Clinical Trials Directory

Trials / Not Yet Recruiting

Not Yet RecruitingNCT07368023

A Retrospective Study of Safety and Efficacy of Locoregional Therapies Combined With Anti-VEGF/TKIs and Immune Checkpoint Inhibitors for All Comers of Intention-to-treat Patients With Unresectable Hepatocellular Carcinoma

Status
Not Yet Recruiting
Phase
Study type
Observational
Enrollment
300 (estimated)
Sponsor
Ningbo Medical Center Lihuili Hospital · Other Government
Sex
All
Age
16 Years
Healthy volunteers
Not accepted

Summary

This is a single-center, retrospective cohort study aiming to evaluate the safety and efficacy of a combined conversion therapy strategy for patients with initially unresectable hepatocellular carcinoma (HCC).The primary objective is to assess the outcomes of intention-to-treat (ITT) patients who received multidisciplinary conversion therapy. This therapy combines locoregional treatments (LRT, such as TACE or radiotherapy) with systemic therapy (anti-VEGF/tyrosine kinase inhibitors and immune checkpoint inhibitors) with the goal of down-staging tumors to allow for subsequent curative resection. The study plans to enroll 300 subjects. The exposure group will include approximately 100 patients with initially unresectable HCC who received the combined conversion therapy between January 2018 and December 2024. A control group of about 200 patients with initially resectable HCC who underwent direct radical surgery during the same period will be used for comparison. Data will be collected retrospectively from hospital electronic medical records and the HCC clinical database, with follow-up until December 2025.

Conditions

Interventions

TypeNameDescription
COMBINATION_PRODUCTLocoregional Therapy (LRT) + Systemic Drug TherapyTreatment regimens, doses, and durations varied based on individual clinical decisions and are collected retrospectively.

Timeline

Start date
2026-01-25
Primary completion
2026-01-31
Completion
2026-05-31
First posted
2026-01-26
Last updated
2026-01-26

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT07368023. Inclusion in this directory is not an endorsement.