Observational Cohort Study of Advanced Non-small Cell Lung Cancer (CAPTRA-LUNG)
Trial Snapshot
- Phase
- Not Applicable
- Status
- Recruiting
- Enrollment
- 5,000
- Locations
- 1
- Primary Endpoint
- Overall Survival (OS)
Study Overview
Brief Summary
Investigators propose to establish and maintain a cohort of patients with advanced non-small cell lung cancer, and to assess the treatment pattern, host genetic, and clinical factors which influence the prognosis and survival, as well as the interaction among these factors on disease diagnosis and treatment, short and long-term outcomes.
Study type: Observational (Patient Registry)
Study design: Observational Model: Cohort
Time Perspective: Prospective and retrospective
Study Design
- Study Type
- Observational
- Observational Model
- Cohort
- Time Perspective
- Other
Eligibility Criteria
- Ages
- 18 Years to — (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •Cohort I: diagnosis of advanced non-small cell lung cancer from 2012-2016;
- •Cohort II: documented positive driver gene mutations; and diagnosis of advanced non-small cell lung cancer;
- •Cohort III: diagnosis of advanced non-small cell lung cancer and in immune-therapy;
- •Cohort IV: diagnosis of advanced non-small cell lung cancer, and with wild-type driver gene or unknown driver gene status;
- •Cohort V: treated with anti-VEGF drug in first line, diagnosis of advanced non-squamous and non-small cell lung cancer in 6 months before recruit;
- •Age>18 years;
- •Provision of written informed consent.
Exclusion Criteria
- •not applicable
Outcomes
Primary Outcomes
Overall Survival (OS)
Time Frame: 3 years
OS was calculated from the diagnosis of advanced non-small cell lung cancer to death from any reasons
Secondary Outcomes
No secondary outcomes reported
