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Ledipasvir/Sofosbuvir for Patients Coinfected With Chronic Hepatitis C and Hepatitis B in Taiwan: Follow-up at 108 Weeks Posttreatment.
Liu, Chun Jen; Sheen, I Shyan; Chen, Chi Yi; Chuang, Wan Long; Wang, Horng Yuan; Tseng, Kuo Chih; Chang, Ting Tsung; Yang, Jenny; Massetto, Benedetta; Suri, Vithika; Camus, Gregory; Jiang, Deyuan; Zhang, Fangqiu; Gaggar, Anuj; Hu, Tsung Hui; Hsu, Yu Chun; Lo, Gin Ho; Chu, Chi Jen; Chen, Jyh Jou; Peng, Cheng Yuan; Chien, Rong Nan; Chen, Pei Jer.
Affiliation
  • Liu CJ; Department of Internal Medicine, Hepatitis Research Center, and Graduate Institute of Clinical Medicine, National Taiwan University College of Medicine and Hospital, Taipei City, Taiwan.
  • Sheen IS; Linkou Chang Gung Memorial Hospital, Taoyuan City, Taiwan.
  • Chen CY; Chia-Yi Christian Hospital, Chia-Yi City, Taiwan.
  • Chuang WL; Kaohsiung Medical University Hospital, Kaohsiung Medical University, Kaohsiung City, Taiwan.
  • Wang HY; MacKay Memorial Hospital, Taipei City, Taiwan.
  • Tseng KC; Dalin Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation, Chia-Yi City, Taiwan.
  • Chang TT; National Cheng Kung University, College of Medicine and Hospital, Tainan City, Taiwan.
  • Yang J; Gilead Sciences, Inc., Foster City, California, USA.
  • Massetto B; Gilead Sciences, Inc., Foster City, California, USA.
  • Suri V; Gilead Sciences, Inc., Foster City, California, USA.
  • Camus G; Gilead Sciences, Inc., Foster City, California, USA.
  • Jiang D; Gilead Sciences, Inc., Foster City, California, USA.
  • Zhang F; Gilead Sciences, Inc., Foster City, California, USA.
  • Gaggar A; Gilead Sciences, Inc., Foster City, California, USA.
  • Hu TH; Kaohsiung Chang Gung Memorial Hospital, Kaohsiung City, Taiwan.
  • Hsu YC; Changhua Christian Hospital, Changhua City, Taiwan.
  • Lo GH; E-Da Hospital, Kaohsiung City, Taiwan.
  • Chu CJ; Taipei Veterans General Hospital, Taipei City, Taiwan.
  • Chen JJ; Chi Mei Hospital, Tainan City, Taiwan.
  • Peng CY; China Medical University Hospital, Taichung City, Taiwan.
  • Chien RN; Keelung Chang Gung Memorial Hospital, Keelung City, Taiwanand.
  • Chen PJ; National Taiwan University College of Medicine and Hospital, Taipei City, Taiwan.
Clin Infect Dis ; 75(3): 453-459, 2022 08 31.
Article in En | MEDLINE | ID: mdl-34864948
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.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Hepatitis C / Hepatitis C, Chronic / Coinfection / Hepatitis B Type of study: Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Humans Country/Region as subject: Asia Language: En Journal: Clin Infect Dis Journal subject: DOENCAS TRANSMISSIVEIS Year: 2022 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Hepatitis C / Hepatitis C, Chronic / Coinfection / Hepatitis B Type of study: Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Humans Country/Region as subject: Asia Language: En Journal: Clin Infect Dis Journal subject: DOENCAS TRANSMISSIVEIS Year: 2022 Document type: Article Affiliation country: