A Study on the Heterogeneity of Efficacy of Interventional Therapy Combined With Systemic Therapy for Liver Cancer Based on Multi-center Real-world Data
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)
rwPFS — up to 2 years The definition of rwPFS is the time from the first administration of combined therapy to the first imaging assessment indicating tumor progression or death, whichever occurs first.
Trial sites (14)
Facility
City
Region
Status
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
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.
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