Chronic hepatitis B in children and adolescents

Massimiliano Paganelli, Xavier Stephenne, Etienne M. Sokal

Pediatric Gastroenterology and Liver Unit, Cliniques St Luc, Universit Catholique de Louvain, Brussels, Belgium
Introduction
Hepatitis B virus (HBV) infection is still one of the most impor-
tant causes of liver disease, with 2 billion people infected world-
wide and more than 600,000 deaths each year, caused in 94% of
cases by chronic infection-related cirrhosis and hepatocellular
carcinoma (HCC) [13]. The World Health Organization (WHO)
estimates more than 360 million persons being chronic carriers
worldwide (6% of the world population). The incidence of HBV
infection has been declining over the last two decades thanks
to the introduction of universal immunization programs and
the implementation of blood-donor screening. Nevertheless, a
signicant number of adults and children are still infected each
year, the latter often developing chronic infection and requiring
an appropriate follow-up. In spite of a rather benign course of
chronic disease during childhood and adolescence, HBV chronic
carriers have a lifetime risk of developing HCC up to 25%, and
an incidence of cirrhosis of 23% per year [4]. Safe and partially
effective antiviral therapies are available, but few are licensed
for use in children, and an accurate selection of subjects to treat
and of the right timing for treatment is needed to optimize
efcacy and reduce viral resistance.
2012 European Association for the Study of the Liver. Published
by Elsevier B.V. All rights reserved.
Epidemiology
HBV is transmitted by percutaneous and mucous membrane
exposure to infectious blood, semen, vaginal secretions and saliva
[5]. The extreme resilience of HBV, allowing its survival for more
than a week on dry surfaces, explains the increased risk of hori-
zontal intrafamilial transmission and the need of carriers coun-
seling and household members vaccination [69]. Nonetheless,
after 20 years from the introduction of immunization programs,
most infants and children are protected against HBV [10], and
chronic carriers should not be isolated in schools or prevented
from practicing sports. Transmission occurs rarely in childcare
settings [7], but the risk is higher in detention centers, where
adolescents are less likely to be immunized and have high-risk
behaviors [11,12].
In highly endemic areas, infection occurs mainly in infancy
and early childhood, with mother-to-child transmission account-
ing for more than half of chronic infections. After exposure, the
risk of developing CHB is indeed higher for newborns (90%) than
for infants and children <5 years of age (2530%) or adolescents
and adults (<5%) [13,14]. To further reduce mother-to-child
transmission, WHO recommends the administration of both the
vaccine and hepatitis B immunoglobulins (HBIG) to newborns
of HBsAg-positive mothers within 24 h from birth (9098% pro-
tection rate) [7,1517]. HBIG administration to newborns of
HBeAg-negative mothers does not change the overall protection
rate but decreases the risk of fulminant hepatitis (higher in this
group), proving to be cost-effective [16,1820].
Newborns of highly viremic HBeAg-positive mothers are at
increased risk of HBV infection despite proper immunization
(breakthrough infection), compared to babies born to HBeAg-
negative mothers (16.8% vs. 1.6%), and are at increased risk for
chronicity [16,21]. Breakthrough infection is more likely to occur
in newborns of mothers with genotype C, who have higher viral
loads. Vaccination programs are therefore changing the HBV
genotype distribution [22]. Intrauterine infection, hyporespon-
siveness to vaccine, and vaccine escape mutants could play a role
as well [16,21,23,24]. The risk of mother-to-child transmission
also depends on maternal serum HBsAg titer and mode of deliv-
ery (10.5% for elective cesarean section vs. 28% for vaginal deliv-
ery) [21,25,26]. Vertical transmission can be further reduced by
treating highly viremic mothers during the last trimester of preg-
nancy with either lamivudine, telbivudine, or tenofovir (12% risk
reduction for lamivudine and 8% for telbivudine) [2730].
HBsAg and HBV DNA can be detected in breast milk of chronic
carriers, but no increased risk of transmission to a breastfed
infant has been shown and breastfeeding is currently recom-
mended after proper infant immunization [3133].
WHO has recommended universal HBV vaccination since
1991, with the rst dose to be administered within 24 h from
birth, followed by at least two doses at 1 and 6 months of life
[15,3436]. By the end of 2010, 179 of the 193 WHO member
states had implemented a nationwide childhood HBV immuniza-
tion program and global HBV vaccine coverage was estimated at
75% [37]. In countries where such programs have been imple-
Journal of Hepatology 2012 vol. 57
j
885896
Keywords: Chronic hepatitis B; Children; Epidemiology; Natural history; Vacci-
nation; Prevention; Treatment.
Received 29 October 2011; received in revised form 16 March 2012; accepted 20
March 2012

Corresponding author. Address: Department of Paediatrics, Universit Catho-

lique de Louvain, 10, Av. Hippocrate, 1200 Brussels, Belgium. Tel.: +32 2 764
1386/87.
E-mail address: [email protected] (E.M. Sokal).
