Abstract
Purpose
This study aimed to clarify the long-term efficacy of the lamivudine treatment in Japanese patients with chronic hepatitis B either with or without lamivudine resistance or with or without adefovir add-on treatment.
Methods
We followed 110 patients who received lamivudine for more than 12 months, including 67 hepatitis B e antigen (HBeAg)-positive and 43 HBeAg-negative patients.
Results
The median follow-up after the onset of lamivudine was 48 (range = 12–86) months. In all the patients with or without lamivudine resistance, the level of alanine aminotransferase (ALT) normalization decreased from 70.0% at 1 year to 36.4% at 5 years and the loss of serum HBV DNA level decreased from 72.7% at 1 year to 31.8% at 5 years. Sixty patients (54.6%) developed a lamivudine-resistant mutation, and this occurrence was more frequently observed in those who were HBeAg-positive (P < 0.01), those with a low level of ALT (P < 0.05), and those with a high level of serum HBV DNA (P < 0.01). Thirty-six of 60 patients received adefovir in addition to lamivudine to treat breakthrough hepatitis. A Cox proportional hazards model analysis revealed the level of baseline HBV DNA to be the best predictive factor for the virus recrudescence (risk ratio = 0.466, 95% confidence interval [CI]: 0.246–0.842, P = 0.011) and the breakthrough hepatitis (risk ratio = 0.444, 95% CI: 0.218–0.879, P = 0.019). We carefully monitored the efficacy of this treatment both in patients who received adefovir and in those who did not since the beginning of the lamivudine treatment. The normalization level of ALT was 61.4% at 5 years and the loss of serum HBV DNA was 61.4% at 5 years since lamivudine was started. A histologic improvement was observed in patients with ALT levels less than two times the upper limit of normal at the time of a second liver biopsy.
Conclusions
Although the efficacy of lamivudine is limited because of breakthrough hepatitis, adefovir was used as a salvage treatment of patients with lamivudine-resistant chronic hepatitis B. In addition, lamivudine was used for the treatment of Japanese patients with chronic hepatitis B with or without lamivudine resistance, and was found to be useful regarding the long-term virologic and biochemical responses.
Keywords: Chronic hepatitis B, Lamivudine, Adefovir
Introduction
The number of patients chronically infected with hepatitis B virus (HBV) is reported to be more than 350 million worldwide [1, 2]. These patients are at an increased risk to develop cirrhosis, hepatic decompensation, and hepatocellular carcinoma [3, 4]. The aims of treatment of chronic hepatitis B are to achieve a sustained suppression in HBV replication and remission in liver disease. The endpoints used to assess the treatment response include the normalization of the alanine aminotransferase (ALT) level, the loss of serum HBV DNA, the loss of hepatitis B e antigen (HBeAg) with or without the detection of antibody to HBeAg (HBeAb), and an improvement in the liver histology.
Interferon, which has been shown to have an antiproliferative effect on the virus, has been used for the treatment of chronic hepatitis B; however, its efficacy has been limited to only a small percentage of preselected patients [5, 6]. Lamivudine is the first nucleoside analog to be approved for the treatment of the patients with chronic hepatitis B. Although the short-term efficacy of lamivudine therapy has been well documented, the occurrence of lamivudine-resistant mutations has also been reported to increase with extended use [7–9]. Adefovir dipivoxil is a nucleotide analogue of adenosine monophosphate and has been shown to be effective in suppressing not only wild-type HBV but also lamivudine-resistant HBV [10, 11].
Lamivudine has been used in Japan since November 2000 for the treatment of patients with chronic hepatitis B. Since December 2004, adefovir, which decreases the incidence of lamivudine-resistant mutations, has been administered to patients demonstrating a flare-up of hepatitis. The aims of this study were to clarify (1) the long-term efficacy of the lamivudine treatment of Japanese patients with chronic hepatitis B with or without adefovir add-on treatment of breakthrough hepatitis due to lamivudine resistance, (2) the rate of both occurrence of the lamivudine-resistant mutant virus and recurrence of hepatitis related to the lamivudine-resistant virus, and (3) the long-term consequences of the lamivudine and adefovir combination therapy for chronic hepatitis B.
