA to conventional RFA, intention-to-treat and as-treated analyses were performed.
Results
Enrolled patients were randomly assigned to the NT-RFA group (37 patients with 38 HCCs) or the conventional RFA group (36 patients with 38 HCCs). Among the NT-RFA group patients, conversion to conventional RFA occurred in four patients (10.8%, 4/37). According to intention-to-treat analysis, both 1- and 3-year cumulative LTP rates were 5.6%, in the NT-RFA group, and they were 11.8% and 21.3%, respectively, in the conventional RFA group (p = 0.073, log-rank). In the as-treated analysis, LTP rates at 1 year and 3 years were 0% and 0%, respectively, in the NT-RFA group sand 15.6% and 24.5%, respectively, in the conventional RFA group (p = 0.004, log-rank). In as-treated analysis using multivariable Cox regression analysis, RFA type was the only significant predictive factor for LTP (hazard ratio = 0.061 with conventional RFA as the reference, 95% confidence interval = 0.000–0.497; p = 0.004). There were no significant differences in the procedure characteristics between the two groups. No procedure-related deaths or major complications were observed.
Conclusion
NT-RFA using TICW electrodes in bipolar mode demonstrated significantly lower cumulative LTP rates than conventional RFA for small HCCs, which warrants a larger study for further confirmation.
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