Current and Future Treatment of Hepatocellular Carcinoma: An Updated Comprehensive Review.

Hepatocellular carcinoma (HCC) is among the leading causes of cancer-related mortality. The principal treatment is surgical resection or liver transplantation, depending on whether the patient is a suitable transplant candidate. However, in most patients with HCC the diagnosis is often late, thereby excluding the patients from definitive surgical resection. Medical treatment includes sorafenib, which is the most commonly used systemic therapy; although, it has been shown to only minimally impact patient survival by several months. Chemotherapy and radiotherapy are generally ineffective. Due to the poor prognosis of patients with HCC, newer treatments are needed with several being in development, either in pre-clinical or clinical studies. In this review article, we provide an update on the current and future medical and surgical management of HCC.

Introduction

Hepatocellular carcinoma (HCC) is currently the sixth most common cancer worldwide, and considered to be the second deadliest cancer for men and sixth for women; according to GLOBOCAN, in 2012 it was estimated that 745,517 deaths were a direct result of HCC.1–4 HCC development, in most cases, arises in the setting of underlying end-stage liver disease, secondary to either viral hepatitis (specifically hepatitis B virus (HBV) or hepatitis C virus) or other non-viral chronic liver diseases.5,6 Given its asymptomatic nature in the early stages of the disease, the majority of HCC cases are detected in advanced stages, leading to incurable disease states.7 Currently, sorafenib is the only approved systemic medication for the treatment of advanced HCC, in addition to other several medical and surgical treatment options (Fig. 1); however, there is a great unmet need for new effective therapies for this condition.

Fig. 1.

Summary of the available medical and surgical treatment options for HCC.

Genetic aberrancy in HCC

In vitro, HCC cells have been shown to be associated with several chromosomal genetic alterations. To date, several aberrant genes encoding proteins have been identified and implicated in HCC pathogenesis, including P53, P16, P73, APC, PTEN, IGF-2, BRCA2, SMAD2, SOCS, beta-catenin, retinoblastoma proteins, c-myc and cyclin D1 proteins.8–10 P53 is considered as one of the most common mutated genes that is expressed in HCC, from among these genes mentioned.11 Other than the specific genetic mutation in HCC, there are several involved signaling/angiogenetic pathways observed in HCC development, including vascular factors produced by tumor cells themselves, growth factors and oncogene receptors. For example, HCC overexpresses epidermal growth factor, which stimulates tyrosine kinase receptor that in return stimulates cell surface signal transmission to the nucleus.

Another similar mechanism that underlies HCC development involves MAPK pathway activation acting through the Ras protein. The Ras protein undergoes activation via phosphorylation, which allows the delivery of signals to the nucleus via downstream components of the pathway, such as ERK1, RAF and MEK.12,13 As mentioned above, HCC is a highly-vascularized tumor with strong angiogenetic activity that is enriched with vascular endothelial growth factor on the surface of tumor cells. Thus, the vascular endothelial growth factor (VEGF) pathway has also been targeted as a treatment for HCC.12

HCC epigenetics

Several epigenetic factors underlie the progression of HCC, including invasion, distant metastasis and hematological dissemination. Epigenetics are related to heritable phenotypic change that does not relate to changes of the genome but rather changes that may result from environmental factors, or other developmental factors. Epigenetic alterations that have been reported in HCC include DNA hyper-/hypo-methylation, histone disruption and non-coding RNAs as manifested by altered expression of mirco-RNAs.14,15 Those epigenetic changes can be used for diagnostic purposes, as well for prognosis. For example, liver specific DNA methylation can guide the clinician for early urgent screening for HCC in cirrhotic patients.16 Furthermore, under-expression of miR-122 was associated with poorer prognosis in HCC patients.17 Similarly, histone modifying genes (EZH2 and SUV39HZ) and protein produced by histone phosphorylation (ARK1 and ARK2) were all poor predictors of outcome and invasiveness.18,19 A recent study by Mansour et al.20 found that hypermethylation of RASSF1A positively correlated with increased tumor size but not with alpha-fetoprotein level, and aggravated the hepatocarcinogenic process; the authors suggested the incorporation of RASSF1A measurement as a screening tool in patients at risk for HCC development.

All those epigenetic biomarkers are promising targets in HCC that may provide clinicians with better diagnostic and prognostic tools; and, in the future, epigenetic-directed therapy might be developed.

