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Retrospective study on the efficacy and safety of TACE combined with lenvatinib and PD-1 inhibitor in patients with advanced hepatocellular carcinoma

Retrospective study on the efficacy and safety of TACE combined with lenvatinib and PD-1 inhibitor in patients with advanced hepatocellular carcinoma

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500102544
Enrollment
Unknown
Registered
2025-05-15
Start date
2025-05-15
Completion date
Unknown
Last updated
2025-05-19

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

Conditions

Advanced hepatocellular carcinoma

Interventions

Study group (Arterial chemoembolization combined with lenvatinib and PD-1 inhibitor):None
Control group (Arterial chemoembolization combined with lenvatinib):None

Sponsors

Shandong Provincial Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: 1. Age >=18 years old; 2. BCLC stage B/C and meeting the diagnostic criteria of the "Guidelines for the Diagnosis and Treatment of Hepatocellular Carcinoma"; 3. The Eastern Cooperative Oncology Group (ECOG) status score ranges from 0 to 1 4.Patients who have undergone radical treatment and experience recurrence can be included; 5.Child Pugh classification of liver function as A or B; 6.At least one measurable target lesion that meets the mRECIST criteria is present in the imaging examination.

Exclusion criteria

Exclusion criteria: 1.Diffuse distribution of HCC; 2. Patients who have received TACE, hepatic artery infusion chemotherapy, radiotherapy, targeted drugs or immunosuppressants in the past; 3.Accompanied by serious medical complications such as heart, lung, kidney, or coagulation dysfunction that cannot be improved through treatment; 4.There are severe manifestations of liver function impairment, such as refractory ascites, hepatic encephalopathy, or jaundice; 5. Patients with complete blockage of the main portal vein by cancer thrombus and no rich collateral circulation formed; 6.Follow up time is less than 3 months or there is no complete clinical data; 7.History of malignant tumors other than liver cancer.

Design outcomes

Primary

MeasureTime frame
Progression-free survival;

Secondary

MeasureTime frame
Overall survival;

Countries

China

Contacts

Public ContactZhu Qiang

Shandong Provincial Hospital

zhuqiang@sdu.edu.cn+86 151 6888 7780

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026