Hepatitis B coinfection is common in HIV-positive individuals and as antiretroviral therapy has made death due to AIDS less common, hepatitis has become increasingly important. Several drugs are available to treat hepatitis B. The most potent and the one with the lowest risk of resistance appears to be tenofovir (TDF). However there are several questions that remain unanswered regarding the use of TDF, including the proportion of patients that achieves suppression of HBV viral load and over what time, whether suppression is durable and whether prior treatment with other HBV-active drugs such as lamivudine, compromises the efficacy of TDF due to possible selection of resistant HBV strains.
A systematic review and meta-analysis following PRISMA guidelines and using multilevel mixed effects logistic regression, stratified by prior and/or concomitant use of lamivudine and/or emtricitabine.
Data was available from 23 studies including 550 HBV/HIV coinfected patients treated with TDF. Follow up was for up to seven years but to ensure sufficient power the data analyses were limited to three years. The overall proportion achieving suppression of HBV replication was 57.4%, 79.0% and 85.6% at one, two and three years, respectively. No effect of prior or concomitant 3TC/FTC was shown. Virological rebound on TDF treatment was rare.
TDF suppresses HBV to undetectable levels in the majority of HBV/HIV coinfected patients with the proportion fully suppressed continuing to increase during continuous treatment. Prior treatment with 3TC/FTC does not compromise efficacy of TDF treatment. The use of combination treatment with 3TC/FTC offers no significant benefit over TDF alone.
Citation: Price H, Dunn D, Pillay D, Bani-Sadr F, de Vries-Sluijs T, et al. (2013) Suppression of HBV by Tenofovir in HBV/HIV Coinfected Patients: A Systematic Review and Meta-Analysis. PLoS ONE 8(7): e68152. doi:10.1371/journal.pone.0068152
Editor: Sang-Hoon Ahn, Yonsei University College of Medicine, Republic of Korea
Received: March 14, 2013; Accepted: May 26, 2013; Published: July 10, 2013
Copyright: © 2013 Price et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: HP is funded by a fellowship from the Medical Research Council. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Approximately 10% of people infected with HIV are coinfected with hepatitis B virus (HBV). Among populations with access to antiretroviral therapy (ART), in whom serious opportunistic infections have become a rare event, liver diseases including HBV infection represent a major cause of morbidity and mortality.  Since the life-cycles of HIV and HBV both utilise a reverse transcriptase enzyme, some drugs that inhibit reverse transcriptase have activity against both viruses. Guidelines now recommend tenofovir (TDF) in combination with lamivudine (3TC) or emtricitabine (FTC) as first-line therapy for patients with HIV/HBV coinfection.  Many studies have reported on the effect of TDF, either with or without 3TC or FTC, in treatment-naïve or experienced patients, however many studies are small and with relatively short follow-up.
It is uncertain what proportion of patients achieves suppression of HBV DNA (viral load) and whether those in whom suppression is not seen after one year may achieve HBV suppression later. It is also unclear to what extent, if at all, those with complete suppression may relapse despite continued treatment, e.g. in case of development of resistance mutations. Finally, it remains uncertain whether sequential treatment, for example with 3TC initially and TDF later, compromises the chance of successful treatment with TDF.
A recent meta-analysis examined all randomised controlled trials of treatment for HBV but excluded patients with HIV coinfection and only compared responses at 12 months.  Outcomes included both virological (undetectable HBV viral load – excluded if the lower limit of detection was greater than 1000 copies/mL) and biochemical responses, HBeAg loss or seroconversion to anti-HBe, HBsAg loss, histological improvement and serious adverse events.
We carried out this meta-analysis of data from patients coinfected with HIV to amalgamate all available evidence and to answer the following questions:
- what proportion of patients achieve HBV viral load suppression on TDF?
- does the rate of suppression differ in those with prior 3TC experience?
- does the rate of suppression differ in those treated with combination therapy compared with TDF monotherapy?
- how common is HBV rebound on TDF?
The systematic review was carried out following the guidance laid out in the PRISMA statement .
Search Strategy and Selection Criteria
Studies included were those that described HBV/HIV coinfected individuals treated with TDF with or without 3TC and/or FTC for a period of at least one year and that gave results of quantification of plasma HBV viral load at yearly intervals (at a minimum) while on TDF treatment. Studies included could be randomised controlled trials or prospective or retrospective cohort studies. Patients with undetectable plasma HBV viral load at baseline were excluded since their inclusion gives a falsely high estimate of the effect of treatment. Baseline HBV viral load data was not given for 20 patients in three studies (see Table 1). The analysis was restricted to patients on TDF treatment, with or without 3TC and/or FTC. In this analysis inclusion bias could be considerable if patients who failed to suppress either stopped taking TDF or had progressive liver disease and so dropped out. This would leave a higher proportion of patients with a good response, overestimating the treatment effect. However very little data required to deal with this has been published. Further analysis of individual patient data was carried out where this was available or was provided in the process of performing the current analysis (Table 1).
