Association between nucleoside analogues and risk of hepatitis B virus–related hepatocellular carcinoma recurrence following liver resection
- PMID: 23162861
- DOI: 10.1001/2012.jama.11975
Association between nucleoside analogues and risk of hepatitis B virus–related hepatocellular carcinoma recurrence following liver resection
Abstract
Context: Tumor recurrence is a major issue for patients with hepatocellular carcinoma (HCC) following curative liver resection.
Objective: To investigate the association between nucleoside analogue use and risk of tumor recurrence in patients with hepatitis B virus (HBV)--related HCC after curative surgery.
Design, setting, and participants: A nationwide cohort study between October 2003 and September 2010. Data from the Taiwan National Health Insurance Research Database. Among 100 938 newly diagnosed HCC patients, we identified 4569 HBV-related HCC patients who received curative liver resection for HCC between October 2003 and September 2010.
Main outcome measures: The risk of first tumor recurrence was compared between patients not taking nucleoside analogues (untreated cohort, n = 4051) and patients taking nucleoside analogues (treated cohort, n = 518). Cumulative incidences and hazard ratios (HRs) were calculated after adjusting for competing mortality.
Results: The treated cohort had a higher prevalence of liver cirrhosis when compared with the untreated cohort (48.6% vs 38.7%; P < .001), but lower risk of HCC recurrence (n = 106 [20.5%] vs n = 1765 [43.6%]; P < .001), and lower overall death (n = 55 [10.6%] vs n = 1145 [28.3%]; P < .001). After adjusting for competing mortality, the treated cohort had a significantly lower 6-year HCC recurrence rate (45.6%; 95% CI, 36.5%-54.6% vs untreated, 54.6%; 95% CI, 52.5%-56.6%; P < .001). Six-year overall mortalities for treated cohorts were 29.0% (95% CI, 20.0%-38.0%) and for untreated 42.4% (95% CI, 40.0%-44.7%; P < .001). On modified Cox regression analysis, nucleoside analogue use (HR, 0.67; 95% CI, 0.55-0.81; P < .001), statin use (HR, 0.68; 95% CI, 0.53-0.87; P = .002), and nonsteroidal anti-inflammatory drugs or aspirin use (HR, 0.80; 95% CI, 0.73-0.88; P < .001) were independently associated with a reduced risk of HCC recurrence. Multivariable stratified analyses verified the association in all subgroups of patients, including those who were noncirrhotic (HR, 0.56; 95% CI, 0.42-0.76) and diabetic (HR, 0.52; 95% CI, 0.31-0.89).
Conclusion: Nucleoside analogue use was associated with a lower risk of HCC recurrence among patients with HBV-related HCC after liver resection.
Comment in
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Does antiviral therapy prevent recurrence of hepatitis B virus–related hepatocellular carcinoma after curative liver resection?JAMA. 2012 Nov 14;308(18):1922-24. doi: 10.1001/jama.2012.12971. JAMA. 2012. PMID: 23147511 No abstract available.
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Antiviral therapy and hepatitis B virus-related hepatocellular carcinoma recurrence.JAMA. 2013 Feb 27;309(8):765. doi: 10.1001/jama.2013.568. JAMA. 2013. PMID: 23443429 No abstract available.
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Antiviral therapy and hepatitis B virus-related hepatocellular carcinoma recurrence.JAMA. 2013 Feb 27;309(8):765-6. doi: 10.1001/jama.2013.571. JAMA. 2013. PMID: 23443430 No abstract available.
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Antiviral therapy and hepatitis B virus-related hepatocellular carcinoma recurrence--reply.JAMA. 2013 Feb 27;309(8):766-7. doi: 10.1001/jama.2013.574. JAMA. 2013. PMID: 23443431 No abstract available.
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Tertiary prevention of hepatitis B-related hepatocellular carcinoma: do we have a verdict?Gastroenterology. 2013 May;144(5):1142-4. doi: 10.1053/j.gastro.2013.03.038. Epub 2013 Mar 22. Gastroenterology. 2013. PMID: 23523833 No abstract available.
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