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Poster Display session

20P - Genomic profiles in EGFR mutant locally advanced or metastatic NSCLC patients post osimertinib first line treatment failure: An interim analysis of GPS study

Date

22 Mar 2024

Session

Poster Display session

Topics

Tumour Site

Non-Small Cell Lung Cancer

Presenters

Yuan-Kai Shi

Citation

Annals of Oncology (2024) 9 (suppl_3): 1-53. 10.1016/esmoop/esmoop102569

Authors

Y. Shi1, D. Lv2, W. Feng3, Y. Yu4, S. Liu5, P. Xing6, J. Zhang7, X. Ren8, J. Yin9, G. Han10, S. Cang11, J. Chen12, L. Meng13, E. Chen14, Y. Zhang15

Author affiliations

  • 1 Chinese Academy of Medical Sciences - National Cancer Center, Cancer Hospital, Beijing/CN
  • 2 Taizhou Hospital of Zhejiang Province, 318000 - Taizhou/CN
  • 3 The First People's Hospital of Foshan, Foshan/CN
  • 4 Cancer Hospital Affiliated to Harbin Medical University, Harbin/CN
  • 5 Clinical Oncology School of Fujian Medical University, Fujian Cancer Hospital, Fuzhou/CN
  • 6 National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing/CN
  • 7 The First Affiliated Hospital of University of Science and Technology of China (Anhui Provincial Hospital), Hefei/CN
  • 8 Tianjin Medical University Cancer Institute and Hospital, 145000 - Tianjin/CN
  • 9 The Third People's Hospital of Chengdu, Southwest Jiaotong University, Chongqing Medical University, 610072 - Chengdu/CN
  • 10 The People's Hospital of Taizhou, Taizhou Medical School, Jiangsu and Nantong University, Taizhou/CN
  • 11 Henan Provincial People's Hospital, 450000 - Zhengzhou/CN
  • 12 The Second Affiliated Hospital of Dalian Medical University, 116000 - Dalian/CN
  • 13 Rizhao People's Hospital, Rizhao/CN
  • 14 Sir Run Run Shaw Hospital, School of Medicine, Zhejiang University, 310000 - hangzhou/CN
  • 15 Zhongshan Hospital - Fudan University, Shanghai/CN

Resources

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Abstract 20P

Background

Osimertinib represents the current standard treatment for advanced EGFR-mutated NSCLC in the first-line (1L) setting. Acquired resistance inevitably occurs. The exploration of genomic profiles in resistant patients (pts) is vital.

Methods

EGFR mutant locally advanced or metastatic NSCLC pts post osimertinib 1L treatment failure were prospectively enrolled. Genomic profiles of paired tissues and plasma samples at progression were analyzed using NGS. Considering tissues as references, the sensitivity and specificity of EGFR amplification (amp), MET amp, EGFR C797S mutation and other non-sensitive EGFR mutations in plasma samples were analyzed.

Results

From Feb 2022 to Oct 2023, 86 pts were analyzed with paired tissue and plasma samples. The median age was 63 years (range, 33-84 years), and 45.3% were males. The majority had ECOG PS 0-1 (97.7%). At progression, EGFR C797S mutation (3.5%), other non-sensitive EGFR mutation (15.1%), EGFR amp (30.2%), MET amp (27.9%), other amps (16.3%), cell cycle gene alterations (25.6%), fusion (11.6%) and other mutations (20.9%) in tissue samples were detected. Two pts (2.3%) had histological transformation, one experienced SCLC transformation, the other one experienced squamous carcinoma transformation. Same genomic profile with different proportions were detected in paired plasma samples, including EGFR C797S mutation (4.7%), other non-sensitive EGFR mutation (17.4%), EGFR amp (10.5%), MET amp (8.1%), other amps (7.0%), cell cycle gene alterations (4.7%), fusion (14.0%) and other mutations (11.6%). Using tissues as references, the sensitivity of EGFR amp, MET amp, EGFR C797S mutation and other non-sensitive EGFR mutation were 34.62%, 16.67%, 66.67% and 76.92%, respectively in paired plasma samples. The specificity were 100.00%, 95.16%, 97.59% and 93.15%, respectively in paired plasma samples.

Conclusions

Genomic profiles were complicated in EGFR mutant locally advanced or metastatic NSCLC pts post osimertinib 1L treatment failure, with the most common being EGFR amp and MET amp. Plasma genotyping is an alternative method to identify resistance profiles when tissues are not available.

Clinical trial identification

NCT05219162.

Editorial acknowledgement

Medical writing and editorial support were provided by Hangzhou Tigermed Consulting Co.,Ltd, which was funded by AstraZeneca China.

Legal entity responsible for the study

AstraZeneca China.

Funding

AstraZeneca China.

Disclosure

All authors have declared no conflicts of interest.

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