Lamivudine Plus Tenofovir Combination Therapy Versus Lamivudine Monotherapy for HBV/HIV Coinfection: a Meta-analysis
Overview
Authors
Affiliations
Background: Currently, there is no consensus on the efficacy and safety of lamivudine (LAM) plus tenofovir disoproxil fumarate (TDF) combination therapy versus lamivudine monotherapy in HBV/HIV coinfected patients.
Methods: A comprehensive literature search was performed in English and Chinese databases. Both relevant dichotomous and continuous variables were extracted, and the combined outcomes were expressed as a risk ratio (RR) or a standard mean difference (SMD).
Results: Eleven eligible studies were included in our analysis. For HBV-relevant outcomes, the proportion of patients with undetectable HBV, the rates of serum alanine aminotransferase (ALT) normalization and hepatitis B e antigen (HBeAg) loss were higher in the combination therapy group than the monotherapy group (RR = 1.42, 95% CI: 1.14-1.76, P = 0.002; RR = 1.36, 95% CI: 1.17-1.58, P < 0.0001; RR = 2.74, 95% CI: 1.20-6.22, P = 0.02). In addition, the rate of HIV RNA-negative conversion was higher in the combination therapy group than the monotherapy group (RR = 1.26, 95% CI: 1.11-1.42, P = 0.0003).
Conclusion: LAM plus TDF combination therapy was more efficacious than LAM monotherapy in HBV/HIV coinfected patients. As time passes, this difference becomes more pronounced.
Ugwu E, Eleje G, Ugwu A, Nwagha U, Ikechebelu J, Umeh U Cochrane Database Syst Rev. 2023; 6:CD013653.
PMID: 37306558 PMC: 10259198. DOI: 10.1002/14651858.CD013653.pub2.
Recent Advances in Hepatitis B Treatment.
Prifti G, Moianos D, Giannakopoulou E, Pardali V, Tavis J, Zoidis G Pharmaceuticals (Basel). 2021; 14(5).
PMID: 34062711 PMC: 8147224. DOI: 10.3390/ph14050417.
FDA approved drugs with pharmacotherapeutic potential for SARS-CoV-2 (COVID-19) therapy.
Drozdzal S, Rosik J, Lechowicz K, Machaj F, Kotfis K, Ghavami S Drug Resist Updat. 2020; 53:100719.
PMID: 32717568 PMC: 7362818. DOI: 10.1016/j.drup.2020.100719.
A long-acting 3TC ProTide nanoformulation suppresses HBV replication in humanized mice.
Wang W, Smith N, Makarov E, Sun Y, Gebhart C, Ganesan M Nanomedicine. 2020; 28:102185.
PMID: 32217146 PMC: 7438263. DOI: 10.1016/j.nano.2020.102185.
Jiang T, Su B, Song T, Zhu Z, Xia W, Dai L Front Pharmacol. 2019; 10:1023.
PMID: 31572195 PMC: 6752181. DOI: 10.3389/fphar.2019.01023.