Literature DB >> 32641247

Prospective Observational Study of Treatment Resistance-related Gene Screening Using Plasma Circulating Tumor DNA in Third-generation EGFR-TKI Osimertinib Therapy (Elucidator).

Akihiro Tamiya1, Shun-Ichi Isa2, Yoshihiko Taniguchi3, Hideyuki Nakagawa4, Shinji Atagi2, Masahiko Ando5, Yasuhiro Koh6.   

Abstract

BACKGROUND: Osimertinib is a third-generation epidermal growth factor receptor (EGFR)-tyrosine kinase inhibitor (TKI) that potently and selectively inhibits EGFR activating and EGFR T790M resistance mutations. Osimertinib was found to be more effective than first-generation EGFR-TKIs in patients with previously untreated advanced non-small-cell lung cancer (NSCLC) harboring EGFR-positive mutations in a prior phase III trial. Osimertinib is, therefore, one of the most important standard therapies for EGFR mutation-positive patients. However, there are few reports about osimertinib resistance mechanisms in first-line EGFR-TKI therapy. Understanding first-line osimertinib resistance mechanisms is essential for future therapeutic strategies in patients with NSCLC with EGFR-positive mutations. To clarify the resistance mechanisms of first-line osimertinib, we proposed to analyze circulating tumor (ct) deoxyribonucleic acid (DNA) by the ultra-sensitive next-generation sequencing method. PATIENTS AND METHODS: We aim to collect ctDNA samples from patients with the following key inclusion criteria: histologically or cytologically proven NSCLC, activating EGFR mutation-positive, planned treatment with first-line osimertinib, and written informed consent. Patients with comorbidities, who are deemed unsuitable for participation by an attending physician, would be excluded. We plan to enroll 180 cases and estimate a final analysis of 120 cases following registration and 2-year observation. ctDNA samples are collected at osimertinib treatment initiation, 3 and 12 months later, and disease progression. The key primary endpoint is to clarify the incidence and ratio of osimertinib resistance. The key secondary endpoint is to examine how the quantity of osimertinib resistance-associated mutations detected in ctDNA at treatment initiation influences disease progression.
Copyright © 2020 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Epidermal growth factor receptor; Next-generation sequencing; Non–small-cell lung cancer

Mesh:

Substances:

Year:  2020        PMID: 32641247     DOI: 10.1016/j.cllc.2020.05.023

Source DB:  PubMed          Journal:  Clin Lung Cancer        ISSN: 1525-7304            Impact factor:   4.785


  1 in total

1.  Circulating tumor DNA accurately predicts disease progression and genotype alterations in postoperative adjuvant EGFR-TKI resistance: a case report.

Authors:  Zhen Zeng; Chengwu Liu; Senyi Deng; Feng Lin; Hatim Husain; Mariacarmela Santarpia; Lunxu Liu
Journal:  Transl Lung Cancer Res       Date:  2022-09
  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.