Hepatitis B-related hepatocellular carcinoma:surveillance strategy directed by immuneepidemiology

Chimaobi M. Anugwom, Manon Allaire, Sheikh Mohammad Fazle Akbar, Amir Sultan, Steven Bollipo,Angelo Z. Mattos, Jose D. Debes,9,0

1Department of Medicine, Division of Gastroenterology, Hepatology and Nutrition, University of Minnesota, Minneapolis 55455,USA.

2Sorbonne Université, Service d’Hépatologie, Hôpitaux Universitaires Pitié Salpêtrière - Charles Foix, AP-HP, Paris 75103, France.

3Inserm U1149, Centre de Recherche sur l’Inflammation, France Faculté de Médecine, Xavier Bichat, Université Paris Diderot,Paris 75108, France.

4Department of Gastroenterology and Metabology, Ehime University Graduate School of Medicine, Toon 791-0295, Japan.

5College of Health Sciences, Addis Ababa University, Tikur Anbessa Specialized Hospital, Addis Ababa 5657, Ethiopia.

6Department of Gastroenterology, John Hunter Hospital, Newcastle, Australia & School of Medicine & Public Health, University of Newcastle, New South Wales 2310, Australia.

7Graduate Program in Medicine: Hepatology, Federal University of Health Sciences of Porto Alegre 90050-170, Brazil.

8Gastroenterology and Hepatology Unit, Irmandade Santa Casa de Misericórdia de Porto Alegre 90020-090, Brazil.

9Department of Medicine, Division of Infectious Diseases, University of Minnesota, Minneapolis, MN 55455, USA.

10Department of Gastroenterology & Hepatology, Erasmus MC, Rotterdam 3015-CE, Netherlands.

Abstract Hepatitis B infection (HBV) is one of the most common causes of hepatocellular carcinoma (HCC) worldwide. The age of occurrence, prognosis and incidence vary dramatically depending on the region of the world. This geographic variation is largely dependent on the contrasting incidence of HBV, age of transmission of the virus, the timing of integration into the human genome, and different HBV genotypes, as well as environmental factors. It results in a wide difference in viral interaction with the immune system, genomic modulation and the consequent development of HCC in an individual. In this review, we describe many factors implicated in HCC development,provide insight regarding at-risk populations and explain societal recommendations for HCC surveillance in persons living with HBV in different continents of the world.

Keywords: HCC, HBV, continent, risk

INTRODUCTION

Hepatocellular carcinoma (HCC) remains the most common primary liver malignancy and the third leading cause of cancer-related death worldwide[1]. Its distribution varies geographically and is dependent on the etiology of underlying liver disease. Non-alcoholic fatty liver disease (NAFLD) and alcohol-related liver disease are primary etiological factors in Western countries whereas hepatitis B infection (HBV) is the predominant culprit in Asia and Africa[2-4].

The role of HBV in the development of HCC is undisputed. Although the presence of cirrhosis is a major risk factor for development of HCC in patients with HBV, the tumor may also occur in the absence of advanced fibrosis. This particular feature of the virus to be a carcinogenper seis mainly attributed to the ability of the HBV DNA to integrate into the host cellular genome, thus inducing genetic damage among other factors[5,6].

According to the 2016 Polaris Observatory Study, the worldwide prevalence of chronic HBV is about 290 million[7]. This prevalence differs widely from one continent to the next, with 80% of the global burden represented by the African, Western Pacific, and Southeast Asia regions[8]. Furthermore, although the development of HCC may occur in up to a quarter of these patients, the incidence of HBV-related HCC also varies geographically [Figure 1]. In Asia, the incidence rate of HCC was 0.2 per 100 person-years in inactive carriers and 3.7 per 100 person-years in patients with compensated cirrhosis, compared to studies done in Europe where rates were 0.02 per 100 person-years in inactive carriers and 2.2 in those with compensated cirrhosis[9,10].

