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 |
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Format: | Artikel |
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. |
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ISSN: | 1542-3565 1542-7714 |
DOI: | 10.1016/j.cgh.2006.09.021 |