This clinical trial aims to use the patient-derived organoid (PDO), Patient-derived organoids-tumor-infiltrating lymphocyte coculture system (PDO-TIL) and patient-derived organotypic tissue spheroids (PDOTS) to simulate the tumor microenvironment in cancer patients. The culture system can be used for pre-clinical validation of drugs and screening of drugs to treat sensitive people and provide individualized treatment for patients with liver cancer. This model is used to explore the molecular mechanism of drug resistance and to find intervention strategies to further improve the response rate of drugs. This study is expected to provide an ideal platform for drug screening and drug resistance research in liver cancer patients, which can replace experimental animal models, and guide personalized medication for liver cancer patients, so as to improve the overall prognosis of patients.
Study Type
OBSERVATIONAL
Enrollment
30
Drug screen with patient-derived organoids, patient-derived organoids-tumor-infiltrating lymphocyte coculture system, or patient-derived organotypic tissue spheroids.
Zhongshan Hospital, Fudan University
Shanghai, Shanghai Municipality, China
RECRUITINGObjective response rate (ORR)
Evaluated by researchers based on the RECIST 1.1 standard
Time frame: 1 years
Progression free survival (PFS)
1 years
Time frame: Evaluated by researchers based on the RECIST 1.1 standard
Relapse-free survival (RFS)
From the date of enrollment to tumor recurrence or Death
Time frame: 1 year
Overall survival (OS)
The date of Death of any causes since the date of enrollment
Time frame: 1 years
To the relief time (TOR)
Evaluated by researchers based on the RECIST 1.1 standard
Time frame: 1 years
Duration of relief (DOR)
Evaluated by researchers based on the RECIST 1.1 standard
Time frame: 1 years
Disease control rate (DCR)
Evaluated by researchers based on the RECIST 1.1 standard
Time frame: 1 years
6-month survival rate
Evaluated by researchers based on the RECIST 1.1 standard
Time frame: 6 months
12-month survival rate
Evaluated by researchers based on the RECIST 1.1 standard
Time frame: 12 months
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