Abbreviations: HBV, hepatitis B virus; HCC, hepatocarcinoma; HBIG, hepatitis B
immunoglobulins; CHB, chronic hepatitis B; ALT, alanine aminotransferases; cc-
cDNA, covalently closed circular DNA; WHO, World Health Organization; ULN,
upper limit of normal; IFN, interferon; FDA, Food and Drug Administration; VR,
virologic response; PegIFN, pegylated interferon.
Review
mented, prevalence of HBV infection decreased dramatically [38
40]. Many countries with high HBsAg seroprevalence (P8%)
before vaccination programs (like China and Taiwan) are now
considered at intermediate (27%) or low prevalence (<2%)
[38,4143]. In Taiwan, prevalence of HBsAg in children younger
than 15 years of age decreased from 9.8% to 0.5% after 20 years
of vaccination [42]. In China, HBsAg prevalence in children aged
114 years decreased by 83% (from 8% in 1992 to 1.36% in
2006) [44]. In a recent study, 4.6% of the total population of the
Unites States has been exposed to HBV (past or chronic infection),
with up to a 50-fold variation as age, ethnicity and country of
birth vary. HBsAg seroprevalence in children and adolescents
aged 612 years and 1317 years is 0.03% and 0.02%, respec-
tively. Prevalence of both exposure and chronic carrier state is
higher among people coming from high or intermediate preva-
lence countries, and among those with lower family income or
with high-risk behavior [45].
Although, among children born in Western Europe and North
America, prevalence of HBV infection is low, pediatricians and
hepatologists are confronted with an increasing number of chil-
dren adopted from higher prevalence countries (Table 1).
Between 2% and 5% of all internationally adopted children, all
coming from P2% prevalence areas, are still infected with HBV
[46,47]. CDC and American Academy of Pediatrics recommend
screening all children adopted from these countries for HBV
(HBsAg, HBsAb, HBcAb), at arrival and after 6 months, in order
to provide vaccination to those without protective antibody lev-
els (anti-HBs P10 mIU/ml) [15,48] or diagnose a previously
unknown infection and proceed to immunization of household
contacts [6,34,49].
Ten genotypes (AJ) and several subtypes have been described
for HBV, with a distinctive geographic distribution. Although in
most of Europe and North America, genotype A is predominant,
many of the children coming from high or intermediate endemic-
ity countries are infected with genotype B, C, D, or F (Table 1), are
at increased risk of complications and may have a worse response
to therapy [5052].
Natural history
Chronic HBV infection is dened as a positive HBsAg for 6 months
or longer. Chronic hepatitis B (CHB) in childhood is a mild dis-
ease, and infected children are mostly asymptomatic, have nor-
mal growth and a normal physical examination [53]. Most
perinatally infected subjects present a positive HBeAg and high
serum levels of HBV DNA, with normal or minimally elevated
serum alanine aminotransferases (ALT). A transplacental transfer
of maternal HBeAg has been proved both in mice and in humans,
and could elicit HBe/HBcAg-specic Th cell tolerance in utero
[40,5456]. Such an induced tolerance could explain the higher
chronicity rate in babies born to HBeAg-positive mothers and
the different rate of chronicity between neonatal and adult infec-
tion. The synthesis of large amounts of HBeAg by the wild type
virus could be necessary to maintain the tolerance [57]. This
immunotolerant phase is characterized by high viral replication
and little liver damage, although in Italian children, after 7 years
of disease, 710% of subjects showed severe hepatitis at liver
biopsy and 1.74.5% had cirrhosis [53,58]. It lasts 1030 years
when infection is acquired perinatally, whereas it is of minimal
duration in subjects infected later in life.
Viral mutants not capable of secreting HBeAg are then slowly
selected (pre-core mutants are detected in 89% of HBeAg-positive
patients) [59]. Selection seems to be secondary to an advantage of
such mutants over wild type HBV, as hepatocytes infected by the
latter are more susceptible to cytotoxic T lymphocyte-mediated
clearance [60]. Pre-core mutants selection leads to a lower secre-
tion of HBeAg. When the decreased amount of secreted tolerogen
is no more sufcient to maintain immunotolerance, the immune
system starts attacking infected hepatocytes [56,57]. ALT levels
rise, reecting the bioptic nding of necroinammation of liver
parenchyma, and HBV DNA levels uctuate. This phase of active
hepatitis leads to seroconversion to anti-HBe antibodies in 60
95% of patients on long-term follow-up [58,61]. ALT levels signif-
icantly increase before HBeAg clearance and may remain elevated
for 6 months after seroconversion [53,6264]. Up to 20% of
spontaneous seroconverters may have ALT are-ups in the years
following seroconversion, which seems to be more likely in
subjects carrying a pre-core mutant [63]. Spontaneous serocon-
version occurs earlier and more frequently in subjects who have
Key Points
Incidence of HBV infection declined over the last two
decades in countries where universal immunization
programs have been implemented
Newborns, infants and young children are at higher risk
for chronicity
To reduce mother-to-child transmission, newborns of
HBsAg-positive mothers should receive both the vaccine
and HBIG at birth
Vertical transmission of HBV to properly immunized
newborns (breakthrough infection) is an unsolved
problem, which is changing HBV genotype distribution
CHB in childhood is a mild disease but can lead to
The goal of antiviral therapy is to reduce the risk of
infection-related complications
Response to the few treatments currently available for
Decision to treat should weight the risk of disease
progression against side effects and the risk of
developing antiviral resistance
A chronic delay in licensing new drugs for children has
limited treatment options
Treatment with IFN should be considered for patients
with elevated serum ALT, high HBV DNA and moderate
Children in the immunotolerant phase should not be
treated outside of clinical trials
Pediatric clinical trials for telbivudine, PegIFN and
tenofovir are currently ongoing
cirrhosis and HCC in few, not yet well identified cases
children is partial and limited to specific subgroups
to severe fibrosis/inflammation at liver biopsy
Review
886 Journal of Hepatology 2012 vol. 57
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885896
acquired HBV horizontally than in those infected perinatally
(1416% vs. 45% per year) [53,58,62,65]. It usually occurs after
puberty, with about 90% of children <15 years of age still HBeAg
positive [65]. It was shown that boys with earlier-onset puberty
seroconverted at younger age (13 vs. 22 years), suggesting that
androgens play a role in this process [64]. Environmental factors,
such as nutritional status, have been suggested to inuence
immune response to HBV, accelerating seroconversion in children
after adoption from developing countries [62]. Genotype C and
maternal HBeAg-positive status were also associated with
delayed spontaneous seroconversion [24,61,62,6668].
