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 Table of Contents  
ORIGINAL ARTICLE
Year : 2011  |  Volume : 7  |  Issue : 4  |  Page : 463-475

An overview of evidence-based management of hepatocellular carcinoma: A meta-analysis


Department of Surgery and Cancer, HPB and Surgery Unit, Imperial College Healthcare NHS Trust London, United Kingdom

Date of Web Publication19-Jan-2012

Correspondence Address:
Mohammad Salhab
Leeds Teaching Hospitals, Chapel Allerton Hospital, Ward 4, Harehills Lane, Leeds, LS7 4SA
United Kingdom
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DOI: 10.4103/0973-1482.92023

PMID: 22269411

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 > Abstract 

Introduction: An increasing trend of incidence in hepatocellular carcinoma (HCC) has been recorded in most developed countries. HCC ranks among the ten most common cancers worldwide. The health costs and burden to the economy implicated by HCC are huge. In recent years, the surveillance programs and screening for the disease, in addition to increasing awareness, led to the detection of smaller precursor lesions of HCC in the liver. The rise of molecular-targeted therapies and the publication of various conflicting guidelines on the management of the disease demand a review of evidence into the curative therapies and medical management of HCC.
Aims: The primary objective was to identify the survival benefit of the primary medical modalities in HCC, as more trials were uncovered between 2005 and 2010. The secondary objective was to conduct a meta-analysis. Selection criteria were implemented to select randomized controlled trials (RCTs), to include in this study. After selection, all the articles were ranked according to their strength.
Materials and Methods: The MEDLINE, CANCERLIT, Embase databases, and the Cochrane Library were reviewed using the national library of health website. The time limit used for searching for RCTs was between January 2005 and December 2010. Overall survival and the cumulative probability of no recurrence were the primary endpoints considered in the studies to be assessed. These endpoints were measured over one, two, or three years, depending on the size of the study and the length of follow-up. The software package comprehensive meta-analysis ver 2.0.exe (Biostat, USA) was used to comply with the results, to conduct the meta-analysis, and help with analyzing the data.
Results: The original general search yielded 193 RCTs between 2005 and 2010. Only 32 studies met the inclusion criteria. However, after the ranking of the studies according to strength, only 17 studies were eventually selected. The 17 studies were subsequently classified according to the following; surgical resection (n = 2); percutaneous treatments (n = 5); chemoembolization (n = 1); systemic treatments (n = 8); and other treatments (n = 1). Randomized studies comparing the percutaneous ethanol injection (PEI) to the surgical resection were inconclusive. However, percutaneous treatments showed results similar to surgical resection in terms of overall survival. The meta-analysis comparing PEI to radiofrequency ablation (RFA) showed RFA to be superior to PEI in terms of overall survival at three years (odds ratio 1.698; 95% CI 1.206 - 2.391; P = 0.002). When adverse events were considered there was no statistically significant difference between the RFA and PEI groups (odds ratio 1.199; 95% CI 0.571- 2.521; P = 0.632).
Conclusion: RFA should be the first-line treatment in patients with a single small HCC tumor ≤ 3 cm. Careful patient selection is crucial prior to transarterial chemoembolization (TACE), as the procedure may be associated with an increased risk of liver failure. Tamoxifen has no role to play in the treatment of HCC. Sorafenib should be the first-line treatment in patients with advanced and inoperable HCC. The role of Sorafenib in the management of early stage HCC remains to be determined.

Keywords: Hepatocellular carcinoma, liver resection, liver transplant, percutaneous treatments


How to cite this article:
Salhab M, Canelo R. An overview of evidence-based management of hepatocellular carcinoma: A meta-analysis. J Can Res Ther 2011;7:463-75

How to cite this URL:
Salhab M, Canelo R. An overview of evidence-based management of hepatocellular carcinoma: A meta-analysis. J Can Res Ther [serial online] 2011 [cited 2014 Oct 31];7:463-75. Available from: http://www.cancerjournal.net/text.asp?2011/7/4/463/92023


 > Introduction Top


Hepatocellular carcinoma (HCC) is among the most common malignancies worldwide, with a high prevalence in Asia and southern Africa. [1] An increasing trend in the incidence of HCC in the western world has been observed in recent years, particularly in the United States and Canada. [2],[3],[4],[5],[6],[7],[8],[9] An increase in the trend of HCC has also been recorded in southern Europe. [10] Although the cause of such increasing trends in the incidence of HCC varies between different parts of the world, it seems that hepatitis C (HCV)-related HCC is the major contributing factor to such increasing trends. [3],[11],[12],[13],[14],[15] This increasing incidence of HCC and HCV in the western world, in addition to the projected increasing health costs, have prompted the need to develop new modalities of treatment, in addition to reviewing the current management of HCC.

Surveillance programs for HCC in patients with cirrhosis and chronic hepatitis have led to the detection of smaller lesions in the liver with some of these lesions being precursors to malignancy. [16] This prompts the need to review the current modalities of treatment of HCC according to the size of the tumor and liver function. [17]

At present, only surgical resection and liver transplantation are considered curative measures, in terms of disease-free survival. [18] However, the strict Milan criteria for transplantation, in addition to poor liver function and limitations of donor availability, have encouraged researchers to investigate other modalities of treatment that might bridge the gap to transplantation or surgical resection and even herald tumor progression. [19] Such treatments include embolization, radiofrequency ablation (RFA), and alcohol injection.

There are relatively few comprehensive reviews or meta-analysis on the management of HCC. [20],[21],[22] The reason for that may be the variable degree of heterogeneity of the results between the different clinical trials that have investigated such modalities of treatment. This makes any prospective meta-analysis difficult to conduct.

Even as patients wait, attempts to bridge the gap to transplantation have been explored with adjuvant therapies. Again, there is a lack of robust evidence in this field, due to the lack of large randomised controlled trials (RCTs). The turn of this century has witnessed changes in HCC disease progression and prognosis. The advent of new therapeutic modalities; in addition to curative resection, emphasise the need to diagnose the disease at an early stage. The implications of new surveillance programs of HCC were enormous in detecting the disease at an early stage. This means that patients with small tumors can now benefit from curative measures. [23] However, the treatment of HCC is far from definitive and is still based at large on only few RCTs. [20],[21]

We have reviewed the literature since January 1978, and up to December 2010 period in an attempt to provide a comprehensive review of treatment modalities of HCC. We have also conducted a meta-analysis that would incorporate tumor size in the results.


 > Materials and Methods Top


The MEDLINE, CANCERLIT, and Embase databases were reviewed, using the national library of health website. In addition, the Cochrane Library Database was consulted to retrieve any previous systemic reviews on the subject. The following key MeSH terms were used to complete the search: "hepatocellular carcinoma", "meta-analysis", "clinical trials", "operative treatment", "medical therapy", "percutaneous ablation", and "embolization". The time limit allotted for searching for RCTs was between January 2005 and December 2010. Additional references were sought from individuals considered an authority on the subject. For the meta-analysis, the trial computer package comprehensive meta-analysis v2 was used. Odds ratios were calculated where appropriate.

Criteria for selection of studies

All RCTs that have been published in English between January 1978 and December 2010 were selected. For the purpose of the meta-analysis, RCTs between 2005 and 2010 were selected [Figure 1]. The inclusion of studies was done on the following basis: (1) RCTs assessing medical interventions as primary treatment of HCC and published as full articles; (2) Time period considered from January 2005 to December 2010; (3) RCTs published in the English language; (4) Studies comparing two or more active treatments, treatment versus conservative management or suboptimal therapies; (5) Use of overall survival or cumulative probability of no recurrence at least one and two years, as clinical end-points. All phase 2 studies, RCTs with unpublished protocols, or those published in abstracts were excluded. All RCTs that included patients with metastatic disease were also excluded. All non-RCTs, such as case control studies and observational studies, were excluded.
Figure 1: Prisma structure of the meta-analysis for display

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To assess the quality of these studies, the modified Jadad standard, adopted by Lopez et al., was used. [20] Each study was ranked out of a total score of 10 points, high rank being > 5 points and low being ≤ 5 [Table 1]. Each study was ranked and assessed independently by two observers.
Table 1: Classification of studies according to design and benefit of treatment modalities

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The classification of the evidence presented in this review follows the National Cancer Institute guidelines and is adopted from the reviews published by Lopez et al., and Llovet et al. [20],[21] This classification has been used in several reviews to present the RCTs according to a certain hierarchy. This hierarchy is displayed according to the benefit of the evidence presented and the treatment modality being assessed [Table 2].
Table 2: One-to-five year survival and one-to-five year tumor-free survival in patients with HCC, who had either PEI or surgical resection[38]

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Outcome measures

Overall survival and the cumulative probability of no recurrence were the primary endpoints considered in the studies to be assessed. These endpoints were measured over one, two, or three years, depending on the size of the study and the length of follow-up.

