Abstract
Background:
In recent years, there has been considerable uncertainty about the optimal treatment option for very early hepatocellular carcinoma (HCC) with tumor size less than 2 cm. Therefore, we performed a systematic review and meta-analysis to evaluate the outcomes of the different treatments.
Methods:
This study was designed in accordance with the Preferred Reporting Items for Systematic Review and Meta-analysis (PRISMA). PubMed, EMBASE, and Cochrane library were searched for calculating the survival rates, and the “time to event” method was used to compare the outcomes of liver resection (LR) and radiofrequency ablation (RFA). All studies focusing on the treatment of solitary HCC up to 2 cm by different techniques were included in our analysis. The Hazard ratios (HR) and 95% confidence intervals (CI) derived from multivariate and univariate analysis were utilized to assess the treatment risks.
Results:
We included 32 studies in our systematic review. The median 5-year overall survival (OS) and recurrence-free survival rate (RFS) for LR were 73% and 47%, respectively, and those for RFA were 73% and 43%, respectively. RFA was found to be associated with increased risk of mortality and recurrence compared to LR (HR = 1.61, 95% CI: 1.35–1.92, P < .0001 for OS and HR = 1.75, 95% CI: 1.56–1.96, P < .0001 for RFS).
Conclusion:
Our meta-analysis demonstrated that LR is superior to RFA in the treatment of solitary HCC up to 2 cm, with reduction in mortality and recurrence risk and improved long-term outcome.
Keywords: hepatocellular carcinoma, solitary, treatment, very early
1. Introduction
Hepatocellular carcinoma (HCC) is the fifth most common type of malignancy and a major cause of cancer-related deaths worldwide.[1,2] The incidence of HCC has slightly decreased in recent years due to the surveillance programs for patients diagnosed with hepatitis virus infection and chronic liver cirrhosis.[3,4] Nevertheless, HCC remains the fourth common malignancy in China because of the large number of hepatitis B patients.[3] Due to the emphasis on surveillance, more cases of early HCCs are being detected currently which means more treatment options are being adopted.[4–6]
The relationship between tumor stage and prognosis has been analyzed for years.[7–9] The American Joint Committee on Cancer (AJCC) cancer staging is one of the most well-known staging systems for the management of cancer patients and recently, in their 8th edition, a solitary HCC ≤ 2 cm has been regarded as T1a stage, irrespective of vascular involvement.[8] Another reliable method is the Barcelona Clinic Liver Cancer (BCLC) system, in which a solitary HCC ≤ 2 cm, with satisfactory liver function and absence of vascular invasion or extrahepatic disease, is defined as very early stage HCC.[7] However, for those HCC patients who are deemed “too early”, liver transplantation (LT) is not recommended as the first line treatment and there are no exceptional points in the waiting list for graft in western countries.[8,10] Liver resection (LR) is recommended as the best choice for HCC patients with normal portal pressure.[7] In addition, radiofrequency ablation (RFA) as one of the local treatments for HCC, is also an optional curative treatment for small HCC. However, the impact of RFA compared to that of LR remains controversial.
In our study, we systematically reviewed the survival rates in literature and used the “time to event” method to perform a meta-analysis, with the aim of investigating the role of RFA in the treatment of patients with very early HCC.
2. Materials and methods
The protocol was approved by the Ethics Committee of the Second People's Hospital of Lanzhou City. This study was designed according to the preferred reporting items for systematic reviews and meta-analysis (PRISMA) guidelines.[11]
2.1. Search strategy and study selection
A systematic review with meta-analysis was undertaken to evaluate and assess the outcome of very early HCC patients with different treatments. We systematically searched the PubMed, EMBASE Medline, and Cochrane Central Register of Controlled Trials (CENTRAL) up to September 25, 2019. Moreover, Google Scholar was used for finding additional related grey literature. The search strategy that we used was as follows: medical subject heading (MeSH) major topic “hepatocellular carcinoma” AND “solitary”, “very early”, “2 cm”, AND “liver resection”, “hepatic resection”, “hepatectomy”(MeSH), “liver transplantation”(MeSH), “transarterial chemoembolization”, “radiofrequency ablation”, “percutaneous ethanol injection”, “microwave ablation”, “stereotactic body radiation therapy”, “sorafenib”. A systematic literature search was performed independently by 2 investigators. There was no language restriction. After completing the search, the records were imported into Endnote (Clarivate Analytic, version X6) for screening the titles and abstracts.