In addition to the inherent risk HBV infection conveys, there is also a multiplicative effect of heavy smoking and alcohol drinking in those with HBV infection, increasing the risk of HCC 9-fold in these individuals[11].It is clear that the prevalence of HBV-related HCC differs worldwide, and the associated immune and epigenetic factors lead a variable incidence and age of occurrence, so the surveillance strategies contrast from one continent to the next. Nonetheless, there are many similarities that underscore the significant health burden of this important health condition. In this review we provide specific insight into HBVassociated HCC in different regions of the world, provide focus on the most important target populations to be at higher risk due to alternate risk factors, and emphasize the recommendations of different liver societies in terms of HCC surveillance.

NORTH AMERICA

The healthcare burden of HBV-related HCC varies across countries in North America. As North America is mostly inhabited by individuals from all over the world, the etiology of HCC is therefore quite variable[12].Hepatitis C infection (HCV), alcohol-related liver disease and NAFLD remain the most common causes among non-immigrants populations. Immigration seems to be propelling the rates of HBV-HCC in North America as individuals from Asia and Africa with HCC commonly have a background of HBV infection[12-14]. Modification of environmental exposures driven by population movement and environment change appears to mitigate the early occurrence of HCC in HBV-infected individuals, but further research on this issue is required[14,15]. An outlier of the North American territory lies in the Alaskan region. Native Alaskans suffer some of the highest rates of HBV-related HCC and is one of the few non-immigrant populations in the world with 5 out of the 8 genotypes of HBV present[16]. Although aflatoxin exposure does not seem to be a prevailing additional risk factor, the presence of genotypes A and F1 has shown to confer a higher risk for HCC progression in this group[17]. In contrast, studies from Mexico suggest a low burden of HBV-HCC. NAFLD is recognized as a major risk factor in the country and thus, it is responsible for a large number of cases with cirrhosis and HCC[18]. Although a large group of HCC cases are also related to alcohol-associated liver disease and HCV, HBV is only implicated in a small number of cases[19-21]. This will be discussed in more detail in the section on Latin America.

Figure 1. Graphic indicating percentage of HBV-related HCC depending on the geographical area of the world.

The implementation of widespread vaccination programs, as well as the use of anti-viral therapy, has succeeded in considerably reducing the incidence of HBV-HCC in North America. However, the morbidity and mortality from HBV-HCC have been shown to be largely affected by suboptimal HCC screening in HBV patients as early detection of HCC increases the likelihood of curative therapies such as surgical resection and liver transplantation[22].

Target population

It’s difficult to predict HCC risk in patients with HBV. Scoring systems that may help stratify patients into low to high risk for HCC include the PAGE-B and the Toronto HCC risk index (THRI). The PAGE-B scoring system was studied to assess the patients’ platelets, age, and gender to calculate a 5-year risk of HCC in a cohort of Caucasian patients with chronic HBV treated with tenofovir or entecavir, showing a c-index of 0.82[23]. The THRI, with the aid of available clinical and laboratory parameters, also predicts the risk of HCC[24]. Despite the validation of these scoring systems, they are not widely used in North America and adherence to surveillance programs is key to detection and management of HCC[25].

Among patients with HBV, HCC surveillance should be instituted in all patients with cirrhosis, regardless of age or race. The American Association for the Study of Liver Disease (AASLD) includes HBsAg-positive adults at high risk for HCC, including Asian or black men over 40 years and Asian women over 50 years of age, persons with a first-degree family member with a history of HCC, or persons co-infected with HDV[26].

Guidelines from the Canadian Association for the Study of the Liver (CASL) are largely similar to those put forth by the AASLD; however, the age for commencement of screening in patients of African origin is 20 years, and the guidelines also include co-infection with HIV[13]. Screening and surveillance for HCC in Mexico is largely governed by the Latin-American association for the Study of the Liver (Asociación Latinoamericana para el Estudio del Hígado - ALEH). The ALEH develops guidelines for the Latin American region, so this will be discussed in detail in the section on Latin America.

