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INTRODUCTION
In East Asia, hepatitis B virus (HBV) infection is endemic and its transmission occurs mainly via the perinatal mode during infancy and early childhood.12 Unlike horizontal infection during adulthood, vertical transmission progresses to chronic hepatitis B (CHB) infection in about 80%–90% of cases.1 Furthermore, HBV proliferation and liver damage remain sustained for many years. The cumulative percentage of children converting to the immune-reactive phase was reported to be 39.7% among patients aged < 18 years and 11.7% among those aged < 12 years.3 Therefore, continuous regular follow-up is necessary to ensure proper treatment and to minimize necro-inflammation and sequelae during the immune-active phase.14 Long-term lamivudine (LMV) treatment in children has significantly improved the seroconversion rate of HBeAg and HBsAg than interferon-alpha in children with genotype C; however, antiviral resistance occurs in 27.5% by 96 weeks of follow-up.56
Newly developed nucleos(t)ide analogues are currently being used, and these are known to have stronger antiviral activity and lower frequency of viral resistance during long-term use than previous drugs. Currently, entecavir (ETV) or tenofovir disoproxil fumarate (TDF) is the first-choice treatment in adults.789 In a randomized, placebo-controlled trial of adolescents with human immunodeficiency virus infection, TDF was effective in normalizing alanine aminotransferase (ALT) levels and suppressing HBV DNA, and was well tolerated not only by treatment-naive patients but also those with treatment experience.10
Nevertheless, TDF was not allowed in children younger than 12 years until now, and a 96 weeks' comparison of the efficacy of TDF and LMV has not been conducted yet in children. The aim of this study was to compare the therapeutic efficacy of TDF with that of LMV in children and adolescents with nucleos(t)ide-naive CHB, among whom genotype C is predominant.
METHODS
Baseline characteristics of patients
This retrospective cohort study involved four centers (Department of Pediatrics of Kyungpook National University Children's Hospital, Kyungpook National University Hospital, Seoul National University Children's Hospital, and Seoul National University Bundang Hospital) in Korea. Nucleos(t)ide-naive patients with CHB treated with TDF (TDF group) were sequentially enrolled from January 2013 to September 2016, when confirmed to be in the immune-reactive phase. The TDF group was compared with a historical control group of patients treated with LMV (LMV group) at Kyungpook National University Hospital from January 2005 to December 2009 (when TDF was not available for children).
Inclusion criteria (all of the listed criteria are mandatory):
1) Age > 8 but < 18 years.
2) HBeAg-positive or HBeAg-negative hepatitis in the immune-reactive phase.
3) Pretreatment HBV DNA level > 106 IU/mL.
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4) Immune-reactive phase, defined as pretreatment ALT levels more than two times the upper limit of the normal value persisting for
5) Refusal of patients to be enrolled in a concurrent global TDF trial (age 2–12 years)
Exclusion criteria:
1) Previous treatment with antiviral agents.
2) Treatment with corticosteroids, cytotoxic agents, or immunosuppressive drugs within the last 6 months.
3) Co-infection with other viruses such as cytomegalovirus, human immunodeficiency virus, Epstein-Barr virus, or hepatitis C virus.
4) Comorbidities with other liver diseases such as immune or metabolic disorders, or steatohepatitis.
5) Present enrollment in a TDF clinical trial (age 2–12 years).
Treatment protocol
The TDF group was compared with the historical control group (LMV group treated before TDF became available for children). TDF was given orally once daily at a dose of 8 mg/kg (maximal dose 300 mg, tablet). LMV was orally administered once daily at a dose of 3 mg/kg (maximal dose 100 mg, tablet or syrup). During all follow-up periods, adverse events were checked by using laboratory data and clinical assessments.
Monitoring
The duration of HBV DNA clearance (< 357 IU/mL) and titer decrements (> 3 log10 IU/mL), ALT normalization (< 40 U/L), and HBeAg loss were monitored after the initiation of each treatment and compared between groups. The detection limit for the HBV DNA assay was 20 IU/mL from 2009, whereas it was 357 IU/mL before 2009. The proportion of inadequate responders (> 2,000 IU/mL) was also compared at 24 weeks of treatment. The aspartate aminotransferase/ALT titers were monitored before and 4 weeks after the start of treatment, and follow-up measurements were conducted at intervals of 8–12 weeks. During the follow-up periods, serum HBsAg, anti-HBs, HBeAg, and anti-HBe levels were assessed by using a commercially available electrochemiluminescence immunoassay method (ARCHITECT PLUS; Abbott, Lake Bluff, IL, USA). The HBV DNA level was monitored by using real-time polymerase chain reaction (PCR) (Exicycler™ 96; BIONEER, Daejeon, Korea; detection limit 20 IU/mL).
