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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

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
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07368023
Enrollment
300
Registered
2026-01-26
Start date
2026-01-25
Completion date
2026-05-31
Last updated
2026-01-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hepatocellular Carcinoma, Hepatocellular Carcinoma Non-resectable

Brief 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.

Interventions

Treatment regimens, doses, and durations varied based on individual clinical decisions and are collected retrospectively.

Sponsors

Ningbo Medical Center Lihuili Hospital
Lead SponsorOTHER_GOV

Study design

Observational model
CASE_CONTROL
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
16 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Aged 16 years or older. * Clinical and/or pathological diagnosis of hepatocellular carcinoma (HCC). China Liver Cancer (CNLC) stage I, II, or IIIA. * Assessed by a multidisciplinary team (MDT) as having initially unresectable HCC.

Exclusion criteria

* Presence of extrahepatic metastasis. * Presence of Cheng's type IV portal vein tumor thrombus (PVTT). * Presence of Cheng's type II or III inferior vena cava tumor thrombus (IVCTT).

Design outcomes

Primary

MeasureTime frameDescription
Conversion RateFrom the start of conversion therapy until the completion of therapy (assessed up to 24 months).Proportion of ITT patients with initially unresectable HCC successfully down-staged to resectability after conversion therapy (per MDT reassessment).
1-, 2-, and 3-year OS in ITT PopulationStarting from conversion therapy, evaluate at 1, 2, and 3 years.Proportion of patients in the ITT population alive at 1, 2, and 3 years after initiation of conversion therapy (Kaplan-Meier method).
Resection Rate After ConversionFrom the start of conversion therapy to the day of surgery (with a maximum evaluation period of 24 months).Proportion of patients who successfully undergo curative resection after down-staging.

Countries

China

Contacts

CONTACTCaide Lu, Professor
lucaide@nbu.edu.cn+8613957800900
CONTACTShuqi Mao, Professor
mmmaoshuqi@163.com+8617855848257
PRINCIPAL_INVESTIGATORCaide Lu, Professor

Ningbo Medical Centre Lihuili Hospital

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026