Meta-analysis

The software package comprehensive meta-analysis ver 2.0.exe (Biostat, USA) was used to input and analyze the data to determine the odds ratios and heterogeneity factors compiled from the different RCTs. The protocol of the systemic review followed the recommendations of Sacks et al,[24] for conducting a meta-analysis. In this review, only fully published RCTs in English, which considered primary treatments for HCC, were included.


 > Results Top


The original general search yielded 193 RCTs between January 2005 and December 2010. Only 32 studies met the inclusion criteria. Six studies were excluded. [25],[26],[27],[28],[29],[30] Three studies were not considered to be phase III RCTs and were therefore also excluded. [28],[29],[30] One study was retracted due to issues with the ethical approval, integrity of the data, and the design of the study. [27],[31] One study was excluded due to the fact that on further investigation of the material and method described in the study, the design did not reveal a randomization process. [26] Two studies were also excluded due to the multiple arms of these studies. [26],[32] One study was excluded as only the protocol was published by the time this review was completed. [33]

Seventeen of the 18 studies included in this review showed good methodological sequence in addition to a thorough description of the randomization process, and thus, were ranked as high in quality [Table 1]. One study fell short in terms of blinding and description of the randomization process. The 17 studies were subsequently classified according to the following: Surgical resection (n = 2); percutaneous treatments (n = 5); chemoembolization (n = 1); systemic treatments (n = 8); and other treatments (n = 1).

Randomized studies comparing percutaneous ethanol injection (PEI) with surgical resection have been inconclusive. However, percutaneous treatments showed results similar to surgical resection, in terms of overall survival. The meta-analysis comparing PEI to RFA showed RFA to be superior to PEI in terms of overall survival at three years (odds ratio 1.698; 95% CI 1.206­­-2.391 P = 0.002) [Figure 2]. The odds ratio for complete response at one year showed no advantage of RFA compared to PEI (odds ratio 1.238; 95% CI 0.872-1.759; P > 0.005) [Figure 3]. When adverse events were considered there was no statistically significant difference between the RFA and PEI groups (odds ratio 1.199; 95% CI 0.571-2.521; P = 0.632) [Figure 4].
Figure 2: Odds ratios following meta-analysis of overall survival rates at three years; RFA versus PEI

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Figure 3: Meta-analysis of Complete response at one year: RFA versus PEI

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Figure 4: Meta-analysis: Odds ratio of adverse events RFA versus PEI

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 > Discussion Top


As previously mentioned, there are relatively few comprehensive reviews or meta-analysis on the management of HCC. [20],[21],[22] In one meta-analysis, published in 1998, the authors excluded surgical procedures and adjuvant medical treatment from their analysis. [22] In addition, different randomized trials with different control groups were combined. The degree of bias, however, was reduced by defining the inclusion and exclusion criteria in advance. All RCTs were analyzed independently by two observers, and these observations were conferred with a third individual, if there were any disagreements. However, the search strategy was limited and there was no mention if the Cochrane review database was consulted for the time periods for the literature search. This meta-analysis included 30 randomized trials, with 23 being excluded for several reasons, including the evaluation of multiple therapies. This meta-analysis subdivided treatments into; (1) systemic cytotoxic treatment; (2) locoregional therapy; and (3) systemic hormonal therapy. It concluded that no treatment within these categories had actually prolonged survival. The authors also could not establish the efficacy of interferon and PEI as modalities of definitive treatment. There was also insufficient evidence presented with regards to interferon and tamoxifen.

A serious attempt to conduct a comprehensive meta-analysis was made by Llovet et al. [21] This however, was lacking in the meta-analysis part, but almost perfect in the literature review section. It was initially a well-structured systemic review of the literature conducted between 1978 and 2002, and included all published RCTs investigating primary treatments of HCC. The authors then limited their meta-analysis to only two modalities of treatment they considered controversial at the time, embolization and tamoxifen. However despite the limitations of the meta-analysis, the literature review was comprehensive. 61 randomized trials were identified during that period and 14 trials were used in the meta-analysis. This article was a landmark in terms of establishing chemoembolization as the new potential standard for treating unresectable HCC. These recommendations were endorsed by the European Association for the Study of the Liver and the American Association for the Study of Liver Diseases. Unfortunately, tamoxifen was shown not to be effective in prolonging survival in patients with progressive disease.

A third article that can be considered as an update to the article Llovet et al., published in 2003, was the one published in 2006 by the same author. [20] This article included 16 RCTs that were published between 2002 and 2005. These trials assessed the roles of percutaneous ablation (PA), and other locoregional treatments, in addition to systemic therapies. This review suggested that there was better local tumor control with the use of RFA in tumors larger than 2 cm.

The above reviews have clearly demonstrated that there is a lack of enough RCTs investigating the treatment modalities of HCC, whether these treatments are curative approaches or adjuvant therapies. Between 1978 and 2005 there seem to be less than 100 RCTs that have investigated primary treatments for HCC. Thus, the strategies and guidelines drawn for the treatment of HCC may be based on insufficient evidence. However, with HCC becoming an increasing problem in the western world, more effort is underway to conduct larger multi-center RCTs in the field, in order to establish the gold standard treatments and adjuvant therapy modalities.

Surgical resection

PA has become the first option for patients with early stage HCC, who are not suitable for resection or transplant. However, although there are no large RCTs comparing ablation to resection or transplantation, PA has been recommended as the first therapeutic option by the J-HCC panel of experts in Japan supported by the Ministry of Japanese Health. [34] PA may be thermal or chemical. Thermal ablation involves destroying tumor cells by heat. This can be achieved using lasers, high intensity focused ultrasound, microwaves, radiotherapy, or even cryoablation. Chemical ablation involves injecting chemicals into the tumor cells using a very fine needle. The chemical then induces injury to the organelles causing vascular thrombosis, osmotic shifts, in addition to other complex effects that destroy the tumor cells. Chemicals that have been used in clinical trials include ethanol, acetic acid or even boiling saline. Although PA is usually performed using an ultrasound, CT-guided ablations are common. CT is also used to assess the efficacy of treatment one month following PA. The choice of the ablative method may depend on the tumor size.

Retrospective studies have shown surgical resection to be superior to PA, namely RFA. [35],[36],[37],[38],[39] Two ambitious RCTs attempted to compare resection and PA. [40],[41] One trial recruited 76 patients with one or two tumors ≤ 3 cm and Child-Pugh A/B cirrhosis; and compared PEI with surgical resection. [40] The other trial involved 90 patients and compared RFA to surgical resection in patients with a solitary mass of ≤ 5 cm. [40] Both studies were underpowered and the suitability of the patients selected for either procedure was questionable. In addition to an allocation bias in both trials, many patients withdrew consent and were not followed on an intention-to-treat basis.