Definition of response
Virologic response was defined as an undetectable HBV DNA level as determined with real-time PCR assay (< 357 IU/mL). Virologic breakthrough was defined as a confirmed increase in HBV DNA level of > 1 log10 IU/mL in comparison with the nadir (lowest value) HBV DNA level during treatment. Complete response was defined as the combination of HBeAg loss, HBV DNA clearance, and normalization of the ALT level after the start of treatment.
Statistical analysis
Data were analyzed by using χ2 test or Fisher's exact test to examine the significance of the association between categorical variables. Independent t-tests or Welch's t-tests were performed for the comparison of continuous variables such as age, HBV DNA values, and pretreatment ALT.
All statistical analyses were performed with statistical software (Statistical Package for the Social Sciences, version 18; SPSS Inc., Chicago, IL, USA). A P value of < 0.05 was defined as statistically significant.
Ethics statement
Written informed consent was obtained from the TDF group, but not obtained from the LMV historical control group. The study protocol was reviewed and approved by Institutional Review Boards of Kyungpook National University Medical Center (IRB file No. 2016-12-025) and Seoul National University Hospital (IRB file No. 1608-032-783).
RESULTS
Baseline characteristics
Sixteen patients (male:female, 6:10; age range, 10.1–17.5 years; mean ± standard deviation [SD], 14.1 ± 2.1) were enrolled for TDF treatment. The historical control group was composed of 24 patients (male:female, 14:10; age range, 8.0–15.2 years; mean ± SD, 12.5 ± 1.9) treated with LMV at Kyungpook National University Hospital from January 2005 to December 2009 before the TDF era.
The baseline demographics of the subjects are shown in Table 1. Except for age, there was no statistically significant difference between the groups in HBV DNA values, pretreatment ALT, or sex. The mean pretreatment HBV DNA level of four HBeAg-negative patients in the TDF group was 7.4 ± 0.5 log10 IU/mL (range, 6.6–7.8 log10 IU/mL), which was not statistically different from the mean level in HBeAg-positive patients in the TDF group (7.3 ± 0.7 log10 IU/mL; range, 6.1–8.2 log10 IU/mL; P = 0.777). The mean (± SD) age at treatment was 14.1 ± 2.1 years in the TDF group and 12.5 ± 1.9 years in the LMV group (P = 0.020). All 16 patients in the TDF group and 24 patients in the LMV group were followed for 96 weeks.
Table 1
Baseline demographics of the TDF- and LMV-treated CHB groups
ALT level
The mean pretreatment ALT level was 224 ± 161.2 U/L (range, 81–619 U/L) in the TDF group, whereas the mean level was 178.3 ± 118.6 U/L (range, 81–597 U/L) in the LMV group. The pretreatment ALT levels of biopsy-proven patients were all > 80 U/L.
By week 24, the proportion of all patients who had normal ALT levels was 93.8% (15/16) in the TDF group and 95.8% (23/24) in the LMV group (P = 0.767). ALT normalization (< 40 U/L) was achieved in both the TDF and LMV groups: 93.8% (15/16) and 100% (24/24) at 48 weeks (P = 0.215), and 100% (16/16) and 62.5% (15/24) at 96 weeks (P = 0.007) (Fig. 1).
Fig. 1
Proportion of patients among HBeAg-positive and HBeAg-negative patients receiving TDF versus those who received LMV who achieved virologic, biochemical, and serologic responses at 48 and 96 weeks.
TDF = tenofovir disoproxil fumarate, LMV = lamivudine, HBV = hepatitis B virus, CHB = chronic hepatitis B, ALT = alanine aminotransferase.
aComplete response: HBeAg negativization and HBV DNA clearance (< 357 IU/mL) among HBeAg-positive patients with CHB.
Antiviral potency of TDF compared with LMV
HBV DNA clearance (HBV DNA level < 357 IU/mL)
The HBV DNA clearance (< 357 IU/mL) in the TDF and LMV groups, respectively, was as follows: 62.5% (10/16) and 25.0% (6/24) at 12 weeks (P = 0.018), 81.3% (13/16) and 37.5% (9/24) at 24 weeks (P = 0.006), 93.8% (15/16) and 50.0% (12/24) at 48 weeks (P = 0.004), and 100% (16/16) and 54.2% (13/24) at 96 weeks (P = 0.002) (Fig. 1).
