Clinical Trials Study
Copyright ©2014 Baishideng Publishing Group Inc.
World J Hepatol. Jul 27, 2014; 6(7): 520-526
Published online Jul 27, 2014. doi: 10.4254/wjh.v6.i7.520
Table 1 Baseline characteristics of patients with genotypes 1, 3 and 4
ParameterGenotype 1Genotype 3Genotype 4
(n = 27)(n = 56)1(n = 17)
Age (yr)41.9 ± 13.241.7 ± 10.946.3 ± 9.3
Weight (kg)60.5 ± 12.063.3 ± 11.563.7 ± 10.8
Male number (%)219 (70.3%)11 (19.7%)11 (64.7%)
Hemoglobin (g/dL)14.1 ± 1.613.8 ± 1.914.2 ± 1.2
White blood cell count (109/L)6682 ± 16827086 ± 18867201 ± 1886
Neutrophils (%)58.4 ± 8.456.0 ± 11.853.3 ± 8.0
Platelet count (103/L)200 ± 80199 ± 78170 ± 50
Alanine Aminotransferase (U/L)88.1 ± 41127.7 ± 87.4104.9 ± 61.1
HCV RNA log10 IU/mL5.5 ± 1.25.4 ± 1.15.5 ± 0.9
Table 2 Percentage of patients who responded in terms of rapid virologic response, early virologic response, end of the treatment virologic response, and sustained virologic response in genotypes 1, 3 and 4 by intention-to-treat analysis
ParameterGenotype 1Genotype 31Genotype 4
(n = 27)(n = 56)(n = 17)
RVR25.9%71.4%58.8%
EVR74.1%87.5%88.2%
ETVR59.2%78.6%70.5%
SVR44.4%64.3%52.9%
Table 3 Percentage of patients who responded in terms of rapid virologic response, early virologic response, end of treatment virologic response, and sustained virologic response in genotypes 1, 3 and 4 by per protocol analysis
ParameterGenotype 1Genotype 31Genotype 4
(n/N)(n/N)(n/N)
RVR25.9% (7/27)74.1% (40/54)58.8% (10/17)
EVR74.1% (20/27)100% (49/49)88.2% (15/17)
ETVR84.2% (16/19)89.8% (44/49)75.0% (12/16)
SVR60.0% (12/20)76.6% (36/47)60.0% (9/15)
Table 4 Percentage of patients with normalization of alanine aminotransferase levels during different study periods n (%)
WeeksGenotype 1Genotype 31Genotype 4
(n = 27)(n = 56)(n = 17)
416 (59.2)27 (48.2)8 (47.0)
1217 (62.9)29 (51.7)8 (47.0)
2417 (62.9)35 (62.5)9 (52.9)
4817 (62.9)40 (71.4)11 (64.7)
7217 (62.9)-12 (70.6)
Table 5 Patients with adverse events
Adverse eventn (%) of patients
Genotype 1Genotype 31Genotype 4
(n = 27)(n = 56)(n = 17)
Injection-site reactions9 (33.3)16 (28.6)7 (41.2)
Flu-like symptoms24 (88.8)49 (87.5)14 (82.3)
Tiredness4 (14.8)5 (8.9)2 (11.7)
Weight loss1 (3.7)3 (5.4)1 (5.8)
Chest discomfort1 (3.7)2 (3.6)2 (11.7)
Arthralgia3 (11.1)0 (0)1 (5.8)
Alopecia2 (7.4)10 (17.9)3 (17.6)
Anorexia2 (7.4)7 (12.5)3 (17.6)
Nausea3 (11.1)8 (14.3)3 (17.6)
Vomiting2 (7.4)3 (5.4)0
Dyspepsia1 (3.7)3 (5.4)2 (11.7)
Gastritis1 (3.7)0 (0)0
Mucous stool1 (3.7)0 (0)0
Diarrhea1 (3.7)4 (7.1)1 (5.8)
Melena1 (3.7)6 (10.7)0
Ascites1 (3.7)0 (0)0
Thrombocytopenia2 (7.4)5 (8.9)1 (5.8)
Anemia9 (33.3)13 (23.2)6 (35.3)
Neutropenia12 (44.4)15 (26.8)8 (47.0)
Anxiety1 (3.7)3 (5.4)1 (5.8)
Depression2 (7.4)4 (7.1)3 (17.6)
Insomnia1 (3.7)1 (1.8)2 (11.7)
Hypothyroidism2 (7.4)2 (3.6)2 (11.7)
Giddiness1 (3.7)1 (1.8)2 (11.7)
Dry throat1 (3.7)1 (1.8)0 (0)
Cough2 (7.4)2 (3.6)2 (11.7)
Sinusitis1 (3.7)0 (0)0 (0)
Bleeding gums2 (7.4)1 (1.8)0 (0)
Palpitation1 (3.7)0 (0)0 (0)
Pruritus0 (0)0 (0)1 (5.8)
Yellow-colored sputum0 (0)0 (0)1 (5.8)
Urinary tract infection1 (3.7)0 (0)0 (0)
Death0 (0)1 (1.8)0 (0)
No. of patients reporting AEs24 (88.8)49 (87.5)14 (82.3)
Discontinued due to SAEs0 (0)2 (3.6)0 (0)
Temporary discontinuation of therapy4 (14.8)3 (5.4)3 (17.6)
Temporary dose reduction11 (40.7)16 (29.6)5 (29.4)