Treatment efficacy of pegylated interferon plus ribavirin therapy in chronic hepatitis C patients with mixed genotype 1/2 infection

被引:9
作者
Huang, Ching-I [1 ,2 ,5 ]
Huang, Chung-Feng [1 ,3 ,5 ]
Huang, Jee-Fu [4 ,5 ,6 ]
Dai, Chia-Yen [4 ,5 ,7 ]
Yeh, Ming-Lun [5 ]
Hsieh, Ming-Yen [2 ]
Lin, Zu-Yau [4 ,5 ]
Chen, Shinn-Cherng [4 ,5 ]
Wang, Liang-Yen [4 ,5 ]
Yu, Ming-Lung [4 ,5 ]
Chuang, Wan-Long [4 ,5 ]
机构
[1] Kaohsiung Med Univ Hosp, Inst Clin Med, Coll Med, Kaohsiung Municipal Ta Tung Hosp, Kaohsiung, Taiwan
[2] Kaohsiung Med Univ Hosp, Kaohsiung Municipal Ta Tung Hosp, Dept Internal Med, Kaohsiung, Taiwan
[3] Kaohsiung Med Univ Hosp, Kaohsiung Municipal Ta Tung Hosp, Dept Occupat Med, Kaohsiung, Taiwan
[4] Kaohsiung Med Univ, Sch Med, Fac Internal Med, Coll Med, Kaohsiung, Taiwan
[5] Kaohsiung Municipal Hsiaokang Hosp, Dept Internal Med, Hepatobiliary Div, Kaohsiung, Taiwan
[6] Kaohsiung Municipal Hsiaokang Hosp, Dept Internal Med, Kaohsiung, Taiwan
[7] Kaohsiung Med Univ Hosp, Dept Prevent Med, Kaohsiung, Taiwan
关键词
HCV; IL-28B; mixed infection; RGT; treatment; SUSTAINED VIROLOGICAL RESPONSE; INTERLEUKIN-28B GENETIC-VARIANTS; COMBINATION THERAPY; TREATMENT DURATION; PEGINTERFERON; MULTICENTER; IDENTIFICATION; POLYMORPHISMS;
D O I
10.1111/jgh.12467
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background and AimThe treatment efficacy of patients with mixed hepatitis C virus (HCV) genotype 1/genotype 2 (HCV-1/2) remains unknown. We aimed to elucidate the sustained virological response (SVR) rate in patients with HCV-1/2 infection. MethodsOne hundred and ten HCV-1/2 patients treated with response-guided peginterferon/ribavirin therapy (24 weeks for patients with a rapid virological response [RVR] and low viral loads; 48 weeks for patients without a RVR or high viral loads) were allocated. Two hundred HCV-1 patients were selected as a historical control. Interleukin-28B (IL-28B) rs8099917 genotype was tested for the association with an SVR. ResultsThe rates of RVR, sustained virologic response (SVR), and relapse rate were 71.8%, 87.3%, and 11.1%, respectively. The SVR rate was significantly higher in patients with an abbreviated regimen as compared with those with 48-week regimen (95.5% vs 75.0%, P=0.002), and both were similar to the HCV-1 historical control. Stepwise logistic regression analysis revealed that lower baseline viral loads were the single factor predictive of an RVR (odds ratio/95% confidence intervals [OR/CI] of 41.62/9.72-178.19, P<0.001). The achievement of an RVR was the single best factor predictive of an SVR (OR/CI: 7.5/1.33-42.27, P=0.02). Nevertheless, an abbreviated regimen became the single factor associated with an SVR if treatment regimen was taken into consideration (OR/CI: 11.0/1.25-96.79, P=0.03). The SVR rate did not differ between patients with rs8099917 TT and TG/GG genotype (91.7% vs 87.5%, P=0.63). ConclusionsThe treatment efficacy of patients with HCV-1/2 was satisfactory. The role of IL-28B genetic variants in the population with response-guided therapy was limited.
引用
收藏
页码:1012 / 1018
页数:7
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