Methodology and frequency of surveillance

According to the AASLD and CASL, the modalities for detection of HCC in HBV patients include transabdominal ultrasound scan (US) and measurement of serum alpha-feto protein (AFP). Although it is difficult to carry out a comparison between US and serum AFP in HCC surveillance, the addition of AFP to US seems to increase its sensitivity[26,27]. AFP may also be reserved for areas where US is absent or not easily accessible [Table 1].

Notwithstanding their well-known diagnostic accuracy, the cost effectiveness of cross-sectional imaging modalities such as the computed tomography (CT) scan and magnetic resonance imaging (MRI) in HCC surveillance has not been shown and therefore, these should be reserved for patients with suboptimal ultrasound results.

The frequency of surveillance for HBV patients at risk for HCC using US with or without serum AFP, is every 6 months[13,26].

LATIN AMERICA

According to the estimates of the World Health Organization for Latin America, liver cancer has the 9th highest incidence among all malignant neoplasms, with 39,495 new cases in 2020 (6.0/100,000 inhabitants).Moreover, it figures as the 6th cause of cancer-related deaths in the region, which was associated with 37,566 deaths in the same year (5.7/100,000 inhabitants)[28].

An initial Latin American survey looking at HCC which included 240 patients from 9 countries, found that 85.4% of patients had cirrhosis, and HBV infection was present in 13.7% of patients[29]. A larger study,including 1405 patients with HCC from 29 Brazilian centers (men accounting for 78%) showed a median age of 59 years for HCC diagnosis, with 98% of patients having cirrhosis and 18% having HBV[30]. In a more recent cohort from the South American Liver Research Network assessing 1336 patients with HCC from 14 South American centers, 68% of individuals were male, with a median age of 64 years, and HBV was associated with the liver disease in 14% of cases[31]. In that cohort, HBV association with HCC was higher in Peru and Brazil, and HCC was diagnosed in patients with HBV at earlier ages (38% under 50 years of age)than in those with other liver diseases[32]. It is also noteworthy that, in a Peruvian study, individuals developed HCC despite having low HBV DNA loads[33].

An underestimated situation associated with HCC development refers to occult HBV infection (OBI). It is possible that OBI leads to hepatocarcinogenesis through the integration of HBV DNA in liver DNA[34,35].Some studies have verified the presence of OBI among Latin American patients with HCC[33,36].

Some risk factors for hepatocarcinogenesis have been studied in patients with HBV in Latin America. The most common HBV genotype in the region is F, which has been associated with early-age HCC among Alaska natives[32,33,37]. Furthermore, the HBV A1762T/G1764A double mutant strain, which is associated with HCC development, has been described in Latin American populations, though in variable frequencies[33,38].Moreover, coinfection with hepatitis D virus (HDV) in this geographical region seems to be associated with much higher rates of complications of liver disease, including HCC, than in other regions. This might be attributed to the predominance of genotype 3 of HDV, which is exclusive of the north-western regions of South America, especially the Amazon Basin, and this genotype is specifically associated with a poorprognosis[39]. On the other hand, HIV co-infection does not seem to play an important role in the development of viral hepatitis-related HCC[40].

Table 1. Recommendations for HCC surveillance according to different societies

Besides properly treating HBV infection, some other measures are of great importance for preventing HCC development or improving its prognosis. The most relevant preventive measure is universal vaccination against HBV. In a Peruvian experience, HCC-related mortality decreased from 9.2 to 3.3/100,000 inhabitants after the institution of a vaccination program[41]. On the other hand, when chronic liver disease has been established, close attention must be paid to HCC surveillance. Unfortunately, in different Latin American cohorts, only half of all HCC cases were diagnosed while patients were under surveillance programs[29,31,42]. Nevertheless, when individuals were under surveillance, HCC was diagnosed in earlier stages[29,42,43], and survival rates were significantly higher[31,43].