TDF received approval for the treatment of HIV infection from the United States Food and Drug Administration (FDA) in October 2001 and from the European Medicines Agency in February 2002. (FDA approval for the treatment of chronic HBV infection was granted in August 2008.) The first reports of the use of TDF in treating HBV infection were presented in 2002. Web of Science, Embase and Medline were searched, including all years. Conference abstracts from The Liver Meeting (American Association for the Study of Liver Diseases), The International Liver Congress (European Association for the Study of the Liver) and the Conference on Retroviruses and Opportunistic Infections were searched for the years 2002–2010.
To search databases, a combination of key terms was used including “hepatitis”, “HIV”, and “tenofovir”, limited to articles with human subjects and written in English (Appendix S1). Conference abstracts were searched online or by hand. Other publications that were discovered from the reference lists in publications reviewed were also included.
Studies were screened initially by title and then data was collected by HP from the full article of all published studies and from conference posters, or conference abstracts if posters were not available. Some studies met the eligibility criteria except that the published report did not include data on the number with undetectable HBV viral load at one year, or information on prior or concomitant drug exposure. The authors of these studies were contacted by email and asked to provide additional data if available. Additional, unpublished data was obtained from the authors of 11 of the 23 sources included (Table 1). The authors of one conference report provided an article that superseded the conference report and which had been accepted and published online but that had not been discovered in the search .
Data collected consisted of type of study, source of study funding, number of HBV/HIV coinfected participants, number HBeAg positive at study entry, prior 3TC/FTC exposure, drug regimens used during study period, length of follow-up, type of HBV viral load test used and lower limit of detection, numbers tested for HBV viral load at yearly intervals, and numbers with undetectable HBV viral load at yearly intervals. To maximise power and in the absence of any evidence suggesting a difference in effect on HBV between 3TC and FTC, exposure to these two were grouped together.
Results were stratified by treatment into four groups. Group A consisted of patients who had no prior exposure to 3TC/FTC and who were treated with TDF without concomitant 3TC/FTC, Group B those without prior exposure to 3TC/FTC treated with TDF in combination with 3TC/FTC, Group C those with prior exposure to 3TC/FTC but treated with TDF without 3TC/FTC, and Group D those with prior exposure to 3TC/FTC treated with TDF in combination with 3TC/FTC.
Statistical analysis was carried out using STATA version 10.1. The main outcome measure used was the proportion of patients tested who had a HBV viral load below the limit of detection at each of any available yearly time intervals. 95% confidence intervals for these proportions were calculated for each time point in each study and for the aggregate results.
To detect potential sources of bias, assay cut-off was plotted against proportion suppressed at one year. Publication bias was examined using funnel plots, in which asymmetry with a lack of poorly performing studies (to the left) would suggest such studies were not published.
Multilevel mixed effects logistic regression (XTMELOGIT command) was used to assess the effect of prior exposure to, and combination treatment with 3TC/FTC on the probability of viral suppression, with individual studies fitted as a random effect to account for clustering (Appendix S2). This implicitly weights each study by the amount of information it contains. Since there was no association of assay cut-off with rate of suppression the model was not adjusted for cut-off. The significance of between study heterogeneity was assessed by a likelihood-ratio test comparing the mixed effects model with a standard logistic regression model.
Models were re-run with an interaction term to examine whether the effect of concomitant 3TC/FTC was the same in both those naïve and those exposed to prior 3TC/FTC. As sensitivity analyses, the model was re-run (i) including only larger studies (reporting at least ten patients), (ii) including all studies apart from one that appeared as an outlier on the funnel plot.  and (iii) with a term for study design.
All authors had access to the data in the study and reviewed and approved the manuscript.
The initial searches produced 2,110 references which, after duplicates were removed, referred to 1,607 publications. Publications were then screened by title and if necessary by abstract to remove those clearly not meeting the eligibility criteria. This left 379 published articles. The full text of articles and posters was then checked for eligibility (or abstracts if the full article or poster was not available). 356 were removed as ineligible (as described in Figure 1) and 23 included in the analysis.
