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Usefulness of Body Position Change during Local Ablation Therapies for Hepatocellular Carcinoma

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29 January 2024

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31 January 2024

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Abstract
Objective: Local ablation therapies (radiofrequency ablation (RFA), and microwave ablation (MWA)) are important as curative treatment option in patient with early-stage hepatocellular carcinoma (HCC) and option for intrahepatic tumor volume reduction in those with unresectable HCC. Various techniques; contrast-enhanced ultrasound (CEUS), real-time virtual sonography (RVS), artificial pleural and ascites fluid infusion, and body position change (BPC) have been used to accurately and safely perform local ablation therapies. However, there have been few reports on the usefulness of BPC. Therefore, this study focused on the usefulness of BPC during local ablation therapies in patients with HCC. Methods: We evaluated the technical success rates, treatment time, and prognosis of 283 nodules treated with local ablation therapies. Furthermore, we defined nodules adjacent to large vessels or extrahepatic organs, or poorly visible nodules using US as HCC in high-risk locations. High-risk locations HCC were classified into phase 1 (before active use of BPC, January 2018 to December 2019) and phase 2 (after active use of BPC, January 2020 to January 2022). Results: One hundred seventy-six nodules (62%) were classified as high-risk location group. Compared to non-high risk HCC, treatment-assist techniques, such as BPC (61 vs. 24 %, p<0.001), artificial pleural fluid infusion (24 vs. 5.6%, p<0.001), artificial ascites infusion (50 vs. 11%, p<0.001), fusion imaging (28 vs. 8.4%, p<0.001) and CEUS (26 vs. 4.7%, p<0.001) were performed more frequently for high-risk HCC. The technical success rates were 96% (271/283 nodules), 96% (167/173 nodules) and 95% (102/107 nodules), for all nodules, the high-risk location group and the non-high risk location group, respectively. In the high-risk location group, the technical success rates of the group without BPC were lower than that with BPC (91 vs. 99%, p=0.015). Only BPC was a related factor for the technical success rate for high-risk locations HCC (OR 10 (1.2-86), p=0.034). In contrast, no differences were found in the treatment time, the local tumor progression rates, intrahepatic distant recurrence rates, and overall survival between the group with BPC and that without BPC in the high-risk location HCC. Conclusion: BPC during local ablation therapies in patients with HCC in high-risk locations was safe and efficient. Body position should be adjusted for HCC in high-risk locations to maintain good US visibility and ensure safe puncture route in patients undergoing local ablation therapies.
Keywords: 
Subject: Biology and Life Sciences  -   Life Sciences

1. Introduction

Hepatocellular carcinoma (HCC) is the sixth most commonly diagnosed cancer and the fourth leading cause of cancer-related death [1]. The main treatments for HCC include local ablation therapies (such as radiofrequency and microwave ablation (RFA and MWA, respectively)), surgical resection, transarterial chemoembolization, and liver transplantation. Local ablation therapy is particularly beneficial for patients with hepatic decompensation or those who are ineligible for surgical resection because of complications [2]. This therapy has less impact on residual liver function than resection, making it an important treatment option for early-stage HCC [3,4,5,6].
The 3- and 5-year survival rates for patients treated with RFA were 88.9% and 76.6% for liver damage A and 75.2% and 56.5% for liver damage B, respectively. Similarly, the 3- and 5-year survival rates of patients with HCC treated by MWA were 72%–73% and 57%–60%, respectively [7,8,9]. The SURF trial investigated the effects of surgical resection and RFA in patients with HCC with a maximum diameter of <3 cm and a number of tumors of less than 3. The median recurrence-free survival was 2.98 and 2.76 years in the resection and RFA groups (hazard ratio 0.96, p = 0.793), respectively [10]. Furthermore, randomized controlled prospective trials have demonstrated the equivalence of these two therapies. Hence, when performing local ablation therapies, it is important to accurately control HCC equivalent to resection and minimize complications.
Advancements in ultrasound (US) technology and various techniques have enhanced the accuracy and safety of local ablation therapies. These include RFA with contrast-enhanced US (CEUS), real-time virtual sonography (RVS), artificial pleural and ascites fluid infusion, and body position change (BPC). Implementation of these methods has seemingly improved the safety and completion rates of local ablation therapies. The efficacy of RFA along with CEUS, RVS, and artificial fluid infusion has been supported in previous reports [11,12,13,14,15,16,17,18]. However, the benefit of BPC in patients treated with RFA and MWA was not adequately investigated. Therefore, this study focused on the usefulness of BPC during local ablation therapy in patients with HCC.

2. Materials and Methods

2.1. Patients

This study included 283 nodules in 230 patients with HCC who received RFA therapies at our institution between January 2018 and 2022 (Figure 1). The inclusion criteria were as follows: patients (1) >18 years old; (2) with performance status of 0 or 1; (3) who had surgically unresectable HCC lesions or who voluntarily chose nonsurgical treatment; (4) with three or fewer lesions and ≤5 cm in diameter; (5) with total serum bilirubin concentration of <3 mg/dL; and (6) without extrahepatic metastasis or vascular tumor invasion. Patients with (1) a platelet count below 50 ∗ 109/L, (2) prothrombin activity below 50%, (3) refractory ascites, and (4) nodules suspected of poorly differentiated HCC on pretreatment imaging and patients (5) receiving a combination of local and other therapies were excluded from this study [19,20,21].
HCC was diagnosed on the basis of pathological examination results; classical HCC findings (contrast enhancement in the arterial phase and portal vein phase washout) on dynamic computed tomography (CT), gadolinium ethoxybenzyl diethylenetriamine penta-acetic acid-contrast-enhanced magnetic resonance imaging (MRI), or contrast-enhanced ultrasonography (CEUS); and clinical examination results strongly indicative of HCC, such as elevated alpha-fetoprotein (AFP) levels, AFP-L3 index, or des-gamma-carboxy prothrombin (DCP) levels. In this study, patients with hepatitis B virus (HBV), hepatitis C virus (HCV), and non-B non-C hepatitis were defined as those having detectable HBV-DNA or receiving nucleoside analog therapy and those with detectable HCV-RNA or sustained virological response.
The study was conducted in accordance with the Declaration of Helsinki and was approved by the Human Ethics Review Committee of the University of Yamanashi. Written informed consent was obtained from all patients.

