Actively Recruiting

Age: 18Years +
All Genders
ID06491862

RACE-2L: Real-World Assessment of Clinical Practice and Outcomes in Non-squamous Non-Small Cell Lung Cancer After Failure of Platinum-based Chemotherapy in Brazil

Led by AstraZeneca · Updated on 2026-05-22

250

Participants Needed

11

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are conducting a retrospective, noninterventional study to review medical records of patients diagnosed with advanced or metastatic non-squamous non-small cell lung cancer (NSCLC) who have received systemic treatment after failing platinum-based chemotherapy. This study includes patients with or without actionable genomic alterations (AGA) and aims to describe the patient population and treatment patterns between January 2017 and December 2024. Subgroup analyses will be performed on specific NSCLC subtypes, such as EGFR mutant, ALK translocation, and others if sample size allows. The study involves reviewing records of patients who have failed platinum-based chemotherapy and immunotherapy (for non-AGA patients) or platinum-based chemotherapy and at least one line of targeted therapy (for AGA patients). The index date is defined as the first dose of any agent after platinum chemotherapy failure. The study covers one cohort regardless of AGA status and includes analysis of various NSCLC genetic subtypes. There is no intervention or treatment administered as part of this observational study. Participants' medical records will be examined to collect data on diagnosis, treatments received, and outcomes. The primary outcome is to describe patient characteristics and treatment patterns over the defined period. Since this is a retrospective review, no active participation or treatment is required from patients. The study is expected to be completed by June 2026, with data collection focusing on routine clinical practice and outcomes after platinum chemotherapy failure.

CONDITIONS

Brief Title

RACE-2L: Real-World Assessment of Clinical Practice and Outcomes in Non-squamous NSCLC After Failure of Platinum-based Chemotherapy in Brazil

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Confirmed diagnosis of advanced or metastatic non-squamous NSCLC stage IIIB/IIIC not eligible for curative therapies or stage IV/M1 with or without actionable genomic mutations
  • Age 18 years or older at first diagnosis of advanced/metastatic NSCLC
  • For patients with actionable genomic alterations, must have received platinum-based chemotherapy and at least one approved targeted therapy
  • For patients without actionable genomic alterations, must have received sequential or concurrent immunotherapy and platinum-based chemotherapy
  • Must have received at least one line of active therapy after failing platinum-based chemotherapy
Not Eligible

You will not qualify if you...

  • Patients with other primary cancers (except basal cell carcinoma and melanoma) within one year before index date
  • Patients who participated in any investigational clinical trial or early access program for cancer treatment from 2018 onward

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Long-term Monitoring

Duration - Data collected from January 1st, 2017 to December 31st, 2024

Participants who have previously received standard treatments for advanced non-squamous NSCLC are observed through retrospective medical record review to assess treatment patterns and outcomes.

No visits; data are collected retrospectively from medical records

Trial Site Locations

Total: 11 locations

1

Research Site

Belo Horizonte, Minas Gerais, Brazil, 30110-934

Not Yet Recruiting

2

Research Site

Belo Horizonte, Minas Gerais, Brazil, 30380-420

Not Yet Recruiting

3

Research Site

Natal, Rio Grande do Norte, Brazil, 59062-000

Actively Recruiting

4

Research Site

Porto Alegre, Rio Grande do Sul, Brazil, 90560-032

Not Yet Recruiting

5

Research Site

São José do Rio Preto, São Paulo, Brazil, 15090-000

Not Yet Recruiting

6

Research Site

São Paulo, Brazil, 01308-050

Actively Recruiting

7

Research Site

São Paulo, Brazil, 01323-001

Not Yet Recruiting

8

Research Site

São Paulo, Brazil, 01323-020

Actively Recruiting

9

Research Site

São Paulo, Brazil, 01333-010

Actively Recruiting

10

Research Site

São Paulo, Brazil, 01509-010

Not Yet Recruiting

11

Research Site

São Paulo, Brazil, 05652-900

Actively Recruiting

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Research Team

A

AstraZeneca Clinical Study Information Center

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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