Two RCTs that have been included in this review have compared percutaneous treatments to surgical resection. [40],[41] In the first RCT published in 2005, PEI was compared to surgical resection. [40] Survival and recurrence, following either treatment, were measured as primary endpoints. Seventy-six patients with one or two tumors with a diameter ≤ 3 cm, and with hepatitis, but no cirrhosis; or Child class A or B cirrhosis, but no ascites or bleeding tendency were recruited in total. The patients were randomized to receive PEI (n = 38) or surgical resection (n = 38). Follow-up ranged from one year to five years. In the group that received PEI, 18 patients developed recurrence of HCC. In the surgical resection group, 15 patients developed recurrence. The authors of the study then went on to define what they considered as a true recurrence of HCC. True recurrence was accepted in the case of an undetectable tiny tumor before treatment and when treated the tumor was considered to be completely eradicated. Therefore, of the 18 patients in the PEI group who had recurrence, 11 were considered to be true recurrence. Of the 15 patients in the surgical resection group who had recurrence, 13 patients were considered to have had true recurrence. The results for the one to five years survival rates were 100%, 100%, 96.7%, 92.1%, and 46% for the PEI group and 97.4%, 91.3%, 88.1%, 88.1%, and 81.8% for the surgical resection group. The differences were not statistically different for both tumor-free survival and the overall survival rates [Table 2]. A Cox regression analysis of further risk factors showed that a tumor diameter of > 2 cm ( p0 = 0.0252) and elevated AFP of > 200 ng/ml correlated with higher recurrence rates, whereas, Child's class B liver dysfunction correlated with shorter survival (P = 0.0134).

Similarly, another larger randomized trial of 180 patients compared percutaneous ablative therapy (PLAT) to surgical resection for the treatment of solitary HCC, with a diameter ≤ 5 cm. [34] Despite 90 patients being randomized to each arm of the study, only 71 patients actually received ablative therapy, as 19 patients withdrew consent. All 19 patients received surgical resection. Only 88 patients in the surgical resection group actually underwent surgery, as two patients were found to have a disseminated tumor. Follow-up was over four years. There were no significant statistical differences in terms of the overall survival or disease-free survival at one, two, three or four years of follow-up [Table 3]. Interestingly; 21 patients (23.3%) who received PLAT needed further treatment with PEI or RFA, because the follow-up CT results showed incomplete tumor necrosis. However, according to the authors 91.5% of the patients showed complete tumor necrosis following percutaneous treatments.
Table 3: One-to-four year survival and one-to-four year tumor-free survival in patients with HCC, who had either local ablative therapy or surgical resection.[39]

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Percutaneous treatments

PEI introduced in the 1980's, is the most commonly studied form of PA for HCC. This is because it is technically easier, with only a fine needle needed for delivery. Cohort studies and retrospective series analysis have shown that patients with Child-Pugh class A cirrhosis and either a single tumor smaller than 5 cm or as many as three lesions < 3 cm may achieve a five-year survival of 50%. [33],[42] However, in smaller tumors of up to 3 cm, the results have been much better; 80% complete response. [43] The major limitation of PEI is the high local recurrence rate, which may reach 33-43% at three years. [42] Another form of ablation that has gathered pace in medical research is RFA. The RFA technique was first described by Rossi et al., in 1993. [44] Clinical trials comparing RFA to PEI have shown that RFA is superior in terms of preventing recurrence and improved tumor necrosis, despite fewer treatment sessions. RFA is the preferred percutaneous ablative method in small HCC tumors. [45] In one randomized trial of 139 patients in Child-Pugh classes A / B, with one to three nodes of HCC (diameter 1.5-3.0 cm), RFA was superior to PEI with a one-year complete response rate of 65.7% and 36.2%, respectively. [40] Another randomized trial with 187 patients with HCC of ≤ 3 cm showed similar results. [41] Retrospective analysis also showed RFA to be more cost-effective. [46] Another randomized trial that involved 232 patients with HCC, who had up to three lesions, each ≤ 3 cm in diameter, and liver cirrhosis, Child-Pugh class A or B, showed that RFA was superior to PEI in terms of survival with 74 and 57%, respectively, at four years. [33] In some studies of small HCC tumors less than 2 cm in diameter, there was no difference between RFA and PEI in terms of efficacy. [47],[48] A meta-analysis of five randomized trials concluded that RFA was superior to PEI in terms of one-, two-, or three-year survival rates, in addition to cancer-free rates. [45] This study also concluded that RFA was superior to PEI in achieving necrosis margins, and thus, destroying tumor cells. [49] A large RCT that would stratify patients by tumor size and compare both modalities of treatment would help settle the debate of which ablative method to use, depending on the size of the tumor. Currently there are studies that investigated the combination of both RFA and PEI in the treatment of high-risk patients with large tumors, and these studies showed more effectiveness in terms of survival with a combination therapy rather than single therapy used alone. [41],[50],[51],[52] The effectiveness and morbidity of such a combination therapy need to be studied further by a large randomized trial.

A previous sensitivity analysis from two RCTs by Sarin et al. [53] and Bartolozzi et al., [54] showed that PEI as a single treatment or in combined with TACE did not offer an advantage in terms of survival benefit at one year compared to controls. [22] However, both studies were very small and were limited to large HCC tumors (> 3 cm).

Although PEI has been established as a standard alternative treatment for small HCC tumors, RFA as a technique has developed rapidly over recent years and promises better local control of liver tumors. Therefore, randomized trials that compare both techniques in terms of overall survival and adverse events are needed.

A recent review of percutaneous treatments suggested that RFA offers no additional benefits when compared to PEI, in the management of small HCC tumors. [55] However, the evidence presented in the above-mentioned review was mainly based on four level II RCTs and one level III RCT. Therefore, the evidence gathered is not strong enough.

Four RCTs were included in this meta-analysis. [56],[57],[58],[59] The characteristics of these studies are described in [Table 4]. The study by Lin et al., [60] was not included in the meta-analysis due to differences in randomized groups, but was included in the discussion.
Table 4: Characteristics of the studies included in the meta-analysis of RFA versus PEI since 2005.

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The above-mentioned studies were not homogenous in terms of population or endpoints. Three studies were from Asia and only one from Europe. The primary and secondary endpoints varied between the studies and included disease-free survival, complete response, overall survival, and major complications. Although the definition of the follow-up period was not the same between the trials, the difference was less than a week, and therefore, would not affect the results of the meta-analysis when a three-years period is considered. All studies followed up patients for at least three years, and therefore, the overall survival at three years was chosen as the primary endpoint for this meta-analysis.

The endpoints of the meta-analysis included the complete response rate at one year, overall survival at three years, and adverse complications. The odds ratio for complete response at one year showed no advantage for RFA compared to PEI (odds ratio 1.238; 95% CI 0.872 - 1.759; P > 0.005) [Figure 2]. The heterogeneity among the four trials was significant when the complete response rate was considered as an endpoint (Q = 17.43; P = 0.001). RFA was, however, superior to PEI in terms of overall survival at three years (odds ratio 1.698; 95% CI 1.206 - 2.391; P = 0.002) [Figure 1]. In this case the heterogeneity between the four trials was not significant (Q = 1.715; P = 0.634). When adverse events were considered, there was no statistically significant difference between the RFA and PEI groups (odds ratio 1.199; 95% CI 0.571 - 2.521; P = 0.632) [Figure 3]. The heterogeneity between the four trials in terms of adverse events was not significant (Q = 2.574; P = 0.276). A subgroup analysis by tumor size would have been beneficial, however, this was difficult due to the lack of uniform data from the studies included in the meta-analysis.

