Table 1.
Nucleos(t)ide analogue | Regimen | Pros | Cons |
Lamivudine | 100 mg daily | First licensed agent | Highest incidence of resistant mutations of M204V/I substitution (20% at year 1, 70% at year 5) |
Well established safety and efficacy record | |||
Lowest cost | Adverse effects including hepatitis flare ups, hepatic decompensation and even death | ||
Adefovir dipivoxil | 10 mg daily | Low drug resistance rate, and no cross resistance with other nucleos(t)ide analogs | Incidence of resistant mutations of N236T and/or A181V substitution (29% at year 5) |
Adverse effects including renal tubular acidosis with hypophosphataemia when treatment is prolonged | |||
Telbivudine | 600 mg daily | Higher seroconversion rate | Incidence of resistant mutations of M204I mutation (5% at year 1) |
Adverse effects including myopathy and neuropathy | |||
Entecavir | 1.0 mg daily | Anti-HBV effect | Incidence of resistant mutations of T184G or M250V (1.2% at year 5) (I169T and M250V, or T184G and S202I if also lamivudine-resistant) |
Lowest rate of resistance | |||
Most expensive | |||
Tenofovir disoproxil | 300 mg daily | More potent in reducing HBV load in patients with prior failure or resistance to lamivudine and/or adefovir | No resistant mutations reported at year 3 |
HBV: Hepatitis B virus.