2.2. RFA Techniques and Devices

Percutaneous local ablation therapy was performed on an inpatient basis. Two experienced operators previewed the targeted nodule using US (planning US) the day before treatment. The US visibility of the target tumor was graded by the operators on a 4-point scale: invisible, poor, fair, and good [22]. Thereafter, the operators assessed the presence of a safe access route for electrode placement.
The devices used for RFA were the Cool-tip RFA system (Covidien, USA), VIVA RF system (STARmed, Korea), and Emprint ablation system (Covidien/Medtronic, USA) [23]. After local anesthesia administration, the electrode was inserted under US guidance (Aplio 500, Toshiba, Tokyo, Japan) using a dedicated US transducer for puncture (PVT-350BTP, Toshiba, Japan). In the case of 3-cm internally cooled tip RF electrodes, the output was initiated at 60 W and increased by 20 W/min until tissue impedance overshooting occurred. With 2-cm internally cooled tip RF electrodes, the output started at 40 W and then increased by 10 W/min until tissue impedance overshooting occurred. In the case of the adjustable VIVA RF electrode, we used the general mode, automatically monitoring the impedance rise and adjusting the radio wave output. In the case of the Emprint electrode, we adjusted the radio wave output, as shown in the table, using probes ranging from short (15 cm) to standard (20 cm) and long (30 cm).
All ablation procedures were performed by one of three experienced physicians with 12 years of experience in performing US-guided percutaneous ablation.

2.3. HCC in High-Risk Locations

HCC nodules were classified as HCC in high-risk locations based on US if they were adjacent to large vessels or extrahepatic organs or if they were poorly visible on US. Nodules were considered adjacent to large vessels if they were located <5 mm from the first or second branch of the portal vein, the base of hepatic veins, or the inferior vena cava. However, nodules located <5 mm from the diaphragm, heart, lung, gallbladder, right kidney, or gastrointestinal tract were considered adjacent to extrahepatic organs. The distance between the edge of the nodule and the large vessel or extrahepatic organ was measured on CT images reconstructed at 1-mm intervals.

2.4. Treatment-Assist Techniques for HCC in High-Risk Locations

To protect against thermal injury during the procedure, an artificial pleural fluid infusion method with 5% glucose was used if the targeted nodules were close to the diaphragm or lungs. The artificial ascites effusion method was used if the nodules were close to other extrahepatic organs in the abdominal cavity [24]. For patients whose B-mode US could not identify the nodule, we used artificial pleural effusion, artificial ascites, CEUS, RVS, or BPC [25,26,27]. An image analysis system (Volume Analyzer Synapse VINCENT, version 5.1, Fujifilm Medical Systems, Tokyo, Japan) was used to create fusion images [22,28].
For BPC, patients were examined in various positions, including supine, half side lying (right and left), head up, and upright [29,30]. Patients with no problems with image characterization of HCC using US and a safe puncture route were treated in the supine position. The right half side lying position was used primarily for HCCs in segments S2, 3, and 4, whereas the left half side lying position was used for those in segments S6, 7, and 1. The head up and upright positions were used for those in the S7 and 8 segments, particularly in the liver dome.
Starting in October 2019, after one hepatologist received training at the high-volume center, we actively used BPC during ablation therapies. Patients were classified into phase 1 (January 2018–December 2019) and phase 2 (January 2020–January 2022) before and after the proactive use of BPC.

2.5. Assessment of Treatment Response and Follow-Up

A hepatologist and two radiologists assessed the therapeutic response. Treatment response was assessed using plain CT at 1–3 days after the ablation and dynamic CT at 1 month after the ablation. Later, dynamic CT or EOB-MRI was performed every 3 months. A curative case was defined as one in which all HCC nodules were treated by ablation. In cases of suspected recurrence, imaging studies were conducted. Local tumor progression was defined as the appearance of a viable tumor contiguous with the original nodal site during follow-up. All intrahepatic recurrences, excluding local tumor progression, were defined as intrahepatic distant recurrences.

2.6. Statistical Analysis

Median and range were used to report continuous data. To analyze group differences, the study used the Mann–Whitney U test, Kruskal–Wallis test, and nonparametric ANOVA. When one-way ANOVA yielded significant outcomes, Fisher’s exact test was used to examine the differences between specific groups. The Kaplan–Meier method was used to determine both progression-free survival and overall survival (OS), with the log-rank test used for analysis. Statistical significance was defined as a p-value < 0.05. Statistical analyses were performed using EZR (Saitama Medical Center, Jichi Medical University, Saitama, Japan), a graphical user interface for R (The R Foundation for Statistical Computing, Vienna, Austria) [31].

3. Results

3.1. Patients

This study involved 283 nodules in 230 patients with a median follow-up period of 52 (45–55) months. Table 1 shows the baseline characteristics of patients receiving RFA therapy. The maximal diameter of the tumors ranged between 4 and 38 mm (median = 12 mm). The number of nodules to be treated was 1 (186 cases), 2 (78 cases), or 3 (19 cases). The most common tumor location was segments 7 and 8 (each 23%). However, 62% of the nodules were classified in the high-risk location group. The following procedures were performed more frequently in the high-risk location group than in the low-risk group: BPC (61% vs. 24%, p < 0.001), artificial pleural fluid infusion (24% vs. 5.6%, p < 0.001), artificial ascites infusion (50% vs. 11%, p < 0.001), fusion imaging (28% vs. 8.4%, p < 0.001), and CEUS (26% vs. 4.7%, p < 0.001). The use of treatment-assist techniques such as BPC (2.9 vs. 3.6, p<0.001), artificial pleural fluid infusion (2.9 vs. 3.6, p<0.001), artificial ascites infusion (2.8 vs. 3.6, p<0.001), fusion imaging (2.1 vs. 3.3, p<0.001) and CEUS (2.0 vs. 3.5, p<0.001) improved the intraoperative US visibility for high-risk HCC using the four-point scale, compared to the baseline US the day before treatment.

