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Completed

NCT Number: NCT05517083

Feasibility of Intratumoral Washing Fluid for Detecting EGFR Mutations in Lung Cancer

The purpose of this study is to evaluate the relevance of intratumoral washing for detection of EGFR mutation (including T790M positivity).

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Key information

Age range

20 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Pusan National University hospital

Busan, South Korea

About this study

This is a prospective, single-arm, open-label study to assess evaluate the relevance of intratumoral washing by ultrathin bronchoscopy (outer diameter; 3mm) for detection of EGFR mutation (including T790M positivity) using cobas real-time PCR and droplet digital PCR (DDPCR) in patients with NSCLC.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age ≥ 20 years
  • Obtained written informed consent
  • Patients diagnosed with NSCLC by histology or cytology and inoperable stage IV at the time of study enrollment
  • Patients with the following EGFR gene mutations: E19Del, L858R alone or concurrent rare EGFR gene mutations (T790M, G719X, exon 20 insertion, S768I)
  • Patients previously treated with EGFR-TKIs such as gefitinib, erlotinib, afatinib, dacomitinib as first line therapy
  • Patients who had shown clinical benefits (CR, PR, SD) from EGFR-TKIs and had been confirmed PD on those therapy according to RECIST v 1.1.
  • Patients who underwent liquid biopsy (plasma) for EGFR mutation at the time of PD on EGFR-TKIs
  • Patients who plan to undergo tissue biopsy for EGFR mutation at the time of PD on EGFR-TKIs

Exclusion criteria

  • Patients who withdraw informed consent
  • Patients who are unable to undergo liquid biopsy (plasma) and tissue biopsy for EGFR mutation based on the investigator's judgement

Treatment and study plan

Ultarthin bronchoscopy with intratumoral washing

Diagnostic Test

Each subject with NSCLC will undergo bronchooscopic procedure. First, ultrathin bronchoscope is inserted and placed within tumor under radial EBUS, virtual bronchoscopic navigation, and fluoroscopy guidance. Then, intratumoral washing is performed. Subsequently, transbronchial lung biopsy is performed under radial EBUS, virtual bronchoscopic navigation, and fluoroscopy guidance.

Primary outcomes

  1. The DNA and EGFR mutation (including T790M positivity) detection rate in intratumoral washing fluid

    Time frame: through study completion, an average of 1 year

    Defined as the number of DNA and EGFR mutation (including T790M positivity) detection divided by the total attempts of intratumoral washing by ultrathin bronchoscopy.

Secondary outcomes

  1. The concordance rate of EGFR mutation (including T790M positivity) detection rate among intratumoral washing fluid, plasma, and tissue

    Time frame: through study completion, an average of 1 year

    The concordance rate of EGFR mutation (including T790M positivity) detection rate in intratumoral washing fluid, compared with plasma and tissue (gold standard).

  2. The EGFR mutation (including T790M positivity) sensitivity and specificity in intratumoral washing fluid

    Time frame: through study completion, an average of 1 year

    The sensitivity and specificity of EGFR mutation (including T790M positivity) in intratumoral washing fluid compared with tissue (gold standard).

  3. Objective response rate

    Time frame: through study completion, an average of 1 year

    Objective response rate (ORR) including rate of complete response (CR) and partial response (PR) based on RECIST 1.1.

  4. Disease control rate

    Time frame: through study completion, an average of 1 year

    Disease control rate (DCR) including rate of CR, PR and stable disease (SD) based on RECIST 1.1.

  5. Progression-free survival

    Time frame: through study completion, an average of 1 year

    Progression-free survival (PFS) the time from first dose of the study drug until the date of progressive disease (PD) based on RECIST 1.1 or death by any cause.

Sponsors and collaborators

Lead sponsor

Pusan National University Hospital

Other

Registry information

Official study title

Feasibility of Intratumoral Washing Fluid for Detecting EGFR Mutations in Advanced Non-small Cell Lung Cancer

Important dates

Study start
2022
Primary completion
2023
Study completion
2024
First posted
Aug 26, 2022
Registry last updated
Aug 20, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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