Former and current medical treatment

Sorafenib

The development of targeted therapies for HCC has been ongoing for many years, leading to the development of sorafenib in 1990. Due to the dearth of medical therapy for HCC, sorafenib was rapidly approved by the Food and Drug Administration (FDA), irrespective of the degree of cirrhosis.21 Sorafenib is an oral multi-kinase inhibitor that inhibits cell proliferation through a strong inhibition of the serine/threonine kinase RAF. Moreover, it was shown to inhibit pro-angiogenic VEGF and platelet-derived growth factor receptor (Fig. 2).22,23 Sorafenib was initially approved by the FDA for treatment of metastatic renal cell carcinoma, and later it was approved for management of HCC and metastatic differentiated thyroid carcinoma.24

Fig. 2.

Mechanism of action of sorafenib.

Sorafenib inhibits the action of tyrosine kinase Raf and other factors involved in vasculogenesis (vascular endothelial growth factor receptor and platelet-derived growth factor receptor), which in turn inhibits activation of other downstream multikinases that are normally essential for cell growth, angiogenesis, proliferation and metastasis of HCC cells.

The efficacy of sorafenib has been demonstrated in several studies. In the SHARP randomized controlled trial, the overall survival in the sorafenib treatment group was 10.7 months, as compared to 7.9 months of the placebo group, with a good safety profile in HCC patients,25 making sorafenib the only approved systemic agent for the treatment of advanced HCC. There is a great unmet need for new, effective therapies for this condition. However, even though sorafenib is currently regarded as the best option in advanced HCC, it is only able to prolong survival for a few months.

Systemic chemotherapy and radiotherapy

Previously, HCC was treated with chemotherapy and radiotherapy. However, the reported literature has shown poor results associated with those treatment options. Thus, their use is still controversial and only applicable in the context of palliative treatment. HCC is traditionally considered as a highly chemo-resistant tumor. However, conventional chemotherapy is still considered for palliation therapy, which may improve the patient’s quality of life. Among the chemotherapeutic drugs used in HCC, doxorubicin is one of the most commonly used, even though in up to 90% of cases it did not show response and it did not improve survival partial. Other commonly used chemotherapeutic drugs include 5-fluorouracil in combination and cisplatin either alone or in combination therapy.8,26 Overall, other investigated chemotherapeutic drugs, such as capecitabine, mitoxantrone, placlitaxel, gemcitabine and irinotecan, have failed to show promising results.27–29

Similar to that seen with chemotherapy, HCC is radiotherapy-resistant and treatment with systemic radiotherapy plays only a minor role in HCC cases. The diverse genetic aberration in HCC, as well as the expression of the P53 gene and other genes and/or proteins involved in cell death and proliferation pathways, might provide the basis for the development of resistance for radiation.30,31 Systemic radiotherapy is still used for palliative therapy of HCC metastasis.

Current and future medical treatments

Recently, researchers have focused on the development of HCC-targeted medications. For example, several drugs have been developed targeting angiogenesis, such as sunitinib, brivanib, linifanib, vatalanib, TSU-68, cediranib, bevacizumab and ramucirumab.32 Several other therapies were also under development, including epidermal growth factor receptor inhibitors erlotinib and lapatinib, MEK1/2 competitive inhibitor (selumetinib), mTOR antagonist (everolimus) and multikinase inhibitors (nintedanib and regorafenib). However, all of these medications are still in pre-clinical and early clinical studies and none of them have been yet been shown to be effective or approved for HCC treatment.32

Oncolytic virus therapy

Recently, more attention and research efforts has been put forth towards oncolytic virus therapy, a promising new therapeutic approach for cancer treatment. This treatment strategy is defined as a genetically engineered or naturally occurring virus that can kill cancer cells by activating the immune system, subsequently combating the cancerous cells without harming the normal tissues (Fig. 3). Recent studies have shown that the administration of a second-generation oncolytic herpes simplex virus-type 1 with granulocyte macrophage colony-stimulating factor into malignant melanoma lesions suppresses tumor growth and progression, which was associated with an overall survival benefit.

Fig. 3.

Mechanism of action of oncolytic virus therapy.

After HCC-induced oncolytic virus infection, the virus multiplies within the HCC cells, leading to cell rupture and release of second-generation viruses that infect the surrounding HCC cells, as well to cytokines release which in turn activate the antitumor immune response by recruitment of immune cells (innate and adaptive immune system) that lead to immune clearance and HCC apoptosis.

