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Clinical Trials in China / NCT07156617
Starting soon Observational

A Study on the Heterogeneity of Efficacy of Interventional Therapy Combined With Systemic Therapy for Liver Cancer Based on Multi-center Real-world Data

NCT07156617 · tracked via the Priya Life Science China tracker
Sponsor
Xuhua Duan
Phase
Observational
Started
2025-10-01
Last updated
2025-09-05

Condition(s) studied

Hepatocellular Carcinoma (HCC)

Investigational drug(s) / intervention(s)

Interventional therapySystemic therapy

Interventional therapy: Interventional therapy

Systemic therapy: Targeted Therapy drugs include but are not limited to Lenvatinib, Apatinib, etc. Immunotherapy drugs include but are not limited to Camrelizumab, Tislelizumab

Study summary

The system assesses the heterogeneity of HCC patients in terms of therapeutic outcomes (such as rwPFS, ORR, PRO) and adverse reactions during the process of interventional therapy combined with systemic treatment. It explores the clinical characteristics and biomarker levels of patients related to heterogeneity and builds a machine learning model to predict the risk of adverse reactions, providing evidence support for the construction of a patient-centered individualized decision-making system.

Eligibility

Sex
ALL
Min age
18 Years
Max age
Healthy volunteers
No
Inclusion Criteria: * 1\. Age ≥ 18 years old, gender not restricted; 2. Diagnosed with HCC through pathological or imaging examination, and meeting the diagnostic criteria of the "Primary Liver Cancer Diagnosis and Treatment Guidelines (2024 Edition)"; 3. Has received or plans to receive interventional therapy combined with systemic treatment (including but not limited to DEB-TACE combined with targeted therapy, DEB-TACE combined with targeted therapy and immunotherapy, DEB-TACE combined with targeted therapy and immunotherapy other local interventional treatments (such as HAIC, ablation, particle implantation, etc.)); 4. Has completed baseline clinical information and treatment records, can cooperate with the follow-up arrangement, and has the willingness and ability to complete the entire research process; 5. Signed the informed consent form. Exclusion Criteria: * 1\. Diagnosed with liver metastatic cancer or other primary malignant tumors that are not HCC, or with concurrent other active primary malignant tumors; 2. Clearly have severe cognitive impairment, mental illness or confusion, and are unable to cooperate with the visit or fill out the scale; 3. Expected survival period is less than 3 months or clinical judgment indicates that follow-up cannot be completed; 4. Liver function is in decompensation, with Child-Pugh classification as C; 5. The investigator considers any other situation that is not suitable for participating in this study.

Primary outcome measure(s)

Trial sites (14)

FacilityCityRegionStatus
The Second Affiliated Hospital of Hainan Medical Universsity Haikou Hainan
Xingtai No.5 Hospital Xingtai Hebei
Deng zhou People's Hospital Dengzhou Henan
The Second People's Hospital of Jiaozuo Jiaozuo Henan
Huai He Hospital of Henan University Kaifeng Henan
Luo Yang Central Hospital Luoyang Henan
The First Affiliated Hospital of Henan University of science and Technology Luoyang Henan
First People's Hospital of Shangqiu Shangqiu Henan
The First Affiliated Hospital of Zhengzhou University Zhengzhou Henan
Zhou Kou Central Hospital Zhoukou Henan
Wuxi No.5 People's Hospital Wuxi Jiangsu
Jiangxi Provincial People's Hospitail Nanchang Jiangxi
The First Affiliated Hospital of Nanchang University Nanchang Jiangxi
Second People's Hospital of Jiaozuo Jiaozuo China

More Xuhua Duan trials in China

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07156617 on ClinicalTrials.gov ↗ ← All trials in China