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©2010 Baishideng.
World J Hepatol. Jun 27, 2010; 2(6): 226-232
Published online Jun 27, 2010. doi: 10.4254/wjh.v2.i6.226
Published online Jun 27, 2010. doi: 10.4254/wjh.v2.i6.226
Table 1 Clinical background of patients
Background | |
n of patients | 71 |
Male [n (%)] | 31 (44) |
Age (yr) | 63 (32-78) |
Body weight > 60 kg [n (%)] | 33 (46) |
HCV-RNA (Log IU/mL) | 6.1 (5.1-7.2) |
Alanine aminotransferase (U/L) | 97 (27-513) |
Platelet count [× 104/μL] | 13.9 (9.1-30.6) |
9.0 to 13.0 [n (% )] | 28 (39) |
≥ 13.0 [n (% )] | 43 (61) |
Albumin (g/dL) | 3.9 (3.5-4.5) |
Hemoglobin (g/dL) | 13.6 (10.5-16.9) |
Interferon-naïve [n (%)] | 44 (62) |
Peginterferon-α2a/-α2b (n) | 34/37 |
Initial dose of ribavirin | 38/30/3 |
600/800/1 000 (mg/d) (n) |
Table 2 Clinical background by therapeutic response
Dosing duration of peginterferon plus ribavirin | ||||
1-24 wk | 20-24 wk | |||
SVR non-SVR | P value | SVR non-SVR | P value | |
n of patients | 21 | 17 | ||
40 | 14 | |||
Male [n (%)] | 12 (57) | 0.0636b | 10 (59) | 0.1493c |
13 (33) | 4 (29) | |||
Age (yr) | 58 (35-74) | 0.0030a | 58 (35-74) | 0.0134a |
65 (37-78) | 63 (58-71) | |||
Body weight > 60 kg [n (%)] | 13 (62) | 0.0441b | 10 (59) | 0.0669c |
14 (35) | 3 (21) | |||
HCV-RNA (Log IU/mL) | 5.8 (5.1-6.9) | 0.1685a | 6.0 (5.2-6.9) | 0.9967a |
6.1 (5.1-7.2) | 6.1 (5.2-6.6) | |||
Alanine amino-transferase (U/L) | 97 (52-269) | 0.7699a | 86 (57-138) | 0.6410a |
93 (27-513) | 80 (28-260) | |||
Platelet count (× 104/μL) | 16.8 (10.9-30.6) | 0.0020a | 17.0 (10.9-30.6) | 0.0007a |
13.3 (9.1-24.0) | 11.4 (9.1-15.4) | |||
Albumin (g/dL) | 3.9 (3.5-4.4) | 0.7410a | 3.9 (3.5-4.2) | 0.9211a |
3.9 (3.5-4.5) | 3.9 (3.5-4.5) | |||
Hemoglobin (g/dL) | 14.4 (11.4-15.4) | 0.0126a | 14.5 (11.4-15.4) | 0.1379a |
13.1 (10.5-15.4) | 13.5 (10.7-15.4) | |||
Interferon-naïve [n (%)] | 12 (57) | 0.6847b | 9 (53) | 0.8150b |
25 (63) | 8 (57) | |||
Peginterferon-α2a/-α2b (n) | 12/9 | 0.2016b | 9/8 | 0.4607c |
16/24 | 10/4 | |||
Dosing duration of peginterferon (wk) | 24 (4-24) | 0.0009a | 24 (21-24) | 0.5082a |
15 (2-24) | 24 (21-24) |
Table 3 Nominal logistic regression analysis of clinical background variables related to an sustained virologic response (SVR)
Variable | Odds ratio (95% CI) | P value1 |
Dosing duration of peginterferon: 1-24 wk (n = 61) | ||
Age < 65 yr | 1.3210 (0.2140-8.1481) | 0.7586 |
Body weight > 60 kg | 3.7283 (0.6986-25.865) | 0.1257 |
Platelet count ≥ 130 000/μL | 15.301 (2.5378-155.22) | 0.0018 |
Hemoglobin ≥ 14.0 g/dL | 4.7957 (0.9337-30.599) | 0.0606 |
Dosing duration of Peg-IFN 20-24 wk (vs 1-19 wk) | 33.551 (5.5858-352.77) | < 0.0001 |
Dosing duration of peginterferon: 20-24 wk (n = 31) | ||
Age < 65 yr | 1.1028 (0.1670-6.6558) | 0.9149 |
Platelet count ≥ 130 000/μL | 11.680 (2.3064-79.474) | 0.0024 |
Table 4 HCV-RNA response during treatment and outcome
Response outcome | IFN-β1n (%)1 | HCV-RNA1 | RVR n (%) | cEVR n (%) | ETR n (%) |
Dosing duration of peginterferon: 1-24 wk (n = 61) | |||||
Yes | 43 (70) | 6.0 (5.1-7.1)b | 15 (25) | 36 (59) | 39 (64) |
SVR | 21 (49)a | 5.8 (5.1-6.9) | 7 (47) | 20 (56)c | 21 (54)d |
Non-SVR | 22 (51)a | 6.0 (5.1-7.1) | 8 (53) | 16 (44)c | 18 (46)d |
No | 18 (30) | 6.2 (5.5-7.2)b | 46 (75) | 25 (41) | 22 (36) |
SVR | 0 (0)a | - | 14 (30) | 1 (4)c | 0 (0)d |
Non-SVR | 18 (100)a | 6.2 (5.5-7.2) | 32 (70) | 24 (96)c | 22 (100)d |
Dosing duration of peginterferon: 20-24 wk (n = 31) | |||||
Yes | 25 (81) | 6.0 (5.2-6.9) | 11 (35) | 24 (77) | 24 (77) |
SVR | 17 (68)e | 6.0 (5.2-6.9) | 7 (64) | 17 (71)f | 17 (71)g |
Non-SVR | 8 (32)e | 5.7 (5.2-6.6) | 4 (36) | 7 (29)f | 7 (29)g |
No | 6 (19) | 6.4 (5.5-6.6) | 20 (65) | 7 (23) | 7 (23) |
SVR | 0 (0)e | - | 10 (50) | 0 (0)f | 0 (0)g |
Non-SVR | 6 (100)e | 6.4 (5.5-6.6) | 10 (50) | 7 (100)f | 7 (100)g |
- Citation: Okushin H, Morii K, Uesaka K, Yuasa S. Twenty four-week peginterferon plus ribavirin after interferon-β induction for genotype 1b chronic hepatitis C. World J Hepatol 2010; 2(6): 226-232
- URL: https://www.wjgnet.com/1948-5182/full/v2/i6/226.htm
- DOI: https://dx.doi.org/10.4254/wjh.v2.i6.226