3.2. Technical Success of Local Ablation Therapy

The total technical success rate was 96% (167/173 nodules) and 95% (102/107 nodules) for the high- and low-risk location groups, respectively. Notably, within the high-risk location group, nodules treated with BPC achieved a significantly higher technical success rate than those without BPC (99% vs. 91%, p = 0.015; Figure 2a). Our analysis identified BPC as the only factor related to the technical success rate for the high-risk location group (OR = 10 (1.2–86), p = 0.034; Table 2).

3.3. Procedure Time

The treatment duration according to the nodule number is reported in Figure 2b. The high-risk location group in patients with 1 target lesion demonstrated longer treatment duration than the low-risk location group (61 min vs. 43 min, p < 0.001). However, no differences were found in the procedure time between the groups with and without BPC in the high-risk location group (p = 0.36; Figure 2b).

3.4. Local Tumor Progression

The local tumor progression rates for all nodules during the follow-up period were 4.4%, 8.2%, and 12% at 1, 3, and 5 years, respectively (Figure 3a). The local tumor progression rate showed no significant difference between the high- and low-risk location groups (p = 0.18; Figure 3b). Similarly, there was no significant difference in the local tumor progression rate between the groups without and with BPC in the high-risk location group (p = 0.64; Figure 2c and Figure 3c).

3.5. Intrahepatic Distant Recurrence

The intrahepatic distant recurrence rates for all nodules during the follow-up period were 37%, 66%, and 84% at 1, 3, and 5 years, respectively (Figure 3d). The difference in intrahepatic distant recurrence rates between the high- and low-risk location groups was insignificant (p = 0.18; Figure 3e). Moreover, there was no significant difference in intrahepatic distant recurrence rates between the groups without and with BPC in the high-risk location group (p = 0.65; Figure 2d and Figure 3f).

3.6. Overall Survival

The survival rates for all nodules were 97%, 79%, and 58% after 1, 3, and 5 years, respectively (Figure 3g). No significant difference in OS was detected between the high- and low-risk location groups (p = 0.16; Figure 3h) or between the groups without and with BPC in the high-risk location group (p = 0.83; Figure 2e and Figure 3i).

3.7. Complications

The rates of complications were comparable between the high- (4.0%) and low-risk location groups (5.6%, p = 0.57). Similarly, they were comparable between the groups with and without BPC in the high-risk location group (2.8% vs. 5.8%, p = 0.44).

3.8. Association between the Timing of Treatment and Prognosis in the High-Risk Location Group

In the high-risk location group, the technical success rates of phase 1 by one session were lower than those of phase 2 (89% vs. 100%, p < 0.001; Figure 2a). The treatment duration of phase 1 (n = 61) was longer than that of phase 2 (n = 115) (83 (12–194) min vs. 63 (15–125) min, p < 0.001; Figure 2b). However, the local tumor progression rates, intrahepatic distant recurrence rates, and OS between the phase 1 and 2 groups were comparable (p=0.34, 0.71, 0.34; Figure 2c–e). Compared with phase 1, phase 2 used intraoperative RVS less frequently (18% vs. 48%, p < 0.001), whereas BPC was used more frequently (77% vs. 31%, p < 0.001) along with artificial ascites infusion (60% vs. 31%, p < 0.001; Table 3).

