Ogawa Eiichi, Nomura Hideyuki, Nakamuta Makoto, Furusyo Norihiro, Kajiwara Eiji, Dohmen Kazufumi, Kawano Akira, Ooho Aritsune, Azuma Koichi, Takahashi Kazuhiro, Satoh Takeaki, Koyanagi Toshimasa, Ichiki Yasunori, Kuniyoshi Masami, Yanagita Kimihiko, Amagase Hiromasa, Morita Chie, Sugimoto Rie, Kato Masaki, Shimoda Shinji, Hayashi Jun
Department of General Internal Medicine, Kyushu University Hospital, Fukuoka 8128582, Japan.
The Center for Liver Disease, Shin-Kokura Hospital, Kitakyushu 8038505, Japan.
Cancers (Basel). 2020 Sep 11;12(9):2602. doi: 10.3390/cancers12092602.
Advanced fibrosis/cirrhosis and related biomarkers have been recognized as useful predictors of the development of hepatocellular carcinoma (HCC) by patients with chronic hepatitis C (CHC) following hepatitis C virus (HCV) cure by direct-acting antivirals (DAAs). However, it remains unclear if DAAs themselves have an influence on or facilitate the development of HCC. This multicenter cohort study included CHC patients without a history of HCC who achieved HCV elimination by DAAs. Cohorts of 835 patients treated with a sofosbuvir (SOF)-based regimen and 835 treated with a SOF-free regimen were matched 1:1 by propensity scoring with nine variables to evaluate differences in HCC incidence. The median observation period was 3.5 years. Sixty-nine cases of HCC were found during 5483.9 person-years (PY) over the entire follow-up period. The annual incidence was similar for both groups (SOF-based 1.25 and SOF-free 1.27 per 100 PY, respectively: adjusted hazard ratio (HR) 1.26, 95% confidence interval (CI) 0.75-2.12, = 0.39). However, the annual incidence within the first two years was higher for patients treated with SOF than for those without, but did not reach significance (1.50 and 0.97 per 100 PY incidence rates, respectively: adjusted HR 2.05, 95% CI 0.98-4.25, = 0.06). In summary, DAA treatment with SOF was not associated with an increase in the development of de novo HCC.
在慢性丙型肝炎(CHC)患者通过直接作用抗病毒药物(DAA)治愈丙型肝炎病毒(HCV)后,晚期纤维化/肝硬化及相关生物标志物已被公认为肝细胞癌(HCC)发生的有用预测指标。然而,DAA本身是否会影响或促进HCC的发生仍不清楚。这项多中心队列研究纳入了无HCC病史且通过DAA实现HCV清除的CHC患者。对835例接受基于索磷布韦(SOF)方案治疗的患者和835例接受不含SOF方案治疗的患者队列,通过倾向评分法对九个变量进行1:1匹配,以评估HCC发病率的差异。中位观察期为3.5年。在整个随访期的5483.9人年(PY)中发现了69例HCC病例。两组的年发病率相似(基于SOF的组为每100 PY 1.25例,不含SOF的组为每100 PY 1.27例:调整后风险比(HR)为1.26,95%置信区间(CI)为0.75 - 2.12,P = 0.39)。然而,接受SOF治疗的患者在头两年的年发病率高于未接受SOF治疗的患者,但未达到显著差异(发病率分别为每100 PY 1.50例和0.97例:调整后HR为2.05,95%CI为0.98 - 4.25,P = 0.06)。总之,使用SOF的DAA治疗与新发HCC的发生增加无关。