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Study on Drug Sensitivity and Resistance Analysis of First-Line Systemic Anti-Tumor Agents in Hepatocellular Carcinoma Using Immune Co-Cultured Organoids

Study on Drug Sensitivity and Resistance Analysis of First-Line Systemic Anti-Tumor Agents in Hepatocellular Carcinoma Using Immune Co-Cultured Organoids

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500110185
Enrollment
Unknown
Registered
2025-10-10
Start date
2025-10-10
Completion date
Unknown
Last updated
2025-10-13

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

Conditions

Patients with B and C stages according to the 2022 Barcelona Clinic Liver Cancer (BCLC) staging system

Interventions

Patients with B and C stages according to the 2022 update of the Barcelona Clinic Liver Cancer (BCLC) staging system:without involving

Sponsors

Affiliated Hospital of Chengdu University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 18–80 years, both genders eligible; 1.Pathologically or cytologically confirmed hepatocellular carcinoma (HCC), with BCLC stage B or C according to the 2022 guidelines; 2.Ability to obtain sufficient fresh tumor tissue (via surgical resection or biopsy) and autologous PBMCs (peripheral blood mononuclear cells) for organoid establishment; 3.ECOG Performance Status: 0–2; 4.No prior systemic first-line antitumor therapies (e.g., targeted agents, immunotherapies) administered before surgical intervention; 5.Voluntary participation with signed informed consent form (ICF), demonstrating compliance and willingness to adhere to follow-up protocols;

Exclusion criteria

Exclusion criteria: 1.Patients with other concurrent malignant tumors; 2.Patients who have undergone liver transplantation; 3.Immunocompromised patients with active infections in other anatomical sites; 4.Patients with severe hepatorenal diseases, cardiovascular diseases, hematologic disorders, or other comorbidities; 5.Patients who have received first-line systemic antitumor therapies or other treatments prior to the initial tissue sampling; 6.Judged by the investigators to be unsuitable for participation in this study;

Design outcomes

Primary

MeasureTime frame
Generational stability;Drug Resistance Index;DEGs Screening;

Countries

China

Contacts

Public ContactXiangke Niu

Affiliated Hospital of Chengdu University

niu19850519@163.com+86 28 8643 6383

Outcome results

None listed

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