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Clin Mol Hepatol. 2024;30(3):500-514.

Extrahepatic malignancies and antiviral drugs for chronic hepatitis B: A nationwide cohort study.

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제1저자 허문행, 이동현 · 교신저자 이정훈

소속 (4)
  1. Department of Internal Medicine and Liver Research Institute, Seoul National University College of Medicine, Seoul, Korea.
  2. Department of Internal Medicine, Seoul Metropolitan Government Seoul National University Boramae Medical Center, Seoul, Korea.
  3. Genome Insight Inc., San Diego, CA, USA.
  4. Medical Research Collaborating Center, Seoul National University Hospital, Seoul, Korea.

Abstract

BACKGROUND/AIMS Chronic hepatitis B (CHB) is related to an increased risk of extrahepatic malignancy (EHM), and antiviral treatment is associated with an incidence of EHM comparable to controls. We compared the risks of EHM and intrahepatic malignancy (IHM) between entecavir (ETV) and tenofovir disoproxil fumarate (TDF) treatment.

METHODS Using data from the National Health Insurance Service of Korea, this nationwide cohort study included treatment-naïve CHB patients who initiated ETV (n=24,287) or TDF (n=29,199) therapy between 2012 and 2014. The primary outcome was the development of any primary EHM. Secondary outcomes included overall IHM development. E-value was calculated to assess the robustness of results to unmeasured confounders.

RESULTS The median follow-up duration was 5.9 years, and all baseline characteristics were well balanced after propensity score matching. EHM incidence rate differed significantly between within versus beyond 3 years in both groups (P<0.01, Davies test). During the first 3 years, EHM risk was comparable in the propensity score-matched cohort (5.88 versus 5.84/1,000 person-years; subdistribution hazard ratio [SHR]=1.01, 95% confidence interval [CI]=0.88-1.17, P=0.84). After year 3, however, TDF was associated with a significantly lower EHM incidence compared to ETV (4.92 versus 6.91/1,000 person-years; SHR=0.70, 95% CI=0.60-0.81, P<0.01; E-value for SHR=2.21). Regarding IHM, the superiority of TDF over ETV was maintained both within (17.58 versus 20.19/1,000 person-years; SHR=0.88, 95% CI=0.81-0.95, P<0.01) and after year 3 (11.45 versus 16.20/1,000 person-years; SHR=0.68, 95% CI=0.62-0.75, P<0.01; E-value for SHR=2.30).

CONCLUSION TDF was associated with approximately 30% lower risks of both EHM and IHM than ETV in CHB patients after 3 years of antiviral therapy.

Keywords

Antiviral treatmentEntecavirHepatitis B virusNon-liver cancerTenofovir

Figures

Figure 1.
Figure 1. Patient flow diagram. Specific diagnostic and procedural codes are presented in Supplementary Table 1. CHB, chronic hepatitis B; ETV, entecavir; HCV, hepatitis C virus; HDV, hepatitis D virus; HIV, human immunodeficiency virus; NA, nucleos(t)ide-analogue; NHIS, National Health Insurance Service; TDF, tenofovir disoproxil fumarate.
Figure 2.
Figure 2. Cumulative incidence of extrahepatic malignancies in propensity score-matched cohort. Analysis was performed after propensity score matching. Intrahepatic malignancy development and death were treated as competing events. ETV, entecavir; TDF, tenofovir disoproxil fumarate.
Figure 3.
Figure 3. Risk of extrahepatic malignancy in the propensity score-matched cohort according to prespecified subgroups. SHR, subdistribution hazard ratio; CI, confidence interval; ETV, entecavir; Pinteraction, P-value for interaction; TDF, tenofovir disoproxil fumarate. *High, middle, and low socioeconomic statuses indicate socioeconomic status within the ≥75th, 25th–75th, and <25th percentiles, respectively.

그림 출처: PubMed Central 공개 논문 (PMC11261230)

Comment · 정정

Conflict of interest statement

Conflicts of Interest . Moon Haeng Hur: Nothing to declare; Dong Hyeon Lee: Nothing to declare; Jeong-Hoon Lee: Receives research grants from Yuhan Pharmaceuticals and GreenCross Cell, lecture fees from GreenCross Cell, Daewoong Pharmaceuticals, and Gilead Korea; Mi-Sook Kim: Nothing to declare; Jeayeon Park: Nothing to declare; Hyunjae Shin: Nothing to declare; Sung Won Chung: Nothing to declare; to declare; Heejoon Jang: Nothing to declare; Yun Bin Lee: Receives research grants from Samjin Pharmaceuticals and Yuhan Pharmaceuticals; Su Jong Yu: Receives research grants from Yuhan Pharmaceuticals and Daewoong Pharmaceuticals; Sang Hyub Lee: Nothing to declare; Yong Jin Jung: Nothing to declare; Yoon Jun Kim: Receives research grants from BTG, Boston Scientific, AstraZeneca, Gilead Sciences, Samjin, BL&H, and Bayer, and lecture fees from Roche, Abbvie, Eisai, Boston Scientific, BMS, BTG, Bayer, MSD, Novo Nordisk, Green Cross Cell, Boehringer Ingelheim, and Gilead; Jung-Hwan Yoon: Receives research grants from Bayer, Daewoong Pharmaceutical, and Bukwang Pharmaceutical.

그 밖의 정보
출판 형태
Journal Article
저널
Clinical and molecular hepatology · eISSN 2287-285X
전자 출판
2024-05-10
MeSH
Humans · Antiviral Agents* / therapeutic use · Hepatitis B, Chronic* / drug therapy / complications · Female · Male · Middle Aged · Adult · Tenofovir* / therapeutic use · Guanine* / analogs & derivatives / therapeutic use · Incidence · Cohort Studies · Republic of Korea / epidemiology · Propensity Score · Proportional Hazards Models · Liver Neoplasms · Risk Factors · Aged
Substances
Antiviral Agents · entecavir · Tenofovir · Guanine
연구비
National IT Industry Promotion Agency S0252-21-1001 · Ministry of Science and ICT · Liver Research Foundation of Korea · Seoul National University Hospital 04-2019-3090 · Yuhan Pharmaceuticals · GreenCross Cell · Samjin Pharmaceuticals · Daewoong Pharmaceuticals · BTG · Boston Scientific · AstraZeneca · Gilead Sciences · BL&H · Bayer · Bukwang Pharmaceutical
참고문헌
49편