Patients and methods
Eligible patients were enrolled at Fukuoka University Hospital. The key inclusion criteria were seropositivity for hepatitis B surface antigen and serum HBV DNA. Both HBeAg-positive and HBeAg-negative patients were included. Lamivudine was administered orally at a dose of 100 mg daily for the treatment of the patients who had elevated ALT levels, namely, more than 1.5 times the upper limit of normal. Exclusion criteria included decompensated liver disease, a coexisting serious medical or psychiatric illness, a history of alcohol or drug abuse within 1 year before entry, and coinfection with hepatitis C virus or human immunodeficiency virus, and advanced hepatocellular carcinoma. We examined the effects of the lamivudine treatment on the normalization of the ALT levels, the loss of HBeAg, HBeAg seroconversion, and the loss of serum HBV DNA at 1, 2, 3, 4, and 5 years, respectively. To determine the factors that influenced the occurrence of lamivudine-resistant mutation in HBV, we also examined the pre-treatment clinical factors.
Among the patients who developed a lamivudine-resistant virus, the patients who showed an elevated ALT levels of more than two times the upper limit of normal and that continued for longer than 2 months received adefovir at an oral dose of 10 mg daily in addition to lamivudine. In those patients who had adefovir in addition to lamivudine for the treatment of recurrence hepatitis, we examined the effect of the adefovir treatment on the normalization of the ALT levels and the loss of serum HBV DNA since the time the adefovir treatment was started. Furthermore, we studied the efficacy of this combination therapy on the normalization of the ALT levels and the loss of serum HBV DNA at 1, 2, 3, 4, and 5 years, respectively, since the time the lamivudine treatment was started.
The histologic improvement was analyzed in 15 patients who underwent a second liver biopsy. The patients were subjected to a liver biopsy using a Menghini needle guided by ultrasonography. Formalin-fixed liver specimens were stained with hematoxylin and eosin for morphologic evaluations, with Masson’s trichrome staining for the assessment of fibrosis.
HBeAg and HBeAb were detected via a chemiluminescent enzyme immunoassay (ARCHITECT HBeAg and ARCHITECT HBeAb, Abbott Japan, Tokyo, Japan). The serum HBV DNA levels in all patients before and during lamivudine treatment were measured via Transcription Mediated Amplification (DNA probe [FR]-HBV; Fujirebio Inc, Tokyo, Japan). The HBV levels were expressed as the log genome equivalent per milliliter (LGE/ml) and the upper and lower detection limits of the assay were 8.7 and 3.7 log copies/ml, respectively. The incidence of lamivudine mutations in the tyrosine-methionine-aspartate-aspartate (YMDD) motif was measured by means of a polymerase chain reaction-enzyme linked mini-sequence assay (PCR-ELMA; SMITEST HBV-YMDD Mutation Detection Kit, Medical and Biological Laboratories, Nagano, Japan).
Statistical analysis
Fisher’s exact test was used for sex and HBeAg positivity for comparisons between groups. Comparisons of the means ± standard deviations were performed using Student’s t-test for age, the ALT level, and the serum HBV DNA level. A P-value of less than 0.05 was considered to be statistically significant. For multivariate analyses, the Cox proportional hazards model analysis was used. Ninety-five CIs were used throughout.
