Toyoda Hidenori, Hiraoka Atsushi, Uojima Haruki, Nozaki Akito, Shimada Noritomo, Takaguchi Koichi, Abe Hiroshi, Atsukawa Masanori, Matsuura Kentaro, Ishikawa Toru, Mikami Shigeru, Watanabe Tsunamasa, Itobayashi Ei, Tsuji Kunihiko, Arai Taeang, Yasuda Satoshi, Chuma Makoto, Senoh Tomonori, Tsutsui Akemi, Okubo Tomomi, Ehira Takuya, Kumada Takashi, Tanaka Junko
Department of GastroenterologyOgaki Municipal HospitalOgakiJapan.
Gastroenterology CenterEhime Prefectural Central HospitalMatsuyamaJapan.
Hepatol Commun. 2021 May 5;5(7):1290-1299. doi: 10.1002/hep4.1716. eCollection 2021 Jul.
Hepatocellular carcinoma (HCC) can develop in patients with chronic hepatitis C even after the achievement of sustained virologic response (SVR). We characterized HCC after SVR, comparing it with HCC that developed in patients during persistent hepatitis C virus (HCV) infection. Characteristics, survival rates, and recurrence rates after curative treatment in 178 patients who developed initial HCC after SVR diagnosed between 2014 and 2020 were compared with those of 127 patients with initial HCC that developed during persistent HCV infection diagnosed between 2011 and 2015; HCC was detected under surveillance in both groups. HCC was less advanced and liver function worsened less in patients with SVR than in patients with persistent HCV. The survival rate after diagnosis was significantly higher for patients with SVR than for patients with persistent HCV (1-, 3-, and 5-year survival rates, 98.2%, 92.5%, and 86.8% versus 89.5%, 74.7%, and 60.8%, respectively; < 0.001). By contrast, the recurrence rate after curative treatment was similar between groups (1-, 3-, and 5-year recurrence rates, 11.6%, 54.6%, and 60.4% versus 24.0%, 46.7%, and 50.4%, respectively; = 0.7484). Liver function improved between initial HCC diagnosis and recurrence in patients with SVR ( = 0.0191), whereas it worsened in the control group ( < 0.001). In addition, patients with SVR could receive curative treatment for recurrence more frequently than patients with persistent HCV (80.4% versus 47.8%, respectively; = 0.0008). Survival of patients with HCC after SVR was significantly higher than that of patients in whom HCC developed during persistent HCV infection, despite similar rates of recurrence after curative treatment. A higher prevalence of curative treatment for recurrent HCC and improved liver function contributed to this result.
即使在实现持续病毒学应答(SVR)之后,慢性丙型肝炎患者仍可能发生肝细胞癌(HCC)。我们对SVR后的HCC进行了特征描述,并将其与丙型肝炎病毒(HCV)持续感染患者中发生的HCC进行比较。将2014年至2020年间诊断为SVR后首次发生HCC的178例患者与2011年至2015年间诊断为HCV持续感染期间首次发生HCC的127例患者进行了比较,两组均在监测中发现HCC。与HCV持续感染患者相比,SVR患者的HCC分期较低,肝功能恶化程度较轻。SVR患者诊断后的生存率显著高于HCV持续感染患者(1年、3年和5年生存率分别为98.2%、92.5%和86.8%,而HCV持续感染患者分别为89.5%、74.7%和60.8%;P<0.001)。相比之下,两组间根治性治疗后的复发率相似(1年、3年和5年复发率分别为11.6%、54.6%和60.4%,而HCV持续感染患者分别为24.0%、46.7%和50.4%;P=0.7484)。SVR患者在初次HCC诊断至复发期间肝功能有所改善(P=0.0191),而对照组肝功能则恶化(P<0.001)。此外,SVR患者比HCV持续感染患者更频繁地接受复发的根治性治疗(分别为80.4%和47.8%;P=0.0008)。尽管根治性治疗后的复发率相似,但SVR后发生HCC的患者生存率显著高于HCV持续感染期间发生HCC的患者。复发性HCC根治性治疗的较高患病率和肝功能改善促成了这一结果。