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Significance of pre-treatment serum alpha-fetoprotein in hepatocellular carcinoma of non-viral aetiology

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dc.contributor.author Siriwardana, R.C. en_US
dc.contributor.author Niriella, M.A. en_US
dc.contributor.author Dassanayake, A.S. en_US
dc.contributor.author de Silva, A.P. en_US
dc.contributor.author Gunetilleke, B. en_US
dc.contributor.author de Silva, H.J. en_US
dc.date.accessioned 2017-10-16T10:20:29Z en_US
dc.date.available 2017-10-16T10:20:29Z en_US
dc.date.issued 2016 en_US
dc.identifier.citation Sri Lanka Medical Association, 129th Anniversary International Medical Congress. 2016: 221 en_US
dc.identifier.issn 0009-0895 en_US
dc.identifier.uri http://repository.kln.ac.lk/handle/123456789/17835 en_US
dc.description Poster Presentation Abstract (PP 122), 129th Anniversary International Medical Congress, Sri Lanka Medical Association, 25-27 July 2016 Colombo, Sri Lanka en_US
dc.description.abstract INTRODUCTION: Alpha-fetoprotein (AFP) is a biomarker for hepatocellular carcinoma (HCC). The significance of pre-treatment AFP (pt-AFP) in non-viral HCC (nvHCC) is not clear. METHOD: Patients with nvHCC, referred to a Hepatobiliary Clinic from September 2011-2015 were screened. Clinical evaluation, liver biochemistry, pt-AFP and contrast enhanced CT abdomen were performed. HCC was diagnosed using American Association for the Study of Liver Disease guidelines and TNM staged. nvHCC was diagnosed in HCC, negative for HBsAg and anti-HCVAb. Child-Turcotte-Pugh (CTP) and Model for End-stage Liver Disease (MELD) scores were calculated. All values are presented as median (range). Differences between groups were tested using Pearson’s Chi-square, Mann Whitney U and Kruskal-Wallis tests. Cumulative survival and recurrence rates were calculated by the Kaplan-Meier method. Difference between survival was evaluated by the log-rank test. A p<0.05 was considered significant. RESULTS: Three hundred and eighty nine patients with nvHCC [age 64 (12-88) years; 344 (88.4%) males] were screened. Two hundred and thirty three (59.9%) had diabetes; 187 (48.1%) were regular, 79 (20.3%) social, 123 (31.6%) non-consumers of alcohol]. Three hundred and twenty nine (84.6%) had cirrhosis [Child A (57.3%), B (32.4%), C (10.3%); median CTP 6 (1-14), MELD 11(5-28)]. One hundred and seventy seven (45.5%) HCCs were TNM stage 3, with median diameter 6cm (0.9-26.5). Two hundred and thirty three (59.9%) had no vascular or visceral invasion. Median AFP was 25.46ng/ml (1.16-100,000) [AFP<10ng/ml: n=160(41.2%), AFP>400ng/ml: n=89(22.9%)]. Females (p<0.05), vascular invasion (p<0.001), diameter>5cm (p<0.05), late TNM stage (p<0.001) and non-surgical candidates had higher AFP levels. Diffuse (p<0.001), invasive (p<0.001) and late stage tumours (p<0.001) had AFP>400ng/ml. AFP<400ng/ml was associated with longer survival compared to AFP>400ng/ml (16 vs. 7 months, p<0.001). CONCLUSIONS: Although pt-AFP was not helpful for diagnosis of nvHCC, AFP>400ng/ml was associated with aggressive tumour behaviour and poor prognosis. en_US
dc.language.iso en_US en_US
dc.publisher Sri Lanka Medical Association en_US
dc.subject Carcinoma, Hepatocellular en_US
dc.subject Carcinoma, Hepatocellular-etiology en_US
dc.subject alpha-Fetoproteins en_US
dc.subject alpha-Fetoproteins-therapeutic use en_US
dc.title Significance of pre-treatment serum alpha-fetoprotein in hepatocellular carcinoma of non-viral aetiology en_US
dc.type Conference Abstract en_US


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