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HEPATOLOGY, VOLUME 62, NUMBER 1 (SUPPL) AASLD ABSTRACTS 451A<br />

480<br />

Value of PIVKA II and AFP serum level kinetics for treatment<br />

monitoring in patients with hepatocellular carcinoma<br />

(HCC): a French pilot study<br />

Audrey Payance 1 , Mohamed Bouattour 1 , Mohamed Achahboun 2 ,<br />

Miguel Albuquerque 2 , Laurent Castera 1 , Pierre Bedossa 2 , Olivier<br />

Soubrane 3 , Francois Durand 1 , Valerie Paradis 2 ; 1 HEPATOLOGY,<br />

BEAUJON HOSPITAL, Clichy, France; 2 Pathology, BEAUJON<br />

HOSPITAL, Clichy, France; 3 HPB Surgery and Liver Transplan,<br />

BEAUJON HOSPITAL, Clichy, France<br />

Background and Aims: In Asia, prothrombin induced by vitamin<br />

K absence-II (PIVKA-II) is largely used as a diagnostic and<br />

prognostic biomarker for hepatocellular carcinoma (HCC).<br />

We already confirmed the diagnostic value of PIVKA-II for<br />

European patients with early HCC. Herein, our aim was to<br />

study the dynamics of PIVKA-II serum level in the follow-up of<br />

European patients with HCC, according to treatment monitoring.<br />

Material and Methods: Patients with histologically proven<br />

HCC diagnosed in our center from January 2013 to August<br />

2014 were included. For each patient, serum PIVKA-II and<br />

afetoprotein (AFP) levels were assessed with an enzyme-linked<br />

immunosorbent assay at two different times. We defined two<br />

groups of patients: 1) “treated patients” group with first serum<br />

sample obtained within two months before treatment (D0) and<br />

the second within 2-3 months after treatment initiation (M2-3),<br />

2) “non-treated patients” as a control group, with two serum<br />

samples, at diagnosis (T1) and 2-3 months subsequently (T2).<br />

Baseline serum levels of AFP and PIVKA-II and dynamics during<br />

follow-up were compared between the two groups. Results are<br />

presented as median (interquartile range). Results: A total of<br />

32 patients with HCC developed on chronic liver disease were<br />

included (men, 85 %; median age, 59 years; BCLC stage: A<br />

47% - B 28%- C 19% - D 6%). Aetiologies of underlying liver<br />

disease were alcohol consumption, viral hepatitis B, viral hepatitis<br />

C, non alcoholic steato-hepatitis and genetic hemochromatosis<br />

in 14 (44%) ; 8 (25%), 13 (41%), 4 (12%), 2 (6%) of<br />

patients respectively. In 23 patients, HCC treatment was performed<br />

including chemoembolization (n=14), radiofrequency<br />

ablation (n=3), surgical resection (n=1), sorafenib (n=4), and<br />

radioembolisation (n=1). For all patients, median baseline AFP<br />

and PIVKA II serum levels were 11.6 ng/ml (4.8 - 139.8 ng/<br />

ml) and 416 mAU/ml (100.5 - 5894.25 mAU/ml), respectively.<br />

In the “treated patients” group, PIVKA II serum levels<br />

decreased statistically significantly from D0 to M2-3 (D0: 811<br />

mAU/ml (100.5-11559.75) vs M2-3: 292 mAU/ml (46.25<br />

- 7391); p = 0.031)). However, no significant decrease was<br />

observed regarding AFP serum levels between D0 and M2-3<br />

(D0: 18.9 ng/ml (4.8-392) vs M2-3: 16.3 ng/ml (4.5-103);<br />

p=0.831). Finally, no changes of AFP and PIVKA II serum levels<br />

from baseline T1 to T2 were observed in the control group.<br />

Conclusions: Significant decrease of PIVKA II serum levels following<br />

treatment of HCC was observed. These results suggest<br />

that this biomarker, in contrast to AFP, could be useful for monitoring<br />

treatment in patients with HCC. Further investigations are<br />

needed to validate these results.<br />

Disclosures:<br />

Mohamed Bouattour - Advisory Committees or Review Panels: Bayer Schering<br />

Pharma; Speaking and Teaching: Bayer Schering Pharma<br />

Laurent Castera - Speaking and Teaching: Gilead, BMS, Janssen, Echosens,<br />

Abbvie, Biopredictive<br />

Francois Durand - Advisory Committees or Review Panels: Astellas, Novartis,<br />

BMS; Speaking and Teaching: Gilead<br />

The following authors have nothing to disclose: Audrey Payance, Mohamed<br />

Achahboun, Miguel Albuquerque, Pierre Bedossa, Olivier Soubrane, Valerie<br />

Paradis<br />

481<br />

Liver-directed (LD) Therapy for Intermediate Stage<br />

Hepatocellular Carcinoma: Survival Across Treatment<br />

Strategies<br />

Alvaro E. Castillo 1 , Willscott E. Naugler 2 , Kenneth J. Kolbeck 3 ,<br />

Khashayar Farsad 3 , Susan L. Orloff 1 , Kevin Billingsley 4 , C. Kristian<br />

Enestvedt 1 ; 1 Surgery, Oregon Health and Science University,<br />

Portland, OR; 2 Internal Medicine, Oregon Health and Science<br />

University, Portland, OR; 3 Dotter Interventional Institute, Oregon<br />

Health and Science University, Portland, OR; 4 Division of Surgical<br />

Oncology, Oregon Health and Science University, Portland, OR<br />

Treatment strategies favor LD options for BCLC intermediate<br />

stage HCC. Evaluate the outcomes of different multidisciplinary<br />

treatment strategies in BCLC B patients. A retrospective cohort<br />

analysis of HCC patients referred to our institutional Multidisciplinary<br />

Liver Tumor Board. All with Barcelona Clinic Liver<br />

Cancer (BCLC) stage B who underwent either trans-arterial<br />

chemoembolization (TACE), radiation therapy (XRT)/TACE,<br />

Yttrium-90 (Y-90) alone and Y-90/TACE were selected. Resection,<br />

ablation or transplantation was excluded. Univariate analysis<br />

was used to compare demographics, tumor characteristics,<br />

and treatment modalities. Multivariate analysis of clinical factors<br />

associated with survival was performed using Cox proportional<br />

hazards modeling. Survival was compared using the<br />

Kaplan Meier log-rank method. Eighty eight BCLC B patients<br />

were included. Comparison by treatment groups showed<br />

no difference in severity of disease or demographics except<br />

for bilirubin which was higher for the TACE and TACE/XRT<br />

groups when compared to Y-90 and Y-90/TACE (p=0.024).<br />

Those who received Y-90 had larger tumors (median 6.5 cm,<br />

p=

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