Cholangiocarcinoma
ICD-10 C22.1 · ICD-11 2C12.0Y

Treatment of Perihilar Cholangiocarcinoma (<3 cm) in Chronic Liver Disease

A distinct subset of patients with perihilar cholangiocarcinoma — those with a tumour under 3 cm, underlying chronic liver disease (most commonly primary sclerosing cholangitis), and no evidence of extrahepatic spread — may be candidates for a specific treatment approach with intent for long-term disease-free survival.

Clinical Scenario

Perihilar cholangiocarcinoma less than 3 cm in the setting of chronic liver disease — most commonly primary sclerosing cholangitis — with no extrahepatic disease confirmed.

Treatment Approach

In carefully selected patients who meet strict eligibility criteria, a surgical transplant-based strategy is the treatment of record. Full selection criteria, pre-treatment workup, and protocol details are available in the complete structured regimen.

Instant Access to Structured Evidence-Based Regimens

References

Liver transplantation for selected patients with pCCA in the presence of chronic liver disease (most commonly primary sclerosing cholangitis), less than 3 cm in size with no evidence of extrahepatic disease results in long-term disease-free survival.

Liver transplantation is a potential treatment option for selected patients with pCCA or iCCA.

DOI: 10.1136/gutjnl-2023-330029

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