Impact of clinically evident portal hypertension on the course of hepatocellular carcinoma in patients listed for liver transplantation

被引:48
作者
Faitot, Francois [1 ]
Allard, Marc-Antoine [1 ]
Pittau, Gabriella [1 ]
Ciacio, Oriana [1 ]
Adam, Rene [1 ,3 ,4 ]
Castaing, Denis [1 ,2 ,3 ]
Cunha, Antonio Sa [1 ,2 ,3 ]
Pelletier, Gilles [1 ,2 ,3 ]
Cherqui, Daniel [1 ,2 ,3 ]
Samuel, Didier [1 ,2 ,3 ]
Vibert, Eric [1 ,2 ,3 ]
机构
[1] Hop Paul Brousse, AH HP, Ctr Hepatobiliaire, F-94804 Villejuif, France
[2] INSERM, U1193, Villejuif, France
[3] Univ Paris 11, Villejuif, France
[4] INSERM, Unite UMRS776, Villejuif, France
关键词
VENOUS-PRESSURE GRADIENT; ENDOTHELIAL GROWTH-FACTOR; TRANSIENT ELASTOGRAPHY; CIRRHOTIC-PATIENTS; HEPATIC RESECTION; ALPHA-FETOPROTEIN; VEGF LEVEL; SURVIVAL; DECOMPENSATION; PREDICTION;
D O I
10.1002/hep.27864
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Liver transplantation (LT) is the best curative treatment for early hepatocellular carcinoma (HCC) in patients with cirrhosis. However, the current shortage of organs causes prolonged waiting times and poorer intention-to-treat (ITT) survival (i.e., after listing) owing to tumor progression and dropout. Portal hypertension (PH) is a recognized risk factor of HCC development in patients with cirrhosis and its recurrence after resection. The aim of this study was to evaluate the potential impact of PHT on the results of LT on an ITT basis. Patients with cirrhosis listed for LT for HCC were included and their outcomes after listing were compared according to the presence or absence of PH defined as presence of esophageal varices or ascites or low platelet count and splenomegaly. Among 243 consecutively listed patients, 70% were affected by PH, which was associated with a significantly higher risk of tumor progression (38% vs. 22%; P=0.017) and a higher risk of dropout (22% vs. 8%; P=0.01). Transarterial chemoembolization (TACE) was similarly applied to the two groups (60% vs. 67%; P=0.325). An absence of TACE was the only other independent risk factor of dropout owing to tumor progression. Under an ITT analysis, PH reduced overall survival (OS), but there was no difference in OS and time to recurrence post-LT. The only pathological feature that could potentially explain this observation was the lower complete response to TACE in the PHT group (12% vs. 36%; P=0.001). Conclusion: PH should be regarded as a major risk factor of dropout owing to tumor progression and should be taken into consideration when managing patients with HCC who are waiting for LT. (Hepatology 2015;62:179-187)
引用
收藏
页码:179 / 187
页数:9
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