TY - JOUR
T1 - Impact of clinically evident portal hypertension on clinical outcome of patients with hepatocellular carcinoma treated by transarterial chemoembolization
AU - Kim, Nam Hee
AU - Lee, Taeheon
AU - Cho, Yong Kyun
AU - Kim, Byung Ik
AU - Kim, Hong Joo
N1 - Publisher Copyright:
© 2018 Journal of Gastroenterology and Hepatology Foundation and John Wiley & Sons Australia, Ltd
PY - 2018/7
Y1 - 2018/7
N2 - Background and Aim: The aim of this study is to determine the impact of clinically evident portal hypertension (CEPH) on prognosis of hepatocellular carcinoma (HCC) patients with Child–Pugh A cirrhosis who underwent transarterial chemoembolization (TACE). Methods: A retrospective data analysis was performed for a total of 388 treatment-naïve HCC patients with Child–Pugh A cirrhosis who underwent TACE as first-line treatment from January 2000 to June 2014. Cumulative occurrence rate of complete response (CR), progression-free survival (PFS), and overall survival (OS) were compared between patients with CEPH and those without CEPH (esophageal/gastric varices or low platelet count [< 100 000 per mm3] associated with splenomegaly). Results: Among 388 patients, 252 (64.9%) had CEPH, while 136 (35.1%) had no evidence of CEPH at the time of HCC diagnosis. Cumulative probability of the occurrence of CR was significantly lower in patients with CEPH than that in patients without CEPH (P < 0.001). Median PFS was significantly shorter in patients with CEPH than that in patients without CEPH (5 vs 31 months, P < 0.001). Five-year OS rate was significantly lower in patients with CEPH than that in patients without CEPH (41.5% vs 77.5%, P < 0.001). Multivariate analysis indicated that the presence of CEPH was the most powerful poor prognostic factor for the occurrence of CR (adjusted hazard ratio [aHR], 0.16; 95% confidence interval [CI], 0.09–0.28; P < 0.001), PFS (aHR, 5.01; 95% CI, 3.08–8.12; P < 0.001), and OS (aHR, 2.95; 95% CI, 1.66–5.23; P < 0.001). Conclusions: The presence of CEPH should be considered as a major negative prognostic factor for patients with HCC who will undergo TACE.
AB - Background and Aim: The aim of this study is to determine the impact of clinically evident portal hypertension (CEPH) on prognosis of hepatocellular carcinoma (HCC) patients with Child–Pugh A cirrhosis who underwent transarterial chemoembolization (TACE). Methods: A retrospective data analysis was performed for a total of 388 treatment-naïve HCC patients with Child–Pugh A cirrhosis who underwent TACE as first-line treatment from January 2000 to June 2014. Cumulative occurrence rate of complete response (CR), progression-free survival (PFS), and overall survival (OS) were compared between patients with CEPH and those without CEPH (esophageal/gastric varices or low platelet count [< 100 000 per mm3] associated with splenomegaly). Results: Among 388 patients, 252 (64.9%) had CEPH, while 136 (35.1%) had no evidence of CEPH at the time of HCC diagnosis. Cumulative probability of the occurrence of CR was significantly lower in patients with CEPH than that in patients without CEPH (P < 0.001). Median PFS was significantly shorter in patients with CEPH than that in patients without CEPH (5 vs 31 months, P < 0.001). Five-year OS rate was significantly lower in patients with CEPH than that in patients without CEPH (41.5% vs 77.5%, P < 0.001). Multivariate analysis indicated that the presence of CEPH was the most powerful poor prognostic factor for the occurrence of CR (adjusted hazard ratio [aHR], 0.16; 95% confidence interval [CI], 0.09–0.28; P < 0.001), PFS (aHR, 5.01; 95% CI, 3.08–8.12; P < 0.001), and OS (aHR, 2.95; 95% CI, 1.66–5.23; P < 0.001). Conclusions: The presence of CEPH should be considered as a major negative prognostic factor for patients with HCC who will undergo TACE.
KW - clinically evident portal hypertension
KW - complete response
KW - hepatocellular carcinoma
KW - overall survival
KW - progression-free survival
KW - transarterial chemoembolization
UR - https://www.scopus.com/pages/publications/85043508817
U2 - 10.1111/jgh.14083
DO - 10.1111/jgh.14083
M3 - Article
C2 - 29314222
AN - SCOPUS:85043508817
SN - 0815-9319
VL - 33
SP - 1397
EP - 1406
JO - Journal of Gastroenterology and Hepatology (Australia)
JF - Journal of Gastroenterology and Hepatology (Australia)
IS - 7
ER -