ALBI Score

Albumin-Bilirubin Grade — Objective Liver Function Assessment
Objective two-variable liver function score for hepatocellular carcinoma and cirrhosis. Uses only bilirubin and albumin to grade hepatic reserve, outperforming Child-Pugh in HCC treatment selection.
Hepatology HCC Cirrhosis Liver Function
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Formula

ALBI = (log₁₀[Bilirubin μmol/L] × 0.66) + (Albumin g/L × −0.085)

If bilirubin in mg/dL: multiply by 17.1 to convert to μmol/L before applying formula. Both variables are objective laboratory values — no subjective clinical assessment required.

Interpretation

Grade ALBI Range Liver Function Clinical Implication
Grade 1 ≤ −2.60 Well-compensated Curative therapies appropriate
Grade 2 −2.60 to −1.39 Moderate dysfunction Select therapies with caution
Grade 3 > −1.39 Significant dysfunction Systemic/palliative approach

Clinical Application

The ALBI score was developed and validated by Johnson et al. (2015) as an objective, evidence-based alternative to the Child-Pugh score for assessing liver function in patients with hepatocellular carcinoma (HCC). The score uses only two routine laboratory parameters — serum bilirubin and albumin — both of which are continuous, objective variables free from the interobserver variability inherent in clinical assessments of ascites and encephalopathy.

In HCC treatment selection, ALBI grade is used alongside tumour staging systems (BCLC, Barcelona Clinic Liver Cancer) to determine patient suitability for curative resection, transplantation, ablation, transarterial chemoembolisation (TACE), or systemic therapy. Grade 1 patients with preserved liver function tolerate aggressive therapies well, while Grade 3 patients carry substantial risk of hepatic decompensation even with minimally invasive interventions.

The score has been validated in cohorts exceeding 1,000 HCC patients across multiple continents, including Western, Asian, and mixed populations. It demonstrates superior discriminative ability for survival compared to Child-Pugh class in numerous studies, particularly in distinguishing outcomes within Child-Pugh class A — a group previously considered homogeneous.

Comparison with Child-Pugh

The Child-Pugh score, while widely used, incorporates subjective assessments (ascites grade, hepatic encephalopathy grade) that introduce significant interobserver variability. The ALBI score addresses these limitations with a fully objective approach. Key advantages of ALBI over Child-Pugh include:

  • Entirely objective — no clinical examination required for score calculation
  • No assessment of ascites or encephalopathy, eliminating interobserver variability
  • Continuous score allows finer prognostic discrimination within Child-Pugh class A
  • Better separation of survival curves in HCC patients across BCLC stages
  • Reproducible across centres and countries without calibration differences
  • Suitable for remote or telemedicine-based assessment using laboratory values alone
  • Independently validated in multiple prospective and retrospective multicentre cohorts

Despite these advantages, ALBI has not entirely replaced Child-Pugh in clinical practice. Child-Pugh remains important for assessing patients with clinically overt ascites or encephalopathy, and many international guidelines and trial eligibility criteria continue to use Child-Pugh class A/B as an entry criterion.

Limitations

  • Validated primarily in HCC populations; applicability to other liver diseases (e.g., acute-on-chronic liver failure, alcoholic hepatitis) is less well established
  • Does not account for portal hypertension, platelet count, or prothrombin time — all of which independently affect operative risk and treatment tolerance
  • May underestimate liver dysfunction in patients with haemolysis (falsely elevated bilirubin) or malnutrition affecting albumin independently of synthetic function
  • Grade 2 encompasses a wide heterogeneous range of liver function; the PALBI score was developed specifically to subdivide this group more precisely
  • Not validated as a standalone tool for guiding decisions in liver transplantation allocation
  • Bilirubin unit conversion error is a potential source of calculation mistakes at the point of care

References

  1. Johnson PJ, Berhane S, Kagebayashi C, et al. Assessment of liver function in patients with hepatocellular carcinoma: a new evidence-based approach — the ALBI grade. J Clin Oncol. 2015;33(6):550–558. doi:10.1200/JCO.2014.57.9151
  2. Hiraoka A, Michitaka K, Kumada T, et al. Usefulness of albumin-bilirubin grade for evaluation of prognosis of 2,584 Japanese patients with hepatocellular carcinoma. J Gastroenterol Hepatol. 2016;31(5):1031–1036.
  3. Chan AWH, Kumada T, Toyoda H, et al. Integration of albumin-bilirubin (ALBI) score into Barcelona Clinic Liver Cancer (BCLC) system for hepatocellular carcinoma patients. J Gastroenterol Hepatol. 2016;31(7):1300–1306.
  4. Pinato DJ, Sharma R, Allara E, et al. The ALBI grade provides objective hepatic reserve estimation across each BCLC stage of hepatocellular carcinoma. J Hepatol. 2017;66(2):338–346.