SIRT or TACE Plus Lenvatinib and PD-(L)1 Inhibitor in High Burden HCC

CompletedOBSERVATIONAL
Enrollment

238

Participants

Timeline

Start Date

June 1, 2022

Primary Completion Date

January 31, 2025

Study Completion Date

January 31, 2025

Conditions
Hepatocellular Carcinoma Non-resectable
Interventions
COMBINATION_PRODUCT

SIRT-L-P

Patients received 1-2 session of SIRT. Lenvatinib and PD-(L)1 inhibitor was initiated within 7 days after the first SIRT and continued until unacceptable toxicity, disease progression, initiation of new therapy, or loss to follow-up.

COMBINATION_PRODUCT

TACE-L-P

Patients received TACE. TACE was repeated for viable tumors demonstrated by follow-up imaging in patients without worsening liver function or contraindications (on-demand TACE). Lenvatinib and PD-(L)1 inhibitor was initiated within 7 days after the first SIRT and continued until unacceptable toxicity, disease progression, initiation of new therapy, or loss to follow-up.

Trial Locations (1)

510260

The Second Affiliated Hospital of Guangzhou Medical University, Guangzhou

All Listed Sponsors
collaborator

Jinshazhou Hospital of Guangzhou University of Chinese Medicine

UNKNOWN

collaborator

First Affiliated Hospital of Army Military Medical University

UNKNOWN

collaborator

Hainan Cancer Hospital

OTHER

lead

Second Affiliated Hospital of Guangzhou Medical University

OTHER