HBsAg-positive, HBeAg-negative, and anti-HBe-positive
patients are considered inactive carriers, express absent or low
viral replication, with low or undetectable HBV DNA, and have
inactive liver histology, with normal ALT levels. Inactive carriers
with no signs of cirrhosis at seroconversion did not show pro-
gression to cirrhosis over 2429 year follow-up [53,58].
On the contrary, 15% of HBeAg-positive children developed
cirrhosis [53,58,69]. Between 2% and 5% of children with CHB
developed HCC during childhood [24,58,70]. Incidence of HCC
in high prevalence areas was signicantly reduced after the
implementation of immunization programs [71]. Children devel-
oping HCC are more likely to be males (70%), with cirrhosis (80%)
and undergoing early seroconversion, suggesting that necroin-
ammation during seroconversion to anti-HBe may be severe
and lead to cirrhosis and HCC [24,58,70]. Long-term risk of both
HCC and cirrhosis is directly correlated to viral replication and
serum HBV DNA levels [72,73]. The role of viral genotype on
the risk of developing HCC is still to be dened: in children,
80% of HCCs are present in cirrhotic genotype B patients, whereas
young adults with HCC are mostly non-cirrhotic [24,66]. In
adults, genotypes C and F increase the risk for HCC [66,7476].
Furthermore, such a risk is higher in persons with a family history
of HCC, and a new susceptibility locus has been recently
Table 1. Estimated HBsAg seroprevalence and HBV genotype in countries of origin of internationally adopted children. (See below-mentioned references for further
information.)
Country [Ref.] HBsAg prevalence
%
Predominant
genotypes
Adopted children per year
Total <16 yr United States
a
Italy
b
France
c
Canada
d
China [41] 7.2 1.8 B, C 3401 116 100 230
Russian Federation [149] 1.4-8 - D 1079 707 301 66
Ethiopia [150] 4.7 - A 2511 274 352 159
Haiti [151,152] 5 - A 133 0 992 94
Korea [153,154] 5.9 0.9 C 865 4 6 87
Colombia [155] 5.7 3.1 F 235 592 369 25
Vietnam [156] 10 7.5 B, C 9 251 469 29
Ukraine [157] 1-2 - D 450 426 59 35
Brazil [158,159] 1 0.8 A, D, F 26 318 13 1
Taiwan [16,42] 1.1* 0.5 B, C 282 3 3 6
India [160] 2-8 - A, D 241 124 21 36
Philippines [152] 10 - B, C 216 30 14 96
Poland [149,157] 1-2 - A 50 193 26 0
Nigeria [161-163] 4-12 12.4 E 189 5 23 6
Kazakhstan [164] 3.8 - D 181 28 46 45
Bulgaria [149] 2-7 - D 40 128 8 2
Ghana [165] 11.4 - A 117 0 2 9
Belarus [166] 4.8 - D 0 99 0 1
Cambodia [167] 8 2-14 B, C 0 87 2 1
Peru [149] 0.8-5.2 - F 35 83 1 3
Hungary [149] <1 - A, D 5 78 5 0
Others 993 584 692 261
Total 11,058 4130 3504 1192

Prevalence obtained from a study on 18-year old freshmen.

