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Table 1 Clinical characteristics of study population

From: Hepatitis B relapse after entecavir or tenofovir alafenamide cessation under anti-viral prophylaxis for cancer chemotherapy

Variables, n (%) or mean ± S.D (range)

Entecavir

N = 144

TAF

N = 83

p value

Age (years)

54.5 ± 10.5

55.5 ± 9.8

0.473

Gender (male: female), n

44:100

34:49

0.112

Use of rituximab, n (%)

16 (11.1%)

6 (7.2%)

0.341

Use of steroid, n (%)

15 (10.4%)

4 (4.8%)

0.142

Use of anthracycline, n (%)

51 (35.4%)

25 (30.1%)

0.415

Hematologic malignancy, n (%)

17 (11.8%)

10 (12%)

0.957

Distant metastasis

21 (14.6%)

16 (19.2%)

0.356

Liver metastasis

7 (4.9%)

3 (3.6%)

0.750

AST (U/L)

35.0 ± 55.8

28.4 ± 19.5

0.298

ALT (U/L)

43.0 ± 96.8

31.6 ± 32.3

0.299

Total bilirubin (mg/dL)

0.63 ± 0.38

0.71 ± 0.46

0.153

Platelet × 103/μL

248.4 ± 83.8

250.3 ± 102.7

0.881

FIB-4

1.39 ± 0.94

1.42 ± 0.91

0.822

HBV DNA (log10 IU/mL)

2.85 ± 1.66

2.80 ± 1.54

0.836

 Low-viremia group, n (%)

36 (25%)

24 (28.9%)

0.541

 Moderate-viremia group, n (%)

61 (42.4%)

29 (34.9%)

 

 High-viremia group, n (%)

47 (32.6%)

30 (36.1%)

 

Treatment duration (weeks)

60.6 ± 25.1

55.7 ± 18.6

0.116

Consolidation duration (weeks)

30.2 ± 10.8

31.1 ± 10.8

0.555

  1. ALT Alanine transaminase, AST Aspartate transaminase, SD standard deviation, TAF tenofovir alafenamide
  2. High-viremia group: Baseline HBV DNA levels of > 2000 IU/mL, Moderate-viremia group: baseline HBV DNA levels of ≧20 and < 2000 IU/mL, Low-viremia group: baseline HBV DNA levels of < 20 IU/mL