The second-generation oncolytic human simplex virus type-1 is the first oncolytic virus therapy approved in both the USA and Europe. Clinical studies are being performed in several oncolytic viruses, including vaccinia virus JX-594 (pexastimogene devacirepvec) for HCC, granulocyte macrophage colony-stimulating factor-expressing adenovirus CG0070 for bladder cancer, and Reolysin (pelareorep), a wild-type variant of reovirus, for head and neck cancer; and, in Japan, a phase II clinical trial of a third-generation oncolytic human simplex virus type-1 in glioblastoma patients is still ongoing. Interestingly, oncolytic virus therapy seems to be the anticipated breakthrough in cancer therapy generally and in HCC specifically.33

Immunotherapy

The immune system is a crucial player in the combat against malignancies. Since its introduction into clinical practice, immunotherapy has revolutionized cancer treatment. Two checkpoint inhibitors have been developed for cancer treatment, the cytotoxic T-lymphocyte-associated protein 4 (CTLA-4) and the programmed cell death protein 1 pathway (PD-1/PD-L1); this approach is now considered as a cornerstone treatment regimen in cancer therapy. The first CTLA-4 inhibitor was ipilimumab, which showed a significant survival benefit in patients with advanced melanoma,34 which led to its approval by the USA FDA in 2011.

In HCC, immune tolerance is present owing to several immunosuppression mechanisms that lead to augmented inhibitory checkpoint molecules. Among those signals that lead to immune tolerance are CTLA-4,35 PD-1 and its ligand (PD-L1),36 lymphocyte-activation gene 3,37 and T-cell membrane protein 3 and its ligand (galectin-9).38 A recent study reported overexpression of lymphocyte-activation gene 3 in HBV patients, and showed it to cause a reduction in CD8+ T lymphocyte infiltration of HCC.37 Moreover, Li et al.38 showed that targeting of the T-cell membrane protein 3/galectin-9 pathway can be an effective potential therapy of HCC related to HBV.

Several preclinical and clinical studies have been published regarding immunotherapy in HCC. Chen et al.39 showed that administration of CTLA-4 inhibitor augments antitumor immunity in a murine HCC model, with a tumor rejection rate of 90% and a curative rate of 50% in metastatic HCC. Another clinical study reported a partial response of 17.6% and disease control of 76.4% of CTLA-4 inhibitor (tremelimumab) in patients with hepatitis C virus-associated HCC with Child–Pugh grades A and B who failed traditional HCC therapy.40 In that study, the most common side effects were fatigue and anorexia, which occurred in almost one-half of patients, and a transient elevation of liver enzymes mainly after the first dose of therapy.

Similar to CTLA-4 inhibitor, PD-1/PDL-1 has been investigated in several studies. PD-1/PDL-1 is mainly found on T and B lymphocytes, T-regulatory cells and natural killer cells. This molecule mediates T cell function inhibition, thus inhibiting tumor cell apoptosis.41,42 A recent study has shown an association of increased disease progression and poorer prognosis with intra-tumor and circulating PD-1/PDL-1 in patients with HBV.36 Similarly, Gao et al.43 have shown a poor prognosis of HCC with high intra-tumor expression of PD-1/PDL-1, as compared to low-level expression. Moreover, PDL-1 overexpression was the most important independent factor for postoperative recurrence on multivariate analysis. A recent published large multicenter study which evaluated nivolumab, a fully human IgG4 monoclonal PD-1 inhibitor antibody, in patients with histologically-proven advanced HCC showed overall effective antitumor activity and tolerated safety profile.44

Surgical treatments: minimally invasive procedures

In cirrhotic patients with HCC who are not candidates for major surgical therapeutic procedures, minimally invasive procedures, including radiofrequency ablation (RFA), trans-arterial chemoembolization (TACE), highly-focused ultrasound (HIFU), microwave ablation (MWA) and irreversible electroporation (IRE), can be offered. These techniques are performed with imaging control, and maximum efficiency for nodules is less than 3 cm of diameter, for which the complete response rate is around 80%. However, a high number of recurrences has been reported with those techniques.45,46