a
Data refer to year 2010 (Bureau of Consular Affairs, US Department of State. US Intercountry Adoption [Internet]. adoption.state.gov 2011; [cited 10.01.12] Available from:
http://adoption.state.gov/about_us/statistics.php). HBsAg seroprevalence in the United States is 0.27% (0.03% in 612 years old) [45].
b
Data refer to year 2010 (Commission for intercountry adoptions. Data and perspectives in intercountry adoptions in Italy. Report on les from January 1 to December 31,
2010. Commission for intercountry adoptions; 2011. Available from: http://commissioneadozioni.it/it/per-una-famiglia-adottiva/rapporto-statistico.aspx). HBsAg sero-
prevalence in Italy is 0.9% [168].
c
Data refer to year 2010 (Agence franaise de ladoption. Statistiques de ladoption international 2010. [Internet]. France Diplomatie 2011; [cited 10.01.12] Available from:
http://www.diplomatie.gouv.fr). HBsAg seroprevalence in France is 0.65% [169].
d
Data refer to year 2008 (HCCH Hague Conference Statistics. Canada: annual adoption statistics 20052009. [Internet]. HCCH 2012; [cited 10.01.12] Available from: http://
www.hcch.net). HBsAg seroprevalence in Canada is 0.30.6% (0.4% for preadolescents) [170].
JOURNAL OF HEPATOLOGY
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885896 887
described in 1p36.22 [77,78]. Seroconversion to anti-HBe reduces
the overall risk of developing HCC later in life, but an annual
incidence of 0.2% has been described in HBeAg-negative adults
(1.6% of asymptomatic HBsAg carriers) [79].
In 5% of anti-HBe-positive children, a pre-core mutant is
selected, with persistent viral replication, abnormal ALT levels
and histologically active hepatitis (HBeAg-negative chronic hepa-
titis). The latter progresses slowly in children, whereas adult
patients are at increased risk of cirrhosis and HCC [53,58,79,80].
A stronger immune response with a faster turnover of infected
cells could account for such an increased severity, and could be
secondary to the reducedsecretionof the tolerogenHBeAg [55,81].
In long-term longitudinal studies, it was shown that 714% of
inactive carriers lost HBsAg and became anti-HBs-positive. Spon-
taneous seroconversion to anti-HBs is a rare event in childhood
(1%/year and 0.6%/year in horizontally and perinatally infected
children, respectively) [53,58,62,80]. HBsAg clearance and anti-
HBs seroconversion mark the resolution of HBV infection, and
are accompanied by improved liver histology. Long-term progno-
sis after HBsAg seroclearance is excellent if it occurs before the
development of cirrhosis or HCC and in the absence of concomi-
tant infections [82]. Nevertheless, cccDNA persists indenitely in
hepatocytes, and low-level viral replication or reactivation upon
immunosuppression are still possible.
Who and when to treat
Even though several guidelines have been published by major
international societies on the management of adult patients with
CHB, treatment strategies for children are still evolving and are
mostly based on consensus of expert panels (Fig. 1) [8386].
Decision to start a therapy must take into account the mild evo-
lution of the disease during childhood for most of the patients
and the potentially severe complications in few, not yet well
identied cases, and it is complicated by the limited number of
drugs labeled for use in children.
The goal of the anti-HBV therapy, in children as in adults, is to
reduce the risk of progressive liver disease, cirrhosis, and HCC. It
can be achieved by suppressing viral replication through durable
HBeAg seroconversion and undetectable serum HBV DNA levels.
Reduction of viremia levels leads to decreased liver inammation
Children with CHB
Normal
ALT
Persistently elevated
ALT
HBeAg+ HBeAg-
High HBV DNA
Immunotolerant
phase
Low HBV DNA
Inactive carrier
Follow-up
Follow-up
Immune active
phase
Liver biopsy
Mild inflammation/
fibrosis
Moderate/severe
inflammation/
fibrosis
HBeAg+ HBeAg-
High HBV DNA High HBV DNA Low HBV DNA
Treatment
Family history
of HCC?
HBeAg- chronic
hepatitis
Exclude other
diagnosis
No Yes
Decompensated
liver disease
Fig. 1. Who and when to treat: algorithm for treatment of children and adolescents with chronic hepatitis B.
Review
888 Journal of Hepatology 2012 vol. 57
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885896
and subsequent normalization of ALT levels. The nal goal is anti-
HBs seroconversion, as it stops disease progression and reduces
the risk of HCC, although it occurs in a minority of treated sub-
jects [87].
Need for treatment should be evaluated at each follow-up
visit, in order to treat as soon as early signs of liver damage are
detected. Children with CHB should undergo physical examina-
tion and measurement of serum ALT, HBeAg/anti-HBe, and
alpha-fetoprotein levels every 6 months. ALT should be moni-
tored every 3 months at diagnosis (for 1 year) and if persistently
elevated, and every 12 months in HBeAg-negative patients with
low viral load (<2000 IU/ml). HBV DNA levels should be assessed
every 12 months, along with a complete blood count, a full liver
panel and a liver ultrasound [83,85,88]. Lifetime follow-up is
warranted even for inactive carriers, because of the risk of cirrho-
sis (7.8% of patients at 25 years), HCC (2.2%) and reactivation of
HBV infection, with seroreversion to HBeAg positivity (14% of
patients) or progression to HBeAg-negative hepatitis (1524%)
[79,89].
