4.8 Article

Liver cancer risk after HCV cure in patients with advanced liver disease without non-characterized nodules

期刊

JOURNAL OF HEPATOLOGY
卷 76, 期 4, 页码 874-882

出版社

ELSEVIER
DOI: 10.1016/j.jhep.2021.11.023

关键词

HCC; SVR; DAA; cancer; advanced liver disease; F3; cirrhosis; HCC screening program; ALBI score; AFP

资金

  1. Societat Catalana de Digestologia (SCD)
  2. Instituto de Salud Carlos III [PI15/00145, PI18/0358, FI19/00222, PI20/00609, PI18/00542, PI18/00768, PI18/00079]
  3. Spanish Health Ministry (National Strategic Plan against Hepatitis C.)
  4. Gilead [IN-ES987-5349]
  5. Asociacion Espanola para el Estudio del Higado
  6. Societat Catalana Digestologia
  7. Spanish Health Ministry
  8. Contractes Clinic de Recerca Emili Letang-Josep Font 2020 - Hospital Clinic de Barcelona
  9. European Association for the Study of the Liver (EASL)
  10. AECC [PI044031]
  11. [PERIS_IPIF19-SLT008/18/00182]

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Research on HCV-infected patients shows that cirrhotic patients without non-characterized liver nodules at sustained virologic response still face the risk of hepatocellular carcinoma. Patients in F3 fibrosis stage have a lower cancer risk, but more prospective studies are needed for verification.
Background & Aims: Recognition of non-characterized liver nodules (NCLN) prior to direct-acting antivirals (DAAs) is associated with increased hepatocellular carcinoma (HCC) risk in patients with HCV. The risk of HCC has not been defined in F3/F4 patients in whom NCLN have been ruled-out before starting DAAs and at sustained virological response (SVR). This study aimed to estimate HCC incidence in this population. Methods: We performed a prospective study including HCV-infected patients with F3/F4 fibrosis, without a history of HCC, and who achieved SVR after DAAs. Patients were only included if they had undergone ultrasound imaging that excluded the presence of HCC/NCLN within 30 days after SVR. All patients were evaluated every 6 months until developing primary liver cancer, death or withdrawal of informed consent. HCC incidence was expressed per 100 patient-years (/100PY). Adherence to screening program was calculated every 6 months for the first 48 months. Results: A total of 185 patients (63/122, F3/F4) were included. Among those with cirrhosis, 92% were Child-Pugh A and 42.7% had clinically significant portal hypertension (CSPH). Albumin-bilirubin score was 1 in 84.9% and 2 in 15.1% of patients, respectively. The median clinical and radiologic follow-up was 52.4 months and 48 months, respectively. Ten patients developed HCC: HCC incidence was 1.46/100PY (95% CI 0.79-2.71) in the whole cohort, 2.24/100PY (95% CI 1.21-4.17) in F4 only and 3.63/100PY (95% CI 1.95-6.74) in patients with CSPH. No HCC was registered in patients with F3. Median time between SVR and HCC occurrence was 28.1 months; 12 non-primary liver cancers were also identified. Conclusions: Patients with cirrhosis without NCLN at SVR remain at risk of HCC development. The absence of HCC in patients with F3 reinforces their marginal cancer risk, but prospective studies are needed to exclude them from screening programs. Lay summary: Patients with HCV-related cirrhosis, without non-characterized liver nodules at sustained virologic response, remain at risk of hepatocellular carcinoma despite viral cure. However, the cancer risk after successful direct-acting antiviral treatment is marginal in patients with F3 fibrosis without non-characterized liver nodules. If confirmed in larger prospective studies, current screening recommendations may need to be revisited in this group of patients. (C) 2021 Published by Elsevier B.V. on behalf of European Association for the Study of the Liver.

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