High pretreatment static and dynamic alpha‐fetoprotein values predict reduced overall survival in hepatocellular carcinoma

Background Hepatocellular carcinoma is one of the most lethal cancers worldwide. Novel prognostic and/or predictive biomarkers are urgently needed to improve patient management. Alpha‐fetoprotein (AFP) is a well‐established and widely used biomarker for hepatocellular carcinoma. However, diagnostic...

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Veröffentlicht in:United European gastroenterology journal 2021-04, Vol.9 (3), p.388-397
Hauptverfasser: Czauderna, Carolin, Schmidtmann, Irene, Koch, Sandra, Pilz, Lukas, Heinrich, Sophia, Otto, Gerd, Mittler, Jens, Lang, Hauke, Kloeckner, Roman, Düber, Christoph, Sprinzl, Martin F., Worns, Marcus A., Galle, Peter R., Marquardt, Jens U., Weinmann, Arndt
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Sprache:eng
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Zusammenfassung:Background Hepatocellular carcinoma is one of the most lethal cancers worldwide. Novel prognostic and/or predictive biomarkers are urgently needed to improve patient management. Alpha‐fetoprotein (AFP) is a well‐established and widely used biomarker for hepatocellular carcinoma. However, diagnostic accuracy of static AFP values is limited and the clinical potential is a matter of ongoing scientific discussion. Objective We here evaluated the prognostic impact of pretreatment static and dynamic AFP variables on overall survival of hepatocellular carcinoma patients in a Western cohort. Methods Patients with confirmed hepatocellular carcinoma (n = 809) treated at the Johannes Gutenberg University Mainz between 1998 and 2014 and two available pretreatment AFP‐values (AFP‐slope) were retrospectively analysed. Clinicopathological baseline parameters, pretreatment static values and AFP‐slope were assessed. Prognostic impact was determined by Kaplan–Meier analyses and Cox regression models. Results High static and dynamic AFP variables prior to therapy were associated with reduced survival rates of hepatocellular carcinoma patients. Several known clinical parameters such as Child–Pugh B (p < 0.01) and C stage (p 
ISSN:2050-6406
2050-6414
DOI:10.1177/2050640620972611