Local and Peripheral Immune Responsive Landscape Induced by Local Cryoablation in Patients With Lung Adenocarcinoma

Sponsor
China-Japan Friendship Hospital (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT06104709
Collaborator
(none)
10
13

Study Details

Study Description

Brief Summary

The goal of this observational study is to learn about local and peripheral immune and metabolic changes in patients with lung adenocarcinoma undergoing cryoablation. The main question it aims to answer are:

  • local and peripheral immune changes in patients with lung adenocarcinoma undergoing cryoablation.

  • local and peripheral metabolic changes in patients with lung adenocarcinoma undergoing cryoablation.

Peripheral blood, biopsy tissues of patients will be collected at the baseline and after cryoablation. Single-cell sequencing, single-cell immune bank, metabolomics and spatial metabolomics will be used to explore the local and peripheral immune changes and metabolites changes in patients with lung adenocarcinoma before and after cryoablation.

Condition or Disease Intervention/Treatment Phase

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    10 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    Local and Peripheral Immune Responsive Landscape Induced by Local Cryoablation in Patients With Lung Adenocarcinoma
    Anticipated Study Start Date :
    Dec 1, 2023
    Anticipated Primary Completion Date :
    Dec 31, 2024
    Anticipated Study Completion Date :
    Dec 31, 2024

    Arms and Interventions

    Arm Intervention/Treatment
    LUAD patients undergoing cryoablation

    No interventions.

    Outcome Measures

    Primary Outcome Measures

    1. cryoablation completion [1 month]

      patients complete local cryoablation

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 90 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    1. Primary or metastatic lung cancer with definite pathological diagnosis.

    2. Patients are not suitable for thoracotomy due to serious lung or systemic disease.

    3. Peripheral lung cancer involves pleura and chest wall, which cannot be completely removed by surgical resection.

    4. There are indications for surgical resection, but the patient refuses surgery.

    5. Single tumor, maximum diameter ≤5cm; Or the number of tumors ≤3, the maximum diameter ≤3cm.

    6. ECOG-PS score≤2.

    7. Patients with an expected survival of more than three months.

    8. Patients have not participated in other clinical validation within 3 months.

    9. Subjects voluntarily sign informed consent.

    Exclusion Criteria:
    1. Serious heart and brain disease or other mental illness.

    2. Severe pulmonary fibrosis, especially drug-induced pulmonary fibrosis.

    3. Patients with previous severe pulmonary dysfunction, pulmonary ventilation disorder, and multiple pulmonary bulla.

    4. A history of immunodeficiency, including a positive HIV test (enzyme-linked immunoassay and Western spot assay).

    5. Patients treated with chemotherapy, radiotherapy, interventional therapy, ablative therapy or surgery within 30 days before surgical treatment.

    6. There is a serious bleeding tendency, platelets less than 50×109 /L and coagulation function is seriously disturbed.

    7. Coagulation index (PT, TT, APTT) > 2.5 times the upper limit of normal.

    8. Ablation of ipsilateral malignant pleural effusion is not well controlled.

    9. Poor general condition, multiple organ failure, cachexia, severe anemia and nutritional metabolism disorders.

    10. Patients with extensive extrapulmonary metastasis are not suitable for ablative therapy.

    11. People who regularly use sedatives, sleeping pills, tranquilizers or other addictive drugs.

    12. Pregnant or breastfeeding women.

    13. Patients who cannot evaluate the efficacy.

    14. Other conditions determined by the investigators to be unsuitable for inclusion, such as inability to tolerate cryoablation surgery, difficulty in follow-up, and other serious diseases.

    Contacts and Locations

    Locations

    No locations specified.

    Sponsors and Collaborators

    • China-Japan Friendship Hospital

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Gang Hou, Principle Investigator, China-Japan Friendship Hospital
    ClinicalTrials.gov Identifier:
    NCT06104709
    Other Study ID Numbers:
    • ZRJY2021-BJ08-02-06
    First Posted:
    Oct 27, 2023
    Last Update Posted:
    Oct 27, 2023
    Last Verified:
    Oct 1, 2023
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Gang Hou, Principle Investigator, China-Japan Friendship Hospital
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Oct 27, 2023