TACE

TACE has been indicated as the first treatment option for intermediate HCC patients with Barcelona Clinic Liver Cancer (BCLC) stage B.46,47 TACE mediates its antitumor effect by local catheter-guided administration of chemotherapeutic agents mixed with lipiodol which cause selective HCC targeted blood supply embolization and subsequent ischemia and tissue necrosis.1,48 Furthermore, TACE has been used as a bridging therapy for HCC patients awaiting liver transplantation, in order to prevent further tumor progression, thus maintaining the eligibility criteria for liver transplantation.49 TACE has been associated with 2-year survival benefit (HR = 0.53, 95%CI: 0.32–0.89; p = 0.017).50

Recent large meta-analysis (9 randomized controlled trials were included) showed overall improved survival compared to symptomatic treatment (HR = 0.705, 95%CI: 0.5–0.99).51 However, TACE has been associated with adverse events, commonly post-embolization syndrome which is characterized by abdominal pain, elevated temperature and elevated liver enzymes at 1–2 days following the procedure.52 Other adverse events include iatrogenic bile duct injury, hypoxic cholecystitis and liver abscess.53 Moreover, TACE-related mortality has been reported in approximately 0.38%, according to recent study.54 However, in an advanced cirrhosis stage, liver function deterioration can develop, and in one study 17.3% of patients with cirrhosis and ascites developed post-procedural liver failure, with 94% of patients dying within 1 year following TACE.55

RFA

The first application of RFA was in 1990, and FDA approval was obtained in 2001.56,57 Currently, RFA is the most commonly applied minimally invasive treatment for advanced HCC. RFA delivers a rapid electromagnetic pulse that causes thermal injury leading to coagulative necrosis of the tissue. The heat injury is dependent on both the temperature achieved and the duration of heating. Recently, beneficial results have been demonstrated by RFA in local advanced HCC.

Currently, RFA is considered as one of the main treatments of HCC and it can achieve complete response rates in about 90–100% of HCC lesions below 3 cm, with the ability to obtain clear surgical margins. It is considered as an effective alternative for surgical resection in operable BCLC 0–1, according to the European Association for the Study of the Liver disease (EASL)- European Organization for Research and Treatment of Cancer.58 Moreover, there are reports that RFA can be used to hinder the progression of HCC until liver transplant.59 Recently, the international recommendation is not to treat HCC by RFA when the HCC size exceeds 5 cm.23,60

The RFA safety profile is high, as it is associated with minor side effects in about 5% and all of them are self-limited. However, mortality and major complications have been reported in 0.3% and 2% with RFA, respectively, including biliary tree injury, hemorrhage, hepatic abscess and intestinal perforation.61 Another worrisome complication that was reported in almost 0.5% is tumor seeding during the time of needle withdrawal; however, this complication can be prevented by application of low-grade heat in the tract at the time of withdrawal of the needle.

Percutaneous ethanol injection therapy (PEIT)

PEIT is one of the most common chemical ablation techniques for HCC patients who are not candidates for surgery and who have BCLC stage 0-A.62 It is still commonly used, given its low cost and technical simplicity. Ethanol is a cytotoxic material that causes tumorous tissue necrosis, as well tumor microcirculation thrombosis and resultant ischemia. The destructive effect of alcohol is effective due to the extensive vascularity and soft consistency of HCC, which enables the alcohol to diffusely penetrate the tumor tissue.63

PEIT is mostly used in small HCC, at which the necrosis rate of HCC less than 2 cm can reach 90–100%, while the rate decreases to about 70% in HCC of more than 2 cm and less than 3 cm.46 Ethanol injection requires multiple injections on separate days and rarely induces significant necrosis in tumors more than 3 cm, largely because the injected ethanol rarely reaches the entire tumor volume. In one study, PEIT was effective in only 50% of patients with multinodular or large (3–5 cm) HCC; in addition, tumor progression was seen in almost 33% of HCC of more than 3 cm despite several treatment courses.64

HCC size is a very important factor in the selection of locoregional therapy, such as RFA. The American Association for the Study of Liver Disease guidelines state that in HCC less than 2 cm, the efficacy of RFA and PEIT is similar, while in tumors more than 2 cm, RFA benefits outweigh PEIT.46 PEIT is associated with minor side effects and mostly is well tolerated.65 The 1- and 5-year survival rates with PEIT are reported to be 64%–100% and 32%–59%, respectively.66 Furthermore, the presence of septa within the tumor is important as it inhibits the diffusion capacity of ethanol into the tumorous tissue, which reduces the probability of achieving complete response. Thus, tumor size and structure are very crucial to accurate determination and are a perquisite for decision-making in PEIT treatment.

