In a patient with hepatocellular carcinoma, what specific disease stage, liver function (Child‑Pugh class), performance status (ECOG), tumor size/number, portal‑vein involvement, extra‑hepatic spread, hepatic arterial anatomy, platelet count and INR criteria define the indications for transarterial chemo‑embolisation (TACE)?

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Last updated: February 16, 2026View editorial policy

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TACE Indications for Hepatocellular Carcinoma

Primary Indication: Intermediate-Stage Disease

TACE is the standard first-line treatment for intermediate-stage HCC (BCLC B) in patients with preserved liver function, good performance status, multinodular asymptomatic tumors without macroscopic vascular invasion or extrahepatic spread. 1

Specific Patient Selection Criteria

Disease Stage Requirements

  • BCLC Stage B (intermediate): Large or multifocal tumors not amenable to resection, transplantation, or ablation 1
  • BCLC Stage A: May be considered when patients are excluded from transplantation or unfit for surgery/ablation due to tumor location 1, 2
  • Selected BCLC Stage C: Patients with ECOG 0-1 and only segmental/subsegmental portal vein thrombosis (not main portal vein) may be considered with superselective technique 1

Liver Function (Child-Pugh Class)

  • Child-Pugh A: Optimal candidates 1
  • Child-Pugh B7: Acceptable if well-compensated without ascites 1
  • Child-Pugh B ≥8: Absolute contraindication 1
  • Child-Pugh C: Absolute contraindication 1
  • Bilirubin: Must be <2 mg/dL 1

Performance Status

  • ECOG 0-1: Required for TACE 1
  • ECOG ≥2: Absolute contraindication 1

Tumor Characteristics

Tumor Size and Number

  • Optimal: Uni- or pauci-nodular disease, tumors ≤7 cm 1, 2
  • Acceptable: Multiple nodules if tumor burden <50% of total liver volume 1
  • Poor candidates: Extensive tumor with massive replacement of both lobes 1
  • Best survival outcomes: Patients meeting "up-to-seven" criteria (sum of largest tumor diameter in cm plus number of tumors ≤7) 1

Portal Vein Involvement

  • Main portal vein occlusion: Absolute contraindication 1
  • Hepatofugal blood flow: Absolute contraindication 1
  • Segmental/subsegmental portal vein thrombosis: Relative contraindication; TACE may be performed if superselective approach is feasible and hepatopedal collateral flow is present 1
  • Branch portal vein invasion with preserved liver function: cTACE alone or combined with external beam radiation therapy may be considered 1

Extrahepatic Spread

  • No extrahepatic metastases: Required for standard TACE indication 1
  • Limited extrahepatic disease: Relative contraindication; may consider TACE if bulk of disease is intrahepatic and patient likely to die from liver disease rather than metastatic disease 1

Hepatic Arterial Anatomy

  • Superselective catheterization must be technically feasible to target tumor-feeding arteries while preserving non-tumoral tissue 1
  • Untreatable arteriovenous fistula: Absolute contraindication 1

Laboratory Parameters

Platelet Count and Coagulation

  • Platelet count: No specific threshold defined in guidelines, but adequate hemostasis required for arterial puncture 1
  • INR: No specific cutoff stated, but normal coagulation parameters implied for safe arterial access 1

Renal Function

  • Creatinine clearance <30 mL/min: Absolute contraindication 1

Additional Laboratory Contraindications

  • Clinical encephalopathy: Absolute contraindication 1
  • Refractory ascites: Absolute contraindication 1
  • Obstructive jaundice: Absolute contraindication 2

Special Anatomical Considerations

  • Biliary-enteric anastomosis or biliary stents: Contraindication due to high risk of hepatic abscess 1

Additional Clinical Scenarios for TACE

Bridging to Transplantation

  • Waiting time >6 months: TACE may be offered to minimize tumor progression and maintain patients within transplant criteria 1, 2
  • Response to TACE: Can serve as predictor of tumor biology in transplant candidates 1

Downstaging for Transplantation

  • Beyond Milan criteria: TACE may reduce tumor burden to meet eligibility criteria if sufficient radiologic response achieved 3, 2

Treatment Response and Retreatment Criteria

When to Repeat TACE

  • On-demand approach: Repeat at 1-2 month intervals based on tumor response assessment 2, 4
  • Imaging follow-up: CT or MRI at 4-6 weeks post-procedure using mRECIST criteria 2, 4
  • Complete or partial response: Continue TACE on-demand 4
  • Stable disease after one TACE: Repeat once more 4

TACE Refractoriness (When to Stop)

  • No objective response after 2 consecutive TACE sessions within 6 months 1
  • New vascular invasion or extrahepatic metastasis 1
  • Progressive disease or stable disease after 2 TACE sessions: Switch to systemic immunotherapy 4
  • Liver function deterioration to Child-Pugh B8 or higher 2
  • ECOG performance status worsens to ≥2 2

Common Pitfalls to Avoid

  • Avoid treating >50% of liver volume in single session: Significantly increases risk of post-procedural liver failure 1, 4
  • Do not combine TACE with systemic TKIs in intermediate-stage HCC: No survival benefit demonstrated and increases risk of hepatic decompensation 4
  • Do not perform TACE in patients with complete main portal vein thrombosis: High risk of hepatic necrosis and liver failure 1
  • Ensure superselective catheterization in compromised liver function: Non-selective TACE causes excessive parenchymal injury 2, 4

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Treatment Guidelines for Hepatocellular Carcinoma

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

TACE and Portal Vein Embolization for Hepatocellular Carcinoma

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Guideline

Guideline Recommendations for TACE Monotherapy versus Combination Therapy in Intermediate‑Stage Hepatocellular Carcinoma

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

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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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