2.2. Inclusion and exclusion criteria
Studies focusing on solitary HCC up to 2 cm were included in our analysis. Survival results were collected either from Kaplan–Meier Curves or from the description of the results. Case reports and conference abstracts were excluded. Review articles were searched for relevant references. If the results of different studies came from the same center, only 1 study was included.
2.3. Literature screening, data extraction, and quality assessment
Two investigators independently screened the titles and abstracts for inclusion in the study. If the inclusion criteria were not clearly satisfied after going through the abstract, the full-text was further analyzed. Any disagreement regarding a study selection was solved by discussing with a third investigator.
The general study information and demographic data were recorded, including author details, publication year, recruitment period, country, study design, total sample size, and median tumor size. The primary outcomes of overall survival rate (OS), recurrence-free survival rate (RFS), recurrence rate, and VI rate were collected if available. Two authors together assessed the risk of bias in different studies. The Newcastle–Ottawa Scale was used to assess the quality of the cohort studies or case-control studies.
2.4. Statistical analysis
For comparing the impact of LR and RFA, the outcomes analyzed were “time to achieve 5-year OS” or “time to achieve 5-year RFS”. We derived the hazard ratios (HR) and 95% confidence intervals (CI) from multivariate and univariate analyses. If the HR was not described explicitly, we summarized the time-to-event data through survival curves based on the Tierney's method.[12] Fixed effect model was used for calculation of the overall pooled HRs, involving calculation of the observed events minus the expected events and variance of each endpoint in each trial, with the treatment effect expressed as Petos odds with 95% CI. The χ2 test was used for statistical heterogeneity, and I2 statistic was used to evaluate heterogeneity (P value with I2 ≥ 50% indicating presence of heterogeneity). For the studies included in the systematic review, 1-, 3-, and 5-year OS and RFS were summarized using bubble size plots, where sample size was proportional to the bubble size.[13] The meta-analysis and bubble plot construction were performed using Stata 15.0 software (Stata Corporation, College station, TX, USA). A P value < .05 was considered statistically significant for all analyses.
3. Results
3.1. Literature selection
Our search strategy yielded a total of 1456 studies. After screening the abstracts and titles, we were left with 32 articles in our systematic review,[10,14–43] involving 10,517 patients with solitary HCC up to 2 cm who were treated with different treatment strategies. The screening procedure used for the articles is shown in the flowchart in Figure 1.
Figure 1.

The flow diagram of study selection in our systematic review.
3.2. Characteristics of the included studies
The characteristics of the included studies are shown in Table 1, and the OS and RFS rates published in different studies are listed in Table 2 . Three multicenter and 31 single-center retrospective case series were included. However, there were no randomized clinical trials. All papers were written in English. Two studies reported by Kim et al (2016) and Kim et al (2014) were reported from the same center, therefore, only the transarterial chemoembolization (TACE) group study by Kim et al was included in our analysis.[19,24] The publication years ranged from 1993 to 2019, and the patients were recruited from 1981 to 2014. There were 27 studies involving 4938 patients who reportedly underwent LR and 18 studies involving 3531 patients who underwent RFA in this period. Only 1 study coming from the Surveillance, Epidemiology, and End Results database reported the OS for LT. Figure 2 shows the bubble plots for 1-, 3-, 5-year OS (drawn in red bubble) and RFS (drawn in blue bubble) for different treatments; the bubble sizes stands for the patient sample sizes of different studies. The 5-year OS rate ranged from 40% to 91.5% (median 73%) for LR, 40% to 86% (median 73%) for RFA, and 31.3% to 63.1% (median 56%) for TACE. The 5-year RFS rate ranged from 23% to 76% (median 47%) for LR and 13% to 71% (median 43%) for the RFA group.
Table 1.
The characteristics of the studies involved in the systematic review.

Table 2.
The overall survival and recurrence-free survival rate in solitary HCC less than 2 cm.

Figure 2.

The bubble plot of 1-,3-,5-year overall and recurrence-free survival in different treatment from systematic review in patients diagnosing as solitary HCC up to 2 cm. Bubble size indicates relative cohort size (LR = red bubble, RFA = blue bubble).
Table 2 (Continued).
The overall survival and recurrence-free survival rate in solitary HCC less than 2 cm.

