Skip to main content
OpenTrials
Recruiting

NCT Number: NCT06699979

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

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.

Recruiting

Interested in participating?

Request Info

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

The Second Xiangya Hospital of Central South University

Changsha, Hunan, 410011, China

Location status: Recruiting

Location contact

Ping Jiang

CONTACT

[email protected]

+8673185292476

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Cohort 1: Multi-omics study in early-stage synchronous multiple primary lung cancer

Inclusion criteria

  • 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);
  • Good compliance, family members agree to cooperate to receive survival follow-up;
  • Understand and voluntarily sign the informed consent.

Exclusion criteria

  • 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.

Cohort 2: Multi-omics study of lung cancer associated with cystic airspaces

Inclusion criteria

  • Male or female patients:18-75 years old;
  • ECOG score:0-1;
  • Histopathologically confirmed TNM stage I-II NSCLC;
  • CT findings show solitary or multiple nodules with cystic airspaces.

Exclusion criteria

  • 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.

Treatment and study plan

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

Study contacts

Contact information is provided by the study sponsor or research team.

Sponsors and collaborators

Lead sponsor

Central South University

Other

Registry information

Official study title

Comprehensive Multi-Omics Analysis of Early-Stage Lung Cancer Exhibiting Distinct Phenotypes

Important dates

Study start
2024
Primary completion
2026
Study completion
2027
First posted
Nov 21, 2024
Registry last updated
Jul 7, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.