Chemoembolization

Transarterial embolization (TAE) is considered a locoregional palliative treatment and is commonly used in HCC tumors that are not suitable for surgical resection or curative therapy. Once the HCC becomes vascularized, the supply is no longer from the portal vein, but rather from the hepatic artery. TAE results in hepatic obstruction, and thus, induces tumor necrosis. This procedure is performed under radiological control, and when embolizing chemical agents are used mixed with lipiodol, prior to embolization, the procedure is termed 'transarterial chemoembolization' (TACE). Several chemotactic agents have been used and investigated, but more often than not adriamycin or cisplatin are used. [61] TAE has been shown to be effective in inducing tumor necrosis and delaying tumor progression and revascularization of the tumor bed in 15 - 55% of the patients. [61],[62] TACE has shown similar results to TAE, with 16 - 60% response rates. [21],[61],[62] In 2002, two trials, one from Asia and one from Europe, showed benefit in terms of survival rates after using TACE in unresectable HCC tumors. [63],[64] Both trials have used different chemotherapeutic agents and the numbers recruited were still small to make any generalizations. This was also confirmed in cohort studies. [65] A meta-analysis of seven RCTs comparing TACE / TAE to a control group showed only a modest effect in terms of survival, due to the advanced nature of the disease. [21] New studies investigated the use of TACE in combination with percutaneous treatments or other agents. A cohort study of 183 patients, who have received TACE, either alone or in combination with pervastatin, suggested that the use of pervastatin can prolong median survival by up to 20 months. [66] Another cohort study that investigated the combination of TACE with PEI suggested better survival rates at one, three, and five years. [25] A meta-analysis of four randomized trials, in addition to a review of cohort studies, suggested that a combination of TACE and PA improves the survival outcome. [67] However, this report suffered from methodological discrepancies in the pooling of data, and the sub-analysis of data also included evidence from cohort studies. The meta-analysis itself did not include a measure of heterogeneity, and thus, the control arm included patients who received TACE in combination with RFA or PEI. There are no large published RCTs comparing TACE to RFA alone. However, a cohort study of more than 700 patients that included 114 patients eligible for RFA, but received TACE instead, revealed comparable results to using RFA alone, with survival rates at one, three, and five years at 80, 43, and 23%, respectively. [68] High intensity ultrasound was also investigated in one cohort study, suggesting a future role, but not enough numbers had been enrolled in the study to make any valid generalization. [26] A recent meta-analysis of nine RCTs suggested that TACE improves survival, however, on the other hand a meta-analysis of three RCTs that compared TACE to TAE showed that TACE offers no advantages in terms of survival rates. [69] This is contrary to an earlier meta-analysis, which included four trials and showed no advantage of TACE compared to supportive care alone in the unresectable tumors. [70] However, in the latter meta-analysis, only short-term survival rates were considered at three and six months and the RCTs included in the meta-analysis were of poor quality and the numbers of patients included in each trial were scarce and even according to the authors no clear conclusions could be drawn.

It is still not clear whether TACE plays a role in prolonging life and preventing recurrence. A study by Zhou et al., [71] in 2009, compared preoperative TACE to controls (no preoperative treatment) in 108 patients with large resectable HCC tumors (≥ 5 cm). The primary endpoints were measured including recurrence rates, disease-free survival rates, and overall survival rates. The median follow-up was 57 months. Although the study was larger than the previously reported studies, the results showed that preoperative TACE did not improve the surgical outcome, and as a matter of fact may have been detrimental to the surgery, due to complications associated with liver failure and progression of the tumor. There was no statistically significant difference at the one-, three-, and five-year, disease-free or overall survival rates between the two groups.

The main purpose of neoadjuvant therapy prior to definitive surgery was to help reduce the tumor bulk and thus facilitate the surgical procedure, and therefore, reduce the complications rate. In addition to making the surgical intervention easier, TACE also aimed to destroy the microscopic foci of the tumor, hence reducing the chances of recurrence in the future. However, due to the complications associated with the procedure TACE was not used in the early stages of the HCC tumor. Therefore, TACE should not be recommended as the first-line treatment in large or small HCC tumors suitable for surgical resection.

Hormonal treatments

Systemic treatments including external radiotherapy have been investigated extensively in HCC. Oestrogen receptors have been found in up to 33% of HCC tumors. [72] Therefore, tamoxifen was investigated more than any other hormonal compound, as a possible systemic treatment for HCC. However, the results from the RCTs involving tamoxifen were disappointing. [73] This led to the suggestion that HCC is probably not a hormone-responsive disease and thus hormonal compounds may play no role in the treatment of HCC. [74] A meta-analysis of seven RCTs, comparing tamoxifen to conservative treatment, showed no benefit in terms of survival or local HCC responsiveness to treatment. [21] A Cochrane review also reached similar conclusions. [75] In addition to this a comprehensive review of tamoxifen, in 2005, included ten RCTs, and suggested that tamoxifen plays no role in the treatment of HCC, and it must not even be used in the control arm of future RCTs. [76] RCTs in the last five years included, one RCT that compared the use of tamoxifen alone or with TACE, one RCT that compared the use of long-acting octreotide in combination with tamoxifen or tamoxifen alone, and one RCT that compared tamoxifen to a control group. [77],[78],[79] All these trials reached one conclusion; there was no added benefit with the use of tamoxifen alone or in combination with other chemotherapy agents to treat advanced HCC.

Hormonal compounds have not shown any survival benefit. All RCTs comparing tamoxifen alone or in combination with other treatments failed to show any benefit in terms of survival [Table 5].
Table 5: Characteristics of trials comparing tamoxifen to other treatments in HCC

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Despite the negative results surrounding tamoxifen, Barbare et al., [79] suggested that tamoxifen may improve survival in patients with preserved liver condition assessed by Okuda stage I or II. A univariate analysis of Okuda I or II patients showed that median survival may be significantly prolonged by four months between Okuda I (7.6 months) and Okuda II (3.9 months) subgroups (P = 0.0001). However, this subgroup analysis was not planned at the beginning of the trial and Okuda scores do not account particularly for patients with hepatic failure.

On the other hand, Gallo et al., [80] showed in a well-constructed RCT that tamoxifen did not offer any benefit in patients with HCC, even with relatively good prognosis, as stratified by the Okuda scores. All data up to date have shown that tamoxifen is ineffective even when used in combination with other treatments.

Although tamoxifen failed to show any benefit in prolonging survival in advanced HCC, somatostatin and its synthetic analogs may play a role in prolonging survival in patients with advanced disease. However, the results so far are conflicting in terms of RCTs comparing long-acting octreotide (LAO) to a placebo. This can be simplified by considering both RCTs, since 2005 [Table 6].
Table 6: Characteristics of studies comparing long-acting octreotide to placebo in advanced HCC

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The study by Becker et al., [81] was the first RCT to investigate the effects of LAO on survival. However, the study showed no survival benefit in using LAO, in advanced HCC disease. There was also no statistically significant limitation to the progression of the disease in the LAO group. Although LAO was tolerated as a treatment, there was no improvement in the quality of life scores as measured by EORTC QLQ-C30. However, another RCT, which investigated the role of somatostatin and its synthetic analogs in somatostatin receptor tumor cells, showed that survival was prolonged significantly in patients with targeted therapy, as demonstrated by octreoscan. [82] The patients were screened to demonstrate whether the tumor cells were somatostatin sensitive or not. LAO was given to patients with Octreoscan +ve tumors and the controls were given a placebo. Both groups were then compared to the octreoscan -ve group that received no intervention. Although the population of this study was small and there were no comparisons of baseline patient characteristics; the study posed an interesting question of whether HCC tumor cells should be investigated for hormonal sensitivity prior to treatment. Unlike the study by Becker et al., [81] this study also demonstrated a better quality of life in the octreoscan +ve group, as measured by the QLQ-C30 scores. The discrepancy in results between both these studies may have been due to the selection criteria of patients, in addition to the targeted therapy of choice.

Systemic chemotherapy

The use of systemic chemotherapy did not achieve better results in terms of survival rates. Doxorubicin is the most commonly studied form of HCC chemotherapy, whether in combination to other agents or as a single treatment. [20],[83] Doxorubicin has shown response rates of 10-20% in clinical trials, however, no added benefits in terms of prolonging survival in patients with advanced HCC were seen. [20],[21] Of late, a large multi-centered phase III trial of 445 patients with HCC investigated the use of doxorubicin or nolatrexed, but the results were disappointing in terms of survival rates, to an extent that further calls for the exploration of the use of nolatrexed in HCC treatment were no longer recommended. [34] Similarly Cisplatin did not show any promising results in terms of improving survival. [73]

Although there is no approved chemotherapy treatment for HCC, doxorubicin has been considered in trials of advanced HCC since the 1970s. Since 2005, two phase III trials that have considered systemic chemotherapy in patients with unresectable HCC tumor were included in this review. [84],[85] A multicenter phase III trial by Gish et al., [84] recruited 445 patients to receive either nolatrexed or doxorubicin. This study was relatively large and the results were not encouraging, as the median overall survival was less in the nolatrexed group (22.3 weeks) compared to the doxorubicin group (32.3 weeks). However, the difference in the median overall survival was not statistically significant between both groups (P = 0.0068).

