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Prognostic impact of concurrent nonalcoholic fatty liver disease in patients with chronic hepatitis B‐related hepatocellular carcinoma
Author(s) -
Yoon Jun Sik,
Lee Hyo Young,
Chung Sung Won,
Kim Sun Woong,
Chang Young,
Lee Yun Bin,
Cho Eun Ju,
Lee JeongHoon,
Yu Su Jong,
Kim Haeryoung,
Yoon JungHwan,
Kim Yoon Jun
Publication year - 2020
Publication title -
journal of gastroenterology and hepatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.214
H-Index - 130
eISSN - 1440-1746
pISSN - 0815-9319
DOI - 10.1111/jgh.15026
Subject(s) - medicine , nonalcoholic fatty liver disease , hepatocellular carcinoma , gastroenterology , hazard ratio , propensity score matching , proportional hazards model , confidence interval , carcinoma , fatty liver , disease
Background and Aim As the prevalence of nonalcoholic fatty liver disease (NAFLD) is increasing globally, patients with both NAFLD and chronic hepatitis B (CHB)‐related hepatocellular carcinoma (HCC) is also frequently found. This study aimed to investigate the clinical impact of concurrent NAFLD on the prognosis of patients with CHB‐related HCC. Methods Patients with CHB‐related HCC who underwent surgical resection were consecutively selected from August 2009 to December 2013. The association between histologically proven concurrent NAFLD and clinical outcomes were analyzed. Propensity score (PS) matching was adapted to adjust for baseline characteristics. We also investigated the presence of nonalcoholic steatohepatitis (NASH) among patients with NAFLD and its association with clinical outcomes. Results Among 338 CHB‐related HCC patients selected, 196 patients (58.0%) were diagnosed with concurrent NAFLD. The median follow‐up duration was 74.9 months. The patients with NAFLD tended to have better recurrence‐free survival (RFS; log‐rank, P = 0.16) and had significantly better overall survival (OS; log‐rank, P = 0.004) than those without NAFLD. However, the survival benefit of the concurrent NAFLD was not significant in a multivariable Cox analysis (adjusted hazard ratio, 0.94; 95% confidence interval, 0.51–1.73, P = 0.84) or an analysis after PS matching (log‐rank, P = 0.57). Regarding the presence or absence of NASH, no differences in the RFS (log‐rank, P = 0.61) and OS (log‐rank, P = 0.26) were found. Conclusions Concurrent NAFLD was not associated with both RFS and OS in patients with CHB‐related HCC after adjusting for baseline characteristics. Moreover, NAFLD patients with NASH did not have significantly different clinical outcomes compared with NAFLD patients without NASH.