Target population

Latin America is predominantly a continent of low and intermediate endemicity of HBV. Nevertheless, high prevalence can be found in some regions,especially in the Amazon Basin, including northern Brazil, Colombia, Peru and Venezuela[44]. ALEH recommends surveillance for HCC in patients with cirrhosis and in some at-risk populations infected with HBV. Nevertheless, its guidelines do not specify when surveillance should begin in patients with HBV who do not have cirrhosis[45]. Considering the early development of HCC in Latin American patients with HBV, it might be argued that the age for surveillance should probably be anticipated in relation to that of individuals of European ancestry and closer to what is recommended for Asian or African individuals[32]. In this context, the Brazilian Society of Hepatology, for instance, recommends surveillance for patients with HBV who have cirrhosis or other risk factors for HCC, such as Asian or African ethnicity, age over 40 years for men or over 50 years for women, family history of HCC in a first-degree relative, coinfection with HCV or HIV and association with NAFLD[46]. Moreover, other methods should be investigated to improve surveillance and early detection of HCC. PAGE-B risk score has shown good screening performance in Caucasian individuals infected with HBV[23]. As this score is based on easily available variables (platelet count, age and gender) and its use would not increase costs of the health systems in developing countries, it should be studied in Latin American cohorts. The Argentinian Association for the Study of Liver Diseases already suggests its use in order to identify patients who should be submitted to surveillance[47].

Methodology and frequency of surveillance

ALEH recommends surveillance for HCC preferably with semiannual ultrasound in patients with cirrhosis and in some other at-risk populations, among whom are individuals infected with HBV. According to its guidelines, AFP could be used as a biomarker in the absence of quality ultrasound[45]. However, it should be noticed that a recent meta-analysis has demonstrated an increase in sensitivity when both methods are used together[48]. As mentioned above, considering the early development of HCC in Latin American patients with HBV, it could be argued that the age for surveillance should probably be anticipated in relation to ancestry of the individual.

EUROPE

In Europe, the pattern of HCC occurrence shows geographical imbalance with higher incidence in southern Europe, especially in Bosnia and Herzegovina, Italy, France, Republic of Moldova and Romania, with the estimated age-standardized incidence rates in 2018 between 6.5 and 13.8 per 100.000[49]. In the last few decades, the increasing incidence of HCC is ascribed to the emergence of chronic liver disease due to HCV and NAFLD but also to an increase in HBV-related HCC, particularly among immigrants from countries with endemic HBV infection. About half of HCC is related to alcohol consumption in Central and Eastern Europe, and to HCV in Western Europe[50]. The proportion of HBV-related HCC is about 15%-20% across different European countries and seems to be more frequent in Eastern Europe and combined with HCV or HDV co-infection[49]. The prevalence of HBsAg chronic carriers in the general population ranges from 0.1%-7% in European countries with distinct geographic distribution of HBV genotypes. HBV genotype A predominates in Northern Europe and genotype D in Mediterranean countries[51]. In France, the incidence of HCC was 1768 new cases per year in 1980 and increased to 10,705 in 2017, with 44% of HCC due to alcohol, while HBV was responsible for less than 3% of cases[52]. In a French cohort of HBV patients, about two-thirds of them were from Africa or Asia and 13% were co-infected with HDV[53]. A similar trend was also observed in Italy[54].

Vaccination against HBV prevents HBV-related HCC occurrence and it is recommended for all new-born and high-risk groups[55]. Most European countries conduct universal immunization against HBV for neonates and infants. Nonetheless, some northern countries such as Denmark, Finland and Iceland among others have not yet introduced universal immunization against HBV due to the very low endemicity.

Target population

Surveillance for HCC should take into account the incidence in a specific set of individuals and the ease of access to curative therapy. In Europe, the majority of countries follow the HCC European Association for the Study of the Liver (EASL) guidelines proposed in 2018[49]. With HCC, the incidence is higher in more advanced liver disease and about 90% of HCC in Europe occurs on a background of cirrhosis. Costeffectiveness studies indicate that surveillance must be performed in patients with cirrhosis Child-Pugh stage A and B, as well as Child-Pugh C awaiting liver transplantation regardless of the cause of the liver disease. Recent advances in HBV therapy have led to high rates of sustained HBV-DNA suppression[56-58].However, effective HBV treatment reduces but does not eliminate the risk of HCC and surveillance should be continued in HBV patients with cirrhosis according to EASL guidelines[49].