4. Discussion

In this study, BPC during local ablation therapy in patients with HCC in high-risk locations was useful. To our knowledge, this is the first study to statistically show that BPC is safe and efficient in patients receiving local ablation therapies. The body position should be adjusted for HCC in high-risk locations to maintain good US visibility and ensure a safe puncture route in patients undergoing local ablation therapies. Furthermore, it is important to sufficiently predict the US view before treatment.
The Barcelona Clinic Liver Cancer (BCLC) classification and the consensus-based clinical practice guidelines for HCC management proposed by the Japan Society of Hepatology have been widely used to determine the treatment strategy in Japan [32]. Recurrence-free survival did not differ significantly between the surgery and RFA groups in patients with the largest HCC diameter ≤3 cm and ≤3 HCC nodules (p = 0.58) [10]. Therefore, RFA and surgical resection are recommended for patients with BCLC stage A HCC. Especially in today’s aging population, RFA is an important treatment option because it is effective and less invasive. RFA delivers thermal energy via an electric current between the electrode and a ground pad and has been evaluated as a first-line therapy in early HCC. However, a high incidence of local recurrence in approximately 10% of patients, especially when located near large blood vessels, has been reported previously [33]. In contrast, MWA originated in the 1980s and was modified with the improvement of antenna and therapy strategies. It has been the most recent generation ablation system that uses electromagnetic waves that are less prone to the heat sink effect. MWA is as safe and effective as RFA and achieves a high complete ablation rate with the ability to reach a larger target area than RFA [34,35,36]. MWA has an obvious superiority to RFA in larger tumors ≥3 cm in diameter or when it is close to large vessels.
When performing local ablation therapies, it is important to obtain a better sonographic window and plan a safe puncture route. Various body positions have been attempted for better visualization of the entire liver during US examinations [30,37,38]. Among various body positions, supine, right half side lying, left half side lying, head up, and upright were mainly used according to the site of the tumor and the patient’s body size empirically. Although BPC is frequently used during US examinations of the liver, this topic has not been sufficiently explored. Therefore, our study focused on providing statistical evidence of the usefulness of BPC during RFA therapies.
As shown in this study, in the high-risk location group, the technical success rates of the group without BPC were lower than those with BPC. Moreover, only BPC was a factor related to the technical success rate for the high-risk location group. In contrast, no differences were found in the treatment duration between the groups with and without BPC. Performing BPC alone is useful for local ablation therapies of high-risk location HCCs, even without the use of other modalities. We believe that the total procedure time is shorter and the rate of complete ablation achieved in one session is higher in the group with BPC, even if it takes more time and effort to perform BPC. Therefore, it is important to have an adequate treatment plan before starting local ablation therapies and to ensure a safe and secure puncture route.
Other treatment-assist techniques include artificial pleural effusion, artificial ascites, CEUS, and RVS. Artificial ascites and pleural effusion are frequently used to protect adjacent organs from thermal damage and obtain a better sonographic window. RVS has been used since 2003, and because of improved accuracy in image synchronization, it is used to confirm the position of HCC before puncture and to check the area to be ablated after treatment [22,39]. Recently, US–US overlay fusion guidance for local controllability was reported to be highly effective for safety margin achievement [40]. Moreover, the usefulness of combination techniques such as RVS-guided RFA with artificial ascites has been reported in a few reports [41]. Conversely, CEUS is frequently used for HCC in coarse liver parenchyma using the Kupffer phase [42]. It may also be useful for evaluating treatment response immediately after local therapies in the future, when more patients with poor renal function are probably elderly and have comorbidities and concomitant systemic therapies. In this study, there was no improvement in the success rates with these other modalities. This may be due to the unplanned use of other modalities, i.e., cases in which intraoperative US visibility was inadequate and a hasty decision was made to use other modalities.
One of the three hepatologists conducting local ablation therapies in this study received a practical training program at a high-volume center for 6 months. Ablation therapies from January 2020 onward, incorporating his training experience, have achieved higher control rates, safely, and shorter procedure times compared to before. Undergoing an intensive training program on local ablation therapies is an extremely valuable experience. Although it is difficult to accurately assess the outcomes of the training program at a high-volume center, it is an important opportunity for non-high-volume centers to improve their competence, as our institution experienced in this study. Therefore, the good results of this study are certainly not solely due to the aggressive addition of BPC, and further studies are needed.
In modern treatment for HCC, where immune checkpoint inhibitors for unresectable HCC have been added as a new treatment option, treatment planning for each individual HCC nodule, even in patients with advanced HCC, may lead to improved prognosis rather than broadly classifying the stages. Moreover, RFA can activate tumor-specific T lymphocytes and enhance the killing ability of natural killer cells toward hepatoma cells [43,44]. Local ablation therapies are no longer just for early-stage HCC but will now be required to be used in combination with other therapies in advanced HCC. Accordingly, the establishment of treatment-assist techniques to achieve safer and more accurate complete ablation is essential.
This study had several limitations. First, this is a single-center study with a few cases. Second, bias may exist in patient selection. Most nodules suspected of having poorly differentiated HCC on pretreatment imaging are selected for surgical resection; however, there are a few cases in which the imaging and pathological diagnoses diverge. Additionally, most of the nodules have not undergone tumor biopsy and may have contained high-grade nodules such as poorly differentiated HCC. Third, as noted in Section 4, this study is not considered a result solely of the effective use of BPC. However, we believe that BPC is certainly useful during local ablation therapies for high-risk locations of HCC, even when various hepatologists with varying years of experience and competence are involved.

5. Conclusions

To the best of our knowledge, this study is the first to statistically propose that BPC is safe and efficient in patients receiving local ablation therapies. The appropriate use of BPC when performing local ablation therapies may allow for more precise treatment in a shorter time and safely.

Author Contributions

Conceptualization, H.T.; Methodology, H.T.; Validation, H.T.; Formal Analysis, H.T.; Data Curation, H.T., Y.K., L.O., M.M., Y.S., M.S., S.K., T.Y., S.T., and S.M.; Writing – Original Draft Preparation, H.T.; Writing – Review & Editing, H.T.; Visualization, H.T.; Supervision, N.E.

Funding

This research received no external funding.

Institutional Review Board Statement

The study was conducted according to the guidelines of the Declaration of Helsinki, and approved by the Institutional Review Board (or Ethics Committee) of University of Yamanashi (protocol code 1326).

Informed Consent Statement

Informed consent was obtained from all subjects involved in the study.

Data Availability Statement

The data presented in this study are available on request from the corresponding author.

