Objective To investigate the influence of different virologic responses on long-term survival rate and incidence rate of liver cancer in patients with decompensated hepatitis B cirrhosis.Methods A total of 378 patients with decompensated hepatitis B cirrhosis who were admitted to The Affiliated Hospital of Xuzhou Medical University from September 2010 to September 2016 were enrolled, and according to whether HBV DNA was continuously undetectable during antiviral therapy, they were divided into sustained virologic response group with 243 patients and non-sustained virologic response group with 135 patients. The patients were stratified according to the application of different antiviral drugs. Baseline data were recorded and the patients were followed up to the occurrence of end events or study endpoint to record death and hepatocellular carcinoma(HCC). The independent samplest-test was used for comparison of normally distributed continuous data between two groups, and the Mann-WhitneyUtest was used for comparison of non-normally distributed continuous data between two groups; the chi-square test was used for comparison of categorical data between groups. The Kaplan-Meier method was used to plot survival curves, and the log-rank test was used to compare survival rates between groups.Results Compared with the non-sustained virologic response group, the sustained virologic response group had a significantly lower 5-year cumulative incidence rate of HCC(7.4% vs19.3%,χ2 =10.627,P= 0. 001) and a significantly higher 5-year transplant-free survival rate(93. 4% vs 80. 7%,χ2 =12.594,P<0.001). For the sustained virologic response group, there were no significant differences between the entecavir group and the non-entecavir group in the 5-year transplant-free survival rate(94.7% vs 90.2%,χ2 =1.122,P= 0. 290) and the 5-year cumulative incidence rate of liver cancer(6.4 % vs 9.7%,χ2 =0.552,P= 0. 458). For the non-sustained viral response group, there were also no significant differences between the entecavir group and the non-entecavir group in the 5-year transplant-free survival rate(78. 4% vs 82. 8%,χ2 =1.526,P= 0. 217) and the 5-year cumulative incidence rate of liver cancer(21. 5% vs 17. 1%,χ2 =1.844,P= 0. 174).Conclusion Antiviral therapy can improve the prognosis of patients with decompensated hepatitis B cirrhosis, and sustained virologic response can reduce the incidence rate of liver cancer and prolong survival time.
[1] FATTOVICH G, GIUSTINA G, SCHALM SW, et al. Occurrence of hepatocellular carcinoma and decompensation in western European patients with cirrhosis type B. The EUROHEP Study Group on Hepatitis B virus and cirrhosis[J]. Hepatology, 1995, 21(1):77-82.
|
[2] PENG CY, CHIEN RN, LIAW YF. Hepatitis B virus-related decompensated liver cirrhosis:Benefits of antiviral therapy[J]. J Hepatol, 2012, 57(2):442-450.
|
[3] SINGAL AK, FONTANA RJ. Meta-analysis:Oral anti-viral agents in adults with decompensated hepatitis B virus cirrhosis[J]. Aliment Pharmacol Ther, 2012, 35(6):674-689.
|
[4] Chinese Society of Hepatology and Chinese Society of Infectious Diseases, Chinese Medical Association. The guideline of prevention and treatment for chronic hepatitis B:A 2015 update[J]. J Clin Hepatol, 2015, 31(12):1941-1960.(in Chinese)中华医学会肝病学分会,中华医学会感染病学分会.慢性乙型肝炎防治指南(2015年更新版)[J].临床肝胆病杂志,2015, 31(12):1941-1960.
|
[5] FATTOVICH G, BORTOLOTTI F, DONATO F. Natural history of chronic hepatitis B:Special emphasis on disease progression and prognostic factors[J]. J Hepatol, 2008, 48(2):335-352.
|
[6] JANG JW, CHOI JY, KIM YS, et al. Effects of virologic response to treatment on short-and long-term outcomes of patients with chronic hepatitis B virus infection and decompensated cirrhosis[J]. Clin Gastroenterol Hepatol, 2018, 16(12):1954-1963. e3.
|
[7] FONTANA RJ, HANN HW, PERRILLO RP, et al. Determinants of early mortality in patients with decompensated chronic hepatitis B treated with antiviral therapy[J]. Gastroenterology,2002, 123(3):719-727.
|
[8] CHEN CJ, YANG HI, SU J, et al. Risk of hepatocellular carcinoma across a biological gradient of serum hepatitis B virus DNA level[J]. JAMA, 2006, 295(1):65-73.
|
[9] JU YC, JUN DW, CHOI J, et al. Long term outcome of antiviral therapy in patients with hepatitis B associated decompensated cirrhosis[J]. World J Gastroenterol, 2018, 24(40):4606-4614.
|
[10] KIM TS, SINN DH, KANG W, et al. Hepatitis B virus DNA levels and overall survival in hepatitis B-related hepatocellular carcinoma patients with low-level viremia[J]. J Gastroenterol Hepatol, 2019, 34(11):2028-2035.
|
[11] PAPATHEODORIDIS GV, MANOLAKOPOULOS S, TOULOUMI G,et al. Virological suppression does not prevent the development of hepatocellular carcinoma in HBeAg-negative chronic hepatitis B patients with cirrhosis receiving oral antiviral(s)starting with lamivudine monotherapy:Results of the nationwide HEPNET.Greece cohort study[J]. Gut, 2011, 60(8):1109-1116.
|
[12] HOSAKA T, SUZUKI F, KOBAYASHI M, et al. Long-term entecavir treatment reduces hepatocellular carcinoma incidence in patients with hepatitis B virus infection[J]. Hepatology, 2013, 58(1):98-107.
|
[13] PAPATHEODORIDIS GV, MANOLAKOPOULOS S, TOULOUMI G, et al. Hepatocellular carcinoma risk in HBeAg-negative chronic hepatitis B patients with or without cirrhosis treated with entecavir:HepNet. Greece cohort[J]. J Viral Hepat, 2015,22(2):120-127.
|
[14] HOU JL, ZHAO W, LEE C, et al. Outcomes of long-term treatment of chronic HBV infection with entecavir or other agents from a randomized trial in 24 countries[J]. Clin Gastroenterol Hepatol, 2020, 18(2):457-467. e21.
|
[15] NAM JY, CHANG Y, CHO H, et al. Delayed viral suppression during antiviral therapy is associated with increased hepatocellular carcinoma rates in HBeAg-positive high viral load chronic hepatitis B[J]. J Viral Hepat, 2018, 25(5):552-560.
|