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Table 3 Factors associated with sustained viral response to interferon-alpha therapy

From: High versus standard doses interferon-alpha in the treatment of naïve chronic hepatitis C patients in Taiwan: a 10-year cohort study

 

Total No.

Non-SVR† No. (%)

SVR† No. (%)

P value

Patient Number

200

136(68.0)

64(32.0)

 

Gender

   

NS‡

Male

103

69(70.0)

34(33.0)

 

Female

97

67(69.1)

30(30.9)

 

Age (year)

 

47.6 ± 10.0

44.2 ± 13.5

NS

History of transfusion

   

NS

No

141

97(68.8)

44(31.2)

 

Yes

59

39(66.1)

20(33.9)

 

Liver histopathology

    

   Total score of necroinflammatory activity

4.10 ± 2.59

4.21 ± 2.31

NS

Fibrosis score

   

<0.01

F3–4

70

57(81.4)

13(18.6)

 

F0–2

130

79(60.8)

51(39.2)

 

Pretreatment ALT value (IU/L)

87.8 ± 86.5

143.5 ± 153.5

<0.01

Pretreatment serum level of HCV RNA§

6.17 ± 0.61

5.62 ± 0.56

<0.0001

HCV genotype

    

   1b

80

63(78.8)

17(21.3)

<0.01

   Non-1b

120

73(60.8)

47(39.2)

 

Interferon preparation

   

NS

   Recombinant IFN-α-2a

37

29(78.4)

8(21.6)

 

   Recombinant IFN-α-2b

95

62(65.3)

33(34.7)

 

   Lymphoblastoid IFN-α-n1

68

45(66.2)

23(33.8)

 

Interferon regimen

   

<0.05

3-MU group¶

76

58(76.3)

18(23.7)

 

6-MU group¶

124

78(62.1)

46(37.1)

 
  1. † SVR: sustained virological response.
  2. ‡ NS: not significant.
  3. §Presented as log (equivalent/mL).
  4. ¶ 3-MU group: interferon-α 3 million units thrice weekly for 24 weeks; 6-MU group: interferon-α 6 million units thrice weekly for 24 weeks.