Ledipasvir/Sofosbuvir for Patients Coinfected With Chronic Hepatitis C and Hepatitis B in Taiwan: Follow-up at 108 Weeks Posttreatment

Author:

Liu Chun-Jen1,Sheen I-Shyan2,Chen Chi-Yi3,Chuang Wan-Long4,Wang Horng-Yuan5,Tseng Kuo-Chih6,Chang Ting-Tsung7,Yang Jenny8,Massetto Benedetta8,Suri Vithika8,Camus Gregory8,Jiang Deyuan8,Zhang Fangqiu8,Gaggar Anuj8,Hu Tsung-Hui9ORCID,Hsu Yu-Chun10,Lo Gin-Ho11,Chu Chi-Jen12,Chen Jyh-Jou13,Peng Cheng-Yuan14ORCID,Chien Rong-Nan15,Chen Pei-Jer16

Affiliation:

1. Department of Internal Medicine, Hepatitis Research Center, and Graduate Institute of Clinical Medicine, National Taiwan University College of Medicine and Hospital, Taipei City, Taiwan

2. Linkou Chang Gung Memorial Hospital, Taoyuan City, Taiwan

3. Chia-Yi Christian Hospital, Chia-Yi City, Taiwan

4. Kaohsiung Medical University Hospital, Kaohsiung Medical University, Kaohsiung City, Taiwan

5. MacKay Memorial Hospital, Taipei City, Taiwan

6. Dalin Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation, Chia-Yi City, Taiwan

7. National Cheng Kung University, College of Medicine and Hospital, Tainan City, Taiwan

8. Gilead Sciences, Inc., Foster City, California, USA

9. Kaohsiung Chang Gung Memorial Hospital, Kaohsiung City, Taiwan

10. Changhua Christian Hospital, Changhua City, Taiwan

11. E-Da Hospital, Kaohsiung City, Taiwan

12. Taipei Veterans General Hospital, Taipei City, Taiwan

13. Chi Mei Hospital, Tainan City, Taiwan

14. China Medical University Hospital, Taichung City, Taiwan

15. Keelung Chang Gung Memorial Hospital, Keelung City, Taiwanand

16. National Taiwan University College of Medicine and Hospital, Taipei City, Taiwan

Abstract

Abstract Background For patients coinfected with hepatitis C virus (HCV) and hepatitis B virus (HBV), HCV treatment with direct-acting antivirals can lead to HBV reactivation. We evaluated HBV reactivation during ledipasvir/sofosbuvir treatment and 108-week follow-up. Methods In Taiwan, 111 patients with HCV genotype 1 or 2 and HBV received ledipasvir/sofosbuvir (90mg/400mg) once daily for 12 weeks. HBV virologic reactivation was defined as postbaseline increase in HBV DNA from either less than the lower limit of quantification (LLOQ, 20 IU/mL) to equal to or more than LLOQ or equal to or more than LLOQ to >1 log10 IU/mL. HBV clinical reactivation was HBV virologic reactivation with alanine aminotransferase (ALT) >2× upper limit of normal. Factors associated with development of HBV virologic or clinical reactivation were evaluated with logistic regression analysis. Results All patients (100%, 111/111) maintained HCV suppression through 108 weeks after treatment. HBV virologic reactivation occurred in 73% of patients (81/111). Clinical reactivation occurred in 9% (10/111). The majority of HBV virologic reactivations (86%, 70/81) occurred by follow-up week 12, whereas clinical reactivation was generally more delayed. Eight (7%, 8/111) initiated HBV therapy. In regression analyses, baseline HBV DNA and hepatitis B surface antigen (HBsAg) levels were associated with HBV virologic reactivation and baseline ALT and HBV DNA, and HBsAg levels were associated with HBV clinical reactivation. Conclusion Among HCV/HBV coinfected patients treated with direct-acting antivirals for HCV, HBV virologic reactivation occurred in a majority of patients during treatment and follow-up. In most patients, HBV virologic reactivation was asymptomatic; only a small proportion initiated HBV treatment. Notably, clinical reactivation may still occur >3 months after end of therapy. Clinical Trials Registration NCT02613871.

Funder

Gilead Sciences

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Microbiology (medical)

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