Decision to treat should be based on the following parame-
ters: ALT levels, HBeAg positivity, HBV DNA levels, liver histology,
family history of cirrhosis, and/or HCC, co-existing liver diseases,
and patients treatment history. Serum ALT level is the most use-
ful marker of liver damage and should be used to identify
patients who could be considered for possible antiviral therapy.
Published evidence suggests that patients with normal or mildly
elevated ALT respond poorly to available treatments [90,91]. Ben-
et of treating children with normal ALT has not been estab-
lished, and the risk of developing antiviral resistance could turn
it deleterious when considering the future of these patients
[92]. Therefore, children in the immunotolerant phase should
not be treated outside of clinical trials, and should be monitored
and treated when the increase of ALT levels reveals immune acti-
vation. The three largest clinical trials of antiviral drugs in chil-
dren used ALT levels higher than 1.5 times the laboratory ULN
or more than 60 IU/L, whichever was lower, as inclusion criteria
[90,91,93]. Unfortunately, the upper limit of normal (ULN) for
ALT levels has not yet been established for children [94].
Serum ALT level has to be elevated for at least 6 months
(12 months if HBeAg-negative), in order to avoid treating patients
who are undergoing spontaneous HBeAg seroconversion. Persis-
tent ALT elevation mandates assessment of serum HBV DNA lev-
els. High HBV DNA values warrant treatment, whereas low HBV
DNA levels should lead to the exclusion of other causes of liver
disease. The cut-off value for HBV DNA has not been dened,
and arbitrary values are used in clinical trials and guidelines. As
children have a higher HBV replication rate, a value of
20,000 IU/ml has been chosen by different authors [85,95]. How-
ever, lower values have been associated with progressive liver
disease in adults and latest management guidelines identied
2.000 IU/ml to be a good cut-off [83].
In adult patients older than 40 years of age, treatment can be
started solely upon detection of a high viral load, as it is an inde-
pendent risk factor of cirrhosis and HCC [72,73]. No data exist in
children to support such an approach. Therefore, as response to
currently available treatments for children is partial and limited
to specic subgroups, histologic assessment of the grade of
inammation and the stage of brosis remains recommended
before treating a child. Response to both interferon(IFN)-alfa
and nucleos(t)ide analogues is more likely when at least moder-
ate necroinammation or moderate brosis are found at liver his-
tology [90,96]. Although the benet of treatment has not been
established for children with mild inammation or brosis, a
family history of HCC may warrant treatment even in children
with mild histological changes, as they are at increased risk of
developing HCC [77].
There are other special populations of children at increased
risk of rapid disease progression (cirrhosis, HBV-related glomeru-
lonephritis, co-infection with HDV, HCV, or HIV). These patients
could benet from treatment even if ALT, HBV DNA levels, and
liver histology do not match the above listed cut-offs. An antiviral
treatment should be always considered in recipients of a liver
graft from an anti-HBc-positive donor and to prevent (or treat)
a recurrent HBV infection in children undergoing liver transplan-
tation [83,9799]. Furthermore, prophylactic treatment should
be administered to HBsAg-positive patients who have to receive
immunosuppressive or cytotoxic therapy, as it decreases the risk
of mortality and morbidity related to HBV reactivation [100].
Several studies conducted in adults showed a better response
to interferon for viral genotypes A and B, compared to D and C,
respectively [25,101103]. On the contrary, no signicant differ-
ence was found when nucleoside analogues were used [104]. No
studies have investigated the role of genotype on treatment
response in pediatric patients, and genotype determination
before treatment is not currently recommended [86].
Treatment options
The US Food and Drug Administration (FDA) approved four med-
ications for treatment of children with CHB: IFNa, lamivudine,
adefovir, and entecavir. IFNa can be used in children older than
12 months of age, lamivudine starting at 3 years of age, adefovir
in children aged 12 years and older and entecavir starting from
16 years of age. Each of these treatments, together with others
currently studied or used off-label in reference centers, has
advantages and disadvantages (Table 2), and different response
and resistance rates (Fig. 2).
Interferon-alfa
IFNa-2b has been the rst drug to be approved and it has been
used to treat CHB in children for about 15 years. Efcacy in chil-
dren is similar to that in adults. In the largest multinational ran-
domized controlled trial of IFNa therapy in children, 26% of
patients achieved virologic response (VR: undetectable HBV
DNA and loss of HBeAg) after 24 weeks of treatment, compared
to 11% of untreated controls, and an additional 7% responded dur-
ing the 24 weeks after treatment cessation. Response rate rose to
35% when only patients with ALT at least twice the ULN were
considered. ALT levels decreased in all responders, and they were
normal in 44% of cases at the end of treatment. Histological activ-
ity index improved in responders and loss of HBsAg occurred in
10% of treated children, as compared to 1.2% in the control group.
Likeliness of a response was associated with low HBV DNA levels
before treatment, younger age and female sex [90]. A better
response in young patients was subsequently conrmed in chil-
dren younger than 5 years of age [105].
