Comprehensive Demographics and Clinical Profile of NSCLC Patients
CA209-1529
1 other identifier
observational
500
0 countries
N/A
Brief Summary
Advances in the treatment of non-small cell lung cancer in the last decade have been significant. Currently, there are several first-line therapeutic options. The molecular biology of the disease, biomarkers and the patient's clinical characteristics can assist in decision making. The study in question aims to retrospectively evaluate the patterns of choice in the first line treatment of metastatic non-small cell lung cancer without driver mutations, from 2019 to 2022 in 7 centers in Brazil.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jan 2025
Shorter than P25 for all trials
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
December 5, 2024
CompletedFirst Posted
Study publicly available on registry
December 10, 2024
CompletedStudy Start
First participant enrolled
January 20, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 1, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
August 1, 2025
CompletedJanuary 15, 2025
January 1, 2025
1 month
December 5, 2024
January 13, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
treatment regimen decision option one
immunotherapy versus chemotherapy, this outcome will be evaluated based on data from medical records and available laboratory results
In 30 days
treatment regimen decision option two
dual immunotherapy, this outcome will be evaluated based on data from medical records and available laboratory results
In 30 days
Secondary Outcomes (1)
Survival analysis
In 24 months
Eligibility Criteria
Patients with a histological diagnosis of advanced non-small cell lung cancer, over 18 years of age
You may qualify if:
- Over 18 years old;
- Histological diagnosis of advanced non-small cell cancer;
- Clinical and demographic data available in medical records;
You may not qualify if:
- Patients with localized disease that can be treated locally;
- Non-epithelial histology;
- small cell carcinoma
- neuroendocrine tumor
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- D'Or Institute for Research and Educationlead
- Bristol-Myers Squibbcollaborator
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Sofia V Mendes, MD
Instituto D'Or de Pesquisa e Ensino
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- OTHER
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
December 5, 2024
First Posted
December 10, 2024
Study Start
January 20, 2025
Primary Completion
March 1, 2025
Study Completion
August 1, 2025
Last Updated
January 15, 2025
Record last verified: 2025-01
Data Sharing
- IPD Sharing
- Will not share