3.3. Survival comparison between LR and RFA
A total of 10 studies compared of the survival outcomes of LR and RFA.[16–19,28,30,31,33,42,43] Among them, 9 articles contained OS rates (Fig. 3) and 9 articles contained RFS rates (Fig. 4). For comparison of the OS of the 2 treatment methods, a total of 2556 patients were analyzed and 1984 patients lived more than 5 years. There was no clear evidence of statistical heterogeneity between trials (I2 = 23.1%, P = .238). Patients treated with RFA were observed to have a higher mortality than those treated with LR (HR = 1.61, 95%:1.35–1.92, P < .0001).
Figure 3.

The forest plots of studies included comparing the overall survival rate between RFA and LR.
Figure 4.

The forest plots of studies included comparing the recurrence-free survival rate between RFA and LR.
For analyzing the RFS, a total of 2409 patients were included and 1077 patients lived for more than 5 years without any recurrence. There was also no significant heterogeneity between trials (I2 = 8.3%, P = .366). The combined results demonstrated a significant increase in RFS associated with the use of LR for treatment of solitary HCC up to 2 cm (HR = 1.75, 95% CI = 1.56–1.96, P < .0001), which represents a 1.75-fold increase in the risk of recurrence if RFA is used for treatment.
4. Discussion
In our meta-analysis, we used the “time to event” method by utilizing the HRs available in various studies to compare the outcomes of LR and RFA in patients with very early HCC. Our findings revealed that treatment with RFA may have a higher risk of recurrence and mortality compared to LR.
The classification and treatment strategies for “very early HCC” patients have been controversial for many years. It has been the general opinion that these patients have a good outcome and therefore, LT should not be considered as the first-line treatment. Consequently, in some centers, these patients are not considered in the LT waiting list because they may deprive the advanced HCC patients. Additionally, these patients have different treatment options to choose from, and in some centers, even if non-curative treatment was adopted, the patients had a favorable outcome. Nevertheless, curative treatment has still been the major approach in treating very early HCC patients. However, a Korean study recently demonstrated that there was no significant difference in the overall survival rate between RFA and TACE for very early stage HCC, although RFA was associated with a better tumor response and delayed tumor progression.[24] Nevertheless, TACE is not considered the first-line treatment for small HCCs unless the patients are unable to tolerate surgery due to suboptimal liver function, anesthesia factors, advanced age, or other personal conditions.
With respect to curative treatment, the choice between RFA and LR is still debatable due to the absence of randomized controlled trials focusing on very early stage HCC patients. According to the BCLC guidelines, patients diagnosed with solitary HCC ≤ 2 cm with normal portal pressure should be treated by LR.[7] However, the majority of HCC patients have a background of cirrhotic liver disease, and portal hypertension is quite common, which is the chief contraindication for LR due to the risk of post-operative hepatic decompensation.[44] Therefore, RFA could be a possible treatment option in such patients. As a local and less-invasive treatment, it is usually considered as a bridging therapy for LT. A few studies have demonstrated that the RFS is better in patients who have undergone LR than in those who have undergone RFA.[18,19,30] Similarly, Wang et al demonstrated that the LR group of patients had a better overall survival than the RFA group.[30] In contrast, 4 other studies found no significant difference in OS and RFS on comparing the 2 treatments.[16,17,28,31,33] In our study, we did not find any significant difference between RFA and LR in terms of overall survival and recurrence-free survival rate in patients with very early HCC. Consequently, a meta-analysis was needed to explore the outcome in these patients. Some previous meta-analyses have analyzed the different treatment options focusing on tumors < 3 cm, or only comparing the 1-, 3-, 5-year survival rates.[45–47] However, in survival analysis, patients censored in the study period should be considered as factors. Therefore, we used the “time to event” method utilizing the HRs obtained from literature to compare the outcomes of T1a stage patients. In our meta-analysis, patients who underwent LR had a better OS and RFS compared to patients who underwent RFA. This might be because anatomical resection may reduce the incidence of intrahepatic recurrence as reported by some studies.[30] Moreover, in our study, we used bubble plots, with sample size as bubble size to indicate the 1-, 3-, 5-year survival rates for different treatments and therefore, the intuitive changes between survival rate, study samples, and treatment could be seen.
Our study does have some limitations. For the meta-analysis, even though we used the “time to event” method to decrease the influence of censoring in the survival analysis, the lack of randomized controlled studies still affected the results and the quality of current evidence remains low. Moreover, even though there was no significant difference in heterogeneity between studies, the variations in therapy techniques are unavoidable in different studies.
In conclusion, our meta-analysis revealed that LR is superior to RFA in the treatment of solitary HCC up to 2 cm, and is associated with decreased mortality and recurrence risk with improved long-term outcome.
