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424A AASLD ABSTRACTS HEPATOLOGY, October, 2015<br />

425<br />

Staging Hepatocellular Carcinoma in Non-Cirrhotic<br />

Patients<br />

Philippe Kolly 1,2 , Helen Reeves 3,4 , Marina Knöpfli 2 , Jean-Francois<br />

Dufour 1,2 ; 1 Hepatology, Department of Clinical Research, University<br />

of Bern, Bern, Switzerland; 2 University Clinic for Visceral<br />

Surgery and Medicine, Inselspital Bern, Bern, Switzerland; 3 The<br />

Northern Institute for Cancer Research, Newcastle University,<br />

Newcastle-upon-Tyne, United Kingdom; 4 The Liver Unit, Freeman<br />

Hospital, Newcastle-upon-Tyne, United Kingdom<br />

To design a staging system for HCC in non-cirrhotic patients,<br />

we used a pooled set of 864 patients combining 2 prospective<br />

European cohorts. Among them, 221 had a non-cirrhotic<br />

liver. Cirrhosis was excluded based on clinical presentation<br />

and imaging. The staging and treatment algorithm was constructed<br />

by using Cox regression, regression tree analysis and<br />

evidenced based literature. We created the Non-Cirrhotic Liver<br />

Cancer (NCLC) staging system. Based on the ECOG PS, tumor<br />

burden (size and number of nodules), presence of vascular<br />

invasion and metastasis, this staging system proposes 4 stages.<br />

Each stage is associated with treatment options, separated in<br />

first and second intention treatments (Fig.). We assessed the<br />

discriminatory power of the staging system by Log-Rank (p<br />

< 0.001). The prognostic ability of the staging system was<br />

assessed with Harrell’s concordance index (0.729). HCC<br />

developing in non-cirrhotic patients represents 10-40% of<br />

HCC. With the growing incidence of NAFLD-associated HCC,<br />

this proportion will rise. The BCLC staging system, which has<br />

been endorsed by AASLD and EASL, has not been developed<br />

for non-cirrhotic patients. The statistical analysis revealed that<br />

the performance status and the tumor burden are discriminating<br />

parameters to classify non-cirrhotic patients with HCC in 4<br />

different stages with different prognostics and treatment allocation.<br />

A staging system for HCC developing in non-cirrhotic<br />

patients has become essential. The NCLC has been designed<br />

specifically for this purpose and will need to be further developed.<br />

Figure legend: NCLC staging and treatment algorithm.<br />

This algorithm stages HCC in non-cirrhotic patients according<br />

to ECOG PS, tumor burden and the existence of vascular invasion<br />

or metastasis. It suggests 4 stages and the corresponding<br />

treatments, separated in first and second intention.<br />

426<br />

Clinical significance of microRNA-31 expression in<br />

human hepatocellular carcinoma<br />

Keun Hur 1 , Se Young Jang 2 , Soo Young Park 2 , Gyeonghwa Kim 1 ,<br />

Yong-Hun Choi 1 , Yu Rim Lee 2 , Su Hyun Lee 2 , Sun Kyung Jang 2 ,<br />

Won Young Tak 2 , Young Oh Kweon 2 ; 1 Department of Biochemistry<br />

and Cell Biology, Kyungpook National University School of<br />

Medicine, Daegu, Korea (the Republic of); 2 Department of Internal<br />

Medicine, Kyungpook National University Hospital, Daegu, Korea<br />

(the Republic of)<br />

Background & aims Hepatocellular carcinoma (HCC) is one<br />

of the most leading cause of cancer-related death worldwide.<br />

It is therefore important to understand the mechanistic roles of<br />

biomolecules involved in HCC development. MicroRNAs (miR-<br />

NAs) are small noncoding RNAs that act as an important regulator<br />

of gene expression in various tumor development as well<br />

as metabolic diseases. This study aim to investigate the role<br />

of miR-31 in HCC and non-alcoholic steatohepatitis (NASH).<br />

Methods We analyzed clinical specimens from HCC, matched<br />

normal liver, and NASH tissues. MicroRNAs expression levels<br />

were evaluated by quantitative real-time PCR (qRT-PCR) and<br />

miR-31 expression was normalized relative to RNU6B expression.<br />

In addition, we determined the clinical significance of<br />

the miR-31 expression in matching tissue and serum samples<br />

from HCC patients. Results MiR-31 expression was significantly<br />

upregulated in HCC and NASH tissues compared with normal<br />

liver tissues (p=0.0015). In HCC patients, lower level of<br />

miR-31 (p

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