Results
Patients (n = 327) who were seropositive for hepatitis B surface antigen were from our hospital and all were Japanese patients. Among these cases, 141 patients received lamivudine as the therapy for chronic hepatitis B and 110 eligible patients have been followed for more than 1 year (67 patients who were HBeAg-positive and 43 patients who were HBeAg-negative) (Table 1). This study reviewed the cumulative outcome of the patients with chronic hepatitis B who were treated with lamivudine, and the patients who had been followed for more than 2, 3, 4, and 5 years numbered 94, 79, 63, and 44, respectively. The median follow-up after the start of lamivudine was 48 (range = 12–86) months. In all patients, including those who were either HBeAg-positive or HBeAg-negative, the normalization of ALT levels decreased with the duration of lamivudine treatment from 70.0% at 1 year to 56.4%, 48.3%, 49.2%, and 36.4% at 2, 3, 4, and 5 years and the loss of serum HBV DNA decreased from 72.7% at 1 year to 53.2%, 41.8%, 39.7%, and 31.8% at 2, 3, 4, and 5 years, respectively (Table 2). These results included all the patients with or without lamivudine resistance. In our intention-to-treat analysis, the patients who had an efficacy of adefovir salvage treatment of breakthrough hepatitis were excluded from the efficacy group of lamivudine treatment. In the HBeAg-positive patients, the normalization of the ALT levels decreased during the lamivudine treatment from 71.6% at 1 year to 55.7%, 42.6%, 41.9%, and 22.6% at 2, 3, 4, and 5 years, respectively (Table 2). Their loss of serum HBV DNA was 22.6% and HBeAg seroconversion was 22.6% during the 5-year period of lamivudine treatment. In the HBeAg-negative patients, the normalization of the ALT levels was 67.4% at 1 year and 57.6%, 60.0%, 65.0%, and 69.2% at 2, 3, 4, and 5 years and the loss of serum HBV DNA was 76.7% at 1 year and 69.7%, 66.0%, 53.0%, and 53.8% at 2, 3, 4, and 5 years, respectively.
Table 1.
Patients baseline demographics and disease characteristics (n = 110)
| HBeAg-positive n = 67 |
HBeAg-negative n = 43 |
All patients n = 110 |
|
|---|---|---|---|
| Gender, male:female (%male) | 43:24 (64.2%) | 29:14 (67.4%) | 72:38 (65.6%) |
| Age (years) | |||
| Mean ± SD | 41.0 ± 12.5 | 47.9 ± 9.4 | 43.7 ± 11.9 |
| Median | 42 | 47 | 45 |
| Range | 18–68 | 27–69 | 18–69 |
| Alanine aminotransferase (IU/l)a | |||
| Mean ± SD | 208.5 ± 246.9 | 185.4 ± 238 | 199.3 ± 244.8 |
| Median | 110 | 89 | 92 |
| Range | 45–1148 | 45–907 | 45–1148 |
| HBV DNA (LGE/ml) | |||
| Mean ± SD | 7.52 ± 1.06 | 6.16 ± 1.95 | 6.99 ± 1.62 |
| Median | 7.6 | 6.9 | 7.3 |
| Range | 4.3–8.7 | 3.7–8.4 | 3.7–8.7 |
HBeAg: Hepatitis B e antigen
aThe upper limit of the normal range is 30 IU per liter
Table 2.
