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Staging Strategies and Their Association With Prognosis and Therapy in Lung Cancer With Cystic Airspaces

C

Central South University

Status

Enrolling

Conditions

Lung Cancer Associated With Cystic Airspaces

Study type

Observational

Funder types

Other

Identifiers

NCT07066813
LYEC2025-K0017

Details and patient eligibility

About

The goal of this observational study is to determine the most accurate tumor size measurement method for T-staging and prognostic assessment in lung cancer with cystic airspaces (LCCA). The main questions it aims to answer are:

  • What is the optimal T-staging approach for accurately classifying lung cancer with cystic airspaces (LCCA) and predicting patient outcomes?
  • How do imaging features of cystic lesions correlate with their pathological characteristics?
  • What is the relationship between imaging features of cystic airspace-associated lesions and patient prognosis?
  • Can optimizing the T-staging method improve clinical decision-making in patients with LCCA?

Enrollment

500 estimated patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Histologically confirmed non-small cell lung cancer (NSCLC), as verified by biopsy or postoperative pathological examination;
  2. Patients who have undergone surgical lung resection;
  3. Patients with complete preoperative chest CT imaging data;
  4. Preoperative chest CT showing a well-defined gas-containing (air-filled) cystic component within the tumor.

Exclusion criteria

  1. History of pulmonary diseases that could produce cystic lung lesions (e.g., tuberculosis, pulmonary fungal infections, bullae, emphysema, Lymphangioleiomyomatosis [LAM], or Birt-Hogg-Dubé [BHD] syndrome);
  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. Patients with concurrent other malignancies;
  4. Patients with missing or poor-quality preoperative chest CT imaging data.

Trial design

500 participants in 3 patient groups

group 1
Description:
radiologic T stage based on the maximum tumor diameter including cystic components
group 2
Description:
radiologic T stage based on the diameter of the solid/invasive portion only
group 3
Description:
pathologic T stage derived from the resected specimen

Trial contacts and locations

1

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Central trial contact

Chen Chen

Data sourced from clinicaltrials.gov

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