Another study considered comparing a different regimen of chemotherapy to doxorubicin as baseline. The study by Yeo et al., [85] recruited 188 patients who were randomized equally to receive doxorubicin or cisplatin / interferon alpha-2b / doxorubicin / fluorouracil (PIAF). Again there was no statistically significant difference in terms of overall survival, despite the response rates being slightly better in the PIAF group compared to the doxorubicin group (20.9% and 10.5%, respectively). PIAF, however, was associated with a higher rate of myelotoxicity.

Molecular Targeted Therapy: Sorafenib

There is no proven effective systemic therapy for patients with advanced HCC. However, this may be about to change with the advent of a new therapy that targets tumor cells by halting tumor proliferation and angiogenesis, in addition to increasing the rate of tumor-programmed cell death. In recent years several pathways that control angiogenesis and cell proliferation were identified.

A new drug with anti-tumor effects has been recently approved for use in the treatment of advanced HCC. [86],[87],[88] Sorafenib, a multikinase inhibitor showed promising results in phase III trials, in terms of prolonging survival rates in unresectable HCC tumors, with a significant increase of more than three months compared to a placebo. [89],[90] This is the first systemic therapy to show such a benefit in terms of survival. However, the problems seem to be with the degree-associated toxicity. This may have led to discontinuation of treatment in a relatively moderate number of cases. Most serious events recorded were cardiac in nature. However the combination of sorafenib with other systemic therapies is currently under investigation, including the combination of sorafenib with percutaneous treatments.

Preclinical studies have confirmed that Sorafenib can be used as a multi-kinase inhibitor, to mainly target the Raf kinases and receptor tyrosine kinases associated with angiogenesis (VEGFR-2 / -3, PDGFR-β). [91] The most frequently reported drug-related adverse events at any grade were fatigue, anorexia, diarrhea, rash / desquamation, and hand - foot skin reactions [Table 7]. [92],[93] Phase II trials of Sorafenib showed modest benefit in patients with Child-Pugh A or B and advanced HCC. [94],[95] Phase II trials recommended that Sorafenib should be used in combination with other regimens and systemic therapies, to achieve maximal potential benefit. [94],[95]
Table 7: Percentage of adverse events reported by four phase I clinical trials

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Phase III / IV trials of Sorafenib showed that median overall survival was significantly prolonged by 2.3 - 2.8 months [Table 8]. [89],[90],[96] The SHARP (Sorafenib HCC Assessment Randomized Protocol) study was a multicenter trial that recruited patients mainly from the US and Europe. [89],[96] The SHARP study demonstrated clearly that Sorafenib offers benefit in terms of median overall survival. Therefore, the European Medicinal Agency licensed the use of Sorafenib in patients with advanced HCC, in October 2007. The Food and Drug Administration followed suit and licensed Sorafenib for the treatment of advanced HCC, in November 2007. In 2008, the State Food and Drug Administration (SFDA) of China approved the use of Sorafenib in the treatment of patients with unresectable or metastatic HCC.
Table 8: The median overall survival rates with confidence intervals

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However, whether Sorafenib can achieve the same results in Child-Pugh class B patients with HCC is questionable. Most patients recruited in phase III trials were Child-Pugh class A, and therefore, the benefit of increased overall survival may not be generalized to patients with Child-Pugh class B [Table 8].

The international STORM (Sorafenib as Adjuvant Treatment in the Prevention of Recurrence of Hepatocellular Carcinoma) trial aims to investigate the role of Sorafenib in reducing the chances of tumor recurrence following radical therapy. The target population will include patients who receive local ablation and surgical resection, and the study aims to recruit 1100 patients in total.


 > Conclusion and Future Studies Top


The management of HCC remains dependent on the classification of HCC, the grade of the associated liver cirrhosis, and the number and size of the tumor/s. The current management of HCC includes radical or curative treatments, chemoembolization, and systemic therapies. Radical or curative treatments include liver resection, liver transplantation or RFA. There are no large randomized trials to decide on the best curative therapy in early HCC. However, this review shows that percutaneous treatments may offer an advantage in terms of less adverse events and shorter hospital stay, compared to liver resection, although there is no difference in terms of tumor recurrence or overall survival. Nevertheless the current evidence available is not sufficient to determine the best primary radical therapy. There are no sufficient randomized trials comparing the different modalities of radical therapies, to conduct a meta-analysis.

There is no agreement on a particular protocol or technique for percutaneous and ablative therapies; however, this meta-analysis shows that RFA is superior to PEI. Therefore, this review recommends that RFA should be the first-line treatment in patients with a single small HCC tumor of size ≤ 3 cm.

TACE may be associated with significant hazardous effects and the benefit in terms of shrinking the tumor mass prior to surgery may be compromised with an increased risk of liver failure. Therefore, patients need to be carefully selected prior to undergoing this procedure. In addition, this technique needs to be standardized in future studies.

Tamoxifen has no role to play in the treatment of HCC. Despite the intense research into the use of tamoxifen in advanced HCC, all the results have been disappointing. Tamoxifen also plays no beneficial role as an adjuvant to other treatments. Therefore, no further trials investigating tamoxifen are required.

Although Sorafenib is currently recommended as first-line treatment in advanced and inoperable HCC, it may also offer a potential benefit in patients with early disease, as an adjuvant therapy. The results of the randomized trials into the efficacy of Sorafenib in early and advanced disease are eagerly anticipated.

Finally, there should be a wider call for more randomized trials, investigating the modalities of treatments in HCC. There are not enough trials that compare different first-line treatments of primary HCC. It also remains difficult to clearly determine the benefits in terms of efficacy and safety of any treatment in the light of variations used in the definitions and sizing of HCC tumors.

 
 > References Top

1.Parkin DM, Bray F, Ferlay J, Pisani P. Global cancer statistics, 2002. CA Cancer J Clin 2005;55:74-108.  Back to cited text no. 1
    
2.El-Serag HB. Hepatocellular carcinoma: An epidemiologic view. J Clin Gastroenterol 2002;35:S72-8.  Back to cited text no. 2
    
3.El-Serag HB. Hepatocellular carcinoma: Recent trends in the United States. Gastroenterology 2004;127:S27-34.  Back to cited text no. 3
    
4.Jepsen P, Vilstrup H, Tarone RE, Friis S, Sørensen HT. Incidence rates of hepatocellular carcinoma in the U.S. and Denmark: Recent trends. Int J Cancer 2007;121:1624-6.  Back to cited text no. 4
    
5.El-Serag HB. Epidemiology of hepatocellular carcinoma. Clin Liver Dis 2001;5:87-107, 6.  Back to cited text no. 5
    
6.El-Serag HB. Epidemiology of hepatocellular carcinoma in USA. Hepatol Res 2007;37:S88-94.  Back to cited text no. 6
    
7.Altekruse SF, McGlynn KA, Reichman ME. Hepatocellular carcinoma incidence, mortality, and survival trends in the United States from 1975 to 2005. J Clin Oncol 2009;27:1485-91.  Back to cited text no. 7
    
8.El-Saadany S, Tepper M, Mao Y, Semenciw R, Giulivi A. An epidemiologic study of hepatocellular carcinoma in Canada. Can J Public Health 2002;93:443-6.  Back to cited text no. 8
    
9.Dyer Z, Peltekian K, van Zanten SV. Review article: The changing epidemiology of hepatocellular carcinoma in Canada. Aliment Pharmacol Ther 2005;22:17-22.  Back to cited text no. 9
    
10.Capocaccia R, Sant M, Berrino F, Simonetti A, Santi V, Trevisani F; EUROCARE Working Group. Hepatocellular carcinoma: Trends of incidence and survival in Europe and the United States at the end of the 20th century. Am J Gastroenterol 2007;102:1661-70.  Back to cited text no. 10
    