IFNa is thought to simply accelerate seroconversion, as many
patients who do not respond to treatment may still seroconvert
to anti-HBe later in life. In three different series of 108, 107,
and 174 children with CHB, IFNa treatment was shown to
JOURNAL OF HEPATOLOGY
Journal of Hepatology 2012 vol. 57
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885896 889
accelerate HBeAg seroconversion, but treated and untreated
patients had a similar rate of HBeAg clearance at long-term fol-
low-up (Fig. 3) [53,62,106]. These data were conrmed in a
recent study on Asian children [107]. Furthermore, children of
Asian origin seroconverted slower than those of other ethnic ori-
gin, but they reached the same proportion of seroconversion in
the long-term [62]. In a series of 74 children followed-up for
7 years, treated patients with elevated baseline ALT levels
Table 2. Available treatments for chronic hepatitis B in pediatric age.
Treatment Licensing Dose Duration Advantages Disadvantages
IFN 12 mo 5-10 M units/m
2
sc
3 x/wk
6 mo No resistance
Usable in young children
Short treatment
Heavy side effects
Parenteral administration
Not usable if decompensated
cirrhosis or transplantation
Lamivudine 3 yr 3 mg/kg po
once daily
(max 100 mg/d)
1 yr Few side effects
Usable in young children
Oral administration
Usable in 3
rd
trimester of
pregnancy
High resistance rate (increasing with
time of treatment)
Adefovir 12 yr 10 mg po
once daily
1 yr
(+ 6 mo after HBeAg
seroconversion)
Partially effective in lamivu-
dine resistant patients
Oral administration
Not approved for children <12 yr
Emergence of resistant mutations
Entecavir 16 yr
+ Phase III
(2-17 yr)
0.5 mg/d once
daily (1 mg/d for
lamivudine-
resistant pts)
1 yr
(+ 6 mo after HBeAg
seroconversion)
Partially effective in lamivu-
dine resistant patients
Oral administration
Resistance rate on the long term
Not approved for children <16 yr
No available preparation for young
children
PegIFN Phase III
(2-18 yr)
180 g/wk 6 mo No resistance
Once weekly administration
Short treatment
Heavy side effects
Parenteral administration
Not usable if decompensated
cirrhosis or transplantation
Telbivudine Phase I
(2-18 yr)
600 mg/d
once daily
1 yr Few side effects
Oral administration
Usable in 3rd trimester of
pregnancy
High resistance rate
Tenofovir Phase III
(12-17 yr)
300 mg/d
once daily
1 yr High response rate
Few side effects
Oral administration
No resistance identified
Usable in 3rd trimester of
pregnancy
No available preparation for young
children
Reduced mineral density in children
pts, Patients.
80
70
60
50
40
30
20
10
0
%

o
f

t
r
e
a
t
e
d

p
a
t
i
e
n
t
s
Studies Author et al.,
Year,
[Ref.]
Wong,
1993
[171]
Jonas,
2002
[91]
Jonas,
2008
[93]
Marcellin,
2003
[173]
Dienstag,
1999
[172]
Chang,
2006
[134]
Lau,
2005
[174]
Marcellin,
2008
[142]
*No studies
IFN Lamivudine Adefovir Entecavir PegIFN Tenofovir
P A P A P A P A P A P A
Sokal
1998
[90]
* * *
Fig. 2. Comparison between available treatments in term of HBeAg seroconversion (light blue bars), undetectable HBV DNA (blue bars) and resistant mutations
emergence (dark blue bars). Pediatric clinical trials (P) are compared to studies on adult patients (A). (See below-mentioned references for further information.)
Review
890 Journal of Hepatology 2012 vol. 57
j
885896
showed a higher long-term seroconversion rate, whereas ele-
vated ALT at baseline did not signicantly inuence the long-
term natural seroconversion rate in untreated children [108].
HBsAg clearance was observed in 415% of children treated
with IFN (1525% of responders), compared to 010% of controls
[53,62,90,106108]. The difference in HBsAg seroconversion rate
between treated and untreated patients was shown to be signif-
icant in the randomized controlled trial, whereas none of long-
term studies was able to nd such a difference to be statistically
signicant. Nevertheless, children who responded promptly to
IFN were more likely to lose HBsAg than late or no-responders
[106].
Overall, although pediatric studies failed to show an impact of
treatment over time, large casecontrol studies and meta-analy-
ses in adults showed that IFNa reduced the risk of cirrhosis (RR
0.65) and HCC (RR 0.590.66) in the long-term [109111].
European consensus recommendations for IFNa treatment
suggest to treat HBeAg-positive children aged 2 years or older,
with abnormal ALT and low-intermediate HBV DNA levels. The
recommended regimen is 510 million units per square meter,
three times weekly for 6 months [86,112]. The benet of priming
with corticosteroids has not been proven [113,114]. IFNa is con-
traindicated in children with decompensated cirrhosis, cytopenia,
autoimmune disorders, cardiac or renal failure, and in trans-
planted patients [112]. As VR may be achieved in the 6 months
following the end of treatment, at least 612 months should pass
by before another therapy is started.
Side effects of IFNa treatment included fever and u-like
symptoms, behavioral disorders, gastrointestinal disorders and
neutropenia [90]. Furthermore, IFNa was shown to temporarily
affect growth [115]. All side effects resolve after treatment is
stopped.