Study characteristics are given in Table 1. Although data was included from six randomised controlled trials, allocation of TDF vs. TDF plus 3TC was randomised in only two. ,  Some studies included patients in more than one treatment group (for example both patients with and without prior exposure to 3TC), giving 43 study arms in total (Table 2 and Figure 2).
In cases where insufficient data was published to categorise participants for this meta-analysis (for example if it was impossible to separate according to prior/concomitant treatment or if individuals with undetectable HBV viral load at baseline were included ), authors were contacted for further information. Those studies for which published data has been augmented by additional information are so labelled in Table 1.
Studies used assays with widely varying cut-offs for the detection of HBV (Table 1). This could have introduced bias, with the use of more sensitive assays resulting in an apparent lower rate of suppression. However plotting the proportion undetectable against the logarithm of the cut-off value showed no clear pattern (Figure 3) and the cut-off was ignored in further analyses.
The overall proportion suppressed was 57.4% (95% CI: 53.0–61.7%), 79.0% (95% CI: 73.6–83.8%), and 85.6% (95% CI: 79.2–90.7%) after one, two, and three years of treatment with TDF (Table 3).
It was possible to assess rates of virological suppression by HBeAg status for patients from ten of the included studies. , , , , , –, ,  For HBeAg positive and negative patients respectively the proportion fully suppressed was 51.8%, 82.0%, 86.6% and 76.3%, 82.1%, 75.0% at one, two and three years (Figure 4). After one year of treatment, a higher proportion of HBeAg negative than HBeAg positive individuals had a fully suppressed HBV viral load (p = 0.005). However, after one year the rates of suppression were not significantly different.
Table 4 shows the effects of prior and concomitant 3TC/FTC on virological suppression. Effects are given for all patients and also stratified by prior or concomitant treatment with 3TC/FTC as appropriate. Overall, at one year prior exposure to 3TC had an odds ratio of 0.69 (95% CI: 0.45 to 1.08) and treatment with 3TC/FTC in addition to TDF of 1.24 (95% CI: 0.68 to 2.24), neither being statistically significant. The effect of prior exposure to 3TC/FTC was similar, but also not statistically significant, at each of one, two, and three years. The effect of concomitant treatment with 3TC/FTC favoured dual therapy at one year but TDF monotherapy at years two and three, but these effects were again not statistically significant. The odds ratios in the stratified analyses were similar to the effects overall but with even wider confidence intervals. There was no evidence of an interaction between prior and concomitant 3TC/FTC treatment (p = 0.98 at 1 year, p = 0.14 at 2 years and p = 0.99 at 3 years). Between-study heterogeneity, allowing for the effects of prior and concomitant 3TC/FTC treatment, was significant (p<0.01) at year 1 but not at year 2 (p = 0.48) or at year 3 (p = 1.0).
The proportion suppressed increased over time and reached 100% overall (Table 2). The number of patients in follow-up at each year declined, however of the 379 patients in studies with more than one year of follow-up, individual patient data was available for 187 (49.3%) and in these patients dropping out (i.e. no later HBV viral load test result being available) was more likely at every time point for patients with suppressed HBV than for those with detectable HBV (non-significant – data not shown).
Virological rebound on TDF was rare, with no cases seen in 16 of 23 studies. Three studies reported a single patient with an increase in HBV viral load on TDF treatment, , ,  three had two patients, , ,  and one had three  though in three of these studies the size of the increases were not reported, in two the increases were very small (0.1 to 0.3 log), and only two had patients with an increase of at least one log (one in each study). ,  Unfortunately no discussion of these two cases was given, in particular there were no data on drug compliance and treatment adherence.
The funnel plot (Figure 5) shows the standard error against the proportion undetectable at one year, with the vertical line marking the summary estimate of the treatment effect (derived using fixed-effect meta-analysis).  The plot is symmetrical with no suggestion of publication bias. There is considerable heterogeneity in the effect found in larger studies (appearing higher up on the graph with a lower standard error), with one apparent outlier with a low proportion undetectable despite large size (de Vries-Sluijs,  Group D). Separate funnel plots of each arm in the analysis also show no publication bias (not shown). Repeating the regression analysis after excluding the outlier study arm and after excluding small studies (with less than ten patients) made no significant difference to the results. The model included a term for study design and showed that study design had no significant impact on the results, with p values of 0.76, 0.54 and 0.42 at 1, 2 and 3 years in the overall analysis.
This review of HBV/HIV coinfected patients treated with TDF results demonstrates lasting virological suppression of HBV replication to below the level of detection, with the proportion suppressed increasing to 100% over time, though with small numbers at later time points. Few patients experience virological failure on treatment.