In HBV patients without cirrhosis, the exact degree of HCC risk seems to be influenced by a series of viral parameters (high levels of HBV replication, genotype, and e-antigen seropositivity), individual features(male and older age), family history and geographical origin[59-62]. In fact, patients from Asia and Africa present higher risk of HCC, especially if they have been exposed to aflatoxin B1 or if they present a family history of HCC[63-65]. European guidelines do not recommend routine surveillance for patients with a family history of HCC. However, similar to AASLD guidelines, the French guidelines propose HCC screening in patients with HCC in a first-degree relative[66]. Different models have been proposed to evaluate the risk of developing HCC in HBV patients, but these studied Asian subjects and appeared suboptimal in Caucasian patients[67]. In Europe, the EASL guidelines recommend the use of the PAGE-B classification in Caucasian patients with or without nucleotide or nucleoside (NUC) treatment[49]. This scoring system (discussed above) stratifies HCC risk in HBV patients into three groups - low, intermediate and high risk; and those with a PAGE-B score < 9 rarely develop HCC under NUC therapy, and would not require surveillance[23]. It is important to note, however, that even if surveillance may not be indicated at initial observation, such patients should be assessed yearly to evaluate for any progression of HCC risk. In non-cirrhotic HBV patients, surveillance is recommended in those at intermediate or high risk of HCC identified by a PAGE-B score ≥ 10 and in patients with F3 fibrosis regardless of etiology based on individual risk assessment according to European guidelines[49].

Method and frequency of surveillance

When surveillance is indicated, the EASL guidelines recommends semi-annual ultrasound-based screening without serum AFP[49]. Surveillance every 3 months was not associated with an increase in overall survival in a French randomized series[68]. On the contrary, patients with a new diagnosis of HCC whose last screening ultrasound was more than seven months old presented with more advanced disease and decreased overall survival[69]. The use of biomarkers such as AFP, lectin-binding AFP-3 (AFP-L3) and des-gammacarboxyprothrombin (DCP), is not recommended in routine surveillance per EASL guidelines as they are suboptimal in terms of cost-effectiveness, but AFP in combination with ultrasound is recommended in the French guidelines[66]. Similar to American and Asian guidelines, CT scan and MRI should be performed only in patients with suboptimal ultrasound scans.

AFRICA

In Africa, HCC is a well-recognized scourge in the healthcare service. According to the GLOBOCAN report, an estimated 70,542 new cases and 66,944 deaths occurred from HCC in Africa in 2020[70]. However,HCC-related deaths are likely underreported in the area.

Most cases of HCC in Africa occur with a background of HBV infection which accounts for approximately 55% of cases[71]. A special scenario is in Egypt where HCV is the most common cause, representing 84% of HCC[71]. The reason for this is proposed to be the iatrogenic transmission of HCV during the era of injectable treatment for schistosomiasis[72].Other peculiar proposed etiologies for HCC are exposure for aflatoxin which is a common contaminant of grain products especially during storage period. The practice of open markets for grain and condiments in sub-Saharan Africa coupled with the high moisture content in storage contributes to elevated levels of the mycotoxin in food products[73]. Another recognized entity is African iron overload syndrome which is related to the methods used during alcoholic beverage preparation mainly in west Africa. In this case,metallic pots used to make these beverages are considered to contain high amount of iron and this leads to excessive iron overload overtime with excessive iron deposition in the liver which in turn leads to higher degrees of cirrhosis and malignancy. Homebrewed beer in this method contains iron in amounts of 46-82 mg/L compared to 0.5mg/L in standard commercial beers[74].

HCC in general is considered to occur at an early age in sub-Saharan Africa compared to the east Asia or western world. This is partly because HBV-associated HCC occurs earlier than that of other causes of liver disease[75,76]. Moreover, a study conducted in seven African countries has shown that HCC occurs at a median age of 46 in sub-Saharan Africa compared to 58 years of age in Egypt[71]. The reasons for this variation are not clear but proposed mechanisms are multifactorial combination of country of birth, early age of acquisition of HBV, integration of the virus, exposure to carcinogens, and specific HBV genotype or sub-genotypes[73].

