Recommendations for the use of nucleos(t)ide analogues in clinical practice

DrugAdvantageDisadvantageRecommendation
Lamivudine
(LAM)
Low treatment costs
Oral solution available
for children or individual
dosage in case of renal impairment
Hight risk of
resistance in long-
term monotherapy
Cross-resistance to ETV and LdT
Use as first-line therapy
only in selected patients
with low viral load
Use in pregnancy possible
Adefovir dipivoxil
(ADV)
Experience in combination with LAM No cross-resistance to LAMModerate antiviral activity Primary nonresponse in 10–20% of cases Slow viral kinetics during therapy Risk of viral resistance in longterm monotherapy NephrotoxicityNot to be used as firstline or mono therapy
Telbivudine (LdT)High antiviral efficacy No cross-resistance to entecavirModerate risk for viral resistance in long-term monotherapy Neuropathy and myopathyFirst-line therapy Can be combined with TDF
Entecavir (ETV)High antiviral efficacy Low risk for viral resistance in longterm monotherapy in lamivudine-naïve patients Combination therapy with TDF as rescue therapy Oral solution available for individual dosage in case of renal impairmentIn LAM – experienced patients high risk for the development of viral resistance and virologic failure in long-term monotherapyFirst-line therapy Can be combined with TDF Recommended for pre-emptive treatment in patients with immunosuppression
Tenofovir disoproxil fumarate (TDF)High antiviral efficacy Low risk for viral resistance in long-term monotherapy Oral solution available for individual dosage in case of renal impairmentRare Nephrotoxicity* Decrease in bone mineral densityFirst- and any second-line therapy Can be combined with ETV, LdT or LAM if needed Recommended for pre-emptive treatment in patients with immunosuppression
Tenofovir alafenamide (TAF)Comparable antiviral efficacy as TDF in HBeAg positive and negative patients Smaller risk of bone density loss or kidney damage than TDFFirst- and second line treatment for patients with compensated liver disease
*in HBV mono-infected patients no renal toxicity was observed in 8 years of TDF treatment
Author Profile

Dr. D.Zeqiraj medical doctor at QKUK- Pristina, department of Infectious disease.