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Impact of Concomitant Genetic Alterations in EGFR Mutated Adenocarcinoma by NGS Analysis: A Multicenter Study

K

Konkuk University Medical Center

Status

Enrolling

Conditions

EGFR Activating Mutation
Adenocarcinoma of Lung

Treatments

Other: Next generation sequencing

Study type

Observational

Funder types

Other
Industry

Identifiers

NCT04122833
ML41560

Details and patient eligibility

About

The concomitant co-mutation with epidermal growth factor receptor (EGFR) mutation might influence the clinical outcomes. The investigators will identify the impact of concommitant mutation on clinical outcome in patients with advanced -EGFR mutated adenocarcinoma.

The investigators will compare the genetic alterations between tumors of pre and post Tyrosin Kinase Inhibitor(TKI) treatments and predict the resistance mechanism for EGFR-TKIs by next-generation sequencing(NGS) analysis.

Full description

The current standard therapies in the treatment of advanced EGFR-mutated lung cancer patients are the 1st or 2nd EGFR-TKIs. Although 70-80% of patients treated by EGFR-TKIS show good responses, they have progression after around 12 months. The concomitant co-mutation with EGFR mutation might influence the drug response of EGFR TKI. The investigators will compare the progression-free survival (PFS) of EGFR-TKI according to co-occuring mutations.

The patients experience the change of molecular profiles after using the TKI. Therefore, the investigators will investigate the molecular profiles through NGS panel with foundation medicine in the tissue of pre/post EGFR-TKI, compare the change of the molecular profiles and tumor mutation burden(TMB), and identify novel mechanisms of drug resistance.

The investigators will collect the tumor tissues and blood of around 80 patients in multi-centers prospectively. Then, They will be sent to FoundationOne in the US and perform NGS analysis. The type of EGFR-TKIs would be selected according to physicians' preference. NGS will be performed twice before the EGFR-TKIs treatment and after the progression.

Enrollment

80 estimated patients

Sex

All

Ages

19+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Signed Informed Consent Form
  2. Age ≥19 years
  3. EGFR-mutated stage IV lung adenocarcinoma patients
  4. Archival biopsy tissues which are from core needle biopsies, endobronchial ultrasound (EBUS) guided- lymph node biopsy or lymph node excisional biopsy at baseline and at radiologic progression
  5. Availability of the 10 unstained slides and 1 H&E slides at pre/ post TKI treatment
  6. Samples should contain a minimum of 20% viable tumor cells that preserve

Exclusion criteria

Tumor tissue from bone metastases that have been decalcified are not acceptable.

Trial contacts and locations

2

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Central trial contact

Kye Young Lee, MD. Ph.D; In Ae Kim, MD. Ph.D

Data sourced from clinicaltrials.gov

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