Despite the substantial effect of HCC in the continent, management of the condition has been dismal.Outcome of therapy is limited by lack of therapeutic options and palliative therapy. In limited scenarios where therapy is available, mortality rates are higher compared to the rest of the world[75,77]. Because of this,emphasis is given to addressing the causes of HCC in particular viral hepatitis, with most providers focusing on early treatment of hepatitis as well as vaccination. A major obstacle in controlling HBV infection in Africa is the lack of provision of birth dose vaccination for HBV in most countries[78]. HBV vaccination has been incorporated in most routine Extended Program for Immunization (EPI) in Africa. However, in this program, the first dose is administered at 6 weeks of age and there is a potential window period of transmission before the administration of the vaccine[79]. It is thought that this initial approach was adopted to decrease costs and due to an early notion of low HBV transmissibility due to hepatitis B e antigen(HBeAg) negative prevalence. However, considering the poor coverage of antenatal screening of HBV in sub-Saharan Africa, the provision of the birth dose vaccine is considered to improve the prevention of HBV infection in the continent[80]. It should be noted though that a birth dose vaccine entails higher cost on the healthcare system as it requires cold-chain service, and this is a major limiting factor across the continent.

Target population

Target populations for HCC screening in the continent are patients with HBV infection and those with established cirrhosis. As discussed above, due to the young onset of HCC in the continent, the target age group is relatively larger, which incurs significant cost to potential screening programs. As a region per se all populations in Africa are at high risk for HBV-associated HCC. However, based on the known association of HBV and aflatoxin exposure leading to HCC, hot spot areas for aflatoxins should be a focus in terms of populations to specifically target, particularly regions where pre-harvest interventions to reduce aflatoxin in grain have not been implemented. In this regard, certain areas in Kenya and the Gambia are considered high in aflatoxins, but proper studies have not been performed in most regions of the continent[81,82].Historically, western Africa also bears a higher proportion of HBV-infected individuals and therefore this region should be a special focus for assessment and screening[83,84]. It is likely, however, that a vaccine-related epidemiological balance as well as intrinsic continental mobility has led to a more homogenous risk of HBV-related HCC in most of sub-Saharan Africa. Moreover, the relatively uniform spread of HIV and therefore HBV-HIV coinfection has also played a differential role in modifying the epidemiology. This is becoming clear with newer studies showing high incidence of HCC in eastern and southern regions of the continent[71,85].

Methodology and frequency of surveillance

There is a lack of continental bodies for recommendations of surveillance programs in Africa. In most scenarios, there is local adaptation of global guidelines with emphasis on local applicability vis-à-vis cost implication. The preferred screening methods for HCC in Africa similar to the rest of the world is ultrasound and AFP level[86]. Improvement in Ultrasound technology and the potential use of portable ultrasound machines do offer an opportunity to implement surveillance programs in the continent[87].Regardless, providing these machines across the continent as well as training of personnel requires a comprehensive effort and multilateral cooperation.

ASIA

Asia is the most populous continent in the world. Moreover, there is high heterogeneity throughout Asia in the health care delivery system, including infrastructure for diagnosis and surveillance, and the management of cancers[88,89]. Highly modernized health systems for the entire population are available in some Asian countries, such as Japan, Singapore, Hong-Kong, South Korea, and Taiwan. In contrast, knowledge,attitude, and performance (KAP) pertaining to health education is poor in many rich countries in the Middle East and the rest of Asia. Finally, considerable numbers of people in most south Asian countries may never be treated by a qualified doctor during their lifetime.

