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Prospective Epidemiological Study of Metastatic Non Small Cell Lung Cancer (NSCLC) in Latin America

Prospective Epidemiological Study of Metastatic Non Small Cell Lung Cancer (NSCLC) in Latin America

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04227457
Acronym
LATINO Lung
Enrollment
700
Registered
2020-01-13
Start date
2018-07-25
Completion date
2023-08-04
Last updated
2024-02-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Lung Cancer

Keywords

Lung Cancer

Brief summary

To describe the overall survival of advanced NSCLC in Latin America.

Detailed description

* To describe demographic and socioeconomic characteristics of patients newly diagnosed with advanced NSCLC * To describe diagnostic methods, pathological profile and disease stage at diagnosis of advanced NSCLC * To describe the practice patterns of therapeutic agents for treatment of advanced NSCLC * To describe treatment responses, progression and survival times. * To describe reasons for treatment discontinuation * To identify associations between patient demographics, socioeconomic, pathology, treatment sequences and overall survival; * To define the patient experience of advanced NSCLC and identify unmet needs in their diagnose and treatment.

Interventions

None listed

Sponsors

Bristol-Myers Squibb
CollaboratorINDUSTRY
Latin American Cooperative Oncology Group
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Patients aged 18 years or older; 2. Newly diagnosed Non-Small Cell Lung Cancer (NSCLC) during the period of the study (which includes 3 months prior to site activation by LACOG, although they can have received anti-cancer treatment during that time); 3. Histologically or cytologically confirmed advanced NSCLC: 1. Stage IIIB that progressed after curative therapy (chemoradiation and/or surgery); 2. Stage IV metastatic disease (de novo or distant relapse) 4. Any NSCLC histological subtype and molecular mutation; 5. Any Eastern Cooperative Oncology Group (ECOG) Performance Status (0 to 4) at diagnosis; 6. Patients assigned by treating physician to any therapy (i.e. chemotherapy, targeted agents, immunotherapy) or palliative care; 7. Access to patient medical chart for data collection; 8. Willing and able to provide written informed consent and privacy authorization for the release of personal health information.

Design outcomes

Primary

MeasureTime frameDescription
Overall survival of advanced NSCLC in Latin AmericaAnnually, during 3 yearsTime from randomization or initiation of treatment to patient death

Secondary

MeasureTime frameDescription
Description of socioeconomic characteristics of patients newly diagnosed with advanced NSCLCAnnually, during 3 yearsDescription of the socioeconomical characteristics of the Latin America population with newly advanced NSCLC
Description of pathological profile of advanced NSCLCAnnually, during 3 yearsAnalysis of histology and molecular markers of advanced NSCLC
Description of the practice patterns of therapeutic agents for treatment of advanced NSCLCAnnually, during 3 yearsDescription of the practice patterns of therapeutic agents for treatment of advanced NSCLC
Description of the treatment responsesAnnually, during 3 yearsDescription of the treatment responses
Description of Treatment discontinuationAnnually, during 3 yearsDescription of the reasons for treatment discontinuation

Countries

Argentina, Brazil, Chile, Colombia, Mexico

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026