Pegylated interferon-alfa (PegIFN) has not yet been approved
for the treatment of CHB in children. Polyethylene glycol addition
to IFNa enhances its half-life, allowing a once-weekly adminis-
tration. Such a formulation is licensed for the use in children with
chronic hepatitis C. In adults with CHB, PegIFN proved to have
superior efcacy than conventional IFNa, with the same safety
prole [116]. Clinical trials of PegIFN in children with CHB are
ongoing. Preliminary reports in children with HCV infection
showed that it was well tolerated, while leading to better
response rates than IFNa [117,118].
Lamivudine
Lamivudine is a pyrimidine nucleoside analogue approved for
children aged 3 years and older. In the largest pediatric random-
ized, controlled trial, VR was achieved by 23% of patients receiv-
ing lamivudine after 1-year treatment (compared to 13% in the
control group). Response increased to 35% when considering only
children with ALT levels of at least twice the ULN [91]. An open
label extension study was then carried out on the same cohort,
reaching a total of 2 or 3 years of treatment. At the end of the
extension period, response rate was 56% for children receiving
lamivudine in the absence of resistant mutations (being 5% in
patients with a YMDD mutant HBV). Resistance rate increased
over time (24% after 1 year of treatment, 49% at 2 years, and
64% at 3 years) [119]. Likeliness of response was greater in
patients with higher ALT levels and histologic activity index at
baseline. In children, no data is yet available on the long-term
impact of treatment with lamivudine (or any other nucleoside
analogue) on the natural history of the disease.
Lamivudine is well tolerated with no signicant side effects.
The recommended treatment dose is 3 mg/kg/day (maximum
100 mg/day), administered orally once daily. Such a dose pro-
vides levels of exposure and trough concentrations similar to
the 100 mg dose in adults [120]. Optimal treatment duration is
more difcult to determine. Published data suggest continuing
treatment until VR is achieved, and possibly for 6 months follow-
ing seroconversion [119]. As a longer treatment duration leads to
higher resistance rates, it is recommended to discontinue lamivu-
dine after 6 months if a complete suppression of viral replication
is not achieved or if YMDD mutations emerge. As post-treatment
ALT ares are possible, children should be carefully followed and
an alternative therapy should be started in the rare cases of
severe and protracted ALT elevation [121].
Combination of lamivudine with IFNa (either concurrent or
sequential) proved to be more effective that the single drugs alone
in adult patients with elevated ALT levels [122,123]. The two
drugs were shown to have a synergistic effect on cells in vitro
[124]. In children, fewer data are available. Three studies investi-
gated combined therapy in 32, 33, and 45 treatment-nave chil-
dren with elevated ALT levels. Although no difference was found
between different combination strategies, the children reached
3060% seroconversion to anti-HBe and 917% to anti-HBs
[125127]. An 8-week treatment with lamivudine followed by
10-month combination therapy with lamivudine and IFNhas been
tested on 23 immunotolerant children: complete suppression of
viral replication was achieved in 78% of subjects and 22% of chil-
dren seroconverted to anti-HBe. The concurrent administration of
IFNa appeared to be protective against mutations emergence
[128]. No difference was seen on histological response between
monotherapy and combined therapy [129]. As no large clinical
trials have been conducted so far, advantages of combination
therapy over monotherapy in children are still to be conrmed.
Adefovir
Adefovir dipivoxil is a purine analogue approved to treat
children with CHB aged 12 years and older. In a large pediatric
80
100
60
40
20
0
P
a
t
i
e
n
t
s

(
%
)60%
65%
94%
86%
80%
69%
86%
75%
35%
54%
Studies
Author et al.,
Year,
[Ref.]
Follow-up (yr)
n treated/
untreated
Bortolotti,
2000,
[106]
5
107/59
Marx,
2002,
[62]
13
27/147
Vo Thi Diem,
2005,
[108]
7
37/37
Iorio,
2007,
[53]
12
41/67
Hsu,
2008,
[107]
6
17/21
Fig. 3. HBeAg seroconversion rates in children treated with INF-alfa (light
blue bars) as compared to untreated subjects (dark blue bars). Differences
between the two groups in each study are not statistically signicant.
JOURNAL OF HEPATOLOGY
Journal of Hepatology 2012 vol. 57
j
885896 891
randomized controlled trial, 23% of patients aged 1217 years
achieved VR after 48-week treatment with adefovir (compared
to 0% of placebo-treated subjects). The efcacy on HBV DNA sup-
pression and ALT normalization was less evident in younger chil-
dren (15% vs. 3%), with differences between groups not being
statistically signicant [93]. Adefovir was well tolerated by chil-
dren of all age groups, with no resistance-associated mutation
registered. However, adefovir resistant mutations are reported
in more than 20% of HBeAg-positive adults after a 5-year treat-
ment [130]. A dose-dependent proximal renal tubular toxicity,
with occasional Fanconi-like renal tubular acidosis, is a known
side effect of adefovir, which has been rarely reported in adults,
but never in children. The nephrotoxicity is usually reversible if
the therapy is rapidly stopped [131,132]. The recommended dose
in patients 1218 years of age is 10 mg orally once daily [133].
