Lung Cancer Clinical Trial
Official title:
Multi-omics Combined With Clinical Data Analysis to Identify Prognostic Biomarkers of Lung Cancer
Multi-omics and Clinical Data Analysis is potential to predict the prognosis of lung cancer patients.
Status | Recruiting |
Enrollment | 500 |
Est. completion date | September 30, 2021 |
Est. primary completion date | September 20, 2021 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 80 Years |
Eligibility | Inclusion Criteria: - Patients diagnosed with lung cancer; - Untreated lung cancer patients; - No history of chronic or serious diseases, such as cardiovascular disease, liver disease, kidney disease, respiratory disease, blood disease, lymphatic disease, endocrine disease, immune disease, mental disease, neuromuscular disease, gastrointestinal system disease, etc. Exclusion Criteria: - Patients with other tumors; - Lung cancer patients who had been treated; - Abnormal liver and kidney function; - Acute and chronic infectious diseases |
Country | Name | City | State |
---|---|---|---|
China | Renji Hospital, Shanghai Jiaotong University school of medicine | Shanghai |
Lead Sponsor | Collaborator |
---|---|
RenJi Hospital |
China,
Zhang Y, Yang M, Ng DM, Haleem M, Yi T, Hu S, Zhu H, Zhao G, Liao Q. Multi-omics Data Analyses Construct TME and Identify the Immune-Related Prognosis Signatures in Human LUAD. Mol Ther Nucleic Acids. 2020 Sep 4;21:860-873. doi: 10.1016/j.omtn.2020.07.024 — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Identify some prognostic biomarkers in lung cancer. | Our study will identify some biomarkers that can predict the prognosis of lung cancer patients.
Our study will construct a new risk score model that provide a candidate model for prognostic evaluation of lung cancer. Our research will provide insights for precision immunotherapy of lung cancer by exploring the differences in clinical characteristics, tumor mutation burden, and tumor immune cell infiltration between different risk score groups. |
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