Acknowledgments

We thank Shuichiro Shiina for kind co-operation.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Sung, H.; Ferlay, J.; Siegel, R.L.; Laversanne, M.; Soerjomataram, I.; Jemal, A.; Bray, F.; Bsc, M.F.B.; Me, J.F.; Soerjomataram, M.I.; et al. Global Cancer Statistics 2020: GLOBOCAN Estimates of Incidence and Mortality Worldwide for 36 Cancers in 185 Countries. CA Cancer J. Clin. 2021, 71, 209–249. [Google Scholar] [CrossRef]
  2. Shiina, S.; Tateishi, R.; Arano, T.; Uchino, K.; Enooku, K.; Nakagawa, H.; Asaoka, Y.; Sato, T.; Masuzaki, R.; Kondo, Y.; et al. Radiofrequency ablation for hepatocellular carcinoma: 10-year outcome and prognostic pactors. Am. J. Gastroenterol. 2012, 107, 569–577. [Google Scholar] [CrossRef]
  3. Shiina, S.; Teratani, T.; Obi, S.; Hamamura, K.; Koike, Y.; Omata, M. Nonsurgical treatment of hepatocellular carcinoma: From percutaneous ethanol injection therapy and percutaneous microwave coagulation therapy to radiofrequency ablation. Oncology 2002, 62 (Suppl. 1), 64–68. [Google Scholar] [CrossRef]
  4. Tateishi R, Shiina S, Teratani T, Obi S, Sato S, Koike Y, et al. Percutaneous radiofrequency ablation for hepatocellular carcinoma. An analysis of 1000 cases. Cancer. 2005;103(6):1201-9. [CrossRef]
  5. Teratani, T.; Yoshida, H.; Shiina, S.; Obi, S.; Sato, S.; Tateishi, R.; Mine, N.; Kondo, Y.; Kawabe, T.; Omata, M. Radiofrequency ablation for hepatocellular carcinoma in so-called high-risk locations. Hepatology 2006, 43, 1101–1108. [Google Scholar] [CrossRef] [PubMed]
  6. Tsuchiya, K.; Asahina, Y.; Tamaki, N.; Yasui, Y.; Hosokawa, T.; Ueda, K.; Nakanishi, H.; Itakura, J.; Kurosaki, M.; Enomoto, N.; et al. Risk factors for exceeding the Milan criteria after successful radiofrequency ablation in patients with early-stage hepatocellular carcinoma. Liver Transplant. 2013, 20, 291–297. [Google Scholar] [CrossRef]
  7. Bai, X.-M.; Cui, M.; Yang, W.; Wang, H.; Wang, S.; Zhang, Z.-Y.; Wu, W.; Chen, M.-H.; Yan, K.; Goldberg, S.N. The 10-year Survival Analysis of Radiofrequency Ablation for Solitary Hepatocellular Carcinoma 5 cm or Smaller: Primary versus Recurrent HCC. Radiology 2021, 300, 458–469. [Google Scholar] [CrossRef]
  8. Dong, B.; Liang, P.; Yu, X.; Su, L.; Yu, D.; Cheng, Z.; Zhang, J. Percutaneous sonographically guided microwave coagulation therapy for hepatocellular carcinoma: Results in 234 patients. Am. J. Roentgenol. 2003, 180, 1547–1555. [Google Scholar] [CrossRef]
  9. Dong, T.-T.; Wang, L.; Li, M.; Yin, C.; Li, Y.-Y.; Nie, F. Clinical Results, Risk Factors, and Future Directions of Ultrasound-Guided Percutaneous Microwave Ablation for Hepatocellular Carcinoma. J. Hepatocell. Carcinoma 2023, ume 10, 733–743. [Google Scholar] [CrossRef]
  10. Takayama, T.; Hasegawa, K.; Izumi, N.; Kudo, M.; Shimada, M.; Yamanaka, N.; Inomata, M.; Kaneko, S.; Nakayama, H.; Kawaguchi, Y.; et al. Surgery versus Radiofrequency Ablation for Small Hepatocellular Carcinoma: A Randomized Controlled Trial (SURF Trial). Liver Cancer 2021, 11, 209–218. [Google Scholar] [CrossRef]
  11. Hiraoka, A.; Ichiryu, M.; Tazuya, N.; Ochi, H.; Tanabe, A.; Nakahara, H.; Hidaka, S.; Uehara, T.; Ichikawa, S.; Hasebe, A.; et al. Clinical translation in the treatment of hepatocellular carcinoma following the introduction of contrast-enhanced ultrasonography with Sonazoid. Oncol. Lett. 2010, 1, 57–61. [Google Scholar] [CrossRef]
  12. Masuzaki, R.; Shiina, S.; Tateishi, R.; Yoshida, H.; Goto, E.; Sugioka, Y.; Kondo, Y.; Goto, T.; Ikeda, H.; Omata, M.; et al. Utility of contrast-enhanced ultrasonography with Sonazoid in radiofrequency ablation for hepatocellular carcinoma. J. Gastroenterol. Hepatol. 2011, 26, 759–764. [Google Scholar] [CrossRef]
  13. Takada, H.; Tsuchiya, K.; Yasui, Y.; Nakakuki, N.; Tamaki, N.; Suzuki, S.; Nakanishi, H.; Itakura, J.; Takahashi, Y.; Kurosaki, M.; et al. Irregular vascular pattern by contrast-enhanced ultrasonography and high serum Lens culinaris agglutinin-reactive fraction of alpha-fetoprotein level predict poor outcome after successful radiofrequency ablation in patients with early-stage hepatocellular carcinoma. Cancer Med. 2016, 5, 3111–3120. [Google Scholar] [CrossRef] [PubMed]
  14. Minami, T.; Minami, Y.; Chishina, H.; Arizumi, T.; Takita, M.; Kitai, S.; Yada, N.; Inoue, T.; Hagiwara, S.; Ueshima, K.; et al. Combination guidance of contrast-enhanced US and fusion imaging in radiofrequency ablation for hepatocellular carcinoma with poor conspicuity on contrast-enhanced US/fusion imaging. Oncology 2014, 87 (Suppl. 1), 55–62. [Google Scholar] [CrossRef]
