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. 2014 Dec 23;60(5):1457–1464. doi: 10.1007/s10620-014-3486-7

Table 1.

Biochemical and virologic response to tenofovir disoproxil fumarate at year 7 (week 336)

By HBeAg status All
HBeAg-negativea HBeAg-positiveb
HBV DNA < 69 IU/mL [% (n/N)]
 LTE-TDFc 77.3 (269/348) 60.3 (149/247) 70.3 (418/595)
 On treatmentd 99.3 (271/273) 99.4 (159/160) 99.3 (430/433)
HBV DNA < 29 IU/mL [% (n/N)]
 LTE-TDFc 77.1 (269/349) 60.3 (149/247) 70.1(418/596)
 On treatmentd 99.3 (271/273) 99.4 (159/160) 99.3 (430/433)
ALT normalization [% (n/N)]
 LTE-TDFc 64.6 (210/325) 46.9 (113/241) 57.1 (323/566)
 On treatmentd 83.5 (213/255) 74.2 (115/155) 80.0 (328/410)
HBeAg loss [% (n/N)] 54.5 (84/154)
 HBeAg seroconversion [% (n/N)] 39.6 (61/154)
HBsAg loss [K-M % (95 % CI)] 11.8 (8.1, 16.9)
 HBsAg seroconversion [K-M % (95 % CI)] 9.7 (6.4, 14.6)

ALT alanine aminotransferase, CI confidence interval, HBeAg hepatitis B e-antigen, HBV hepatitis B virus, K–M Kaplan–Meier

aHBeAg-negative patients were enrolled in Study 102

bHBeAg-positive patients were enrolled in Study 103

cIn the long-term evaluation–TDF only (LTE-TDF) analysis, patients with missing data or emtricitabine added to their treatment regimen were counted as failures

dIn the on-treatment analysis, patients with missing data were excluded and patients with emtricitabine added to their treatment regimen were included in the analysis