PDO/PDO-TIL/PDOTS for Drug Screen
Study Details
Study Description
Brief Summary
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.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
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Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Patients with PDO/PDO-TIL/PDOTS Patients whose tumors were established into patient-derived organoids, patient-derived organoids-tumor-infiltrating lymphocyte coculture systems, or patient-derived organotypic tissue spheroids, and screened for drug-sensitive. |
Other: Drug screen with PDO/PDO-TIL/PDOTS
Drug screen with patient-derived organoids, patient-derived organoids-tumor-infiltrating lymphocyte coculture system, or patient-derived organotypic tissue spheroids.
|
Outcome Measures
Primary Outcome Measures
- Objective response rate (ORR) [1 years]
Evaluated by researchers based on the RECIST 1.1 standard
Secondary Outcome Measures
- Progression free survival (PFS) [Evaluated by researchers based on the RECIST 1.1 standard]
1 years
- Relapse-free survival (RFS) [1 year]
From the date of enrollment to tumor recurrence or Death
- Overall survival (OS) [1 years]
The date of Death of any causes since the date of enrollment
- To the relief time (TOR) [1 years]
Evaluated by researchers based on the RECIST 1.1 standard
- Duration of relief (DOR) [1 years]
Evaluated by researchers based on the RECIST 1.1 standard
- Disease control rate (DCR) [1 years]
Evaluated by researchers based on the RECIST 1.1 standard
- 6-month survival rate [6 months]
Evaluated by researchers based on the RECIST 1.1 standard
- 12-month survival rate [12 months]
Evaluated by researchers based on the RECIST 1.1 standard
Eligibility Criteria
Criteria
Inclusion Criteria:
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≥18 years old, male or female.
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Liver cancer or metastatic liver cancer diagnosed clinically or pathologically, at least one measurable lesion.
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Eastern Cooperative Oncology Group (ECOG) Performance Status 0-1.
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Patient has given written informed consent.
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The function of important organs meets the requirements.
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Non-surgical sterilization or women of childbearing age need to use a medically-accepted contraceptive (such as an intrauterine device, contraceptive or condom) during the study period and within 3 months after the end of the study treatment period.
Exclusion Criteria:
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The patient has any active autoimmune disease or a history of autoimmune disease (such as the following, but not limited to autoimmune hepatitis, interstitial pneumonia, uveitis, enteritis, hepatitis, pituitary inflammation, vasculitis, nephritis, thyroid Hyperfunction; patients with vitiligo; complete remission of asthma in childhood, can be included without any intervention after adulthood; asthma patients who require bronchodilators for medical intervention cannot be included).
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The patient is using immunosuppressive agents or systemic hormonal therapy to achieve immunosuppressive purposes (agents amount > 10 mg/day of prednisone or other therapeutic hormones), and continue to use within 2 weeks before enrollment.
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Have clinical symptoms or diseases that are not well controlled.
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Significant clinically significant bleeding symptoms or a clear bleeding tendency within 3 months prior to randomization.
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Arterial/venous thrombosis in the first 6 months of randomization.
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According to the investigator, the patient has other factors that may affect the results of the study or lead to the termination of the study, such as alcohol abuse, drug abuse, other serious diseases (including mental illness) requiring combined treatment, and serious laboratory abnormalities.
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Zhongshan Hospital, Fudan University | Shanghai | Shanghai | China | 200032 |
Sponsors and Collaborators
- Shanghai Zhongshan Hospital
Investigators
None specified.Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- B2022-063R