  15. Hsieh, Y.-C.; Limquiaco, J.L.; Lin, C.-C.; Chen, W.-T.; Lin, S.-M. Radiofrequency ablation following artificial ascites and pleural effusion creation may improve outcomes for hepatocellular carcinoma in high-risk locations. Abdom. Radiol. 2018, 44, 1141–1151. [Google Scholar] [CrossRef]
  16. Uehara, T.; Hirooka, M.; Ishida, K.; Hiraoka, A.; Kumagi, T.; Kisaka, Y.; Hiasa, Y.; Onji, M. Percutaneous ultrasound-guided radiofrequency ablation of hepatocellular carcinoma with artificially induced pleural effusion and ascites. J. Gastroenterol. 2007, 42, 306–311. [Google Scholar] [CrossRef] [PubMed]
  17. Iwai, S.; Sakaguchi, H.; Fujii, H.; Kobayashi, S.; Morikawa, H.; Enomoto, M.; Tamori, A.; Kawada, N. Benefits of artificially induced pleural effusion and/or ascites for percutaneous radiofrequency ablation of hepatocellular carcinoma located on the liver surface and in the hepatic dome. Hepato-Gastroenterology 2012, 59, 546–50. [Google Scholar] [CrossRef] [PubMed]
  18. Inoue, T.; Minami, Y.; Chung, H.; Hayaishi, S.; Ueda, T.; Tatsumi, C.; Takita, M.; Kitai, S.; Hatanaka, K.; Ishikawa, E.; et al. Radiofrequency ablation for hepatocellular carcinoma: Assistant techniques for difficult cases. Oncology 2010, 78 (Suppl. 1), 94–101. [Google Scholar] [CrossRef] [PubMed]
  19. Numata, K.; Fukuda, H.; Nihonmatsu, H.; Kondo, M.; Nozaki, A.; Chuma, M.; Morimoto, M.; Oshima, T.; Okada, M.; Murakami, T.; et al. Use of vessel patterns on contrast-enhanced ultrasonography using a perflubutane-based contrast agent for the differential diagnosis of regenerative nodules from early hepatocellular carcinoma or high-grade dysplastic nodules in patients with chronic liver disease. Abdom. Imaging 2015, 40, 2372–2383. [Google Scholar] [PubMed]
  20. Nakanishi, M.; Chuma, M.; Hige, S.; Omatsu, T.; Yokoo, H.; Nakanishi, K.; Kamiyama, T.; Kubota, K.; Haga, H.; Matsuno, Y.; et al. Relationship between diffusion-weighted magnetic resonance imaging and histological tumor grading of hepatocellular carcinoma. Ann. Surg. Oncol. 2011, 19, 1302–1309. [Google Scholar] [CrossRef]
  21. Nakachi, K.; Tamai, H.; Mori, Y.; Shingaki, N.; Moribata, K.; Deguchi, H.; Ueda, K.; Inoue, I.; Maekita, T.; Iguchi, M.; et al. Prediction of poorly differentiated hepatocellular carcinoma using contrast computed tomography. Cancer Imaging 2014, 14, 7. [Google Scholar] [CrossRef]
  22. Ahn, S.J.; Lee, J.M.; Lee, D.H.; Lee, S.M.; Yoon, J.-H.; Kim, Y.J.; Yu, S.J.; Han, J.K. Real-time US-CT/MR fusion imaging for percutaneous radiofrequency ablation of hepatocellular carcinoma. J. Hepatol. 2016, 66, 347–354. [Google Scholar] [CrossRef]
  23. Maeda, M.; Saeki, I.; Sakaida, I.; Aikata, H.; Araki, Y.; Ogawa, C.; Kariyama, K.; Nouso, K.; Kitamoto, M.; Kobashi, H.; et al. Complications after Radiofrequency Ablation for Hepatocellular Carcinoma: A Multicenter Study Involving 9,411 Japanese Patients. Liver Cancer 2020, 9, 50–62. [Google Scholar] [CrossRef]
  24. Song, I.; Rhim, H.; Lim, H.K.; Kim, Y.-S.; Choi, D. Percutaneous radiofrequency ablation of hepatocellular carcinoma abutting the diaphragm and gastrointestinal tracts with the use of artificial ascites: safety and technical efficacy in 143 patients. Eur. Radiol. 2009, 19, 2630–2640. [Google Scholar] [CrossRef]
  25. Rhim, H.; Lim, H.K.; Kim, Y.-S.; Choi, D. Percutaneous Radiofrequency Ablation with Artificial Ascites for Hepatocellular Carcinoma in the Hepatic Dome: Initial Experience. Am. J. Roentgenol. 2008, 190, 91–98. [Google Scholar] [CrossRef]
  26. Inoue, T.; Hyodo, T.; Korenaga, K.; Murakami, T.; Imai, Y.; Higaki, A.; Suda, T.; Takano, T.; Miyoshi, K.; Koda, M.; et al. Kupffer phase image of Sonazoid-enhanced US is useful in predicting a hypervascularization of non-hypervascular hypointense hepatic lesions detected on Gd-EOB-DTPA-enhanced MRI: a multicenter retrospective study. J. Gastroenterol. 2015, 51, 144–152. [Google Scholar] [CrossRef] [PubMed]
  27. Numata, K.; Morimoto, M.; Ogura, T.; Sugimori, K.; Takebayashi, S.; Okada, M.; Tanaka, K. Ablation therapy guided by contrast-enhanced sonography with Sonazoid for hepatocellular carcinoma lesions not detected by conventional sonography. J. Ultrasound Med. 2008, 27, 395–406. [Google Scholar] [CrossRef] [PubMed]
  28. Kitada, T.; Murakami, T.; Kuzushita, N.; Minamitani, K.; Nakajo, K.; Osuga, K.; Miyoshi, E.; Nakamura, H.; Kishino, B.; Tamura, S.; et al. Effectiveness of real-time virtual sonography-guided radiofrequency ablation treatment for patients with hepatocellular carcinomas. Hepatol. Res. 2008, 38, 565–571. [Google Scholar] [CrossRef]
  29. Ko, S.E.; Lee, M.W.; Lim, H.K.; Min, J.H.; Cha, D.I.; Kang, T.W.; Song, K.D.; Kim, M.J.; Rhim, H. The semi-erect position for better visualization of subphrenic hepatocellular carcinoma during ultrasonography examinations. Ultrasonography 2021, 40, 274–280. [Google Scholar] [CrossRef] [PubMed]