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The epidemiology of HCC due to HBV is poorly understood, as nationwide surveys on HBV or HCC have been performed in few Asian countries. Thus, a proper understanding of the epidemiology and surveillance of HBV-related HCC is lacking. Published studies and various observations have provided important information. According to a systematic review, Asia accounts for about 75% of all patients chronically infected with HBV worldwide[90]. Also, Asian and Middle Eastern countries are highly endemic for HBV,except Japan, Pakistan, Egypt, and Saudi Arabia[91]. Furthermore, hospital-based, general observational studies, and other well-designed studies have reported a marked increase in HCC-related annual death rates during the past two decades, and the majority of all HCC cases worldwide occur in the Asia-Pacific region[92]. HBV remains the primary cause of cirrhosis of the liver and HCC in Asian countries, despite the number of new HBV infections having decreased significantly in all Asian countries due to the use of vaccines and implementation of other prophylactic measures. The prevalence of HBV-related HCC is mostly lower in the northern and western parts of Asia. In contrast, HBV-related HCC is highly prevalent in China and southeast Asian countries. Taken together, the data indicate that HBV-related HCC is one of the major causes of liver-related morbidity and mortality in Asia[93]. Although the economic impact of HBV and HBV-related HCC is tremendous in Asian countries, policymakers have not acted uniformly to attenuate the increase in cases.

Target population

Transmission of HBV in Asia is mostly vertical, occurring either during birth, perinatally or within 5 years of birth. A male predominance of HBV-related HCC is prevalent, in common with other regions in the world. As a risk factor for the development of HBV-related HCC, aflatoxin can induce early development of HBV-related HCC in some Asian populations[94]. Another notable finding is the development of progressive liver disease, including HCC, in HBeAg-negative chronic HBV-infected patients. High levels of HBV DNA and increased levels of hepatitis B virus surface antigen (HBsAg) have been reported to be associated to HCC by some studies conducted in economically rich Asian countries, but no consensus has been reached regarding the significance of these findings[95,96].HBV genotype plays an important role in the progression to HCC in Asian populations. HBV genotype C is notorious for its association with cancer development. Several studies have reported that patients with HBV genotype C showing mutations in some regions of the HBV genome are more prone to develop HCC than patients with other genotypes lacking these mutations[97,98]. However, this has not been verified in many Asian countries or in cohorts with equally distributed genotypes across different environmental exposures.HBV genotype C is not prevalent in all areas of Asia, or even in all regions of some Asian countries.

Surveillance of HCC is important for containing HBV-related HCC. However, the hallmark of HBV-related HCC surveillance depends on detecting groups at risk. As many of the patients with chronic HBV infection have not been identified in most Asian countries, HBV-related HCC surveillance is the next step. Most Asian countries lack proper surveillance mechanisms for detecting HBV infection. Thus, most patients infected with chronic HBV are unaware of their infection status. Almost all Asian countries are signatories of “Elimination of Hepatitis by 2030”, a Sustainable Development Goals project of the United Nations.Some advanced countries in Asia, such as Japan, Singapore, Taiwan, and Korea, have established mechanisms to identify unknown HBV-infected patients, by various means, and ensure appropriate followup and management. China has made considerable progress with respect to combating HBV infection and HBV-related HCC. India, which has a huge population and a HBV burden, has failed to make similar progress. Several Asian countries with moderate-to-high levels of chronic HBV-infected subjects lack proper surveillance systems.

Methodology and frequency of surveillance

Surveillance of HCC in Asia generally follows the recommendation of Asian-Pacific Association for the study of the Liver (APASL). This includes hepatic ultrasonography, with or without measurement of AFP,performed every 6 months. This may be feasible in most parts of Asia through national- and internationallevel collaborations. In addition, assessment of DCP is recommended in some Asian countries, such as Japan as a routine procedure of surveillance. The cost-effectiveness of surveillance programs in Asian countries would likely be highly variable[99].

OCEANIA

Oceania refers to the geographic region with a total population of 41.5 million people that includes Australia, New Zealand (NZ), Pacific Island Countries and Territories (PICT), encompassing 22 countries.There is a high prevalence of HBV-related morbidity and mortality in the PICT as well as in the Aboriginal and Torres Strait islanders in Australia and Maori people of NZ with significant challenges when aiming for elimination of HBV[100].