Mean duration for HBV DNA clearance
The mean duration for HBV DNA clearance (time interval between treatment initiation and HBV DNA becoming < 357 IU/mL) was 22.5 ± 18.0 weeks in all 16 patients (100%) of the TDF group; however, it was 27.7 ± 19.8 weeks in only 54.2% (13/24) of the LMV group (P = 0.467). In the comparison of 16 HBeAg-positive and HBeAg-negative patients of the TDF group and 21 HBeAg-positive patients of the LMV group, the mean duration for HBV DNA clearance was 22.5 ± 18.0 weeks in 100% (16/16) of the TDF group and 30.5 ± 20.3 weeks in 52.4% (11/21) of the LMV group (P [duration/proportion] = 1.000/0.036) (Table 2). Among HBeAg-positive patients, the mean duration for HBV DNA clearance was 26.0 ± 19.7 weeks in 100% (12/12) of the TDF group and 30.5 ± 20.3 weeks in 52.4% (11/21) of the LMV group (P [duration/proportion] = 0.592/0.004) (Table 3).
Table 2
Duration of treatment and proportion of patients for HBV DNA decrement among HBeAg-positive and HBeAg-negative patients with CHB
Table 3
Duration of treatment and proportion of patients for HBV DNA decrement and HBeAg negativization, among HBeAg-positive patients with CHB
Mean duration for HBV DNA titer decrement > 3 log10 IU/mL
The mean duration for HBV DNA titer decrement (> 3 log10 IU/mL) was 15.0 ± 9.3 weeks in all 16 patients (100%) of the TDF group; however, it was 14.5 ± 5.0 weeks in 79.2% (19/24) of the LMV group (P = 0.857). HBV DNA decrement (> 3 log10 IU/mL) was achieved in 100% (16/16) of patients in the TDF group, but in only 62.5% (15/24) of patients in the LMV group at 48 weeks after the initiation of treatment (P = 0.005). In the comparison of 16 HBeAg-positive and HBeAg-negative patients of the TDF group and 21 HBeAg-positive patients of the LMV group, the mean duration for HBV DNA titer decrement (> 3 log10 IU/mL) was 15.0 ± 9.3 weeks in 100% (16/16) of the TDF group and 15.0 ± 5.4 weeks in 76.2% (16/21) of the LMV group (P [duration/proportion] = 1.000/0.036) (Table 2). Among HBeAg-positive patients, the mean duration for HBV DNA titer decrement (> 3 log10 IU/mL) was 16.0 ± 10.7 weeks in 100% (12/12) of the TDF group and 15.0 ± 5.4 weeks in 76.2% (16/21) of the LMV group (P [duration/proportion] = 0.770/0.067) (Table 3).
Inadequate virologic suppression and partial virologic response
Inadequate virologic suppression (> 2,000 IU/mL) at 24 weeks' follow-up was noted in 12.5% (2/16) of the TDF group and 54.2% (13/24) of the LMV group (P = 0.008). Partial virologic response (357–2,000 IU/mL) was observed in 6.3% (1/16) and 12.5% (3/24) of patients at 24 weeks (P = 0.519).
Serology
Among patients who were HBeAg positive at baseline, 12.5% (2/12) in the TDF group and 23.8% (5/21) in the LMV group achieved complete response (HBeAg loss and HBV DNA < 357 IU/mL) by week 48 (P = 0.629), and 41.7% (5/12) of the TDF group and 28.6% (6/21) of the LMV group achieved complete response by week 96 (P = 0.443) (Fig. 1). Only one child showed HBsAg loss in the LMV group at 43 months after treatment; however, no patient achieved HBsAg and anti-HBs seroconversion until the last follow-up after 96 weeks. Among HBeAg-positive patients, the mean duration of HBeAg negativization was 11.6 ± 8.4 weeks in 41.7% (5/12) of the TDF group and 28.0 ± 23.1 weeks in 28.6% (6/21) of the LMV group (P [duration/proportion] = 0.210/0.443) (Table 3).
Adverse events
There was no adverse event related to treatment during the study period in the TDF group; however, one patient in the LMV group had peripheral neuropathy. Decrement of bone mineral density was not monitored through bone densitometry (dual-energy X-ray absorptiometry scan).
Antiviral resistance and long-term follow-up monitoring
Cumulative antiviral resistance occurred in 33.3% (8/24) and 41.7% (10/24) in the LMV group at 96 and 144 weeks of follow-up, respectively. Their treatment was switched to another option including tenofovir rescue therapy.
Until 192 weeks of treatment start, 8 of 24 patients had achieved complete response and 13 of 24 patients had confirmed mutations in the LMV group. Furthermore, the treatment protocol was changed, such as adding adefovir (or tenofovir) or switching to ETV (+/− adefovir or tenofovir), in 15 patients. In the TDF group, there was no viral mutation until up to 192 weeks of follow-up.