11.Di Bisceglie AM, Lyra AC, Schwartz M, Reddy RK, Martin P, Gores G, et al.; Liver Cancer Network. Hepatitis C-related hepatocellular carcinoma in the United States: Influence of ethnic status. Am J Gastroenterol 2003;98:2060-3.  Back to cited text no. 11
    
12.Mitra AK. Hepatitis C-related hepatocellular carcinoma: Prevalence around the world, factors interacting, and role of genotypes. Epidemiol Rev 1999;21:180-7.  Back to cited text no. 12
    
13.Raza SA, Clifford GM, Franceschi S. Worldwide variation in the relative importance of hepatitis B and hepatitis C viruses in hepatocellular carcinoma: A systematic review. Br J Cancer 2007;96:1127-34.  Back to cited text no. 13
    
14.El-Serag HB, Mason AC. Risk factors for the rising rates of primary liver cancer in the United States. Arch Intern Med 2000;160:3227-30.  Back to cited text no. 14
    
15.Deuffic S, Poynard T, Valleron AJ. Correlation between hepatitis C virus prevalence and hepatocellular carcinoma mortality in Europe. J Viral Hepat 1999;6:411-3.  Back to cited text no. 15
    
16.Sherman M. Approaches to the diagnosis of hepatocellular carcinoma. Curr Gastroenterol Rep 2005;7:11-8.  Back to cited text no. 16
    
17.Barbara L, Benzi G, Gaiani S, Fusconi F, Zironi G, Siringo S, et al. Natural history of small untreated hepatocellular carcinoma in cirrhosis: A multivariate analysis of prognostic factors of tumor growth rate and patient survival. Hepatology 1992;16:132-7.  Back to cited text no. 17
    
18.Ishizaki Y, Kawasaki S. The evolution of liver transplantation for hepatocellular carcinoma (past, present, and future). J Gastroenterol 2008;43:18-26.  Back to cited text no. 18
    
19.Schwartz M, Roayaie S, Uva P. Treatment of HCC in patients awaiting liver transplantation. Am J Transplant 2007;7:1875-81.  Back to cited text no. 19
    
20.Lopez PM, Villanueva A, Llovet JM. Systematic review: Evidence-based management of hepatocellular carcinoma--an updated analysis of randomized controlled trials. Aliment Pharmacol Ther 2006;23:1535-47.  Back to cited text no. 20
    
21.Llovet JM, Bruix J. Systematic review of randomized trials for unresectable hepatocellular carcinoma: Chemoembolization improves survival. Hepatology 2003;37:429-42.  Back to cited text no. 21
    
22.Mathurin P, Rixe O, Carbonell N, Bernard B, Cluzel P, Bellin MF, et al. Review article: Overview of medical treatments in unresectable hepatocellular carcinoma--an impossible meta-analysis. Aliment Pharmacol Ther 1998;12:111-26.  Back to cited text no. 22
    
23.Pascual S, Irurzun J, Zapater P, Such J, Sempere L, Carnicer F, et al. Usefulness of surveillance programmes for early diagnosis of hepatocellular carcinoma in clinical practice. Liver Int 2008;28:682-9.  Back to cited text no. 23
    
24.Sacks HS, Berrier J, Reitman D, Ancona-Berk VA, Chalmers TC. Meta-analyses of randomized controlled trials. N Engl J Med 1987;316:450-5.  Back to cited text no. 24
    
25.Dettmer A, Kirchhoff TD, Gebel M, Zender L, Malek NP, Panning B, et al. Combination of repeated single-session percutaneous ethanol injection and transarterial chemoembolisation compared to repeated single-session percutaneous ethanol injection in patients with non-resectable hepatocellular carcinoma. World J Gastroenterol 2006;12:3707-15.  Back to cited text no. 25
    
26.Wu F, Wang ZB, Chen WZ, Zou JZ, Bai J, Zhu H, et al. Advanced hepatocellular carcinoma: Treatment with high-intensity focused ultrasound ablation combined with transcatheter arterial embolization. Radiology 2005;235:659-67.  Back to cited text no. 26
    
27.Cheng BQ, Jia CQ, Liu CT, Fan W, Wang QL, Zhang ZL, et al. Chemoembolization combined with radiofrequency ablation for patients with hepatocellular carcinoma larger than 3 cm: A randomized controlled trial. JAMA 2008;299:1669-77.  Back to cited text no. 27
    
28.Kobayashi M, Ikeda K, Kawamura Y, Hosaka T, Sezaki H, Yatsuji H, et al. Randomized controlled trial for the efficacy of hepatic arterial occlusion during radiofrequency ablation for small hepatocellular carcinoma--direct ablative effects and a long-term outcome. Liver Int 2007;27:353-9.  Back to cited text no. 28
    
29.Sarin SK, Kumar M, Garg S, Hissar S, Pandey C, Sharma BC. High dose vitamin K3 infusion in advanced hepatocellular carcinoma. J Gastroenterol Hepatol 2006;21:1478-82.  Back to cited text no. 29
    
30.Becker G, Soezgen T, Olschewski M, Laubenberger J, Blum HE, Allgaier HP. Combined TACE and PEI for palliative treatment of unresectable hepatocellular carcinoma. World J Gastroenterol 2005;11:6104-9.  Back to cited text no. 30
    
31.Cheng BQ, Jia CQ, Liu CT, Fan W, Wang QL, Zhang ZL, et al. Chemoembolization combined with radiofrequency ablation for patients with hepatocellular carcinoma larger than 3 cm: A randomized controlled trial (Retraction in: DeAngelis CD, Fontanarosa PB. JAMA 2009;301:1931). JAMA 2008;299:1669-77.   Back to cited text no. 31
    
32.Yang P, Liang M, Zhang Y, Shen B. Clinical application of a combination therapy of lentinan, multi-electrode RFA and TACE in HCC. Adv Ther 2008;25:787-94.  Back to cited text no. 32
    
33.Lencioni R, Crocetti L. A critical appraisal of the literature on local ablative therapies for hepatocellular carcinoma. Clin Liver Dis 2005;9:301-14.  Back to cited text no. 33
    
34.Kokudo N, Makuuchi M. Evidence-based clinical practice guidelines for hepatocellular carcinoma in Japan: The J-HCC guidelines. J Gastroenterol 2009;44 Suppl 19:119-21.  Back to cited text no. 34
    
35.Vivarelli M, Guglielmi A, Ruzzenente A, Cucchetti A, Bellusci R, Cordiano C, et al. Surgical resection versus percutaneous radiofrequency ablation in the treatment of hepatocellular carcinoma on cirrhotic liver. Ann Surg 2004;240:102-7.  Back to cited text no. 35
    
36.Hong SN, Lee SY, Choi MS, Lee JH, Koh KC, Paik SW, et al. Comparing the outcomes of radiofrequency ablation and surgery in patients with a single small hepatocellular carcinoma and well-preserved hepatic function. J Clin Gastroenterol 2005;39:247-52.  Back to cited text no. 36
    
37.Wakai T, Shirai Y, Suda T, Yokoyama N, Sakata J, Cruz PV, et al. Long-term outcomes of hepatectomy vs percutaneous ablation for treatment of hepatocellular carcinoma < or = 4 cm. World J Gastroenterol 2006;12:546-52.  Back to cited text no. 37
    
38.Guglielmi A, Ruzzenente A, Valdegamberi A, Pachera S, Campagnaro T, D'Onofrio M, et al. Radiofrequency ablation versus surgical resection for the treatment of hepatocellular carcinoma in cirrhosis. J Gastrointest Surg 2008;12:192-8.  Back to cited text no. 38
    
39.Abu-Hilal M, Primrose JN, Casaril A, McPhail MJ, Pearce NW, Nicoli N. Surgical resection versus radiofrequency ablation in the treatment of small unifocal hepatocellular carcinoma. J Gastrointest Surg 2008;12:1521-6.  Back to cited text no. 39
    