The efficacy of lamivudine treatment in the patients with or without lamivudine-resistance (n = 110)
| At 1 year (n = 110) | At 2 years (n = 94) | At 3 years (n = 79) | At 4 years (n = 63) | At 5 years (n = 44) | |
|---|---|---|---|---|---|
| All patients (n = 110) | |||||
| ALT normalization | 77 (70.0%) | 53 (56.4%) | 38 (48.3%) | 31 (49.2%) | 16 (36.4%) |
| Loss of HBV DNA | 80 (72.7%) | 50 (53.2%) | 33 (41.8%) | 25 (39.7%) | 14 (31.8%) |
| At 1 year (n = 67) | At 2 years (n = 61) | At 3 years (n = 54) | At 4 years (n = 43) | At 5 years (n = 31) | |
|---|---|---|---|---|---|
| HBeAg-positive patients (n = 67) | |||||
| ALT normalization | 48 (71.6%) | 34 (55.7%) | 23 (42.6%) | 18 (41.9%) | 7 (22.6%) |
| Loss of HBV DNA | 47 (70.1%) | 27 (44.3%) | 19 (35.2%) | 14 (32.6%) | 7 (22.6%) |
| Loss of HBeAg | 20 (29.9%) | 20 (32.8%) | 19 (35.2%) | 13 (30.2%) | 7 (22.6%) |
| HBeAg seroconversion | 16 (23.9%) | 9 (31.1%) | 18 (33.3%) | 13 (30.2%) | 7 (22.6%) |
| At 1 year (n = 43) | At 2 years (n = 33) | At 3 years (n = 25) | At 4 years (n = 20) | At 5 years (n = 13) | |
|---|---|---|---|---|---|
| HBeAg-negative patients (n = 43) | |||||
| ALT normalization | 29 (67.4%) | 19 (57.6%) | 15 (60.0%) | 13 (65.0%) | 9 (69.2%) |
| Loss of HBV DNA | 33 (76.7%) | 23 (69.7%) | 14 (66.0%) | 11 (53.0%) | 7 (53.8%) |
ALT: Alanine aminotransferase
HBeAg: Hepatitis B e antigen
The occurrence of a lamivudine-resistant mutation was seen in 60 patients. The mutation proportion increased from 27.3% at 1 year to 43.6%, 50.1%, 53.6%, and 54.6% at 2, 3, 4, and 5 years of treatment, respectively. Table 3 shows the number of patients who developed virus recrudescence at each year. This occurrence was more frequent in those who were HBeAg-positive (P < 0.01), those with a low ALT level (P < 0.05), and those with a high level of serum HBV DNA (P < 0.01) at the time the lamivudine treatment was started (Table 4). Thirty-six (60.0%) of the 60 patients received adefovir for the treatment of breakthrough hepatitis due to a lamivudine-resistant mutation, whereas the other 24 patients with a slight elevation in the ALT level did not receive adefovir. The patients who received adefovir had significantly higher levels of serum HBV DNA at the time the lamivudine treatment was started than those who did not receive adefovir (Table 5). Cox proportional hazards model analysis was used to determine the factors predicting viral recrudescence and breakthrough hepatitis. The patients who had more than 7.0 LGE/ml of serum HBV DNA level at the time the lamivudine treatment was started showed a significantly frequent occurrence of a lamivudine-resistant mutation (risk ratio = 0.466, 95% CI: 0.246–0.842, P = 0.011; Table 6). The patients who had more than 7.7 LGE/ml of serum HBV DNA at the time the lamivudine treatment was started more frequently received adefovir add-on therapy for breakthrough hepatitis (risk ratio = 0.444, 95% CI: 0.218–0.879, P = 0.019; Table 6).
Table 3.
The occurrence of lamivudine-resistant mutation during 5 years
| Number of patients | Baseline HBV DNA levels Mean ± SD (LGE/ml) |
|
|---|---|---|
| At 1 year | 30 | 7.46 ± 1.15 |
| At 2 years | 18 | 7.56 ± 1.07 |
| At 3 years | 8 | 6.98 ± 2.35 |
| At 4 years | 3 | 7.46 ± 0.70 |
| At 5 years | 1 | 6.3 |
Table 4.
Comparison between those patients who had virus recrudescence and those who did not
| Virus recrudescence (n = 60) |
Non-virus recrudescence (n = 50) |
P | |
|---|---|---|---|
| Age (years) mean ± SD | 43.5 ± 11.4 | 44.4 ± 12.3 | NS |
| Gender: male:female (%male) | 44:16 (73.3%) | 28:22 (56.0%) | NS |
| HBeAg-positive patients | 44 (73.3%) | 23 (46.0%) | <0.01 |
| Alanine aminotransferase (IU/l) | |||
| Mean ± SD | 157.9 ± 218.5 | 246.6 ± 261.6 | <0.05 |
| Serum HBV DNA (LGE/ml) | |||
| Mean ± SD | 7.40 ± 1.36 | 6.49 ± 1.75 | <0.01 |
HBeAg: Hepatitis B e antigen
NS: Not significant
Table 5.