While HBV in Australia and NZ is predominantly among people born overseas, there is also a disproportionately high HBV burden among the indigenous people (Aboriginal and Torres Strait islanders in Australia and Maori in NZ) similar to the situation among indigenous people globally. It is worth noting at this point that HBV Surface antigen (then called Australia antigen) was first documented among Aboriginal and Torres Strait island people in Australia[101]. While the prevalence of HBV is low in Australia at 1.0%, it is 4.11% in NZ owing to the higher proportion of indigenous people and those born in PICT[102].On the other hand, HBV has moderate to high endemicity ranging from 3% in some PICT to 23% in Kiribati[103].

Target population

A retrospective review in 2018 from NZ found that more than half of HCC related to HBV was diagnosed in late stages when curative options are no longer possible. A significant proportion of patients (26%) with advanced HCC related to HBV did not receive HCC surveillance prior to the diagnosis. In this study, the majority of the patients with HCC related to HBV were from Maori (39%), Pacific islander (34%) and Asian(20%) ethnicities. Much work is still needed in improving HCC surveillance in these ethnic and minority groups with healthcare disparities[104]. In a resource-poor Pacific island nation like Kiribati HBV and HDV co-infection is endemic placing a higher risk for HCC in this population. Moreover, there are significant challenges in infrastructure and healthcare functionality making regular HCC surveillance or HCC treatment beyond reach for most of the population[105]. Incidence of HCC continues to rise in Australia with disproportionate numbers in indigenous Australians who comprise 3.3% of the total population. More than 50% of HCC in Australia occurs in people born overseas and across culturally and linguistically diverse populations[102,103,106]. The high incidence of HCC among the indigenous people and those born overseas appears to be related to the high prevalence of HBV in these two groups. Indeed, the prevalence of HBV among indigenous Australians in Northern Territory estimated to be 6%. Data from the state of Victoria in Australia in 2012-2013 showed HBV-related HCC to be 22% of all cases[103]. Overall, available Australian data on HBV-HCC are comparable with global statistics on viral hepatitis-related HCC.

Methodology and frequency of surveillance

Recent Australian consensus recommendations include HCC surveillance (by ultrasound and AFP level)every 6 months among HBV patients with cirrhosis[107]. Screening with ultrasound and AFP every 6 months is also recommended in those with HBV but with no cirrhosis if they are in the appropriate age group from Asia, sub-Saharan Africa or from indigenous populations (Asian men older than 40 years, Asian women older than 50 years, people born in sub-Saharan Africa older than 20 years, aboriginal and Torres Strait Islander people older than 50 years)[103]. However, it is unclear that these recommendations do apply to resource-poor areas with high level of HBV-HDV co-infection such as Kiribati.

CONCLUSIONS

This review attempts to highlight the evident differences in HBV-related HCC across different regions of the world. A variety of important factors, including age of transmission of HBV, environmental factors,genotype and family history among others all contribute to different interactions between the immune system, genomic modifications and the occurrence of HCC at the individual level. It is unclear that different societies take into account the entire multitude of factors implicated in HCC risk in persons living with HBV when providing recommendations. These factors should be taken into account to properly survey HCC based on the individual risk of a population.

DECLARATIONS

Authors’ contributions

Wrote respective portions of the review for their continent: Anugwom CM, Allaire M, Bollipo S, Allaire M,Sultan A

Wrote the introduction, conclusions and designed figure and table: Anugwom CM, Debes JD

Overviewed and edited the entire manuscript: Debes JD

Availability of data and materials

Not applicable.

Financial support and sponsorship

This work was supported by Robert Wood Johnson Foundation, Harold Amos Medical Faculty Development Program, NIH-NCI R21 CA215883-01A1 and University of Minnesota AIRP grant, all to JDD.

Conflicts of interest

All authors declared that there are no conflicts of interest.

Ethical approval and consent to participate

Not applicable.

Consent for publication

Not applicable.

Copyright

© The Author(s) 2021.