NCT06725537

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

35
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
500

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Jan 2025

Shorter than P25 for all trials

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

December 5, 2024

Completed
5 days until next milestone

First Posted

Study publicly available on registry

December 10, 2024

Completed
1 month until next milestone

Study Start

First participant enrolled

January 20, 2025

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 1, 2025

Completed
5 months until next milestone

Study Completion

Last participant's last visit for all outcomes

August 1, 2025

Completed
Last Updated

January 15, 2025

Status Verified

January 1, 2025

Enrollment Period

1 month

First QC Date

December 5, 2024

Last Update Submit

January 13, 2025

Conditions

Keywords

neoplasialungmetastasisfirst line treatment

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

Age18 Years+
Sexall
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

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

MeSH Terms

Conditions

Carcinoma, Non-Small-Cell LungNeoplasmsNeoplasm Metastasis

Condition Hierarchy (Ancestors)

Carcinoma, BronchogenicBronchial NeoplasmsLung NeoplasmsRespiratory Tract NeoplasmsThoracic NeoplasmsNeoplasms by SiteLung DiseasesRespiratory Tract DiseasesNeoplastic ProcessesPathologic ProcessesPathological Conditions, Signs and Symptoms

Study Officials

  • Sofia V Mendes, MD

    Instituto D'Or de Pesquisa e Ensino

    PRINCIPAL INVESTIGATOR

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