Comparison between those patients who received adefovir and those who did not
| Administration of adefovir (n = 36) | No administration of adefovir (n = 24) | P | |||
|---|---|---|---|---|---|
| Age (years) mean ± SD | 45.0 ± 10.5 | 41.3 ± 12.3 | NS | ||
| Gender: male:female (%male) | 29:7 (80.1%) | 15:9 (62.5%) | NS | ||
| HBeAg-positive patients | 25 (69.4%) | 19 (79.2%) | NS | ||
| Alanine aminotransferase (IU/l) | |||||
| Mean ± SD | 148.7 ± 202.5 | 170.0 ± 239.6 | NS | ||
| Serum HBV DNA (LGE/ml) | |||||
| Mean ± SD | 7.64 ± 1.03 | 6.91 ± 1.30 | <0.05 | ||
| YMDD mutation | YIDD | 20 | YIDD | 13 | |
| YVDD | 8 | YVDD | 4 | ||
| YIDD + YVDD | 3 | YIDD + YVDD | 0 | ||
HBeAg: Hepatitis B e antigen
NS: Not significant
YMDD mutation: YMDD motif of the HBV DNA polymerase
YIDD: Methionine to isoleucine
YVDD: Methioneine to valine
Table 6.
Multivariate analysis with Cox proportional hazards model
| Variable | P-value | Risk ratio | 95% CI | |
|---|---|---|---|---|
| Virus recrudescence | HBV DNA ≧ 7.0 LGE/ml | 0.011 | 0.466 | 0.246–0.842 |
| Breakthrough | HBV DNA ≧ 7.7 LGE/ml | 0.019 | 0.444 | 0.218–0.879 |
Only variables that achieved statistical significance (P < 0.05) are shown
CI: Confidence interval
Breakthrough; administration of adefovir for breakthrough hepatitis due to lamivudine resistance
Of these 36 patients who received adefovir, the normalization of ALT levels was 47.2%, 57.9%, and 81.8% at 1, 2, and at 3 years and their loss of serum HBV DNA was 47.2%, 68.4%, and 90.9% at 1, 2, and at 3 years, respectively (Table 7). At the time of this analysis, the median total duration of adefovir treatment was 24 (range = 12–56) months and no adefovir-resistant mutation has been detected in any of these patients.
Table 7.
The efficacy of the adefovir add-on treatment
| At 1 year (n = 36) | At 2 years (n = 19) | At 3 years (n = 11) | |
|---|---|---|---|
| All patients (n = 36) | |||
| ALT Normalization | 17 (47.2%) | 11 (57.9%) | 9 (81.8%) |
| Loss of HBV DNA | 17 (47.2%) | 13 (68.4%) | 10 (90.9%) |
| At 1 year (n = 25) | At 2 year (n = 13) | At 3 years (n = 8) | |
|---|---|---|---|
| HBeAg-positive patients (n = 25) | |||
| ALT Normalization | 12 (48.0%) | 7 (53.8%) | 7 (87.5%) |
| Loss of HBV DNA | 9 (36.0%) | 8 (61.5%) | 7 (87.5%) |
| Loss of HBeAg | 3 (12.0%) | 5 (38.5%) | 6 (75.0%) |
| HBeAg seroconversion | 3 (12.0%) | 5 (38.5%) | 6 (75.0%) |
| At 1 year (n = 11) | At 2 year (n = 6) | At 3 years (n = 3) | |
|---|---|---|---|
| HBeAg-negative patients (n = 11) | |||
| ALT Normalization | 5 (45.5%) | 4 (66.7%) | 2 (66.7%) |
| Loss of HBV DNA | 8 (72.7%) | 5 (83.3%) | 3 (100%) |
ALT: Alanine aminotransferase
HBeAg: Hepatitis B e antigen
Fifty patients who did not develop lamivudine resistance showed the normalization of their ALT levels to be 84.0% at 1 year and 86.1%, 92.0%, 90.9%, and 91.9% at 2, 3, 4, and 5 years and the loss of serum HBV DNA was 92.0% at 1 year and 94.4%, 96.0%, 95.5%, and 100% at 2, 3, 4, and 5 years, respectively. The results were good for the patients who did not develop lamivudine resistance.
