Analysis of the Microenvironment of Lung Cancer and Exploration of the Mechanism of Resistance to Immunotherapy
NCT ID: NCT05636605
Last Updated: 2022-12-20
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
200 participants
OBSERVATIONAL
2018-01-01
2028-12-31
Brief Summary
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Detailed Description
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Immune checkpoint blockers (ICBs) have revolutionized the management of patients with lung cancer. Blocking the interaction between the programmed cell death protein 1 (PD-1) receptor and its primary ligand (PD-L1) has demonstrated remarkable anticancer activity, and anti-PD-1/PD-L1 drugs have been approved both as single agents or in combination with cytotoxic chemotherapy. However, most patients receiving anti-PD-1/PD-L1 monoclonal antibodies do not derive benefit. Hence, there is a crucial need to identify reliable predictive biomarkers of the response to anti-PD-1/PD-L1 agents to develop precision medicine for NSCLC immunotherapy as well as to identify novel mechanisms underlying resistance to ICBs.
To map the cell type-specific landscape of cancer cells and their tumor microenvironment in lung cancer, the investigators plan to conduct a multiomics analysis(such as, Genomics, proteomics, single cell RNA sequencing, space transcriptomics)of tumor tissue and blood, aiming at analyzing tumor heterogeneity, mapping the microenvironment map of lung cancer and exploring the mechanism of sensitivity and resistance to anti-PD1/PD-L1 antibodies.
Conditions
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Study Design
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COHORT
OTHER
Interventions
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Multiomics analysis
Genome, proteomics, single cell RNA sequencing, and space transcriptome sequencing,etc
Eligibility Criteria
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Inclusion Criteria
* Patients have never received any antineoplastic therapy
Exclusion Criteria
* Currently participating in interventional clinical research treatment, or received other research drugs or used research devices within 4 weeks before the first administration
* Active autoimmune diseases requiring systemic treatment (such as the use of disease relieving drugs, glucocorticoids or immunosuppressants) occurred within 2 years before the first administration
* The study was receiving systemic glucocorticoid treatment (excluding local glucocorticoids by nasal spray, inhalation or other means) or any other form of immunosuppressive therapy within 7 days before the first administration; Note: It is allowed to use glucocorticoid with physiological dose (prednisone ≤ 10mg/day or equivalent)
* Known history of allogeneic organ transplantation and allogeneic hematopoietic stem cell transplantation
18 Years
80 Years
ALL
No
Sponsors
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Second Affiliated Hospital, School of Medicine, Zhejiang University
OTHER
The Fourth Affiliated Hospital of Zhejiang University School of Medicine
OTHER
Responsible Party
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Principal Investigators
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Kai Wang, PhD
Role: PRINCIPAL_INVESTIGATOR
The Fourth Affiliated Hospital of Zhejiang University
Locations
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The Fourth Affiliated Hospital of Zhejiang University
Yiwu, Zhejiang, China
Countries
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Central Contacts
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Facility Contacts
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Kai Wang, PhD
Role: primary
Jiangnan Zhao, PhD
Role: backup
Other Identifiers
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K2022179
Identifier Type: -
Identifier Source: org_study_id