Should Patients With NAFLD/NASH Be Surveyed for HCC?


Journal

Transplantation
ISSN: 1534-6080
Titre abrégé: Transplantation
Pays: United States
ID NLM: 0132144

Informations de publication

Date de publication:
01 2019
Historique:
pubmed: 7 8 2018
medline: 23 5 2019
entrez: 7 8 2018
Statut: ppublish

Résumé

Patients with nonalcoholic fatty liver disease (NAFLD) are at risk of developing hepatocellular carcinoma (HCC), but the magnitude of the association still needs to be determined to define the need for a specific surveillance strategy. We based our assessment on a previously published review by White et al (1992-2011) and on a systematic review(2012-2017). The new search identified 328 abstracts. Combining both eras (1992-2011 and 2012-2017), 25 studies were included in the analysis. Four were prospective, 2 described a retrospective analysis of a prospective database, and the others were retrospective. All studies were published after 2004, but the inclusion period of half of them ended before the year 2000. Studies showed variation in the definition of NAFLD, in the incidence of fibrosis/cirrhosis, in the presence of comorbidities (potentially affecting HCC incidence), and in the type and duration of screening. Considering only studies strictly including patients with or without cirrhosis, the reported incidence of HCC in NAFLD patients with cirrhosis was between 6.7 and 15% at 5 to 10 years, whereas the incidence in NAFLD patients without cirrhosis was 2.7% at 10 years and 23 per 100 000 person-years. Hepatocellular carcinoma screening in NAFLD patients with cirrhosis is mandatory. However, the currently observed low (and insufficiently documented) incidence of HCC in NAFLD patients without cirrhosis does not justify a systematic surveillance. Research efforts should focus on developing a score, which could aid the clinician in identifying NAFLD patients without cirrhosis who are at higher risk of developing HCC.

Sections du résumé

BACKGROUND
Patients with nonalcoholic fatty liver disease (NAFLD) are at risk of developing hepatocellular carcinoma (HCC), but the magnitude of the association still needs to be determined to define the need for a specific surveillance strategy.
METHODS
We based our assessment on a previously published review by White et al (1992-2011) and on a systematic review(2012-2017).
RESULTS
The new search identified 328 abstracts. Combining both eras (1992-2011 and 2012-2017), 25 studies were included in the analysis. Four were prospective, 2 described a retrospective analysis of a prospective database, and the others were retrospective. All studies were published after 2004, but the inclusion period of half of them ended before the year 2000. Studies showed variation in the definition of NAFLD, in the incidence of fibrosis/cirrhosis, in the presence of comorbidities (potentially affecting HCC incidence), and in the type and duration of screening. Considering only studies strictly including patients with or without cirrhosis, the reported incidence of HCC in NAFLD patients with cirrhosis was between 6.7 and 15% at 5 to 10 years, whereas the incidence in NAFLD patients without cirrhosis was 2.7% at 10 years and 23 per 100 000 person-years.
CONCLUSIONS
Hepatocellular carcinoma screening in NAFLD patients with cirrhosis is mandatory. However, the currently observed low (and insufficiently documented) incidence of HCC in NAFLD patients without cirrhosis does not justify a systematic surveillance. Research efforts should focus on developing a score, which could aid the clinician in identifying NAFLD patients without cirrhosis who are at higher risk of developing HCC.

Identifiants

pubmed: 30080818
doi: 10.1097/TP.0000000000002361
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

39-44

Auteurs

Maria Reig (M)

Barcelona Clinic Liver Cancer (BCLC) Group, Radiology Department, Hospital Clinic Barcelona, IDIBAPS, University of Barcelona, Barcelona, Spain.

Martina Gambato (M)

Multivisceral Transplant Unit, Department of Surgery, Oncology and Gastroenterology, Padua University Hospital, Padua, Italy.

Nancy Kwan Man (NK)

Department of Surgery, The University of Hong Kong, Pokfulam, Hong Kong.

John P Roberts (JP)

Department of Surgery, University of California, San Francisco, CA.

David Victor (D)

Underwood Center for Digestive Disorders, J.C. Walter Jr. Transplant Center, and Sherrie and Allan Conover Center for Liver Disease and Transplantation, Houston Methodist Hospital, Houston, TX.

Lorenzo A Orci (LA)

Divisions of Transplant and Abdominal Surgery, Department of Surgery, and Hepato-pancreato-biliary Center, University of Geneva Hospitals, Geneva, Switzerland.

Christian Toso (C)

Divisions of Transplant and Abdominal Surgery, Department of Surgery, and Hepato-pancreato-biliary Center, University of Geneva Hospitals, Geneva, Switzerland.

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