Author contributions
FHY and ZWQ designed the study; FHY, ZCG, YJZ, MWH performed the research and collected the data; FHY and ZWQ analyzed and interpreted the data; FHY wrote the first draft of the manuscript; All authors edited the manuscript and approved the final draft.
Footnotes
Abbreviations: AFP = α-fetoprotein, AJCC = the American Joint Committee on Cancer, BCLC = Barcelona Clinic Liver Cancer, CI = confidence intervals, HCC = hepatocellular carcinoma, HR = hazard ratio, LR = liver resection, LT = liver transplantation, OS = overall survival, RFA = radiofrequency ablation, RFS = recurrence-free survival, TACE = transarterial chemoembolization, VI = vascular invasion.
How to cite this article: Fan H, Zhou C, Yan J, Meng W, Zhang W. Treatment of solitary hepatocellular carcinoma up to 2 cm: A PRISMA-compliant systematic review and meta-analysis. Medicine. 2020;99:23(e20321).
The authors have no conflicts of interest to disclose.
All data generated or analyzed during this study are included in this published article [and its supplementary information files].
References
- [1].Siegel R, Ma J, Zou Z, Jemal A. Cancer statistics, 2014. CA 2014;64:9–29. [DOI] [PubMed] [Google Scholar]
- [2].Llovet JM, Burroughs A. Bruix J Hepatocellular carcinoma. Lancet 2003;362:1907–17. [DOI] [PubMed] [Google Scholar]
- [3].Chen W, Zheng R, Baade PD, et al. Cancer statistics in China, 2015. CA 2016;66:115–32. [DOI] [PubMed] [Google Scholar]
- [4].Bruix J, Sherman M. American Association for the Study of Liver D Management of hepatocellular carcinoma: an update. Hepatology 2011;53:1020–2. [DOI] [PMC free article] [PubMed] [Google Scholar]
- [5].Torzilli G, Belghiti J, Kokudo N, et al. A snapshot of the effective indications and results of surgery for hepatocellular carcinoma in tertiary referral centers: is it adherent to the EASL/AASLD recommendations?: an observational study of the HCC East-West study group. Ann Surg 2013;257:929–37. [DOI] [PubMed] [Google Scholar]
- [6].Allemani C, Matsuda T, Di Carlo V, et al. Global surveillance of trends in cancer survival 2000-14 (CONCORD-3): analysis of individual records for 37 513 025 patients diagnosed with one of 18 cancers from 322 population-based registries in 71 countries. Lancet (London, England). 2018;391:1023-75. [DOI] [PMC free article] [PubMed] [Google Scholar]
- [7].EASL-EORTC clinical practice guidelines: management of hepatocellular carcinoma. J Hepatol 2012;56:908–43. [DOI] [PubMed] [Google Scholar]
- [8].Heimbach JK, Kulik LM, Finn R, et al. Aasld guidelines for the treatment of hepatocellular carcinoma. Hepatology 2017. [DOI] [PubMed] [Google Scholar]
- [9].Amin MB, Edge S, Greene F, et al. AJCC cancer staging manual, 8th edn. New York, NY: Springer. 2017. [Google Scholar]
- [10].Sapisochin G, Castells L, Dopazo C, et al. Single HCC in cirrhotic patients: liver resection or liver transplantation? Long-term outcome according to an intention-to-treat basis. Ann Surg Oncol 2013;20:1194–202. [DOI] [PubMed] [Google Scholar]
- [11].Moher D, Liberati A, Tetzlaff J, Altman DG, Group P. Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. PLoS Med 2009;6:e1000097. [DOI] [PMC free article] [PubMed] [Google Scholar]
- [12].Tierney JF, Stewart LA, Ghersi D, et al. Practical methods for incorporating summary time-to-event data into meta-analysis. Trials 2007;8:16. [DOI] [PMC free article] [PubMed] [Google Scholar]
- [13].Lim KC, Chow PK, Allen JC, et al. Systematic review of outcomes of liver resection for early hepatocellular carcinoma within the Milan criteria. Br J Surg 2012;99:1622–9. [DOI] [PubMed] [Google Scholar]
- [14].Xu Y, Shen Q, Wang N, et al. Microwave ablation is as effective as radiofrequency ablation for very-early-stage hepatocellular carcinoma. Chin J Cancer 2017;36:14. [DOI] [PMC free article] [PubMed] [Google Scholar]
