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Lower Observed Hepatocellular Carcinoma Incidence in Chronic Hepatitis B Patients Treated With Entecavir: Results of the ENUMERATE Study.
Ahn, Joseph; Lim, Joseph K; Lee, Hannah M; Lok, Anna S; Nguyen, Mindie; Pan, Calvin Q; Mannalithara, Ajitha; Te, Helen; Reddy, K Rajender; Trinh, Huy; Chu, Danny; Tran, Tram; Lau, Daryl; Leduc, Truong-Sinh; Min, Albert; Trong Le, Loc; Bae, Ho; Van Tran, Sang; Do, Son; Hann, Hie-Won L; Wong, Clifford; Han, Steven; Pillai, Anjana; Park, James S; Tong, Myron; Scaglione, Steve; Woog, Jocelyn; Kim, W Ray.
  • Ahn J; Division of Gastroenterology and Hepatology, Oregon Health and Science University, Portland, Oregon, USA.
  • Lim JK; Department of Digestive Diseases, Yale University, New Haven, Connecticut, USA.
  • Lee HM; Gastroenterology/Hepatology Division, Virginia Commonwealth University, Richmond, Virginia, USA.
  • Lok AS; Division of Gastroenterology and Hepatology, University of Michigan, Ann Arbor, Michigan, USA.
  • Nguyen M; Division of Gastroenterology and Hepatology, Stanford University, Stanford, California, USA.
  • Pan CQ; Department of Medicine, NYU Langone, New York City, New York, USA.
  • Mannalithara A; Division of Gastroenterology and Hepatology, Stanford University, Stanford, California, USA.
  • Te H; Digestive Disease Center, University of Chicago, Chicago, Illinois, USA.
  • Reddy KR; Division of Gastroenterology and Hepatology, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
  • Trinh H; San Jose GI, San Jose, California, USA.
  • Chu D; NYU School of Medicine, New York City, New York, USA.
  • Tran T; Department of Medicine, Cedars Sinai Medical Center, Los Angeles, California, USA.
  • Lau D; Department of Gastroenterology and Hepatology, BIDMC, Boston, Massachusetts, USA.
  • Leduc TS; Leduc Medical Group, Fountain Valley, California, USA.
  • Min A; Division of Gastroenterology, Mount Sinai Beth Israel, New York City, New York, USA.
  • Trong Le L; Woodholme Gastroenterology Associates, Pikeville, Maryland, USA.
  • Bae H; Asian Pacific Liver Center, Los Angeles, California, USA.
  • Van Tran S; Falls Church Family Practice, Falls Church, Virginia, USA.
  • Do S; Digestive Health Associates of Texas, Plano, Texas, USA.
  • Hann HW; Thomas Jefferson University Hospital, Philadelphia, Pennsylvania, USA.
  • Wong C; San Francisco, California, USA.
  • Han S; University of California, Los Angeles, Los Angeles, California, USA.
  • Pillai A; Emory University, Atlanta, Georgia, USA.
  • Park JS; NYU Langone, New York City, New York, USA.
  • Tong M; Emory University, Atlanta, Georgia, USA.
  • Scaglione S; Loyola University, Maywood, Illinois, USA.
  • Woog J; Asian Health Foundation, Philadelphia, Pennsylvania, USA.
  • Kim WR; Division of Gastroenterology and Hepatology, Stanford University, Stanford, California, USA.
Am J Gastroenterol ; 111(9): 1297-304, 2016 09.
Article en En | MEDLINE | ID: mdl-27325221
ABSTRACT

OBJECTIVES:

Data from the United States are lacking regarding the impact of entecavir (ETV) on the risk of hepatocellular carcinoma (HCC). Our aim is to determine whether treatment with ETV is associated with a reduced HCC risk by calculating the expected HCC incidence based on the Risk Estimation for Hepatocellular Carcinoma in Chronic Hepatitis B (REACH-B) model and comparing it with the observed HCC incidence.

METHODS:

The incidence of HCC in US patients treated with ETV between 2005 and 2013 in a retrospective cohort was obtained. The predicted HCC incidence was calculated using the REACH-B model. The standardized incidence ratios (SIRs) were calculated as a ratio of observed over predicted HCC cases.

RESULTS:

Of 841 patients, 646 (65% male, 84% Asian, median age 47 years, 36% hepatitis B e antigen positive, 9.4% with cirrhosis) met the inclusion criteria. Over a median follow-up of 4 years, 17 (2.6%) cases of HCC were diagnosed, including 8 out of 61 (13.1%) patients with cirrhosis and 9 out of 585 (1.5%) without cirrhosis. Compared with those without HCC, the 17 patients with HCC were older at 53 years vs. 47 years and more likely to have cirrhosis at 47.1% vs. 8.4%. Among patients without cirrhosis, the observed HCC incidence was significantly lower than predicted by the fourth year (SIR, 0.37; 95% confidence interval 0.166-0.82). A sensitivity analysis that comprised all patients, including those with cirrhosis, showed that at the maximum follow-up time of 8.2 years, a significantly lower than predicted HCC incidence was noted with an SIR of 0.56 (95% confidence interval 0.35-0.905).

CONCLUSIONS:

Based on the REACH-B model, long-term ETV therapy was associated with a lower than predicted HCC incidence. However, the risk of HCC persisted, and careful HCC surveillance remains warranted despite the anti-viral treatment.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Antivirales / Carcinoma Hepatocelular / Hepatitis B Crónica / Guanina / Neoplasias Hepáticas Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Aged / Aged80 / Female / Humans / Male / Middle aged País como asunto: America do norte Idioma: En Año: 2016 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Antivirales / Carcinoma Hepatocelular / Hepatitis B Crónica / Guanina / Neoplasias Hepáticas Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Aged / Aged80 / Female / Humans / Male / Middle aged País como asunto: America do norte Idioma: En Año: 2016 Tipo del documento: Article