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Clinical Study on the Improvement of Immune Status in Primary Liver Cancer PLC Patients after TACE by ß-1,3/a-1,3-Glucan

Clinical Study on the Improvement of Immune Status in Primary Liver Cancer PLC Patients after TACE by ß-1,3/a-1,3-Glucan

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500115118
Enrollment
Unknown
Registered
2025-12-23
Start date
2025-12-29
Completion date
Unknown
Last updated
2026-01-05

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

Conditions

primary liver cancer

Interventions

Control group:Targeted immunotherapy after TACE
ß-1,3/a-1,3-glucan experimental group:Oral ß-glucan on the basis of TACE combined with targeted immunotherapy

Sponsors

The First People's Hospital of Qinzhou
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Meet the diagnostic criteria for primary liver cancer; 2. All patients with liver cancer were in the initial stage and had not received any other treatment before surgery; 3. All patients had no immune diseases and had not used immune enhancers, immune modulators, antibiotics, probiotics, etc. within one week before TACE; 4. All patients underwent imaging examinations such as CT or MRI, which ruled out distant metastasis. There were indications for TACE surgery; 5. 18 years <age<75 years.

Exclusion criteria

Exclusion criteria: 1. Pregnant or lactating women; 2. Patients with severe primary diseases of the cardiovascular, pulmonary, renal, cerebral, endocrine and hematopoietic systems, as well as patients with mental illnesses; patients complicated with other severe infectious diseases such as pulmonary tuberculosis and acquired immunodeficiency syndrome (AIDS), etc.; 3. Patients with active autoimmune diseases or other immune system diseases; 4. Patients who have previously received other anti-tumor treatments, such as systemic therapy, chemotherapy combined with radiotherapy, etc.; 5. Patients complicated with other malignant tumors or symptomatic brain metastasis.

Design outcomes

Primary

MeasureTime frame
Tumor Markers;Liver Function;

Secondary

MeasureTime frame
cytokines;Complete Blood Count;immune cells subsets;T cell exhaustion markers;Immunoglobulin;gut microbiota;

Countries

China

Contacts

Public ContactYuanli Wang

The First People's Hospital of Qinzhou

wylxinyuan@126.com+86 777 281 9959

Outcome results

None listed

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