Staging Hepatocellular Carcinoma by a Novel Scoring System (BALAD Score) Based on Serum Markers

Background & Aims: Previously proposed staging systems for hepatocellular carcinoma (HCC) involve clinical, imaging, or pathologic factors in the evaluation. We established and validated a novel staging system for HCC that is based on simply serum markers. Methods: The new scoring system is base...

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Veröffentlicht in:Clinical gastroenterology and hepatology 2006-12, Vol.4 (12), p.1528-1536
Hauptverfasser: Toyoda, Hidenori, Kumada, Takashi, Osaki, Yukio, Oka, Hiroko, Urano, Fumihiro, Kudo, Masatoshi, Matsunaga, Takashi
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Sprache:eng
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Zusammenfassung:Background & Aims: Previously proposed staging systems for hepatocellular carcinoma (HCC) involve clinical, imaging, or pathologic factors in the evaluation. We established and validated a novel staging system for HCC that is based on simply serum markers. Methods: The new scoring system is based on 5 serum markers: bilirubin, albumin, Lens culinaris agglutinin-reactive α-fetoprotein (AFP-L3), α-fetoprotein (AFP), and des-γ-carboxy prothrombin (DCP) and thus is termed the BALAD score. The system was validated in 2600 HCC patients from 5 institutions. The power of our system to predict patient survival and its discriminative ability were compared with those of previously reported staging systems. Results: The best tumor marker cutoff values were 400 ng/dL for AFP, 15% for AFP-L3, and 100 milli-arbitrary unit/mL for DCP. The patients were classified into 6 categories on the basis of 5 laboratory values. The categories reflected patient survival well. The discriminative ability was comparable to that of previously reported staging systems. Conclusions: The new staging system for HCC combining serum albumin, serum bilirubin, and 3 tumor markers predicts patient outcomes with excellent discriminative ability. The system is easy to use and objective. In addition, stage can be evaluated with the use of only 1 serum sample. It also allows global comparison of patients with HCC or comparison of patients from different time periods with the same standard.
ISSN:1542-3565
1542-7714
DOI:10.1016/j.cgh.2006.09.021