MWA

Thermo-ablative treatment for HCC has also been reported. MWA consists of electromagnetic waves that range from 1–300 GHz. It can be performed by several routes, including intraoperatively, laparoscopically and percutaneously. MWA has some advantageous features over RFA, including higher temperature degree being transmitted to the target tissue, shorter duration of treatment session and the absence of skin burning risk. Earlier randomized controlled trials that aimed to compare RFA versus MWA reported similar efficacy of the two therapeutic methods; however, RFA was slightly superior to MWA in terms of local tumor control and relatively lower rate of complications.67 Moreover, a recent large study involving more than 1000 patients with malignant hepatic tumors which were treated by MWA reported a major complication rate of 2.6% and with higher minor complication rate, including pain, fever, pleural effusion and skin burns.68

HIFU

HIFU is another noninvasive technique used for the treatment of unresectable HCC, intended to deliver mechanical energetic waves to a targeted volume of HCC and causing tissue destruction by local heat waves. HIFU has been used in the management of benign prostatic hypertrophy and inoperable prostatic cancer69,70 and in uterus myoma.71 Furthermore, HIFU has shown efficacy in treating liver malignancies in both animal and human studies.72,73 The mechanism involves the ultrasound initiating vibrating particles longitudinally and transversally to the direction of spreading. When ultrasound waves are focused to reach high acoustic densities (100–10,000 W/cm2), which rapidly raises local temperature to at least 56 degrees Celsius and above, this leads to parenchymal necrosis induced by heat shock in few seconds.74

The typical HIFU transducer generates a cylindrical focus with a diameter of 1.5 mm and a length of 1 cm in the direction of the wave. Adjacent to the focus, the temperature decreases rapidly, leading to histologically clearly-defined tissue coagulation.75 Several limitations are related to this method, including the delivery of small size of focus volume, necessitating multiple treatment sessions. Another limitation is the formation of microbubbles when high acoustic intensities are used, which interfere with the acoustic field.

Still, large randomized trials are needed before any conclusion can be made in the utility for clinical practice.

IRE

IRE was mainly used as electro-chemotherapy to affect the cell membrane permeability. IRE acts by generating very short electrical pulses that cause loss of membrane potential in human cells by destabilizing them, which subsequently causes formation of larger holes in the cell membrane that finally lead to cell death. Currently, IRE is extensively used in water decontamination and sterilization or preprocessing use; recently, its use in killing of tumor cells has been reported. The IRE technique has the ability to delineate the tumor borders by accurately applying electrical pulse to the tumorous tissue without affecting the adjacent healthy parenchyma; thus, the structures in proximity to the destroyed tissue by IRE are preserved.76–78

Selective internal radiation therapy (SIRT)

More recently, SIRT has been developed for use in HCC patients who are ineligible for other therapies, and specifically in cases such as lesions more than 7 cm in diameter, with vascular invasion and failure of prior TACE. In this technique, HCC are targeted via injection of microspheres, which are labelled with β-emitting radioisotope, such as 90Yttrium, which then delivers the radiation to the liver tumor.79 Several studies have been performed and reported various responses, including partial response, complete response and stable disease.

Salem et al.80 reported treatment with 90Yttrium in a single-center, prospective, longitudinal cohort study of 291 HCC patients. The 30-day mortality rate was 3%. Response rates were 42% and 57% based on World Health Organization and EASL criteria, respectively. The overall TTP was 7.9 months (95%CI, 6–10.3). Survival times differed between patients with Child-Pugh A and B disease (A, 17.2 months; B, 7.7 months; p = 0.002).80 Another study by Hilgard et al.81 reported complete response in 3% of patients, partial response in 37%, stable disease in 53%, and primary progression in 6% of the patients with HCC; the median overall survival was 16.4 months. Another study showed no differences between SIRT and drug-eluting bead TACE.82

Several adverse events have been associated with SIRT, including radiation pneumonitis and pulmonary fibrosis in the setting of hepato-pulmonary shunts.83 Furthermore, SIRT may cause gastrointestinal ulceration. The most common complication is post-radioembolization syndrome, which includes abdominal pain, nausea and fatigue. Fever is mostly transient, lasting up to 1 month after SIRT.84

It is important to accurately select HCC cases for SIRT as it was shown to be associated with radioembolization-induced liver disease, which is characterized by symptoms of liver failure in the absence of HCC progression. This syndrome arises from 1–2 months following procedures and is characterized by ascites and reduced liver function.84 Other less frequently reported adverse events include post-SIRT cholecystitis, abscess and bilioma, which occur in less than 2% of cases.85

In conclusion, SIRT is a promising treatment option for advanced unresectable HCC cases.

