Nguyen Ngan, Patel Kruti, Uhelski Anna Carson, Waters Bradford, Weir Alva
is a Gastroenterologist in the Gastroenterology & Hepatology Department; and is a Hematologist Oncologist, Section Chief Hematology/Oncology, both at the Memphis Veteran Affairs Medical Center in Tennessee. is a Medicine Resident Physician at Johns Hopkins Osler in Baltimore Maryland. Bradford Waters and Alva Weir are Professors; and and are Hematology Oncology Fellows, all at the University of Tennessee Health Science Center, in Memphis.
Fed Pract. 2021 Aug;38(Suppl 3):e58-e63. doi: 10.12788/fp.0165.
Chronic hepatitis C virus (HCV) infection is a common risk factor for hepatocellular cancer (HCC). Patients with HCV infection are at a higher risk of developing HCC because the virus induces fibrosis in the liver, which may lead to cirrhosis. Early treatment of HCV and achieving a sustained virologic response (SVR) may lead to decreased incidence and mortality associated with HCC.
We performed a retrospective review of patients at the Memphis Veterans Affairs Medical Center (VAMC) in Tennessee from November 2008 to March 2019 to determine whether treatment of HCV infection makes a difference in overall survival (OS) among patients who develop HCC. Patients were treated with an interferon-based regimen or direct-acting antiviral agents (DAAs). Among the patients with HCV infection who were treated, we identified those who did achieve or did not achieve SVR.
We identified 111 patients with HCV and HCC; 68 were treated for HCV infection. Forty-eight patients received DAA and 20 patients received an interferon-based regimen and 51 achieved SVR. In a multivariate analysis accounting for severity of liver disease, treated patients had an improved 5-year OS rate, median 1338 days (95% CI, 966-3202) when compared with untreated patients whose median OS was 452 days (95% CI, 242-853) ( = .0005). The treatment group had a longer median progression-free survival (PFS) than did the nontreatment group (460 days [95% CI, 294-726] vs 286 days [95% CI, 205-405], = .04). Patients with SVR had an increased 5-year OS compared with patients without SVR (median 1973 days [95% CI, 1222-NA] vs 470 days [95% CI, 242-853], < .001). HCV treatment type (interferon vs DAA) was not found to be associated with either OS or PFS, regardless of time period. Advanced liver disease stage as characterized by a high model for end-stage liver disease (MELD) score (> 10) or high Child-Pugh score (B or C) was associated with worse survival outcome.
A retrospective analysis of patients with HCV infection and HCC confirms that treatment of HCV infection leads to OS benefit among patients with HCC. We further demonstrate that patients with HCV infection who achieve SVR have an OS benefit over patients unable to achieve SVR. The type of treatment, DAA vs an interferon-based regimen, did not show a significant survival benefit.
慢性丙型肝炎病毒(HCV)感染是肝细胞癌(HCC)的常见危险因素。HCV感染患者发生HCC的风险更高,因为该病毒会诱发肝脏纤维化,进而可能导致肝硬化。早期治疗HCV并实现持续病毒学应答(SVR)可能会降低与HCC相关的发病率和死亡率。
我们对田纳西州孟菲斯退伍军人事务医疗中心(VAMC)在2008年11月至2019年3月期间的患者进行了回顾性研究,以确定HCV感染的治疗是否会对发生HCC的患者的总生存期(OS)产生影响。患者接受了基于干扰素的治疗方案或直接抗病毒药物(DAA)治疗。在接受治疗的HCV感染患者中,我们确定了那些实现或未实现SVR的患者。
我们确定了111例HCV和HCC患者;68例接受了HCV感染治疗。48例患者接受了DAA治疗,20例患者接受了基于干扰素的治疗方案,51例实现了SVR。在一项考虑了肝病严重程度的多变量分析中,与未治疗患者(中位OS为452天[95%CI,242 - 853])相比,接受治疗的患者5年OS率有所提高,中位生存期为1338天(95%CI,966 - 3202)(P = 0.0005)。治疗组的无进展生存期(PFS)中位数比未治疗组更长(460天[95%CI,294 - 726]对286天[95%CI,205 - 405],P = 0.04)。与未实现SVR的患者相比,实现SVR的患者5年OS有所增加(中位生存期为1973天[95%CI,1222 - NA]对470天[95%CI,242 - 853],P < 0.001)。无论时间段如何,均未发现HCV治疗类型(干扰素与DAA)与OS或PFS相关。以终末期肝病模型(MELD)评分高(> 10)或Child-Pugh评分高(B或C)为特征的晚期肝病阶段与较差的生存结果相关。
对HCV感染和HCC患者的回顾性分析证实,HCV感染的治疗可使HCC患者获得OS益处。我们进一步证明,实现SVR的HCV感染患者比未实现SVR的患者具有OS益处。治疗类型,即DAA与基于干扰素的治疗方案,未显示出显著的生存益处。