40.Huang GT, Lee PH, Tsang YM, Lai MY, Yang PM, Hu RH, et al. Percutaneous ethanol injection versus surgical resection for the treatment of small hepatocellular carcinoma: A prospective study. Ann Surg 2005;242:36-42.  Back to cited text no. 40
    
41.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;243:321-8.  Back to cited text no. 41
    
42.Lencioni R, Cioni D, Crocetti L, Bartolozzi C. Percutaneous ablation of hepatocellular carcinoma: State-of-the-art. Liver Transpl 2004;10:S91-7.  Back to cited text no. 42
    
43.Gaiani S, Celli N, Cecilioni L, Piscaglia F, Bolondi L. Review article: Percutaneous treatment of hepatocellular carcinoma. Aliment Pharmacol Ther 2003;17:103-10.  Back to cited text no. 43
    
44.Rossi S, Fornari F, Buscarini L. Percutaneous ultrasound-guided radio-frequency electrocautery for the treatment of small hepatocellular carcinoma. J Interv Radiol 1993;8:97-103.  Back to cited text no. 44
    
45.Galandi D, Antes G. Radiofrequency thermal ablation versus other interventions for hepatocellular carcinoma. Cochrane Database Syst Rev 2004:CD003046.  Back to cited text no. 45
    
46.Seror O, N'Kontchou G, Tin-Tin-Htar M, Durand-Zaleski I, Trinchet JC, Sellier N, et al. Ethanol versus radiofrequency ablation for the treatment of small hepatocellular carcinoma in patients with cirrhosis: A retrospective study of efficacy and cost. Gastroenterol Clin Biol 2006;30:1265-73.   Back to cited text no. 46
    
47.Lencioni RA, Allgaier HP, Cioni D, Olschewski M, Deibert P, Crocetti L, et al. Small hepatocellular carcinoma in cirrhosis: Randomized comparison of radio-frequency thermal ablation versus percutaneous ethanol injection. Radiology 2003;228:235-40.  Back to cited text no. 47
    
48.Livraghi T, Goldberg SN, Lazzaroni S, Meloni F, Solbiati L, Gazelle GS. Small hepatocellular carcinoma: Treatment with radio-frequency ablation versus ethanol injection. Radiology 1999;210:655-61.  Back to cited text no. 48
    
49.Orlando A, Leandro G, Olivo M, Andriulli A, Cottone M. Radiofrequency thermal ablation vs. percutaneous ethanol injection for small hepatocellular carcinoma in cirrhosis: Meta-analysis of randomized controlled trials. Am J Gastroenterol 2009;104:514-24.  Back to cited text no. 49
    
50.Wong SN, Lin CJ, Lin CC, Chen WT, Cua IH, Lin SM. Combined percutaneous radiofrequency ablation and ethanol injection for hepatocellular carcinoma in high-risk locations. AJR Am J Roentgenol 2008;190:187-95.  Back to cited text no. 50
    
51.Vallone P, Catalano O, Izzo F, Siani A. Combined ethanol injection therapy and radiofrequency ablation therapy in percutaneous treatment of hepatocellular carcinoma larger than 4 cm. Cardiovasc Intervent Radiol 2006;29:544-51.  Back to cited text no. 51
    
52.Luo BM, Wen YL, Yang HY, Zhi H, Xiao XY, Ou B, et al. Percutaneous ethanol injection, radiofrequency and their combination in treatment of hepatocellular carcinoma. World J Gastroenterol 2005;11:6277-80.  Back to cited text no. 52
    
53.Sarin SK, Sreenivas DV, Saraya A, Mehta S, Lahoti D, Malhotra V. Improved survival with percutaneous ethanol injection in patients with large hepatocellular carcinoma. Eur J Gastroenterol Hepatol 1994;6:971-4.  Back to cited text no. 53
    
54.Bartolozzi C, Lencioni R, Caramella D, Vignali C, Cioni R, Mazzeo S, et al. Treatment of large HCC: Transcatheter arterial chemoembolization combined with percutaneous ethanol injection versus repeated transcatheter arterial chemoembolization. Radiology 1995;197:812-8.   Back to cited text no. 54
    
55.Sutherland LM, Williams JA, Padbury RT, Gotley DC, Stokes B, Maddern GJ. Radiofrequency ablation of liver tumors: A systematic review. Arch Surg 2006;141:181-90.  Back to cited text no. 55
    
56.Brunello F, Veltri A, Carucci P, Pagano E, Ciccone G, Moretto P, et al. Radiofrequency ablation versus ethanol injection for early hepatocellular carcinoma: A randomized controlled trial. Scand J Gastroenterol 2008;43:727-35.  Back to cited text no. 56
    
57.Lin SM, Lin CJ, Lin CC, Hsu CW, Chen YC. Randomised controlled trial comparing percutaneous radiofrequency thermal ablation, percutaneous ethanol injection, and percutaneous acetic acid injection to treat hepatocellular carcinoma of 3 cm or less. Gut 2005;54:1151-6.  Back to cited text no. 57
    
58.Shiina S, Teratani T, Obi S, Sato S, Tateishi R, Fujishima T, et al. A randomized controlled trial of radiofrequency ablation with ethanol injection for small hepatocellular carcinoma. Gastroenterology 2005;129:122-30.  Back to cited text no. 58
    
59.Zhang YJ, Liang HH, Chen MS, Guo RP, Li JQ, Zheng Y, et al. Hepatocellular carcinoma treated with radiofrequency ablation with or without ethanol injection: A prospective randomized trial. Radiology 2007;244:599-607.  Back to cited text no. 59
    
60.Lin JJ, Jin CN, Zheng ML, Ouyang XN, Zeng JX, Dai XH. Clinical study on treatment of primary hepatocellular carcinoma by Shenqi mixture combined with microwave coagulation. Chin J Integr Med 2005;11:104-10.  Back to cited text no. 60
    
61.Bruix J, Sala M, Llovet JM. Chemoembolization for hepatocellular carcinoma. Gastroenterology 2004;127:S179-88.  Back to cited text no. 61
    
62.Llovet JM, Burroughs A, Bruix J. Hepatocellular carcinoma. Lancet 2003;362:1907-17.  Back to cited text no. 62
    
63.Llovet JM, Real MI, Montaña X, Planas R, Coll S, Aponte J, et al.; Barcelona Liver Cancer Group. Arterial embolization or chemoembolization versus symptomatic treatment in patients with unresectable hepatocellular carcinoma: A randomized controlled trial. Lancet 2002;359:1734-9.   Back to cited text no. 63
    
64.Lo CM, Ngan H, Tso WK, Liu CL, Lam CM, Poon RT, et al. Randomized controlled trial of transarterial lipiodol chemoembolization for unresectable hepatocellular carcinoma. Hepatology 2002;35:1164-71.  Back to cited text no. 64
    
65.Molinari M, Kachura JR, Dixon E, Rajan DK, Hayeems EB, Asch MR, et al. Transarterial chemoembolisation for advanced hepatocellular carcinoma: Results from a North American cancer centre. Clin Oncol (R Coll Radiol) 2006;18:684-92.  Back to cited text no. 65
    
66.Graf H, Jungst C, Straub G, Dogan S, Hoffmann RT, Jakobs T, et al. Chemoembolization combined with pravastatin improves survival in patients with hepatocellular carcinoma. Digestion 2008;78:34-8.  Back to cited text no. 66
    
67.Marelli L, Stigliano R, Triantos C, Senzolo M, Cholongitas E, Davies N, et al. Treatment outcomes for hepatocellular carcinoma using chemoembolization in combination with other therapies. Cancer Treat Rev 2006;32:594-606.  Back to cited text no. 67
    
68.Liem MS, Poon RT, Lo CM, Tso WK, Fan ST. Outcome of transarterial chemoembolization in patients with inoperable hepatocellular carcinoma eligible for radiofrequency ablation. World J Gastroenterol 2005;11:4465-71.  Back to cited text no. 68
    
69.Marelli L, Stigliano R, Triantos C, Senzolo M, Cholongitas E, Davies N, et al. Transarterial therapy for hepatocellular carcinoma: Which technique is more effective? A systematic review of cohort and randomized studies. Cardiovasc Intervent Radiol 2007;30:6-25.  Back to cited text no. 69
    