Fifteen patients who were treated with lamivudine underwent a repeat liver biopsy. The changes in stages of liver fibrosis are shown in Fig. 1. Figure 1a shows the group of the patients whose ALT levels were more than two times the upper limit of normal. Figure 1b shows the group of the patients whose ALT levels were less than two times the upper limit of normal. A progression in the fibrosis stage was observed in two patients and an improvement in the fibrosis stage was observed in 8 patients. Even if the serum HBV DNA level showed positive values, the degree of liver fibrosis improved on the basis of the findings of a second liver biopsy in the patients who were treated with lamivudine if the ALT level was less than two times the upper limit of normal.
Fig. 1.
A follow-up study of liver histology on the patients with chronic hepatitis B treated with lamivudine. (a) Four patients whose alanine aminotransferase levels were more than 2 times the upper limit of normal showed no improvement in liver fibrosis at the second liver biopsy. (b) Nine patients whose alanine aminotransferase levels were less than 2 times the upper limit of normal demonstrated an improvement in liver fibrosis at the second liver biopsy even if the serum HBV DNA was positive. Another 3 patients whose degree of fibrosis was diagnosed to be F1 at the first liver biopsy showed no change in liver fibrosis
To clarify the long-term efficacy of the lamivudine treatment of Japanese patients with chronic hepatitis B with or without adefovir add-on treatment of breakthrough hepatitis due to lamivudine-resistance, we investigated the efficacy of the lamivudine treatment by our new approach. Table 2 shows those patients who had an efficacy of adefovir salvage treatment of breakthrough hepatitis and were excluded from the efficacy group of the patients with lamivudine treatment. In addition, in Table 8, the patients who had the efficacy of adefovir add-on treatment were included in the efficacy group for 5-year period since lamivudine treatment was started. These results included all the patients with or without lamivudine-resistance and all the patients with or without adefovir add-on therapy. In all these patients, including those who were HBeAg-positive and those who were HBeAg-negative, the normalization of the ALT levels was 61.4% at 5 years since lamivudine treatment was started (Table 8). The loss of serum HBV DNA was 61.4% at 5 years since the lamivudine treatment was started. In the HBeAg-positive patients, the normalization of the ALT levels, the loss of serum HBV DNA, and HBeAg seroconversion was 54.8%, 51.6%, and 45.2% at 5 years, respectively, since the lamivudine treatment was started. In the HBeAg-negative patients, the normalization of the ALT levels and the loss of serum HBV DNA was 76.9% and 84.6% at 5 years, respectively, since the lamivudine treatment had been started.
Table 8.
