Multi-omics Study of Early-stage Lung Cancer With Distinct Phenotypes

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorCentral South University

About this trial

The goal of this observational study is to investigate the multi-omics characterization early-stage lung cancer exhibiting distinct phenotypes including lung cancer associated with cystic airspaces, multiple primary lung cancers, and so on. The main questions it aims to answer are:

* What are the differences in pathogenesis of non-small cell lung cancer with different phenotypes explored by multi-omics? * Whether differential genes lead to potential prognostic models and therapeutic targets? Participants will be followed up after surgery to answer prognosis: whether they have recurred, and the time to recurrence.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Male or female patients:18-75 years old;

ECOG score:0-1;

Histopathologically confirmed TNM stage I-II NSCLC;

Considered multiple or solitary primary lung cancer by clinical criteria (Martini-Melamed criteria and ACCP criteria);

Disqualifiers

A history of previous or co-existing malignant tumors;

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;

Refusal to participate in the study.

Male or female patients:18-75 years old;

Trial population

Patients with non-small cell lung cancer with indication for surgery.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

300 Participants
are grouped into 1 trial group
Group A: Non-small cell lung cancer

Trial outcomes

Primary outcomes

1

Immune repertoire sequencing

Time frame
From enrollment to the end of surgery for 3 years
2

DNA methylome sequencing

Time frame
From enrollment to the end of surgery for 3 years
3

RNA sequencing

Time frame
From enrollment to the end of surgery for 3 years

Secondary outcomes

1

Genomic sequencing

Time frame
From enrollment to the end of surgery for 3 years
2

Metabolomics analysis

Time frame
From enrollment to the end of surgery for 3 years
3

Radiomics analysis

Time frame
From enrollment to the end of surgery for 3 years

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Central South University

Lead sponsor

Second Xiangya Hospital of Central South University

Sponsor institution