- [15].Oh IS, Sinn DH, Kang TW, et al. Liver function assessment using albumin-bilirubin grade for patients with very early-stage hepatocellular carcinoma treated with radiofrequency ablation. Dig Dis Sci 2017;62:3235–42. [DOI] [PubMed] [Google Scholar]
- [16].Kutlu OC, Chan JA, Aloia TA, et al. Comparative effectiveness of first-line radiofrequency ablation versus surgical resection and transplantation for patients with early hepatocellular carcinoma. Cancer 2017;123:1817–27. [DOI] [PubMed] [Google Scholar]
- [17].Song J, Wang Y, Ma K, et al. Laparoscopic hepatectomy versus radiofrequency ablation for minimally invasive treatment of single, small hepatocellular carcinomas. Surg Endosc 2016;30:4249–57. [DOI] [PubMed] [Google Scholar]
- [18].Liu PH, Hsu CY, Hsia CY, et al. Surgical resection versus radiofrequency ablation for single hepatocellular carcinoma < = 2 cm in a propensity score model. [Erratum appears in Ann Surg. 2016 May;263:e77; PMID: 27058857]. Ann Surg 2016;263:538–45. [DOI] [PubMed] [Google Scholar]
- [19].Kim GA, Shim JH, Kim MJ, et al. Radiofrequency ablation as an alternative to hepatic resection for single small hepatocellular carcinomas. Br J Surg 2016;103:126–35. [DOI] [PubMed] [Google Scholar]
- [20].Sasaki K, Matsuda M, Ohkura Y, et al. The influence of histological differentiation grade on the outcome of liver resection for hepatocellular carcinomas 2 cm or smaller in size. World J Surg 2015;39:1134–41. [DOI] [PubMed] [Google Scholar]
- [21].Pompili M, De Matthaeis N, Saviano A, et al. Single hepatocellular carcinoma smaller than 2 cm: are ethanol injection and radiofrequency ablation equally effective? Anticancer Res 2015;35:325–32. [PubMed] [Google Scholar]
- [22].Zhou Z, Lei J, Li B, et al. Liver resection and radiofrequency ablation of very early hepatocellular carcinoma cases (single nodule <2 cm): a single-center study. Eur J Gastroenterol Hepatol 2014;26:339–44. [DOI] [PubMed] [Google Scholar]
- [23].Zhang H, Yuan SX, Dai SY, et al. Tumor size does not independently affect long-term survival after curative resection of solitary hepatocellular carcinoma without macroscopic vascular invasion. World J Surg 2014;38:947–57. [DOI] [PubMed] [Google Scholar]
- [24].Kim JW, Kim JH, Sung KB, et al. Transarterial chemoembolization vs. radiofrequency ablation for the treatment of single hepatocellular carcinoma 2 cm or smaller. Am J Gastroenterol 2014;109:1234–40. [DOI] [PubMed] [Google Scholar]
- [25].Takuma Y, Takabatake H, Morimoto Y, et al. Comparison of combined transcatheter arterial chemoembolization and radiofrequency ablation with surgical resection by using propensity score matching in patients with hepatocellular carcinoma within Milan criteria. Radiology 2013;269:927–37. [DOI] [PubMed] [Google Scholar]
- [26].Shindoh J, Andreou A, Aloia TA, et al. Microvascular invasion does not predict long-term survival in hepatocellular carcinoma up to 2 cm: Reappraisal of the staging system for solitary tumors. Ann Surg Oncol 2013;20:1223–9. [DOI] [PMC free article] [PubMed] [Google Scholar]
- [27].Roayaie S, Obeidat K, Sposito C. Resection of hepatocellular cancer </ = 2 cm: results from two Western centers. Hepatology 2013;57:1426–35. [DOI] [PMC free article] [PubMed] [Google Scholar]
- [28].Imai K, Beppu T, Chikamoto A, et al. Comparison between hepatic resection and radiofrequency ablation as first-line treatment for solitary small-sized hepatocellular carcinoma of 3 cm or less. Hepatol Res 2013;43:853–64. [DOI] [PubMed] [Google Scholar]
- [29].Yamashita YI, Tsuijita E, Takeishi K, et al. Predictors for microinvasion of small hepatocellular carcinoma <=2 cm. Ann Surg Oncol 2012;19:2027–34. [DOI] [PubMed] [Google Scholar]
