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Gastroenterol Res Pract. 2018;2018:6948235.

Is Combination Antiviral Therapy Mandatory for Maintenance Therapy in Fully Suppressed Multidrug-Resistant Hepatitis B Patients?

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제1저자 정성원 · 교신저자 김윤준

소속 (1)
  1. Department of Internal Medicine and Liver Research Institute, Seoul National University College of Medicine, Republic of Korea.

Abstract

AIM The efficacy of tenofovir disoproxil fumarate (TDF) monotherapy as maintenance therapy in multidrug-resistant (MDR) hepatitis B virus (HBV) patients after complete virologic suppression (CVS) has not been well evaluated. We evaluated the efficacy of maintenance TDF monotherapy compared with conventional TDF plus entecavir combination therapy after CVS of MDR HBV.

METHODS In this single-center retrospective study, patients with MDR HBV who were previously treated with entecavir plus TDF combination therapy and achieved CVS were included. Patients were either maintained on entecavir plus TDF combination therapy or switched to TDF monotherapy after CVS. The primary endpoint was the virologic breakthrough, and secondary outcomes were liver cirrhosis (LC) or hepatocellular carcinoma (HCC) development. To overcome immortal time bias, time-varying Cox proportional hazard regression analysis was performed.

RESULTS A total of 201 patients were included, and 153 patients were maintained on entecavir plus TDF combination therapy (combination group); 48 patients were converted from combination therapy to TDF monotherapy (single group) after CVS. Five patients experienced a virologic breakthrough, one patient in the single group owing to poor transient compliance and four patients in the combination group (P = 0.51). One new case of LC developed in the single group; five cases of LC developed in the combination group (P = 0.35). No new HCC development occurred in the single group, while seven cases of HCC developments were noted in the combination group. However, these results were not statistically significant (P = 0.54).

CONCLUSIONS For patients with suppressed HBV DNA, the efficacy of TDF monotherapy as maintenance therapy is comparable to that of entecavir plus TDF combination therapy.

Figures

Figure 1
Figure 1 Flow diagram. A total of 279 patients were identified, and 78 patients were excluded by exclusion criteria. The final sample consisted of 201 patients, who were classified into 2 groups according to maintenance therapy (combination group versus single group).
Figure 2
Figure 2 Extended Kaplan-Meier curves of cumulative incidence of virologic breakthrough, stratified by time-varying TDF monotherapy status. The index date was set as the date of complete virologic suppression. Hazard ratio (HR), 95% confidence intervals (CI), and P values were calculated by the time-varying Cox proportional hazard model with the time-varying covariate. CI: confidence interval; HR: hazard ratio; no.: number; TDF: tenofovir disoproxil fumarate.
Figure 3
Figure 3 Extended Kaplan-Meier curves of cumulative incidence of liver cirrhosis development, stratified by time-varying TDF monotherapy status. The index date was set as the date of complete virologic suppression. Hazard ratio (HR), 95% confidence intervals (CI), and P values were calculated by the time-varying Cox proportional hazard model with the time-varying covariate. CI: confidence interval; HR: hazard ratio; LC: liver cirrhosis; no.: number; TDF: tenofovir disoproxil fumarate.
Figure 4
Figure 4 Extended Kaplan-Meier curves of cumulative incidence of hepatocellular carcinoma (HCC) development, stratified by time-varying TDF monotherapy status. The index date was set as the date of complete virologic suppression. Hazard ratio (HR), 95% confidence intervals (CI), and P values were calculated by the time-varying Cox proportional hazard model with time-varying covariate. CI: confidence interval; HCC: hepatocellular carcinoma; HR: hazard ratio; TDF: tenofovir disoproxil fumarate.

그림 출처: PubMed Central 공개 논문 (PMC6311770)

그 밖의 정보
출판 형태
Journal Article
저널
Gastroenterology research and practice · ISSN 1687-6121
전자 출판
2018-12-16
참고문헌
32편