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

Last updated: September 22, 2026
Sponsor: AstraZeneca
Overall Status: Active - Recruiting

Phase

N/A

Condition

N/A

Treatment

N/A

Clinical Study ID

NCT06491862
D133HR00041
  • Ages > 18
  • All Genders

Study Summary

The study will be implemented as a retrospective, noninterventional medical record review of patients from routine practice settings who have been diagnosed with a/m non-squamous NSCLC with or without AGA and received at least 1 line of systemic treatment after failing PTC between January 2017 and December 2024.

Eligibility Criteria

Inclusion

Inclusion Criteria

  • Confirmed diagnosis of non-squamous NSCLC, Stage IIIB/IIIC incurable or IV/M1.

  • Age ≥ 18 years at diagnosis of advanced/metastatic disease.

AGA Cohort: Presence of actionable mutations and all of the following:

  • failure of platinum-based chemotherapy,

  • failure of ≥ 1 line of approved target therapy or no targeted therapy available at the clinic,

  • additional systemic treatment after platinum + target therapy combination.

Non-AGA Cohort: Absence of actionable mutations and all of the following:

  • failure of platinum-based chemotherapy,

  • failure of immunotherapy concurrent or sequential to platinum,

  • additional systemic treatment after platinum + immunotherapy combination.

Exclusion Criteria

  • Patients with evidence of other primary malignancies (except basal cell carcinoma and melanoma) within 1 year prior to the index date will be excluded from both study cohorts.

  • Patients who participated in a clinical investigational study for the treatment of any cancer, including NSCLC, or any early access program from 2018 onwards.

Study Design

Total Participants: 250
Study Start date:
July 25, 2024
Estimated Completion Date:
December 31, 2026

Study Description

The study will be implemented as a retrospective, noninterventional medical record review of patients from routine practice settings who have been diagnosed with advanced/metastaic non-squamous NSCLC with or without AGA and who have failed platinum-based chemotherapy and immunotherapy (for patients without AGA) or platinum-based chemotherapy and at least 1 line of targeted therapy (for patients with AGA). The study will be conducted on one cohort of patients regardless their AGA status. The study index date will be defined as first dose of any agent after PTC, with specific treatments received for AGA and non-AGA patients in the preindex period. We will also conduct a subgroup analysis on NSCLC pre-defined subtypes (sample size permitting): EGFR mutant, ALK translocation, ROS1 translocation, MET1 mutant, HER-2 mutant, BRAF mutant, pan-wild-type PD-L1 >50%.

Connect with a study center

  • Research Site

    Belo Horizonte, Minas Gerais 30380-420
    Brazil

    Site Not Available

  • Research Site

    Belo Horizonte, Minas Gerais 30110-934
    Brazil

    Site Not Available

  • Research Site

    Natal, Rio Grande do Norte 59062-000
    Brazil

    Active - Recruiting

  • Research Site

    Porto Alegre, Rio Grande do Sul 90560-032
    Brazil

    Site Not Available

  • Research Site

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

    Site Not Available

  • Research Site

    São Paulo, 05652-900
    Brazil

    Active - Recruiting

  • Research Site

    São Paulo, 01323-001
    Brazil

    Site Not Available

  • Research Site

    São Paulo, 01509-010
    Brazil

    Site Not Available

  • Research Site

    São Paulo, 01308-050
    Brazil

    Active - Recruiting

  • Research Site

    São Paulo, 01333-010
    Brazil

    Active - Recruiting

  • Research Site

    São Paulo, 01323-020
    Brazil

    Active - Recruiting

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