Global impact of hepatitis B vaccination on the risk of hepatocellular carcinoma: a systematic review and meta-analysis.

IF 2.1 4区 医学 Q3 GASTROENTEROLOGY & HEPATOLOGY
Journal of gastrointestinal oncology Pub Date : 2026-08-31 Epub Date: 2026-07-08 DOI:10.21037/jgo-2026-0202
Jingyao Wang, Jie Xu, Juan Meng, Xiaoyang Shi, Shichao Geng, Xiaolan Wang
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引用次数: 0

Abstract

Background: This systematic review and meta-analysis aimed to synthesize global evidence on the association between hepatitis B virus (HBV) vaccination and incident hepatocellular carcinoma (HCC), including subgroup analyses by country/region, vaccine formulation, and dosing regimen.

Methods: PubMed, Scopus, and Web of Science were searched from inception to July 24, 2025. The study protocol was registered on PROSPERO (ID: 1355073). Studies were eligible if they reported HCC incidence or risk among vaccinated versus unvaccinated populations, included >20 cases, and provided extractable comparative data. Methodological quality was appraised using the National Institutes of Health (NIH) Quality Assessment Tool. Random-effects models (DerSimonian-Laird) were used to pool incidence rate ratios (IRRs) and adjusted relative risks (aRRs), expressed with 95% confidence intervals (CIs).

Results: Sixteen studies encompassing over 5 million participants met inclusion criteria. The pooled unadjusted analysis demonstrated a 65% reduction in HCC incidence among vaccinated individuals (IRR =0.35, 95% CI: 0.26-0.47; I2=76.5%). Protection was consistent across subgroups, including males (IRR =0.25, 95% CI: 0.12-0.53) and females (IRR =0.43, 95% CI: 0.20-0.94). The pooled adjusted estimate confirmed a 67% lower risk of HCC (aRR =0.33, 95% CI: 0.24-0.46; I2=83.4%, with substantial between-study heterogeneity). Plasma-derived vaccines were associated with a significantly reduced HCC risk (aRR =0.34, 95% CI: 0.25-0.47), whereas the pooled estimate for recombinant vaccines was directionally consistent but did not reach statistical significance (aRR =0.16, 95% CI: 0.01-3.72), likely reflecting the limited number of contributing studies. Comparable protection was observed with ≥2-dose or ≥3-dose regimens. No study was rated poor in quality; five were good and nine were fair; the two randomized trials were appraised separately using the Cochrane Risk of Bias 2 tool.

Conclusions: HBV vaccination is associated with a significant and durable reduction in HCC risk, independent of demographic, geographic, or vaccine-related factors. These findings are consistent with the view that universal HBV immunization is among the most effective population-level cancer prevention strategies worldwide.

乙型肝炎疫苗接种对肝细胞癌风险的全球影响:一项系统综述和荟萃分析
背景:本系统综述和荟萃分析旨在综合乙型肝炎病毒(HBV)疫苗接种与肝细胞癌(HCC)发生率之间关联的全球证据,包括按国家/地区、疫苗制剂和给药方案进行亚组分析。方法:检索PubMed、Scopus、Web of Science,检索时间为建站至2025年7月24日。研究方案已在PROSPERO (ID: 1355073)上注册。如果研究报告了接种疫苗人群与未接种疫苗人群的HCC发病率或风险,包括20例病例,并提供可提取的比较数据,则该研究是合格的。采用美国国立卫生研究院(NIH)质量评估工具对方法学质量进行评价。随机效应模型(dersimonan - laird)用于汇总发病率比(IRRs)和校正相对风险(aRRs),以95%置信区间(ci)表示。结果:16项研究超过500万参与者符合纳入标准。未经校正的汇总分析显示,接种疫苗的个体HCC发病率降低了65% (IRR =0.35, 95% CI: 0.26-0.47; I2=76.5%)。亚组间的保护效果一致,包括男性(IRR =0.25, 95% CI: 0.12-0.53)和女性(IRR =0.43, 95% CI: 0.20-0.94)。合并调整后的估计证实HCC风险降低67% (aRR =0.33, 95% CI: 0.24-0.46; I2=83.4%,研究间存在显著异质性)。血浆源性疫苗与显著降低HCC风险相关(aRR =0.34, 95% CI: 0.25-0.47),而重组疫苗的汇总估计方向一致,但未达到统计学意义(aRR =0.16, 95% CI: 0.01-3.72),可能反映了有贡献的研究数量有限。≥2剂或≥3剂方案的保护效果相当。没有研究被评为质量差;五个是好的,九个是一般的;使用Cochrane风险偏倚2工具分别对两项随机试验进行评价。结论:HBV疫苗接种与HCC风险的显著和持久降低相关,独立于人口统计学、地理或疫苗相关因素。这些发现与普遍的乙肝病毒免疫接种是全世界最有效的人群癌症预防策略之一的观点是一致的。
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来源期刊
CiteScore
3.20
自引率
0.00%
发文量
171
期刊介绍: ournal of Gastrointestinal Oncology (Print ISSN 2078-6891; Online ISSN 2219-679X; J Gastrointest Oncol; JGO), the official journal of Society for Gastrointestinal Oncology (SGO), is an open-access, international peer-reviewed journal. It is published quarterly (Sep. 2010- Dec. 2013), bimonthly (Feb. 2014 -) and openly distributed worldwide. JGO publishes manuscripts that focus on updated and practical information about diagnosis, prevention and clinical investigations of gastrointestinal cancer treatment. Specific areas of interest include, but not limited to, multimodality therapy, markers, imaging and tumor biology.
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