Analysis of the Microenvironment of Lung Cancer and Exploration of the Mechanism of Resistance to Immunotherapy

Sponsor
The Fourth Affiliated Hospital of Zhejiang University School of Medicine (Other)
Overall Status
Recruiting
CT.gov ID
NCT05636605
Collaborator
Second Affiliated Hospital, School of Medicine, Zhejiang University (Other)
200
1
132
1.5

Study Details

Study Description

Brief Summary

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.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: Multiomics analysis

Detailed Description

Lung cancer is a highly heterogeneous disease. Cancer cells and cells within the tumor microenvironment together determine disease progression, as well as response to or escape from treatment. Tumor ecosystems are comprised of cancer cells, infiltrating immune cells, stromal cells, and other cell types together with noncellular tissue components, which interact and collectively determine disease progression as well as response to therapy. It is well known that cancer patients elicit very individualized responses to different treatments, demanding better characterization of the whole tumor ecosystem beyond currently applied clinical typing of somatic mutations in cancer cells.

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.

Study Design

Study Type:
Observational
Anticipated Enrollment :
200 participants
Observational Model:
Cohort
Time Perspective:
Other
Official Title:
Analysis of the Microenvironment of Lung Cancer and Exploration of the Mechanism of Resistance to Immunotherapy
Actual Study Start Date :
Jan 1, 2018
Anticipated Primary Completion Date :
Dec 31, 2023
Anticipated Study Completion Date :
Dec 31, 2028

Outcome Measures

Primary Outcome Measures

  1. objective response rate [three years]

    Refers to the proportion of patients whose tumor shrinkage reaches a certain amount and remains for a certain period of time, including CR + PR cases

  2. Major Pathologic Response [three-four months]

    <10% viable tumor in resected lung and lymph nodes

  3. progression-free survival [three years]

    Patients with oncological diseases have a period of time from the start of treatment to the observation of disease progression or death due to any cause

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 80 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Histopathology or hemology diagnostics of lung cancer

  • Patients have never received any antineoplastic therapy

Exclusion Criteria:
  • Within 5 years or at the same time, there are other active malignancies

  • 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

Contacts and Locations

Locations

Site City State Country Postal Code
1 The Fourth Affiliated Hospital of Zhejiang University Yiwu Zhejiang China 310000

Sponsors and Collaborators

  • The Fourth Affiliated Hospital of Zhejiang University School of Medicine
  • Second Affiliated Hospital, School of Medicine, Zhejiang University

Investigators

  • Principal Investigator: Kai Wang, PhD, The Fourth Affiliated Hospital of Zhejiang University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
The Fourth Affiliated Hospital of Zhejiang University School of Medicine
ClinicalTrials.gov Identifier:
NCT05636605
Other Study ID Numbers:
  • K2022179
First Posted:
Dec 5, 2022
Last Update Posted:
Dec 20, 2022
Last Verified:
Dec 1, 2022
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Dec 20, 2022