About this trial
This is a prospective, observational, multicenter study, in which clinical and demographic data will be extracted from medical records. Convenience sample, with an estimated inclusion of 200 patients treated in seven participating centers.
Eligible tumors for this project will be from patients with advanced (unresectable or metastatic) non-small cell lung carcinoma, who will start first-line oncological treatment in one of the participating centers between 2025 and 2026 (between January 2025 and January 2026). Patients must be over 18 years old and data must be available in electronic medical records.
Medical records will be assessed to confirm patients' eligibility. Patients with localized disease amenable to local treatment, non-epithelial histology, small cell carcinoma and neuroendocrine tumor will not be eligible.
A survey will be designed targeting thoracic and generalist medical oncologists, aiming to understand the factors guiding the choice of first-line treatment regimens and to compare these insights with real-world data. The survey will be directed to Brazil, with an estimated of 200 filled files.
Eligibility criteria
Qualifiers
Advanced (unresectable or metastatic) non-small cell lung carcinoma
First-line oncological treatment in one of the participating centers between 2025 and 2026 (between January 2025 and January 2026)
> 18 years old
Data available in electronic medical records.
Disqualifiers
Localized disease amenable to local treatment
Non-epithelial histology
Small cell carcinoma
Neuroendocrine tumor
Trial design
Treatments tested in this trial
- Not listed
Trial groups
Locations
7Sponsors and collaborators
AstraZeneca
Lead sponsor