  30. Morgan TA, Maturen KE, Dahiya N, Sun MRM, Kamaya A. US LI-RADS: ultrasound liver imaging reporting and data system for screening and surveillance of hepatocellular carcinoma. Abdom Radiol (NY). 2018;43(1):41-55. [CrossRef]
  31. Kanda, Y. Investigation of the freely available easy-to-use software ‘EZR’ for medical statistics. Bone Marrow Transplant. 2013, 48, 452–458. [Google Scholar] [CrossRef]
  32. EASL Clinical Practice Guidelines: Management of hepatocellular carcinoma. J Hepatol. 2018;69(1):182-236. [CrossRef]
  33. Kudo, M.; Kawamura, Y.; Hasegawa, K.; Tateishi, R.; Kariyama, K.; Shiina, S.; Toyoda, H.; Imai, Y.; Hiraoka, A.; Ikeda, M.; et al. Management of Hepatocellular Carcinoma in Japan: JSH Consensus Statements and Recommendations 2021 Update. Liver Cancer 2021, 10, 181–223. [Google Scholar] [CrossRef]
  34. Radosevic, A.; Quesada, R.; Serlavos, C.; Sánchez, J.; Zugazaga, A.; Sierra, A.; Coll, S.; Busto, M.; Aguilar, G.; Flores, D.; et al. Microwave versus radiofrequency ablation for the treatment of liver malignancies: a randomized controlled phase 2 trial. Sci. Rep. 2022, 12, 316. [Google Scholar] [CrossRef] [PubMed]
  35. 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. [CrossRef]
  36. Liu, W.; Zheng, Y.; He, W.; Zou, R.; Qiu, J.; Shen, J.; Yang, Z.; Zhang, Y.; Wang, C.; Wang, Y.; et al. Microwave vs radiofrequency ablation for hepatocellular carcinoma within the Milan criteria: a propensity score analysis. Aliment. Pharmacol. Ther. 2018, 48, 671–681. [Google Scholar] [CrossRef]
  37. Conrad, M.R.; Leonard, J.; Landay, M.; Conrad, J.L.A.M.L.; Martel, W.; Stuck, K.; Dworin, A.; Hylland, R.; Irish, C.; Meaney, T.; et al. Left lateral decubitus sonography of gallstones in the contracted gallbladder. Am. J. Roentgenol. 1980, 134, 141–144. [Google Scholar] [CrossRef]
  38. Hough, D.M.; Glazebrook, K.N.; Paulson, E.K.; Bowie, J.D.; Foster, W.L. Value of prone positioning in the ultrasonographic diagnosis of gallstones: prospective study. J. Ultrasound Med. 2000, 19, 633–638. [Google Scholar] [CrossRef]
  39. Makino, Y.; Imai, Y.; Ohama, H.; Igura, T.; Kogita, S.; Sawai, Y.; Fukuda, K.; Takamura, M.; Ohashi, H.; Murakami, T. Ultrasonography Fusion Imaging System Increases the Chance of Radiofrequency Ablation for Hepatocellular Carcinoma with Poor Conspicuity on Conventional Ultrasonography. Oncology 2013, 84 (Suppl. 1), 44–50. [Google Scholar] [CrossRef]
  40. Minami, Y.; Minami, T.; Hagiwara, S.; Ida, H.; Ueshima, K.; Nishida, N.; Murakami, T.; Kudo, M. Ultrasound-ultrasound image overlay fusion improves real-time control of radiofrequency ablation margin in the treatment of hepatocellular carcinoma. Eur. Radiol. 2017, 28, 1986–1993. [Google Scholar] [CrossRef]
  41. Kim, J.H.; Lee, J.Y.; Yu, S.J.; Lee, D.H.; Joo, I.; Yoon, J.-H.; Kim, Y.J.; Yoon, J.H.; Lee, J.M. Fusion imaging-guided radiofrequency ablation with artificial ascites or pleural effusion in patients with hepatocellular carcinomas: the feasibility rate and mid-term outcome. Int. J. Hyperth. 2023, 40, 2213424. [Google Scholar] [CrossRef]
  42. Kudo, M.; Ueshima, K.; Osaki, Y.; Hirooka, M.; Imai, Y.; Aso, K.; Numata, K.; Kitano, M.; Kumada, T.; Izumi, N.; et al. B-Mode Ultrasonography versus Contrast-Enhanced Ultrasonography for Surveillance of Hepatocellular Carcinoma: A Prospective Multicenter Randomized Controlled Trial. Liver Cancer 2019, 8, 271–280. [Google Scholar] [CrossRef]
  43. Zerbini, A.; Pilli, M.; Penna, A.; Pelosi, G.; Schianchi, C.; Molinari, A.; Schivazappa, S.; Zibera, C.; Fagnoni, F.F.; Ferrari, C.; et al. Radiofrequency Thermal Ablation of Hepatocellular Carcinoma Liver Nodules Can Activate and Enhance Tumor-Specific T-Cell Responses. Cancer Res 2006, 66, 1139–1146. [Google Scholar] [CrossRef]
  44. Zerbini, A.; Pilli, M.; Laccabue, D.; Pelosi, G.; Molinari, A.; Negri, E.; Cerioni, S.; Fagnoni, F.; Soliani, P.; Ferrari, C.; et al. Radiofrequency Thermal Ablation for Hepatocellular Carcinoma Stimulates Autologous NK-Cell Response. Gastroenterology 2010, 138, 1931–1942.e2. [Google Scholar] [CrossRef]
Preprints 97594 g001
Figure 1. Flowchart of patient enrollment.
Figure 1. Flowchart of patient enrollment.
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Figure 2. Comparison of outcomes after local ablation therapies. (a) The technical success rates, (b) The treatment time, (c) The local tumor progression rates, (d) The intrahepatic distant recurrence rates, and (e) Overall survival rates.
Figure 2. Comparison of outcomes after local ablation therapies. (a) The technical success rates, (b) The treatment time, (c) The local tumor progression rates, (d) The intrahepatic distant recurrence rates, and (e) Overall survival rates.