The efficacy of lamivudine treatment with or without adefovir add-on (n = 110)
| At 1 year (n = 110) | At 2 years (n = 94) | At 3 years (n = 79) | At 4 years (n = 63) | At 5 years (n = 44) | |
|---|---|---|---|---|---|
| All patients (n = 110) | |||||
| ALT normalization | 77 (70.0%) | 55 (58.5%) | 48 (60.8%) | 42 (66.7%) | 27 (61.4%) |
| Loss of HBV DNA | 80 (72.7%) | 55 (58.5%) | 43 (54.4%) | 36 (57.1%) | 27 (61.4%) |
| At 1 year (n = 67) | At 2 years (n = 61) | At 3 years (n = 54) | At 4 years (n = 43) | At 5 years (n = 31) | |
|---|---|---|---|---|---|
| HBeAg-positive patients (n = 67) | |||||
| ALT normalization | 48 (71.6%) | 34 (55.7%) | 29 (53.7%) | 26 (60.5%) | 17 (54.8%) |
| Loss of HBV DNA | 47 (70.1%) | 27 (44.3%) | 24 (44.4%) | 21 (48.8%) | 16 (51.6%) |
| Loss of HBeAg | 20 (29.9%) | 20 (32.8%) | 20 (37.0%) | 18 (41.9%) | 14 (45.2%) |
| HBeAg seroconversion | 16 (23.9%) | 19 (31.1%) | 19 (35.2%) | 18 (41.9%) | 14 (45.2%) |
| At 1 year (n = 43) | At 2 years (n = 33) | At 3 years (n = 25) | At 4 years (n = 20) | At 5 years (n = 13) | |
|---|---|---|---|---|---|
| HBeAg-negative patients (n = 43) | |||||
| ALT Normalization | 29 (67.4%) | 21 (63.6%) | 19 (76.0%) | 16 (80.0%) | 10 (76.9%) |
| Loss of HBV DNA | 33 (76.7%) | 28 (84.8%) | 19 (76.0%) | 15 (75.0%) | 11 (84.6%) |
ALT: Alanine aminotransferase
HBeAg: Hepatitis B e antigen
Discussion
We herein describe the long-term efficacy of lamivudine treatment over a 5-year period. In all patients, including those who were HBeAg-positive and those who were HBeAg-negative, the normalization of ALT levels and the loss of serum HBV DNA gradually decreased to 36.4% and 31.8% at 5 years, respectively. The efficacy of lamivudine treatment was only about 30%. This result showed that lamivudine monotherapy could not improve the long-term outcomes in the patients with chronic hepatitis B. However, in the HBeAg-negative patients, the effects of lamivudine treatment were maintained for long-term. Although we assessed only a small number of patients in this study, we consider lamivudine monotherapy to be an effective treatment modality for patients with HBeAg-negative chronic hepatitis B to improve the long-term outcomes. On the other hand, because in the HBeAg-positive patients, virus recrudescence was more frequently observed than in the HBeAg-negative patients, the efficacy of the lamivudine treatment for 5 years was only about 20%. HBeAg-positive patients who demonstrated a high value of serum HBV DNA level and a low ALT level at the start of the lamivudine therapy showed a significant correlation with an increase in the occurrence of lamivudine-resistant mutations. Our Cox proportional hazards model analysis shows that to obtain serum HBV DNA levels of less than 7.7 LGE/ml before lamivudine treatment might associate with good outcomes in those patients. These patients are therefore recommended to reduce their serum HBV DNA levels before commencing lamivudine treatment and using interferon α or other therapeutic options [5, 6, 12]. Further large-scale and long-term studies are needed to confirm these observations.
In our study, although most virus recrudescence was observed within 1 year after the lamivudine treatment, 1 patient demonstrated virus recrudescence at 5 years after the lamivudine treatment was started. This is a very important finding and we must therefore carefully monitor the serum HBV DNA levels of the patients even if they show a good long-term response to the lamivudine treatment. Thirty-six of the patients with virus-recrudescence had adefovir added to the lamivudine regimen for the treatment of breakthrough hepatitis. However, the other 24 patients (40%) did not need adefovir to be added to the treatment regimen because they did not demonstrate hepatitis. In our study, even if the serum HBV DNA level was found to be positive, a histologic improvement was obtained in patients with ALT levels that were under 2 times the upper limit of normal at the time of a second liver biopsy. We thus consider that the normalization of ALT levels might therefore be more important than achieving a negative serum HBV DNA state to achieve a remission of liver disease. However, the risks of hepatocellular carcinoma and cirrhosis in the patients with chronic hepatitis B have recently been reported to be related to the serum HBV DNA levels [13, 14]. Our 24 patients who did not have adefovir added to the treatment regimen, even if they had virus recrudescence, all required a long-term follow-up to monitor whether or not they might progress to either cirrhosis or hepatocellular carcinoma.
