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Predictive analysis of therapeutic effect of interventional therapy for hepatocellular carcinoma based on clinical characteristics and radiomics consist of DSA features and dynamic contrast-enhanced CT/MR: a retrospective study.

Predictive analysis of therapeutic effect of interventional therapy for hepatocellular carcinoma based on clinical characteristics and radiomics consist of DSA features and dynamic contrast-enhanced CT/MR: a retrospective study.

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300077657
Enrollment
Unknown
Registered
2023-11-15
Start date
2023-11-20
Completion date
Unknown
Last updated
2023-11-21

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

Conditions

hepatocellular carcinoma

Interventions

Interventional treatment group:NA

Sponsors

Sun Yat-sen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: (1) Typical imaging features of hepatocellular carcinoma, elevated AFP or pathological diagnosis of hepatocellular carcinoma; (2) At least two imaging assessments based on enhanced CT or enhanced MR Before surgery or interventional treatment, and the target lesions can be measured according to RECIST1.1/mRECIST criteria; (3) At least one evaluation of blood tumor markers, liver function and blood routine before treatment; (4) At least one imaging evaluation based on contrast-enhanced CT or contrast-enhanced MR After interventional therapy, which should be completed within 2 months after immunotherapy, and the target lesions can be measured according to ECIST1.1/mRECIST criteria; (5) Received at least one interventional therapy, including TACE, HAIC, TIPS, or PTCD; (6) At least one DSA data was available. (7) Patients who underwent surgical treatment had complete pathological data.

Exclusion criteria

Exclusion criteria: (1) Severe renal impairment and intolerance to contrast media; (2) History of congenital or acquired immune deficiency (such as HIV infection); (3) History of other malignant tumors in the past 3 years or at the same time; (4) History of organ transplantation; (5) Loss of clinical information or follow-up data.

Design outcomes

Primary

MeasureTime frame
overall remission;

Secondary

MeasureTime frame
Overall survival;

Countries

China

Contacts

Public ContactFei Gao

Sun Yat-sen University Cancer Center

zuomx@sysucc.org.cn+86 137 6086 9828

Outcome results

None listed

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