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Title: | Surveillance improves survival of patients with hepatocellular carcinoma: a prospective population-based study. | Austin Authors: | Hong, Thai P;Gow, Paul J ;Fink, Michael;Dev, Anouk;Roberts, Stuart K;Nicoll, Amanda;Lubel, John S;Kronborg, Ian;Arachchi, Niranjan;Ryan, Marno;Kemp, William W;Knight, Virginia;Sundararajan, Vijaya;Desmond, Paul;Thompson, Alexander Jv;Bell, Sally J | Affiliation: | St Vincent's Hospital Melbourne, Melbourne, VIC Austin Health Monash Health, Melbourne, VIC Eastern Health, Melbourne, VIC Western Health, Melbourne, VIC Alfred Hospital, Melbourne, VIC University of Melbourne, Melbourne, VIC |
Issue Date: | 15-Oct-2018 | Publication information: | Medical Journal of Australia 2018; 209(8): 348-354 | Abstract: | To determine the factors associated with survival of patients with hepatocellular carcinoma (HCC) and the effect of HCC surveillance on survival. Prospective population-based cohort study of patients newly diagnosed with HCC in seven tertiary hospitals in Melbourne, 1 July 2012 - 30 June 2013. Overall survival (maximum follow-up, 24 months); factors associated with HCC surveillance participation and survival. 272 people were diagnosed with incident HCC during the study period; the most common risk factors were hepatitis C virus infection (41%), alcohol-related liver disease (39%), and hepatitis B virus infection (22%). Only 40% of patients participated in HCC surveillance at the time of diagnosis; participation was significantly higher among patients with smaller median tumour size (participants, 2.8 cm; non-participants, 6.0 cm; P < 0.001) and earlier Barcelona Clinic Liver Cancer (BCLC) stage disease (A/B, 59%; C/D, 25%; P < 0.001). Participation was higher among patients with compensated cirrhosis or hepatitis C infections; it was lower among those with alcohol-related liver disease or decompensated liver disease. Median overall survival time was 20.8 months; mean survival time was 18.1 months (95% CI, 16.6-19.6 months). Participation in HCC surveillance was associated with significantly lower mortality (adjusted hazard ratio [aHR], 0.60; 95% CI, 0.38-0.93; P = 0.021), as were curative therapies (aHR, 0.33; 95% CI, 0.19-0.58). Conversely, higher Child-Pugh class, alpha-fetoprotein levels over 400 kU/L, and later BCLC disease stages were each associated with higher mortality. Survival for patients with HCC is poor, but may be improved by surveillance, associated with the identification of earlier stage tumours, enabling curative therapies to be initiated. | URI: | https://ahro.austin.org.au/austinjspui/handle/1/19666 | ORCID: | Journal: | Medical Journal of Australia | PubMed URL: | 30309301 | Type: | Journal Article | Subjects: | Hepatitis B Hepatitis C Liver cirrhosis Liver diseases, alcoholic Liver neoplasms Neoplasms, epidemiology Preventive medicine Survival analysis |
Appears in Collections: | Journal articles |
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