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Figure 3. Prognosis after local ablation therapies. (a-c) The local tumor progression rates, (d-f) The intrahepatic distant recurrence rates, (g-i) The overall survival rates. (a,d,g) In all the patients, (b,e,h) By High-risk HCC or not, (c,f,i) with or without body position changing.
Figure 3. Prognosis after local ablation therapies. (a-c) The local tumor progression rates, (d-f) The intrahepatic distant recurrence rates, (g-i) The overall survival rates. (a,d,g) In all the patients, (b,e,h) By High-risk HCC or not, (c,f,i) with or without body position changing.
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Table 1. Baseline characteristics.
Table 1. Baseline characteristics.
All High-risk location group Low-risk location group p value
283 nodules (in 230 patients) 176 nodules 107 nodules
Age (years) 76 (56-91)
Male 161 (70%)
Etiology, HBV/HCV/nonBnonC 18/127/85 (8/55/37%)
Child-Pugh grade, A/B 212/18 (92/8%)
Platelet (×103/μL) 130 (49-332)
AFP (ng/mL) 4.2 (0.80-2657)
DCP (mAU/mL) 23 (8.0-4721)
Primary/recurrence HCC 45/185 (20/80%)
Maximal diameter of the tumors (mm) 12 (4-38) 12 (4-37) 12 (5-38) 0.32
Number of nodules, 1/2/3 186/78/19 122/46/8 (69/26/5%) 64/32/11 (60/30/10%) 0.15
Tumor location, segment 1/2/3/4/5/6/7/8 2/15/23/35/31/46/65/65 (0.7/5.3/8/12/11/16/23/23%) 1/10/16/22/19/22/40/45 (0.6/5.7/9.1/13/11/13/23/26%) 1/5/7/13/12/24/25/20 (0.6/5.7/9.1/13/11/13/23/26%) NA
Baseline US visibility scale, 1/2/3/4 15/52/74/142 (5.3/18/26/50%) 15/52/59/50 (8/30/34/28%) 0/0/15/92 (0/0/14/86%) <0.001
Intraoperative US visibility scale, 1/2/3/4 0/4/74/205 (0/1.4/26/72%) 0/4/65/107 (0/2/37/61%) 0/0/9/98 (0/0/8/92%) <0.001
Treatment-assist techniques 133 (47%) 107 (61%) 26 (24%) <0.001
Body position changing
Artificial pleural fluid infusion 48 (17%) 42 (24%) 6 (5.6%) <0.001
Artificial ascites infusion 100 (35%) 88 (50%) 12 (11%) <0.001
Fusion imaging 59 (21%) 50 (28%) 9 (8.4%) <0.001
Contrast enhanced ultrasonography 51 (18%) 46 (26%) 5 (4.7%) <0.001
HCC: hepatocellular carcinoma, HBV: hepatitis B virus, HCV: hepatitis C virus, AFP: alpha-fetoprotein, DCP, des-gamma-carboxy prothrombin, US: ultrasound.
Table 2. Related factors for the technical success rate for high-risk locations HCC.
Table 2. Related factors for the technical success rate for high-risk locations HCC.
Odds ratio range p value
Age (years) 0.96 0.86-1.1 0.52
Male 0.5 0.057-4.4 0.53
Etiology, virus 1.1 0.25-5.3 0.87
Child-Pugh score 1.03 0.41-2.6 0.95
Platelet (×103/μL) 1 0.99-1.01 0.99
AFP (ng/mL) 1.01 0.99-1.1 0.86
DCP (mAU/mL) 1.04 0.97-1.1 0.29
Primary HCC 1330 0-Inf 0.99
Maximal diameter of the tumors (mm) 1.1 0.91-1.3 0.31
Number of nodules 0.82 0.25-2.7 0.75
Tumor location, left lobe 0.96 0.18-5.1 0.96
Tumor location, proximity to adjacent extrahepatic organs 0.99 0.21-4.5 0.99
Tumor location, proximity to large vessels 5330 0-Inf 0.99
Baseline US visibility scale 0.96 0.43-2.1 0.91
Intraoperative US visibility scale 0.59 0.12-2.9 0.52
Treatment-assist techniques
Body position changing		 10 1.2-86 0.034
Artificial pleural fluid infusion 0.78 0.15-4.2 0.77
Artificial ascites infusion 1.4 0.29-6.2 0.7
Fusion imaging 0.51 0.11-2.4 0.4
Contrast enhanced ultrasonography 2.2 0.26-19 0.48
HCC: hepatocellular carcinoma, AFP: alpha-fetoprotein, DCP, des-gamma-carboxy prothrombin, US: ultrasound.
Table 3. Patient characteristics by the timing of treatment.
Table 3. Patient characteristics by the timing of treatment.
Phase 1 group Phase 2 group p value
100 nodules 183 nodules
Maximal diameter of the tumors (mm) 12 (6-38) 12 (4-37) 0.5
Number of nodules, 1/2/3 67/30/3 (67/30/3%) 119/48/16 (65/26/9%) 0.31
Tumor location, segment 1/2/3/4/5/6/7/8 0/2/2/6/8/9/18/15 (0/2/2/6/8/9/18/15%) 1/8/14/16/11/13/22/30 (0.9/7.0/12/14/10/11/19/26%) 0.3
AFP (ng/mL) 4.4 (1.1-454) 4.4 (0.80-2657) 0.46
DCP (mAU/mL) 24 (10-4721) 23 (8.0-1519) 0.96
Baseline US visibility scale, 1/2/3/4 2/26/30/42 (2/26/30/42%) 13/26/44/100 (7/14/14/55%) 0.012
Intraoperative US visibility scale, 1/2/3/4 0/1/30/69 (0/1/30/69%) 0/3/44/136 (2/24/74%) 0.55
High-risk HCC 61 (61%) 115 (63%) 0.8
Treatment-assist techniques
Body position changing 21 (21%) 112 (61%) <0.001
Artificial pleural fluid infusion 19 (19%) 29 (16%) 0.51
Artificial ascites infusion 21 (21%) 79 (43%) <0.001
Fusion imaging 37 (37%) 22 (12%) <0.001
Contrast enhanced ultrasonography 15 (15%) 36 (20%) 0.42
AFP: alpha-fetoprotein, DCP, des-gamma-carboxy prothrombin, US: ultrasound, HCC: hepatocellular carcinoma.
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