Exploring early-stage lung cancer with different characteristics using multi-omics
Comprehensive Multi-Omics Analysis of Early-Stage Lung Cancer Exhibiting Distinct Phenotypes
This study is trying to understand the different types of early-stage lung cancer by looking at their unique characteristics to see if this can help predict outcomes and find new treatment options for patients.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 300 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Central South University Academic / other |
| Drugs / interventions | chemotherapy |
| Locations | 1 site (Changsha, Hunan) |
| Trial ID | NCT06699979 on ClinicalTrials.gov |
What this trial studies
This observational study aims to investigate the multi-omics characterization of early-stage lung cancer that exhibits distinct phenotypes, including those associated with cystic airspaces and multiple primary lung cancers. The study will analyze differences in the pathogenesis of non-small cell lung cancer (NSCLC) and explore whether differential gene expressions can lead to prognostic models and therapeutic targets. Participants will be followed post-surgery to assess recurrence rates and time to recurrence, providing valuable insights into the disease's behavior.
Who should consider this trial
Good fit: Ideal candidates include patients aged 18-75 with histopathologically confirmed stage I-II NSCLC and an ECOG score of 0-1.
Not a fit: Patients with a history of previous or co-existing malignant tumors or those who have received systemic anti-tumor therapies prior to enrollment may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved prognostic models and targeted therapies for early-stage lung cancer patients.
How similar studies have performed: While this study employs a multi-omics approach, similar studies have shown promise in understanding cancer phenotypes, suggesting potential for success.
Eligibility criteria
Show full inclusion / exclusion criteria
Cohort 1: Multi-omics study in early-stage synchronous multiple primary lung cancer Inclusion criteria: 1. Male or female patients:18-75 years old; 2. ECOG score:0-1; 3. Histopathologically confirmed TNM stage I-II NSCLC; 4. Considered multiple or solitary primary lung cancer by clinical criteria (Martini-Melamed criteria and ACCP criteria); 5. Good compliance, family members agree to cooperate to receive survival follow-up; 6. Understand and voluntarily sign the informed consent. Exclusion criteria: 1. A history of previous or co-existing malignant tumors; 2. Systemic anti-tumor therapies, including chemotherapy, radiotherapy, or targeted therapies (such as monoclonal antibodies, small-molecule tyrosine kinase inhibitors, among others), were administered prior to enrollment; 3. Refusal to participate in the study. Cohort 2: Multi-omics study of lung cancer associated with cystic airspaces Inclusion criteria: 1. Male or female patients:18-75 years old; 2. ECOG score:0-1; 3. Histopathologically confirmed TNM stage I-II NSCLC; 4. CT findings show solitary or multiple nodules with cystic airspaces. Exclusion criteria: 1. A history of previous or co-existing malignant tumors; 2. Systemic anti-tumor therapies, including chemotherapy, radiotherapy, or targeted therapies (such as monoclonal antibodies, small-molecule tyrosine kinase inhibitors, among others), were administered prior to enrollment; 3. Refusal to participate in the study.
Where this trial is running
Changsha, Hunan
- The Second Xiangya Hospital of Central South University — Changsha, Hunan, China (Recruiting)
Study contacts
- Study coordinator: Chen Chen
- Email: chenchen1981412@csu.edu.cn
- Phone: +8673185295188
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.