Guohong Han

Prof. Guohong Han

Department of Liver Diseases and Interventional Radiology, Digestive Diseases Hospital, Xi’an International Medical Center Hospital, Northwestern University, Xi’an, China
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Research Focus & Metrics

Academic Career Length

23Years (2004-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 May 2019 in Journal of Hepatology
Verified
Journal Article
Closed access
QWQiuhe Wang
Qiuhe Wang
DXDongdong Xia
Dongdong Xia
WBWei Bai
Wei Bai
EWEnxin Wang
Enxin Wang
JSJunhui Sun
Junhui Sun
GHGuohong Han
Guohong Han

1 August 2019 in The Lancet Gastroenterology & Hepatology
Verified
Journal Article
Closed access
YLYong Lv
Yong Lv
ZYZhiping Yang
Zhiping Yang
LLLei Liu
Lei Liu
KLKai Li
Kai Li
CHChuangye He
Chuangye He
GHGuohong Han
Guohong Han

1 September 2017 in Journal of Hepatology
Verified
Journal Article
Closed access
QWQiuhe Wang
Qiuhe Wang
YLYong Lv
Yong Lv
MBMing Bai
Ming Bai
ZWZhengyu Wang
Zhengyu Wang
HLHaibo Liu
Haibo Liu
GHGuohong Han
Guohong Han

1 June 2021 in Journal of Hepatology
Verified
Journal Article
Closed access
DBDominik Bettinger
Dominik Bettinger
LSLukas Sturm
Lukas Sturm
LPLena Pfaff
Lena Pfaff
FHFelix Hahn
Felix Hahn
RKRoman Kloeckner
Roman Kloeckner
MSMichael Schultheiss
Michael Schultheiss

7 November 2019 in Hepatology
Verified
Journal Article
Open access
PDF file
GHGuohong Han
Guohong Han
SBSarah Berhane
Sarah Berhane
HTHidenori Toyoda
Hidenori Toyoda
DBDominik Bettinger
Dominik Bettinger
OEOmar Elshaarawy
Omar Elshaarawy
PJPhilip Johnson
Philip Johnson
Background and Aims: The heterogeneity of intermediate‐stage hepatocellular carcinoma (HCC) and the widespread use of transarterial chemoembolization (TACE) outside recommended guidelines have encouraged the development of scoring systems that predict patient survival. The aim of this study was to build and validate statistical models that offer individualized patient survival prediction using response to TACE as a variable. Approach and Results: Clinically relevant baseline parameters were collected for 4,621 patients with HCC treated with TACE at 19 centers in 11 countries. In some of the centers, radiological responses (as assessed by modified Response Evaluation Criteria in Solid Tumors [mRECIST]) were also accrued. The data set was divided into a training set, an internal validation set, and two external validation sets. A pre‐TACE model (“Pre‐TACE‐Predict”) and a post‐TACE model (“Post‐TACE‐Predict”) that included response were built. The performance of the models in predicting overall survival (OS) was compared with existing ones. The median OS was 19.9 months. The factors influencing survival were tumor number and size, alpha‐fetoprotein, albumin, bilirubin, vascular invasion, cause, and response as assessed by mRECIST. The proposed models showed superior predictive accuracy compared with existing models (the hepatoma arterial embolization prognostic score and its various modifications) and allowed for patient stratification into four distinct risk categories whose median OS ranged from 7 months to more than 4 years. Conclusions: A TACE‐specific and extensively validated model based on routinely available clinical features and response after first TACE permitted patient‐level prognostication.

10 November 2018 in Gut
Verified
Journal Article
Closed access
PDF file
YLYong Lv
Yong Lv
LZLuo Zuo
Luo Zuo
XZXuan Zhu
Xuan Zhu
JZJianbo Zhao
Jianbo Zhao
HXHui Xue
Hui Xue
GHGuohong Han
Guohong Han
Objectives Early placement of transjugular intrahepatic portosystemic shunt (TIPS) has been shown to improve survival in high-risk patients (Child-Pugh B plus active bleeding at endoscopy or Child-Pugh C 10–13) with cirrhosis and acute variceal bleeding (AVB). However, early TIPS criteria may overestimate the mortality risk in a significant proportion of patients, and the survival benefit conferred by early TIPS in such patients has been questioned. Alternative criteria have been proposed to refine the criteria used to identify candidates for early TIPS. Nevertheless, the true survival benefit provided (or not) by early TIPS compared with standard treatment in the different risk categories has not been investigated in specifically designed comparative studies. Design We collected data on 1425 consecutive patients with cirrhosis and AVB who were admitted to 12 university hospitals in China between December 2010 and June 2016. Of these, 206 patients received early TIPS, and 1219 patients received standard treatment. The Fine and Gray competing risk regression model was used to compare the outcomes between the two groups that were stratified based on the currently available risk stratification systems after adjusting for liver disease severity and other potential confounders. Results Overall, early TIPS was associated with an 80% relative risk reduction (RRR) in mortality at 6 weeks (adjusted HR=0.20; 95% CI: 0.10 to 044; p<0.001) and 51% RRR at 1 year (adjusted HR=0.49, 95% CI: 0.32 to 0.73; p<0.001) compared with standard treatment. In stratification analyses, the RRRs in mortality did not significantly differ among the risk categories. However, the absolute risk reductions (ARRs) of mortality were more pronounced in high-risk patients. The ARRs at 6 weeks were −2.1%, −10.2% and −32.4% in Model for End-stage Liver Disease (MELD) ≤11, 12–18 and ≥19 patients and were −1.5%, −9.1% and −23.2% in Child-Pugh A, B and C patients, respectively (interaction tests, p<0.001 for both criteria). The ARRs for mortality at 1 year were −1.7%, −5.4% and −32.7% in MELD ≤11, 12–18 and ≥19 patients, respectively, and −3.6%, −5.2% and −20.3% in Child-Pugh A, B and C patients, respectively (interaction tests, p<0.001 for both criteria). After adjusting for liver disease severity and other potential confounders, a survival benefit was observed in MELD ≥19 or Child-Pugh C patients but not in MELD ≤11 or Child-Pugh A patients. In MELD 12–18 patients, a survival benefit was observed within 6 weeks but not at 1 year. In Child-Pugh B patients, a survival benefit was observed in those with active bleeding but not those without active bleeding. However, the evaluation of active bleeding was associated with a high interobserver variability. Furthermore, early TIPS was associated with a significantly reduced incidence of failure to control bleeding or rebleeding and new or worsening ascites, without increasing the risk of overt hepatic encephalopathy. Conclusions Early TIPS was associated with improved survival in patients with MELD ≥19 or Child-Pugh C cirrhosis but not in patients with MELD ≤11 or Child-Pugh A cirrhosis. For MELD 12–18 or Child-Pugh B patients, future studies addressing optimal selection criteria for early TIPS remain highly warranted.