70.Geschwind JF, Ramsey DE, Choti MA, Thuluvath PJ, Huncharek MS. Chemoembolization of hepatocellular carcinoma: Results of a metaanalysis. Am J Clin Oncol 2003;26:344-9.   Back to cited text no. 70
    
71.Zhou WP, Lai EC, Li AJ, Fu SY, Zhou JP, Pan ZY, et al. A prospective, randomized, controlled trial of preoperative transarterial chemoembolization for resectable large hepatocellular carcinoma. Ann Surg 2009;249:195-202.  Back to cited text no. 71
    
72.Garcia-Leiva J, Gamboa-Dominguez A, Ceron-Lizarraga T, Morales-Espinosa D, Meza-Junco J, Arrieta O. Response of negative estrogen-receptor hepatocarcinoma to tamoxifen, and survival of non-resectable patients. Ann Hepatol 2006;5:263-7.  Back to cited text no. 72
    
73.Samuel M, Chow PK, Chan Shih-Yen E, Machin D, Soo KC. Neoadjuvant and adjuvant therapy for surgical resection of hepatocellular carcinoma. Cochrane Database Syst Rev 2009:CD001199.   Back to cited text no. 73
    
74.Di Maio M, Daniele B, Pignata S, Gallo C, De Maio E, Morabito A, et al. Is human hepatocellular carcinoma a hormone-responsive tumor? World J Gastroenterol 2008;14:1682-9.  Back to cited text no. 74
    
75.Nowak A, Findlay M, Culjak G, Stockler M. Tamoxifen for hepatocellular carcinoma. Cochrane Database Syst Rev 2004:CD001024.  Back to cited text no. 75
    
76.Nowak AK, Stockler MR, Chow PK, Findlay M. Use of tamoxifen in advanced-stage hepatocellular carcinoma. A systematic review. Cancer 2005;103:1408-14.  Back to cited text no. 76
    
77.Doffoël M, Bonnetain F, Bouché O, Vetter D, Abergel A, Fratté S, et al.; Fédération Francophone de Cancérologie Digestive. Multicentre randomised phase III trial comparing Tamoxifen alone or with Transarterial Lipiodol Chemoembolisation for unresectable hepatocellular carcinoma in cirrhotic patients. (Fédération Francophone de Cancérologie Digestive 9402). Eur J Cancer 2008;44:528-38.   Back to cited text no. 77
    
78.Verset G, Verslype C, Reynaert H, Borbath I, Langlet P, Vandebroek A, et al. Efficacy of the combination of long-acting release octreotide and tamoxifen in patients with advanced hepatocellular carcinoma: A randomised multicentre phase III study. Br J Cancer 2007;97:582-8.  Back to cited text no. 78
    
79.Barbare JC, Bouche O, Bonnetain F, Raoul JL, Rougier P, Abergel A, et al. Randomized controlled trial of tamoxifen in advanced hepatocellular carcinoma. J Clin Oncol 2005;23:4338-46.  Back to cited text no. 79
    
80.Gallo C, De Maio E, Di Maio M, Signoriello G, Daniele B, Pignata S, et al.; CLIP (Cancer of the Liver Italian Programme) Investigators. Tamoxifen is not effective in good prognosis patients with hepatocellular carcinoma. BMC Cancer 2006;24:196.  Back to cited text no. 80
    
81.Becker G, Allgaier HP, Olschewski M, Zähringer A, Blum HE; HECTOR Study Group. Long-acting octreotide versus placebo for treatment of advanced HCC: A randomized controlled double-blind study. Hepatology 2007;45:9-15.  Back to cited text no. 81
    
82.Dimitroulopoulos D, Xinopoulos D, Tsamakidis K, Zisimopoulos A, Andriotis E, Panagiotakos D, et al. Long acting octreotide in the treatment of advanced hepatocellular cancer and overexpression of somatostatin receptors: Randomized placebo-controlled trial. World J Gastroenterol 2007;13:3164-70.  Back to cited text no. 82
    
83.Almhanna K, Kalmadi S, Pelley R, Kim R. Neoadjuvant therapy for hepatocellular carcinoma: Is there an optimal approach? Oncology (Williston Park) 2007;21:1116-22.  Back to cited text no. 83
    
84.Gish RG, Porta C, Lazar L, Ruff P, Feld R, Croitoru A, et al. Phase III randomized controlled trial comparing the survival of patients with unresectable hepatocellular carcinoma treated with nolatrexed or doxorubicin. J Clin Oncol 2007;25:3069-75.  Back to cited text no. 84
    
85.Yeo W, Mok TS, Zee B, Leung TW, Lai PB, Lau WY, et al. A randomized phase III study of doxorubicin versus cisplatin/interferon alpha-2b/doxorubicin/fluorouracil (PIAF) combination chemotherapy for unresectable hepatocellular carcinoma. J Natl Cancer Inst 2005;97:1532-8.  Back to cited text no. 85
    
86.Lang L. FDA approves sorafenib for patients with inoperable liver cancer. Gastroenterology 2008;134:379.  Back to cited text no. 86
    
87.Kudo M. Hepatocellular carcinoma 2009 and beyond: From the surveillance to molecular targeted therapy. Oncology 2008;75:S1-12.  Back to cited text no. 87
    
88.Simpson D, Keating GM. Sorafenib in hepatocellular carcinoma. Drugs 2008;68:251-8.  Back to cited text no. 88
    
89.Llovet JM, Ricci S, Mazzaferro V, Hilgard P, Gane E, Blanc JF, et al.; SHARP Investigators Study Group. Sorafenib in advanced hepatocellular carcinoma. N Engl J Med 2008;359:378-90.  Back to cited text no. 89
    
90.Cheng AL, Kang YK, Chen Z, Tsao CJ, Qin S, Kim JS, et al. Efficacy and safety of sorafenib in patients in the Asia-Pacific region with advanced hepatocellular carcinoma: A phase III randomised, double-blind, placebo-controlled trial. Lancet Oncol 2009;10:25-34.  Back to cited text no. 90
    
91.Woodburn JR. The epidermal growth factor receptor and its inhibition in cancer therapy. Pharmacol Ther 1999;82:241.  Back to cited text no. 91
    
92.Strumberg D, Clark JW, Awada A, Moore MJ, Richly H, Hendlisz A, et al. Safety, pharmacokinetics, and preliminary antitumor activity of sorafenib: A review of four phase I trials in patients with advanced refractory solid tumors. Oncologist 2007;12:426-37.   Back to cited text no. 92
    
93.Minami H, Kawada K, Ebi H, Kitagawa K, Kim YI, Araki K, et al. Phase I and pharmacokinetic study of sorafenib, an oral multikinase inhibitor, in Japanese patients with advanced refractory solid tumors. Cancer Sci 2008;99:1492-8.  Back to cited text no. 93
    
94.Abou-Alfa GK, Schwartz L, Ricci S, Amadori D, Santoro A, Figer A, et al. Phase II study of sorafenib in patients with advanced hepatocellular carcinoma. J Clin Oncol 2006;24:4293-300.  Back to cited text no. 94
    
95.Yau T, Chan P, Ng KK, Chok SH, Cheung TT, Fan ST, et al. Phase 2 open-label study of single-agent sorafenib in treating advanced hepatocellular carcinoma in a hepatitis B-endemic Asian population: Presence of lung metastasis predicts poor response. Cancer 2009;115:428-36.  Back to cited text no. 95
    
96.Llovet J, Ricci S, Mazzaferro V, Hilgard P, Gane E, Blanc JF, et al. Sorafenib improves survival in hepatocellular carcinoma: Results of a phase III randomized, placebo-controlled trial. J Clin Oncol 2007;25:18S.  Back to cited text no. 96
    


    Figures

  [Figure 1], [Figure 2], [Figure 3], [Figure 4]
 
 
    Tables

  [Table 1], [Table 2], [Table 3], [Table 4], [Table 5], [Table 6], [Table 7], [Table 8]


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