- [30].Wang JH, Wang CC, Hung CH, et al. Survival comparison between surgical resection and radiofrequency ablation for patients in BCLC very early/early stage hepatocellular carcinoma. J Hepatol 2012;56:412–8. [DOI] [PubMed] [Google Scholar]
- [31].Peng ZW, Lin XJ, Zhang YJ, et al. Radiofrequency ablation versus hepatic resection for the treatment of hepatocellular carcinomas 2 cm or smaller: a retrospective comparative study. Radiology 2012;262:1022–33. [DOI] [PubMed] [Google Scholar]
- [32].Sawada T, Kubota K, Kita J, et al. Clinical outcome of hepatectomy for hepatocellular carcinomas </=2 cm. World J Surg 2011;35:377–85. [DOI] [PubMed] [Google Scholar]
- [33].Hung HH, Chiou YY, Hsia CY, et al. Survival rates are comparable after radiofrequency ablation or surgery in patients with small hepatocellular carcinomas. Clin Gastroenterol Hepatol 2011;9:79–86. [DOI] [PubMed] [Google Scholar]
- [34].Takayama T, Makuuchi M, Hasegawa K. Single HCC smaller than 2 cm: surgery or ablation?: surgeon's perspective. J Hepatobiliary Pancreat Sci 2010;17:422–4. [DOI] [PubMed] [Google Scholar]
- [35].Livraghi T, Meloni F, Di Stasi M, 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;47:82–9. [DOI] [PubMed] [Google Scholar]
- [36].Miraglia R, Pietrosi G, Maruzzelli L, et al. Efficacy of transcatheter embolization/chemoembolization (TAE/TACE) for the treatment of single hepatocellular carcinoma. World J Gastroenterol 2007;13:2952–5. [DOI] [PMC free article] [PubMed] [Google Scholar]
- [37].Inoue K, Takayama T, Higaki T, et al. Clinical significance of early hepatocellular carcinoma. Liver Transpl 2004;10:S16–9. [DOI] [PubMed] [Google Scholar]
- [38].Yamamoto M, Takasaki K, Otsubo T, et al. Extent of resection for hepatocellular carcinoma 2 cm or less in greatest diameter. Am J Surg 2002;184:437–40. [DOI] [PubMed] [Google Scholar]
- [39].Arii S, Yamaoka Y, Futagawa S, et al. Results of surgical and nonsurgical treatment for small-sized hepatocellular carcinomas: a retrospective and nationwide survey in Japan. Hepatology 2000;32:1224–9. [DOI] [PubMed] [Google Scholar]
- [40].Asahara T, Dohi K, Katayama K, et al. Factors affecting postoperative prognosis in the solitary-nodule type of hepatocellular carcinoma: experience of 132 cases in our institute. Hiroshima J Med Sci 1998;47:99–104. [PubMed] [Google Scholar]
- [41].Torii A, Nonami T, Harada A, et al. Extent of hepatic resection as a prognostic factor for small, solitary hepatocellular carcinomas. J Surg Oncol 1993;54:13–7. [DOI] [PubMed] [Google Scholar]
- [42].Chu HH, Kim JH, Kim PN, et al. Surgical resection versus radiofrequency ablation very early-stage HCC (≤2 cm Single HCC): a propensity score analysis. Liver Int 2019;39:2397–407. [DOI] [PubMed] [Google Scholar]
- [43].Kim TH, Chang JM, Um SH, et al. Comparison of 2 curative treatment options for very early hepatocellular carcinoma: Efficacy, recurrence pattern, and retreatment. Medicine (Baltimore) 2019;98:e16279. [DOI] [PMC free article] [PubMed] [Google Scholar]
- [44].Sapisochin G, de Sevilla EF, Echeverri J, Charco R. Management of “very early” hepatocellular carcinoma on cirrhotic patients. World J Hepatol 2014;6:766–75. [DOI] [PMC free article] [PubMed] [Google Scholar]
- [45].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 2017;162756. [DOI] [PubMed] [Google Scholar]
- [46].Wang Y, Luo Q, Li Y, et al. Radiofrequency ablation versus hepatic resection for small hepatocellular carcinomas: a meta-analysis of randomized and nonrandomized controlled trials. PLoS One 2014;9:e84484. [DOI] [PMC free article] [PubMed] [Google Scholar]
- [47].He ZX, Xiang P, Gong JP, et al. Radiofrequency ablation versus resection for Barcelona clinic liver cancer very early/early stage hepatocellular carcinoma: a systematic review. Ther Clin Risk Manag 2016;12:295–303. [DOI] [PMC free article] [PubMed] [Google Scholar]
