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HEPATOLOGY, VOLUME 62, NUMBER 1 (SUPPL) AASLD ABSTRACTS 637A<br />

862<br />

Clinical impact of 18 F-FDG-PET/CT in living donor liver<br />

transplantation for advanced hepatocellular carcinoma<br />

Seung Duk Lee, Eung Chang Lee, Seong Hoon Kim; Liver Cancer<br />

Center, National Cancer Center, Republic of Korea, Goyang-si,<br />

Korea (the Republic of)<br />

Background: The relevant number of patients with hepatocellular<br />

carcinoma (HCC) beyond the Milan criteria has undergone<br />

living donor liver transplantation (LDLT). However, the prognostic<br />

factors for these patients with advanced HCC are not<br />

well established. Methods: From March 2005 to May 2013,<br />

280 patients with HCC underwent LDLT in the National Cancer<br />

Center. Among these, patients beyond the Milan criteria<br />

were retrospectively enrolled. We analyzed the prognostic significance<br />

of 18 F-fluorodeoxyglucose positron emission tomography/computed<br />

tomography ( 18 F-FDG-PET/CT) for selecting<br />

appropriate candidates. Results: Among total 280 patients,<br />

147 patients (52.5%) were confirmed to have HCC beyond<br />

the Milan criteria using pathological reports. The patients who<br />

met and exceeded the Milan criteria had 5-year overall survival<br />

(OS) rates of 87.2% and 64.6%, respectively, (p < 0.001). In<br />

multivariable analysis for OS and DFS in patients beyond the<br />

Milan criteria, PET/CT positivity [hazard ratio (HR) 2.714, p<br />

= 0.013 for OS; HR 3.803, p < 0.001 for DFS], total tumor<br />

size over 10 cm (HR 2.333, p = 0.035 for OS; HR 3.334, p<br />

= 0.001 for DFS), and microvascular invasion (HR 2.917, p =<br />

0.025 for DFS) were significant prognostic factors. In particular,<br />

patients beyond the Milan criteria with a PET/CT-negative<br />

status and total tumor size < 10 cm showed similar OS and<br />

DFS in comparison with those within the Milan criteria. Conclusions:<br />

A PET/CT status in LDLT is a useful marker to predict<br />

survival of patients with advanced HCC.<br />

Disclosures:<br />

The following authors have nothing to disclose: Seung Duk Lee, Eung Chang Lee,<br />

Seong Hoon Kim<br />

863<br />

Living or Deceased Donor Liver Transplantation for<br />

Hepatocellular Carcinoma: A Western multicenter, intention<br />

to treat, cohort study<br />

Daniel Azoulay; HPB Surgery and liver transplant, Hopital Mondor<br />

APHP, Creteil, France<br />

Purpose. An intention-to-treat analysis of overall survival (ITT-OS)<br />

in cirrhotic patients with hepatocellular carcinoma (HCC) listed<br />

for either living donor (LDLT) [Group LiLDLT] or deceased donor<br />

liver transplantation (DDLT), [Group LiDDLT] across 5 French<br />

liver transplantation (LT) centers. Methods. Records of 861 cirrhotic<br />

patients with HCC who were consecutively listed for<br />

either LDLT (n=79) or DDLT (n=782) from 2000 to 2009 at 5<br />

French centers were analyzed for ITT-OS using Cox model, and<br />

for tumor recurrence using a competitive risk model. Results.<br />

Tumour staging in both groups was similar. Among the listed<br />

patients, 162 dropped-out (20.7%), all from Group LiDDLT (p <<br />

0.0001). At 5-years, ITT-OS was significantly better for Group<br />

LiLDLT vs Group LiDDLT (73.2% vs 66.7%;p = 0.062). Being<br />

listed for LDLT (HR: 0.62 (0.40-0.98); p = 0.039), and MELD<br />

score ≥ 25 at listing (HR: 1.79 (1.11-2.88); p = 0.017) were<br />

independent predictors of ITT-OS. For the 699 transplanted<br />

patients, 5-year OS post-LT (73.2% and 73.0%, p = 0.407)<br />

and HCC recurrence (10.9 % and 11.2 %, p = 0.753) were<br />

similar between those who had a living donor LT [Group LDLT]<br />

and deceased donor LT [Group DDLT], respectively. Tumor<br />

beyond Milan criteria (HR = 2.67 (1.5-4.7); p < 0.001), and<br />

vascular invasion (HR = 2.52 (1.38;4.59); p = 0.003) were<br />

independent predictors of recurrence whereas the type of LT<br />

was not. Conclusion. LDLT improves ITT-OS by obviating dropout,<br />

is not a risk factor of tumor recurrence, and hence should<br />

be equally encouraged in countries where both, LDLT and DDLT<br />

are available.<br />

Disclosures:<br />

The following authors have nothing to disclose: Daniel Azoulay<br />

864<br />

Third Liver Transplantation - Utility and Principles to<br />

Guide Future Transplants; an Analysis of UNOS data<br />

Vandana Khungar 1 , David S. Goldberg 1 , Peter L. Abt 2 ; 1 Medicine,<br />

Division of Gastroenterology, University of Pennsylvania, Philadelphia,<br />

PA; 2 Surgery, University of Pennsylvania, Philadelphia, PA<br />

Background: Repeat liver transplantation (reLT), whether for<br />

recurrent disease, vascular complications, or chronic rejection,<br />

can be a lifesaving therapy. However, donor livers are<br />

a scarce resource, with up to 20% of patients dying on the<br />

waitlist before receiving their first transplant. As more patients<br />

get further out from their 1 st (or 2 nd ) transplant, the transplant<br />

community will need to consider the utility of 3 rd liver transplants.<br />

Yet no data specifically addressing this question exist.<br />

Methods: We performed a retrospective cohort study of all<br />

adult patients listed for their third transplant, who were on<br />

the waiting list between 2/28/02-12/31/2014, using UNOS<br />

data. Kaplan-Meier analyses and log-rank tests were used to<br />

evaluate post-transplant outcomes among the subset of patients<br />

who received their third transplant. Results: 696 adult patients<br />

were on the waitlist for a 3 rd transplant in this period. 362<br />

(52.0%) received a 3 rd transplant, while 218 (31.3%) were<br />

removed from the list for death or clinical deterioration. The<br />

median recipient age was 47 (IQR: 34-45), median donor<br />

risk index (DRI) was 1.33 (IQR: 1.15-1.58), with 211 (58.3%)<br />

donors being under the age of 40. Median laboratory MELD at<br />

transplant was 29 (21-36). The 1,3, and 5 year post-transplant<br />

patient survival rates were 74.5%, 64.4%, and 57.2% respectively.<br />

Graft and patient survival were not statistically different<br />

between centers who had performed 1-9 3 rd transplants vs<br />

≥10 3 rd transplants (p>0.05). Post-transplant patient survival<br />

differed significantly (p=0.001) based on the transplant recipient’s<br />

location at the time of 3 rd transplant. Conclusions: Patients<br />

undergoing reLT were given optimal organs from young donors<br />

with low DRI. Despite this, their post-transplant survival is lower<br />

when compared to patients undergoing 1 st transplantation.<br />

The survival rates among the subset transplanted from the ICU<br />

are dramatically lower, and raise questions about the utility of<br />

transplantation in these high-risk patients outside of the setting<br />

of primary non function (PNF) or hepatic artery thrombosis<br />

(HAT).

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