DISCUSSION
This is the first study to evaluate the effectiveness of TDF among children, including those aged < 12 years, with CHB in real-life clinical practice. Although there are data on the effectiveness of TDF over placebo from a randomized clinical trial in adolescents with CHB,10 there is currently no relevant data concerning children < 12 years old and no comparison data with the old treatment protocol with LMV. Our study revealed that TDF monotherapy was more effective than LMV monotherapy (historical control) in children with CHB.
In the era of newly developed nucleos(t)ide analogues, TDF and ETV are the first-choice treatment for CHB in adults because of their long-term efficacy and safety.111213 The Food and Drug Administration has approved ETV for children > 2 years old in 2012 and TDF for children > 12 years old in 2015.1014 However, the therapeutic potency and long-term efficacy of TDF compared with LMV have not been previously studied in children.
In the aspect of suppression of HBV DNA, the results of this study were relatively better than those of previous adult studies on TDF.151617 In this study, the proportion of virologic responses was 81.3%, 93.8%, and 100% at 24, 48, and 96 weeks, whereas adult studies reported a virologic response rate of 22.8%–49% at 24 weeks, 71.5%–92% at 48 weeks, and 96% at 96 weeks. The proportion of viral suppression (> 3 log10 IU/mL) was better with TDF than with LMV, among HBeAg-positive and HBeAg-negative patients with CHB.
Our results confirmed that the antiviral efficacy of TDF in children correspond to what has been observed in adults.1618 The rate of complete response was 12.5% (2/12) at 48 weeks and 41.7% (5/12) at 96 weeks after treatment. The reported results from adult studies in Korea and that in Western countries are similar. Kim et al.19 reported that 15.2% achieved an absence of serum HBV DNA and detection of anti-HBe after 12 months of TDF treatment among nucleos(t)ide-naive patients with genotype C CHB. On the other hand, other Korean adult studies reported 3.8% and 9.8% rates of HBeAg loss or seroconversion to anti-HBe at 12 months.1520 Marcellin et al.16 demonstrated a rate of HBeAg seroconversion of 21% at week 48. Idilman et al.21 reported that the cumulative probability of HBeAg loss increased from 16.8% at 1 year to 27.6% at 2 years of TDF therapy. In other long-term studies, HBeAg loss was observed in 34%–45% and HBeAg seroconversion was observed in 25% at 3 years.1722
Long-term treatment with LMV is effective in the aspects of HBV DNA clearance, HBeAg seroconversion rate, and ALT normalization in children, and is capable of achieving HBsAg seroconversion in toddlers.5 However, the use of LMV has been restricted by its propensity to lead to the development of treatment-resistant viral mutations. Treatment-resistant mutations were reported in 10%–19% of children treated with LMV for 1 year and in 23%–69.4% after 2 years.52324
In the aspect of insurance coverage, ETV and TDF has been allowed in Korean children since 2015; thus, some strategies were applied for LMV-resistant children between 2012 and 2015.17 Although TDF is now available for children > 12 years old, LMV is still considered effective for children < 6 years of age in Korea where genotype C is predominant.25 A global study on the efficacy and safety of TDF in children between 2 and 11 years old is ongoing.
Despite concerns on adherence to treatment among children and adolescents,26 no viral breakthrough developed in the TDF group in this study. All cases of virologic breakthrough were related to nonadherence to TDF dosage in an adult study,27 with evidence of no phenotypic or genotypic drug resistance at 144 weeks of follow-up of TDF monotherapy.28
The one patient who did not achieve ALT normalization was thought to have nonalcoholic fatty liver disease because of persistent central obesity during the treatment period. TDF therapy for patients with CHB in Asian countries showed no significant difference compared with studies in Western countries where genotypes A and D prevail.19293031 Although genotypes were not identified in this study, genotype C is nearly 100% prevalent in Korea, where vertical or perinatal infection is the main transmission route.3233 However, the results of this study imply that the therapeutic effect of TDF in children is excellent independent of the genotype.34
This study has some limitations. The first limitation is the relatively small number of patients included. However, these patients could represent the national data because of the extremely low HBV prevalence in Korean children. Selection bias could be present because concurrent enrollment into a TDF phase 3 study was ongoing during this study period, although phase 3 trial participants were not enrolled in this study. Second, the enrolled patients in the TDF group were older than those of the LMV group, and age could negatively affect the therapeutic efficacy of TDF.5 However, despite these limitations, the outcomes in the TDF group were better than those in the LMV group. Nevertheless, this is the first study to evaluate the efficacy of TDF in real-life clinical practice among children with CHB.
In conclusion, TDF therapy in nucleos(t)ide-naive children and adolescents was highly effective for antiviral suppression compared with LMV in real-life clinical practice. No resistance to TDF was observed through 96 weeks. TDF has a higher genotypic barrier to resistance than LMV for children with genotype C.
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