Treatment duration has not been established, but experts agree
to continue for at least 6 months after HBeAg seroconversion.
Adefovir should be discontinued if a complete VR is not achieved
after 24 weeks or if a resistant mutation emerges. As with other
nucleos(t)ide analogues, patients should be monitored after dis-
continuation because post-treatment ares are not uncommon.
Entecavir
Entecavir is a carbocyclic analogue of 2
0
-deoxyguanosine that
proved to be more potent than both lamivudine and adefovir in
adult patients [134,135]. Furthermore, entecavir resistance is rare,
even after 5 years of treatment, and entecavir is active (although
less effective) on lamivudine-resistant strains [136138]. The
safety prole of entecavir is similar to that of lamivudine. Based
on adult studies, entecavir has been approved by the FDA for
treatment of adolescents aged 16 years or older. The recom-
mended dose is 0.5 mg once daily for nucleoside-nave patients
and 1 mg/day for lamivudine-resistant patients. A phase III clini-
cal trial in children as young as 2 years old is underway [139].
New drugs
Telbivudine is an L-nucleoside analogue with a potent antiviral
activity and a safety prole similar to lamivudine (although
myopathy and peripheral neuropathy were reported in adults)
[140]. Resistance rate is lower than lamivudine but higher than
adefovir. For such a reason, telbivudine is only used in combina-
tion with other antiviral drugs. A phase I clinical trial is ongoing
on children 218 years of age [141].
Tenofovir disoproxil fumarate is a nucleos(t)ide analogue
originally licensed for treatment of HIV infection, which is struc-
turally similar to adefovir and of equal antiviral activity. Never-
theless, as it proved to be less nephrotoxic than adefovir, the
approved dose for adults is higher than that of adefovir
(300 mg/day). For such a reason, tenofovir was shown to have a
greater antiviral activity than adefovir in clinical trials (undetect-
able HBV DNA in 76% of patients vs. 13% of adefovir-receiving
subjects after 48 weeks of treatment) [142]. After three years of
treatment, 72% of HBeAg-positive and 87% of HBeAg-negative
patients have HBV DNA levels <400 copies/ml [143]. The safety
prole of tenofovir is similar to that of adefovir, although associ-
ated with decreased bone mineral density in children with HIV
[144]. No genotypic resistance to tenofovir has yet been con-
rmed [143,145]. Tenofovir is currently used to treat HIV infec-
tion in children, and it proved to be well tolerated in phase I
studies conducted in patients 418 years of age [146,147]. As
there is no preparation suitable for young children, a phase III
trial is ongoing on 1217 year old CHB patients [148].
Proposition of a treatment scheme
Outside clinical trials, until new drugs are licensed for pediatric
patients, IFNa is still the drug of choice, unless decompensated
cirrhosis is present. The impossibility of developing a genotypic
resistance against such a drug is a big advantage, even though
adverse effects are more pronounced and a clear benet on the
long-term period remains to be conrmed. Furthermore, IFNa is
the only treatment licensed for treating children younger than
3 years of age, although patients in this age group requiring treat-
ment, are extremely rare. Currently available nucleos(t)ide ana-
logues are second-line therapies, as the risk of emergence of
resistant mutant strains is high. In adolescents older than
16 years of age, entecavir is the best choice, as resistance is less
likely. Such a risk is higher with both lamivudine and adefovir,
the latter being preferable in children aged 1215 years. The
use of lamivudine is currently limited to young children unre-
sponsive to IFNa, in special populations (co-infection with HIV,
transplant recipients or patients with HBV-related glomerulone-
phritis) or to prevent reactivation in children receiving immuno-
suppressive therapies. Combination therapy is promising, but
further data are needed in children.
Newer drugs such as PegIFN and tenofovir are extremely
promising and their licensing for children could change manage-
ment of pediatric CHB. As the emergence of resistant mutant
strains is becoming a major public health problem, pediatric
practitioners should refrain from treating children who are not
likely to benet from a licensed therapy and consider waiting
for safer and more effective drugs made available through clinical
trials or future market approval.
Conclusions
A dramatic reduction of pediatric HBV infection prevalence has
been observed in countries where global immunization programs
have been implemented. Nevertheless, an important number of
children are still infected every year. Prevention and manage-
ment of breakthrough infection, along with a better identication
of children at higher risk for disease progression and complica-
tions, are the current challenges.
Overall, management of pediatric patients with CHB is satis-
factory, but hampered by a chronic delay in licensing new drugs
as compared to adults. As the approval by regulatory agencies is
based on the completion of appropriate clinical trials, studies on
treatments that, in adults, have already been proved safe and
more effective than available drugs should be conducted without
undue delays. The current (2007) European regulation on medi-
cines for children offers the appropriate regulatory framework
to speed up this process.
Conict of interest
The authors declared that they do not have anything to disclose
regarding funding or conict of interest with respect to this
manuscript.
Review
892 Journal of Hepatology 2012 vol. 57
j
885896
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