Some reports have shown that among patients who experienced HBeAg seroconversion during the lamivudine treatment, the durability of the response after the cessation of therapy ranged from 38% to 77% [15–17]. Because lamivudine therapy still continues to be administered in Japan to avoid any posttreatment flare-ups of hepatitis [18–20], our patients continue to receive lamivudine treatment; therefore, our data are not comparable with other studies involving a cessation of treatment.
Previous studies reported that in patients receiving adefovir, the HBV DNA level decreased by 3.5 to 3.9 log10 from the baseline level [21, 22]. In addition, studies from Asia reported that patients with lamivudine resistance have been treated with adefovir either in monotherapy or in combination with lamivudine without any significant differences between the 2 regimens [23, 24]. On the other hand, studies from Europe reported that adding adefovir to lamivudine for the treatment of patients with lamivudine-resistant HBeAg-negative chronic hepatitis B maximizes the anti-viral efficacy because of the absence of viral resistance [25, 26]. In Japan, adefovir has been used as an additional therapy to suppress viral replication with lamivudine-resistant mutations. In all the patients investigated in our study, adefovir was added to the lamivudine regimen. However, no virologic or biochemical breakthrough was reported because no adefovir-resistance occurred in any of our patients. We thus considered that the condition of no adefovir-resistance might have occurred as all our patients received adefovir in combination with lamivudine.
To clarify the long-term efficacy of the lamivudine treatment of Japanese patients with chronic hepatitis B, we investigated the efficacy of lamivudine treatment on the basis of our new approach. In all the patients with or without lamivudine resistance and with or without adefovir add-on treatment, the normalization of the ALT levels was 61.4% and the loss of serum HBV DNA was 61.4% after the 5-year period of treatment from the time of lamivudine-treatment. This study is the first report to clarify the long-term efficacy of lamivudine treatment either with or without adefovir from the time the lamivudine treatment was started. Our study suggests that even in patients with chronic hepatitis B who have a high HBV DNA level and/or who are HBeAg-positive, the combination therapy of lamivudine and adefovir appears to be an effective treatment modality. This is a retrospective observational study with a relatively heterogeneous patient population. Although this study has its limitation, it represents the real situation for the treatment of chronic hepatitis B in Japan. The advantages of this study, such as being a single-center study, where all tests were performed in the same laboratory using the same methods, are thus considered to outweigh these limitations. These preliminary observations need to be validated in future studies with a larger number of patients.
In conclusion, although the efficacy of lamivudine is limited because of breakthrough hepatitis, adefovir was used as a salvage treatment of lamivudine resistance in patients with chronic hepatitis B. Therefore, the use of lamivudine for the treatment of Japanese patients with chronic hepatitis B with or without lamivudine-resistance is thus considered to be a useful treatment modality for obtaining long-term virologic and biochemical responses.
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Footnotes
An erratum to this article can be found at http://dx.doi.org/10.1007/s12072-008-9089-7
Contributor Information
Satoshi Shakado, Email: shakado@cis.fukuoka-u.ac.jp.
Takashi Tanaka, Email: tanaka329@minf.med.fukuoka-u.ac.jp.
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Shinya Nishizawa, Email: Shinya@minf.med.fukuoka-u.ac.jp.
Shinjiro Inomata, Email: inomata@minf.med.fukuoka-u.ac.jp.
Syuichi Ueda, Email: Shushu@minf.med.fukuoka-u.ac.jp.
Teruo Matsumoto, Email: tmatsu@minf.med.fukuoka-u.ac.jp.
Akira Anan, Email: a-anan@minf.med.fukuoka-u.ac.jp.
Yasuaki Takeyama, Email: yaz@fukuoka-u.ac.jp.
Makoto Irie, Email: macirie@minf.med.fukuoka-u.ac.jp.
Kaoru Iwata, Email: iwata-k@fukuoka-u.ac.jp.
Tetsuro Sohda, Email: tetsuro@fukuoka-u.ac.jp.
Shotaro Sakisaka, Email: sakisaka@fukuoka-u.ac.jp.
References
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