Sorafenib combined with TACE

The administration of conventional TACE led to increased survival rates of 80%, 43% and 23% at a time frame of 1, 3, and 5 years, respectively.86 Still, TACE limitation is the highest restriction rate, possibly due to the up-regulation of VEGF and platelet-derived growth factor receptor in hepatic tissues which consequently aggravates the process of angiogenesis. However, a prospective single-center study by Pawlik et al.87 which examined the application of combined TACE with doxorubicin-eluting beads and sorafenib in patients with advanced HCC showed a disease control rate of 95%, according to Response Evaluation Criteria in Solid Tumors Group, and 100% according to EASL, and an objective response rate of 58% according to EASL.

Another few clinical trials have shown promising results. Bai et al.88 has conducted a prospective nonrandomized controlled trial which compare the efficacy of sorafenib in combination with TACE versus TACE alone for the treatment of patients with unresectable intermediate, or advanced hepatocellular carcinoma. The combination significantly increased the median survival during a follow-up period of 21.4 weeks (7.5 vs. 5.1 months; HR = 0.61, 95%CI: 0.423–0.884; p = 0.009), as compared to the TACE group alone.88 Another multicenter retrospective study has shown similar results, with overall median survival being 12 months (95%CI: 10.1–13.9) in the sorafenib and TACE combination group.89 Given these promising data, sorafenib in combination with TACE should be considered for patients affected by advanced HCC.

Radiosurgery

The concept of radiosurgery was developed by Leksell in 1987.90 In this initial version (currently named the Gamma Knife), radiosurgery was used for radiation of brain lesions and upper spine, and recently, a computer assisted radio-surgical technique was developed that enabled treatment administration for other organs, such as liver.91 Thus, this CyberKnife System allows the administration of more focused stereotactic radiation based on real-time visualization of the target lesion. The advantage of radiosurgery is that it is capable of administration of radiation therapy to a well characterized tumor with preservation of the surrounding tissue.92 Previous studies have reported beneficial CyberKnife treatment for colorectal cancer metastasis.93,94 Radiosurgery, as well, might be used as a pre-surgical therapy for down-staging tumors that are not compatible for surgical resection.95 Moreover, radiosurgery can be used for preventing tumor growth during liver regeneration after surgical resection for HCC.96

Radiosurgery is an effective, feasible therapeutic option. This new emerging therapy is mainly useful for patients who are not eligible for surgery, and particularly for tumor down-staging before surgical procedures such as liver transplantation or surgical resection. Further randomized clinical trials are needed to examine the exact prognostic benefits in advanced HCC patients and to more fully delineate the effectiveness of radiosurgery compared to the traditional minimally invasive procedures such as RFA.

Liver Transplantation

The definitive treatment of HCC is liver transplantation, which allows for both treatment of the underlying liver disease and cure of the HCC.97 However, only a small proportion of patients receive a liver due to the strict criteria of liver transplantation in HCC patients (Milan criteria which include patients with one tumor of less than 5 cm or up to three tumors less than 3 cm) and the availability of organs.98 The 4-year survival rate of patients within Milan criteria was 75%.98 However, after a liver transplantation the risk of re-infection persists, and approximately half of the patients develop liver cirrhosis post-transplantation.46,99

To validate Milan criteria, a recent systemic review of 90 studies that followed 17,780 patients over a 15-year period identified the Milan criteria as an independent prognostic factor of outcome after orthotopic liver transplantation.100 A recent study showed an improved selection of patients with HCC for liver transplantation when adding alpha-fetoprotein and des-gamma carboxyprothrombin into the criteria.101 Furthermore, the University of California San Francisco (commonly known as UCSF) has prospectively and retrospectively utilized a newly defined criterion which includes several variables, a single lesion less than or equal to 6.5 cm, or three or fewer nodules with the largest lesion being less than or equal to 4.5 cm and with a total diameter of less than or equal to 8 cm. The UCSF 1- and 5-year survival rates were 90% and 75%, respectively.102 Similarly, the survival and disease recurrence rates were comparable to those of the Milan criteria.103 Another study by Dubay et al.104 found an excellent post-liver transplantation rate of any HCC size and number when aggressive ablative therapies were applied and when the histology ruled out poorly differentiated HCC.

