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HEPATOLOGY, VOLUME 62, NUMBER 1 (SUPPL) AASLD ABSTRACTS 455A<br />

Patients characteristics<br />

fatty liver disease. Overall, the percentage of non-cirrhotic,<br />

non-HBV HCC was 2.93%, non-cirrhotic, non-HBV HCC with<br />

hepatitis C was 1.66%, and non-cirrhotic, non-HBV HCC with<br />

fatty liver disease was 6.6%. Conclusions Non-HBV HCC can<br />

arise in the setting of chronic hepatitis C and fatty liver disease<br />

without advanced fibrosis or cirrhosis. Our prevalence rates<br />

may underestimate the true prevalence owing to the exclusion<br />

of patients without adequate histology available.<br />

Disclosures:<br />

Steven-Huy B. Han - Grant/Research Support: Bristol Myers Squibb, Gilead<br />

The following authors have nothing to disclose: Vivian Ng, Jennifer Phan, Alan<br />

J. Sheinbaum<br />

Disclosures:<br />

Rene Adam - Grant/Research Support: Merck Serono, Roche, Sanofi aventis,<br />

astellas, novartis, Merck Serono, Roche, Sanofi aventis, astellas, novartis, Merck<br />

Serono, Roche, Sanofi aventis, astellas, novartis, Merck Serono, Roche, Sanofi<br />

aventis, astellas, novartis<br />

Didier Samuel - Consulting: Astellas, MSD, BMS, Roche, Novartis, Gilead, LFB,<br />

Janssen-Cilag, Biotest, Abbvie<br />

The following authors have nothing to disclose: Eleonora De Martin, Michel<br />

Rayar, Damien Bergeat, Luis Filipe Abreu de Carvalho, Maximiliano Gelli, Denis<br />