However several reservations should be noted. Firstly most of the studies included were observational in design and patients dropping out were not well characterised. Secondly, in this meta-analysis we compare different treatment groups though allocation to these was randomised in only two studies. ,  Thirdly the numbers of patients included in the meta-analysis declines rapidly over time.
The proportion with undetectable HBV at one year (59%) was lower than the proportion found in HIV negative patients receiving TDF for treatment of HBV infection. For example, a multicentre cohort study found that, of 54 HIV-negative patients treated with TDF and FTC, 60% of whom were HBeAg positive, the probability of attaining an undetectable HBV viral load was 76% at one year and 94% at two years.  Similarly, in a large randomised controlled trial comparing TDF with adefovir, Marcellin found 93% of 250 HBeAg negative and 76% of 176 HBeAg positive patients randomised to TDF had an undetectable viral load (<400 copies/mL) at 48 weeks (97% and 83% respectively of those still on TDF at 48 weeks) .
In the latter study, ten patients (2.3%) had virological breakthrough (defined in that study as detectable HBV after an undetectable result or an increase in HBV viral load by a factor of ten from nadir).  Of the 550 patients in the current study, we identified 12 (2.4%) with a rise in HBV viral load on TDF treatment (although at least five of these 12 had less than a one log rise from nadir) which is comparable to HBV-monoinfected patients. However other published data in coinfected patients have found far higher rates, for example 9 (17%) of 52 patients followed up for a median of 34 months in one retrospective cohort study (which was not included in the current meta-analysis as data on HBV viral load suppression was only given at the end of follow-up and not at yearly time points) .
The high rate of virological suppression and low rate of breakthrough may be related to the low chance of developing TDF-resistance mutations. In HBV/HIV coinfected patients treated with lamivudine as the only drug active against HBV, resistance develops in about 90% after four years  whereas mutations associated with TDF resistance, such as the combination of rtL180M, rtM204V/I and rtA194T  or N236T with A181V,  have only rarely been seen and are of uncertain significance –.
No statistically significant effect of prior 3TC/FTC exposure or of concomitant 3TC/FTC use was found and thus no evidence to support the hypotheses that prior exposure may make subsequent treatment less effective or that concomitant use of 3TC/FTC may give a higher rate of suppression. However given the modest number of patients available for inclusion in the meta-analysis, the confidence intervals were wide and we could not exclude the possibility of moderately strong effects in either direction. In HIV-negative patients TDF monotherapy is as effective for HBV as combination therapy with TDF and 3TC/FTC with suppression rates (<400 copies/mL) of 81% at one year in both arms of an RCT using TDF alone or TDF/FTC combination therapy, and 88% and 85% respectively at three years , .
The main concern with sequential treatments that fail to fully suppress the viral load is that resistance may develop and that cross-resistance could reduce the efficacy of subsequent drugs. TDF resistance is yet to be clearly demonstrated but it may be that the risk of cross-resistance is higher with drugs that are more similar to TDF in structure than 3TC/FTC. However HBV mono-infected patients failing to achieve virologic suppression with adefovir have also been shown to respond well to TDF –.
A second mechanism by which prior treatment exposure could reduce the apparent effectiveness of subsequent TDF is through introducing bias, in that patients failing one regimen for reasons other than lack of potency (such as poor adherence to therapy) may go on to fail other regimens but again, no such reduction in the effect of TDF in those with prior exposure to 3TC/FTC was found and so the effect of any such bias must be small.
As stated above, TDF received FDA approval in late 2001 and thus clinical experience to date is limited to just over one decade. Although this review includes data to a maximum of seven years, a lack of data limited the main regression analyses to three years. Patients with HIV require lifelong treatment and patients with HBV coinfection are likely to require the same. The possibility of safe discontinuation of HBV treatment may be limited to patients who clear serum hepatitis B surface antigen (HBsAg). However the probability of HBsAg loss is low with a rate of approximately 2.5% per year ,  with the predicted median time to HBsAg seroclearance in HBeAg positive patients treated with TDF being 18 years (IQR 10–28 years) .
A limitation of this study is that it does not include analysis of the adverse effects of treatment. Future studies with longer follow-up duration will be required to determine the risk of treatment associated adverse effects, such as renal and bone toxicity, in patients exposed to TDF for many decades.
In conclusion, this meta-analysis shows that tenofovir suppresses HBV to undetectable levels in the majority of HBV/HIV coinfected patients, with the proportion fully suppressed increasing with time on treatment and with little if any virological rebound on treatment. Prior treatment with 3TC/FTC does not alter the efficacy of TDF treatment. Combination treatment with 3TC/FTC offers no significant benefit over tenofovir alone.
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