Surgical resection

In HCC cases without signs of advanced liver fibrosis and portal hypertension, surgical resection is considered the treatment of choice. However, liver surgery in patients with chronic liver disease is associated with an increased risk of hepatic failure, especially after extended resection. Although surgical resection might be a curative option, it is limited by several factors, including high complication rates of blood loss, morbidity and mortality.105 HCC resection is also contraindicated in cirrhotic patients in advanced stages (Child-Pugh scores B and C or model for end-stage liver disease over 10). However, recent studies have reported a low mortality rate of less than 5% in cases of cirrhosis without evidence of portal hypertension.106,107

Due to the high rate of disease recurrence, the 5-year survival rates after partial hepatectomy for HCC range between 60% and 70%. The recurrence rate may be due to the formation of new HCC, or the presence of microvascular invasion or satellite nodules.108,109 Currently, the recommendation of EASL and the European Organization for Research and Treatment of Cancer guidelines7 state that surgery is restricted to those patients in the very early or early stages of disease (BCLC 0-A). Thus, the best candidates for surgical resection are patients with an isolated liver tumor, absence of radiological evidence of vascular invasion and patients with preserved synthetic liver function.110,111

Associated liver partition and portal vein ligation for staged hepatectomy (ALPPS)

ALPPS is considered as another surgical option for hepatic malignancy. The main advantage of ALPPS is future liver remnant (FLR) induction in short time period.112–114 Regenerative capacity is induced by several factors, including hepatic inflow redistribution after portal vein ligation, secretion of several hepato-proliferative factors by liver surgical procedure-induced inflammation that accelerate FLR growth, and transection of bilateral lobes of the liver, preventing collateral circulation formation and further increasing the hepatic inflow to the FLR.115 This advantage in ALPPS overcomes the surgical limitations in classic liver surgery, including technical impossibility when the right portal vein is invaded by tumor and unresectability of tumor due to extensive progression. Thus, the ALPPS procedure has achieved increased interest among liver surgeons.

ALPPS is however associated with complications, including biliary leakage and intraperitoneal infection.116 Overall mortality rate of 59%–64% and hospital mortality rate of 12–16% have been seen in association with ALPPS.115 Therefore, controversy exists regarding the use of this procedure in real clinical practice.117 Furthermore, the overall 90-day mortality of ALPPS according to the international ALPPS registry was 8.8%, in which 75% of deaths were related to acute liver failure that appeared following the surgery. Moreover, a model for end-stage liver disease score more than 10 was an independent factor to increased mortality.118

In current clinical practice, ALPPS might be considered in several clinical scenarios, as follows: inability of performing the classic conventional surgical approach due to portal vein involvement by HCC; progressive HCC where the risk for tumor progression is high between the two stages of the conventional surgical approach; and, in progressive HCC extension to the vena cava or even right atrium. Contraindications for ALPPS include inoperable hepatic metastasis in the FLR, significant portal hypertension and unresectable extrahepatic metastasis.119 Recent studies reported a high perioperative mortality rate of 31% for most HCC patients. Moreover, the evidence of the oncological endpoints and technical availability of ALPPS is scarce, thus this strategy should be considered in only a highly-selected patient population.120 Further studies are needed to examine the exact role of ALPPS in the setting of HCC.

Conclusions

Hepatocellular carcinoma is an aggressive tumor associated with a poor prognosis. Given its asymptomatic nature in the early stages, HCC is mostly diagnosed at advanced stages, often leading to incurable clinical situations. Current and prior treatment options were only modestly associated with increased survival. In fact, the survival benefit with sorafenib was only for a few months. Nowadays, newly emerging therapeutic targets, as well as new drugs and therapeutic modalities have been investigated in pre-clinical and clinical trials. Until the discovery of curative therapy, or at least drug development with significant survival benefit, clinicians should be careful to screen for HCC in cirrhotic patients and diagnosis should be done at early stages, so that if the HCC is identified soon enough for liver transplant, the outcomes will be quite good. Ongoing research should be performed on all potential HCC targets, including at the immunological, molecular and translational levels, in order to reduce the increasing HCC mortality.