RecruitingNCT06365034

Study on the Efficacy and Safety of Conversion Therapy in Patients With Initially Unresectable Hepatocellular Carcinoma

A Single-center, Retrospective Study on the Efficacy and Safety of Conversion Therapy for Patients With Initially Unresectable Hepatocellular Carcinoma


Sponsor

Qianfoshan Hospital

Enrollment

92 participants

Start Date

Mar 1, 2024

Study Type

OBSERVATIONAL

Conditions

Summary

To evaluate the efficacy and safety of conversion therapy in patients with initially unresectable hepatocellular carcinoma (uHCC).


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study tests whether giving immunotherapy (anti-PD-1 or anti-CTLA-4 drugs) as part of a "conversion therapy" approach — to shrink initially inoperable liver cancer enough so it can then be surgically removed — is effective and safe. **You may be eligible if...** - You are 18 or older - You have confirmed advanced liver cancer (hepatocellular carcinoma) that cannot be surgically removed - You have at least one measurable tumor - You have not received any prior immunotherapy - Your overall health status is acceptable (ECOG 0–2) - Your liver function is acceptable (Child-Pugh grade A or B) **You may NOT be eligible if...** - You have a history of immune deficiency or autoimmune disease - You have another active cancer - You previously received immunotherapy (PD-1 or CTLA-4 blocking drugs) - Your liver function is too impaired Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Locations(1)

the Qianfoshan Hospital

Jinan, Shandong, China

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NCT06365034


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