Do patients with Hepatocellular Carcinoma (HCC) have varying Model for End-Stage Liver Disease (MELD) scores?

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Last updated: January 21, 2026View editorial policy

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Do HCC Patients Have Different MELD Scores?

Yes, HCC patients typically have lower MELD scores than non-HCC cirrhotic patients awaiting transplantation, but receive standardized MELD exception points to prioritize them for transplantation based on their cancer-related mortality risk rather than their liver dysfunction severity. 1, 2

The Fundamental Discrepancy

MELD Score Reflects Liver Function, Not Cancer Burden

  • HCC patients generally present with better preserved liver function and lower calculated MELD scores compared to patients with decompensated cirrhosis without HCC. 3
  • The MELD score (ranging from 6-40) is calculated using only three objective laboratory parameters: serum bilirubin, INR, and creatinine—none of which directly measure tumor burden or cancer-related mortality risk. 1, 2
  • In a comparative study, HCC patients were older and more likely to be Asian, but had significantly less severe liver impairment than patients with cirrhosis alone, despite their cancer diagnosis. 3

The Exception Points System

  • Patients with HCC meeting Milan criteria (single tumor ≤5 cm or 2-3 tumors each ≤3 cm without macrovascular invasion) receive standardized MELD exception points of 22. 1, 4
  • This exception system exists precisely because MELD inadequately captures the mortality risk from HCC itself—patients can die from cancer progression despite having relatively preserved liver function. 2, 4
  • The current 22-point exception actually overestimates mortality risk compared to laboratory MELD patients: outcome-based analysis shows HCC patients with 22 exception points have comparable adverse event rates to patients with laboratory MELD scores of only 15-19. 5

Clinical Implications of This Discrepancy

Transplant Access and Outcomes

  • Despite lower actual MELD scores, HCC patients undergo transplantation at significantly higher rates (78.1% vs 51.4%) compared to cirrhotic patients without HCC. 3
  • Intention-to-treat survival at 5 years remains similar between HCC and non-HCC patients (73% vs 78%), suggesting the exception system achieves reasonable equity despite the MELD discrepancy. 3
  • Post-transplant survival is comparable (83% vs 90% at 3 years), though HCC patients face higher disease recurrence rates (19% vs 10%). 3

MELD Score Variability in HCC Patients

  • Among HCC patients undergoing locoregional therapy, MELD scores change dynamically: mean scores increased from 10.1 pre-treatment to 12.9 early post-treatment, then decreased to 11.7 at late follow-up. 6
  • Serial MELD determinations correlate well with Child-Pugh score changes (correlation coefficient 0.605 early, 0.512 late), with approximately 2 MELD points changing per unit of Child-Pugh change. 6
  • MELD score >15 independently predicts poor prognosis in HCC patients (relative risk 2.17), along with tumor size >5 cm, multiple tumors, and Child-Pugh class B/C. 6

Performance of MELD-Based Systems in HCC

Comparative Prognostic Value

  • MELD-based prognostic systems (MELD-CLIP and MELD-JIS) outperform Child-Pugh-based systems for predicting HCC outcomes. 7
  • For 3-month survival, MELD-CLIP and MELD-JIS achieved AUC of 0.69 versus 0.64 for original systems (P=0.004 and P=0.0018 respectively). 7
  • For 6-month survival, MELD-CLIP (AUC 0.64) and MELD-JIS (AUC 0.62) remained superior to original systems (AUC 0.54 and 0.59). 7
  • MELD-based systems performed best specifically among HCC patients receiving locoregional therapy. 7

Alternative Scoring Systems

  • The PALBI (platelet-albumin-bilirubin) grade consistently demonstrates superior discriminatory power compared to MELD across all HCC treatment modalities and BCLC stages. 8
  • MELD score had the lowest AUC compared to ALBI, PALBI, and Child-Pugh classification for predicting 1-year, 3-year, and 5-year survival in HCC patients. 8
  • Within Child-Pugh class A patients (73% of HCC cohort), PALBI identified three distinct prognostic groups while MELD provided less granular stratification. 8

Critical Pitfalls to Avoid

Do Not Use MELD Alone for HCC Transplant Decisions

  • MELD score should never be the sole criterion for transplant listing in HCC patients—the exception points system exists specifically because MELD fails to capture cancer-related mortality. 2, 4
  • Patients with HCC meeting Milan criteria require exception points regardless of their calculated MELD score. 2, 4

Recognize MELD Limitations in HCC Context

  • MELD does not account for tumor characteristics (size, number, vascular invasion, AFP level) that critically impact HCC prognosis. 1
  • Serum creatinine can be unreliable in cirrhotic patients, potentially overestimating renal dysfunction in sarcopenic patients or underestimating it with fluid overload. 1, 2
  • Clinical decompensation (ascites, encephalopathy) significantly impacts prognosis but is not captured by MELD. 1, 9

Monitor for Dynamic Changes

  • MELD scores in HCC patients fluctuate with treatment and disease progression—serial monitoring every 3-6 months is essential. 4, 6
  • Acute increases in MELD may reflect treatment-related hepatotoxicity, infection, or tumor progression requiring immediate evaluation. 6

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

MELD Score and Liver Transplant Allocation

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Comparison of clinical outcomes in chronic hepatitis B liver transplant candidates with and without hepatocellular carcinoma.

Liver transplantation : official publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society, 2007

Guideline

Management Guidelines for Patients with Liver Disease According to MELD

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

MELD and Child-Turcotte-Pugh Scoring Systems

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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