X. Castaing, Daniel Cherqui, Antonio Sa-Cunha, Emmanuel Boleslawski, Karim<br />

Boudjema, Eric Vibert<br />

488<br />

Non-Cirrhotic Hepatocellular Carcinoma in the Absence<br />

of Hepatitis B<br />

Vivian Ng 1 , Jennifer Phan 1 , Alan J. Sheinbaum 2 , Steven-Huy B.<br />

Han 1 ; 1 Pfleger Liver Institute, University of California, Los Angeles,<br />

Los Angeles, CA; 2 Gastroenterology, VA West Los Angeles Healthcare<br />

Center, Los Angeles, CA<br />

Purpose Hepatocellular carcinoma (HCC) accounts for approximately<br />

90% of primary hepatic malignancies worldwide.<br />

In hepatitis B virus (HBV) infection, HCC can develop in the<br />

absence of cirrhosis. However, it is thought that in chronic<br />

hepatitis C virus infection and fatty liver disease, development<br />

of cirrhosis is necessary prior to formation of HCC. To date,<br />

there have only been a small number of case reports showing<br />

that HCC can develop in patients with chronic hepatitis C and<br />

in fatty liver disease without evidence of underlying cirrhosis.<br />

We sought to evaluate whether or not non-cirrhotic HCC exists<br />

and assess underlying risk factors contributing to its development.<br />

Methods We performed a single-center, retrospective<br />

chart review study at a large academic tertiary care hospital.<br />

All patients seen in both the liver cancer clinic and orthotopic<br />

liver transplantation (OLT) clinic for liver cancer in the last 10<br />

years were evaluated. We determined how many patients<br />

had non-cirrhotic HCC based on available pathology reports,<br />

such as explanted liver pathology, liver resection pathology,<br />

and liver biopsy pathology. Patients with hepatitis B, non-<br />

HCC tumors, and patients without both tumor and non-tumor<br />

liver histology available were excluded. Demographic information,<br />

pertinent lab values, and co-morbid conditions were<br />

recorded. Results 1925 unique patients were identified. 1382<br />

patients were excluded from the study, including 303 patients<br />

with hepatitis B, 510 patients with non-HCC tumors, and 569<br />

patients without available tumor and non-tumor histology. Of<br />

the remaining patients, 491 patients underwent (OLT), 70<br />

underwent local ablative therapy, 42 underwent resection of<br />

the HCC, and 17 underwent systemic therapy. All 491 OLT<br />

patients had underlying cirrhosis. Of the 134 patients who<br />

did not undergo (OLT), 35 patients (26.1%) were identified as<br />

having non-cirrhotic HCC. 13 patients (37.1%) had an underlying<br />

diagnosis of hepatitis C, and 6 patients (17.1%) had<br />

489<br />

Albi score predicts survival in patients with BCLC 0/A<br />

stage Hepatocellular Carcinoma (HCC) independently of<br />

Child Pugh (CP) score and treatment allocation<br />

Simona Onali 1 , Aileen Marshall 1 , Dinesh Sharma 1 , Pam O’Donoghue<br />

1 , Emily Dannhorn 1 , Phillip Johnson 2 , James O’Beirne 1 ;<br />

1 Sheila Sherlock Liver Centre, Royal Free Hospital, London, United<br />

Kingdom; 2 Department of Molecular and Clinical Cancer Medicine,<br />

University of Liverpool, Liverpool, United Kingdom<br />

Introduction: BCLC 0/A stage HCC patients are considered<br />

candidates for curative treatments. Within the BCLC classification,<br />

liver function is assessed by CP score despite this score<br />

not being derived from patients with HCC. ALBI is a novel<br />

evidence based score derived from a large cohort of HCC<br />

patients and has been shown to define different prognostic<br />

groups even within CP A. 1 We studied the performance of ALBI<br />

score in a well characterised cohort of patients with BCLC 0/A<br />

stage HCC to determine if ALBI score impacted on prognosis.<br />

Methods: Consecutive patients with BCLC 0/A HCC, evaluated<br />

between 2010-2014 at the Royal Free Hospital were included.<br />

All patients had a performance score of 0 and were undergoing<br />

evaluation for potential resection. Patients were considered<br />

resectable if they had HVPG≤10mmHg or HVPG≥10mmHg<br />

with good liver function as assessed by ICG clearance. ALBI<br />

score was calculated at the time of HVPG and ICG clearance<br />

measurement and divided into 3 grades as per published cutoffs.<br />

Kaplan Meier and Cox regression analysis were used to<br />

assess the impact of ALBI on survival. Results: 67 patients were<br />

included: 64 (95.5%) were CP A, 3 (4.5%) were CP B. 60<br />

(89%) had uninodular tumour and 7 (10.4%) multifocal (≤3<br />

tumours ≤30mm). 46 (69%) underwent resection, 4 (6%) RFA,<br />

9 (14%) TAE, 3 (5%) OLT, 3 (5%) either no treatment or undergoing<br />

evaluation. Median follow up was 9 months (13-54).<br />

10 (15%) patients died during follow up. Cause of death was<br />

HCC-related n= 4, liver failure n=4, non-liver related n=2. In<br />

Kaplan Meier analysis CP score was not associated with difference<br />

in survival. Cox regression analysis revealed ALBI score as<br />

the only significant factor related to survival and was independent<br />

of CP score and treatment allocation (p=0.002, OR=15,<br />

95%CI=3-80). Of patients with ALBI grade 1, 44 (83%) were<br />

considered suitable and underwent resection vs only 2 (14%)<br />

with ALBI 2. One-year survival was 88% in patients with ALBI<br />

grade 1 and 43% in patients with ALBI grade 2 (p=0.002).<br />

Conclusion: In patients with BCLC 0/A stage HCC ALBI score<br />

clearly defines patients with different prognosis regardless<br />

of Child Pugh score and treatment allocation. ALBI grade 2<br />

patients are very rarely suitable candidates for resection. ALBI<br />

score is more informative than Child Pugh score in patients with<br />

early stage HCC and may be useful in determining treatment<br />

allocation References: 1 . Johnson PJ et al. Assessment of Liver<br />

Function in Patients With Hepatocellular Carcinoma: A New

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