Real-world Analysis of Workup at Disease Progression and Implementation of Osimertinib for EGFR+ NSCLC

Sponsor
Thoraxklinik-Heidelberg gGmbH (Other)
Overall Status
Unknown status
CT.gov ID
NCT04105153
Collaborator
AstraZeneca (Industry)
400
1
16.6
24.1

Study Details

Study Description

Brief Summary

Tyrosine kinase inhibitors (TKI) have greatly improved prognosis of epidermal growth factor receptor (EGFR)-positive non-small cell lung cancer (NSCLC), with tumor responses in the majority of cases and a median overall survival currently exceeding 2.5 years. However, clinical courses vary widely and eventual treatment failure is inevitable. The most common resistance mechanism against first- and second-generation EGFR inhibitors is the EGFR T790M mutation, which emerges in about 50% of cases and is amenable to next-line treatment with the third-generation compound osimertinib. However, experience in everyday clinical practice shows that implementation of EGFR TKI sequencing is often problematic, for example because a considerable number of EGFR+ NSCLC patients failing first- and second-generation EGFR inhibitors do not undergo T790M mutation testing at the time of disease progression. This study will use patient records to analyze the clinical course of EGFR+ NSCLC patients treated with first- and second-generation EGFR inhibitors at the Thoraxklinik Heidelberg (Germany) during the past years. The main aim is to analyze the diagnostic and therapeutic measures, including implementation of osimertinib, taken at the time of disease progression as well as their effect on patient outcome in a real-world, routine clinical setting.

Condition or Disease Intervention/Treatment Phase

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    400 participants
    Observational Model:
    Cohort
    Time Perspective:
    Retrospective
    Official Title:
    Real-world Analysis of Workup at Disease Progression and Implementation of Osimertinib for EGFR+ NSCLC
    Actual Study Start Date :
    Apr 15, 2019
    Anticipated Primary Completion Date :
    Jun 1, 2020
    Anticipated Study Completion Date :
    Sep 1, 2020

    Arms and Interventions

    Arm Intervention/Treatment
    TKI-treated advanced EGFR+ NSCLC

    Patients with advanced EGFR-mutated non-small cell lung cancer treated with tyrosine kinase inhibitors

    Outcome Measures

    Primary Outcome Measures

    1. Fraction of EGFR+ NSCLC patients with sequential TKI treatment [assessment will performed retrospectively for all study patients from September 2019 until June 2020]

      the rate of rebiopsy and molecular workup (especially T790M testing) at disease progression under treatment with first-/second-generation EGFR inhibitors the frequency of T790M mutations in the molecular workup of patients with disease progression under first-/second-generation EGFR inhibitors the actual rate of osimertinib implementation after failure of first-/second-generation EGFR inhibitors in the "real-world" setting.

    Secondary Outcome Measures

    1. Progression-free survival (PFS) [assessment will performed retrospectively for all study patients from September 2019 until June 2020]

      Progression-free survival (PFS) of patients treated with first-/second-generation EGFR inhibitors and/or osimertinib in the real-world setting

    2. Time-to-next-treatment (TNT) [assessment will performed retrospectively for all study patients from September 2019 until June 2020]

      Time-to-next-treatment (TNT) of patients treated with first-/second-generation EGFR inhibitors and/or osimertinib in the real-world setting

    3. Time-to-chemotherapy (TTC) [assessment will performed retrospectively for all study patients from September 2019 until June 2020]

      Time-to-chemotherapy (TTC) of patients treated with first-/second-generation EGFR inhibitors and/or osimertinib in the real-world setting

    4. Overall survival (OS) [assessment will performed retrospectively for all study patients from September 2019 until June 2020]

      Overall survival (OS) of patients treated with first-/second-generation EGFR inhibitors and/or osimertinib in the real-world setting

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • histologically confirmed locally advanced (stage III) and not suitable for definitive local treatment, or metastatic (stage IV) NSCLC

    • activating EGFR mutation confirmed

    • treatment with EGFR TKI

    Exclusion Criteria:

    none

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Thoraxklinik-Heidelberg gGmbH - Universitätsklinikum Heidelberg Heidelberg Germany 69126

    Sponsors and Collaborators

    • Thoraxklinik-Heidelberg gGmbH
    • AstraZeneca

    Investigators

    • Principal Investigator: Petros Christopoulos, MD, Thoraxklinik-Heidelberg gGmbH - Universitätsklinikum Heidelberg

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Thoraxklinik-Heidelberg gGmbH
    ClinicalTrials.gov Identifier:
    NCT04105153
    Other Study ID Numbers:
    • S-469/19
    • ESR-19-14460
    First Posted:
    Sep 26, 2019
    Last Update Posted:
    Mar 10, 2020
    Last Verified:
    Sep 1, 2019
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Product Manufactured in and Exported from the U.S.:
    No
    Keywords provided by Thoraxklinik-Heidelberg gGmbH
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Mar 10, 2020