Skip to content

The Real-World Study of systematic therapy for advanced hepatocellular carcinoma: a multicenter, multi-cohort, retrospective study

The Real-World Study of systematic therapy for advanced hepatocellular carcinoma: a multicenter, multi-cohort, retrospective study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500100632
Enrollment
Unknown
Registered
2025-04-11
Start date
2025-04-14
Completion date
Unknown
Last updated
2025-04-14

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

Conditions

hepatocellular carcinoma

Interventions

Combination Therapy Group :None
Sequential Therapy Group:None

Sponsors

Zhongshan Hospital Fudan University Xiamen Branch
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Between January 1, 2019 and January 1, 2024, those who underwent systemic therapy at participating centers in advanced inoperable resectable areas that meet the clinical diagnostic criteria of the Guidelines for the Diagnosis and Treatment of Primary Liver Cancer (2024 Edition) or the American Association of Hepatology (AASLD) Guidelines for the Diagnosis and Treatment of Liver Cancer. 2. Have at least one measurable lesion according to the efficacy evaluation criteria for solid tumors (RECIST1.1). 3. Patient age>=18 years. 4. The patient's medical history data is complete and traceable. 5. Application of systemic therapy > = 1 treatment cycle, systemic therapy includes: immune checkpoint inhibitors (including PD-(L)1, CTLA-4), TKI drugs, and macromolecule targeted therapy drugs. [Oral TKI drugs for at least 1 month.] ] 6. Combined local treatment: All combined local treatments should be reflected in the data collection to facilitate further statistical analysis of the data.

Exclusion criteria

Exclusion criteria: 1. Patients who are unable to obtain relevant examinations, examinations or follow-up information required for the study due to incomplete medical history information. 2. Child C or ECOG > 2 points 3. Less than 1 cycle of systemic treatment drugs and less than 1 month of oral targeted drugs. 4. Combined with other malignant tumors requiring active treatment; 5. Survival time at the time of enrollment < 3 months; 6. Any other conditions that, in the judgment of the investigator, consider the patient to be unsuitable for inclusion in this study;

Design outcomes

Primary

MeasureTime frame
Progression-free survival;Overall survival;

Secondary

MeasureTime frame
Objective response rate;Disease control rate;Security;Pharmacoeconomic evaluation;

Countries

China

Contacts

Public ContactZhang Boheng

Zhongshan Hospital Fudan University Xiamen Branch

zhang_boheng@126.com+86 136 8197 2165

Outcome results

None listed

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