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Poster display session: Biomarkers, Gynaecological cancers, Haematological malignancies, Immunotherapy of cancer, New diagnostic tools, NSCLC - early stage, locally advanced & metastatic, SCLC, Thoracic malignancies, Translational research

4774 - Molecular landscape of osimertinib resistance revealed by targeted panel sequencing and patient-derived cancer models in non-small cell lung cancer patients.

Date

20 Oct 2018

Session

Poster display session: Biomarkers, Gynaecological cancers, Haematological malignancies, Immunotherapy of cancer, New diagnostic tools, NSCLC - early stage, locally advanced & metastatic, SCLC, Thoracic malignancies, Translational research

Presenters

Min Hee Hong

Citation

Annals of Oncology (2018) 29 (suppl_8): viii493-viii547. 10.1093/annonc/mdy292

Authors

M.H. Hong1, M.H. Kim2, S. Kim3, S.G. Heo4, H. Kang4, C. Park4, J.C. Barrett5, D. Stetson6, J. Chmielecki6, A. Markovets7, H.R. Kim8, B.C. Cho9

Author affiliations

  • 1 Division Of Medical Oncology, Department Of Internal Medicine, Yonsei Cancer Center, Severance Hospital, Yonsei University College of Medicine, 03722 - Seoul/KR
  • 2 Division Of Medical Oncology, Department Of Internal Medicine, Yonsei Cancer Center, Severance Hospital, Yonsei University College of Medicine, 135-720 - Seoul/KR
  • 3 Institute For Cancer Research, JE-UK Institute for Cancer Research, Gumi-City/KR
  • 4 Institute For Cancer Research, JE-UK Institute for Cancer Research, Gumi-city/KR
  • 5 Translational Science, AstraZeneca, 2451 - Waltham/US
  • 6 Translational Science, AstraZeneca, Waltham/US
  • 7 Bioscience, AstraZeneca, Waltham/US
  • 8 Division Of Medical Oncology, Department Of Internal Medicine, Yonsei Cancer Center, Severance Hospital, Yonsei University College of Medicine, 03799 - Seoul/KR
  • 9 Division Of Medical Oncology, Department Of Internal Medicine, Yonsei Cancer Center, Severance Hospital, Yonsei University College of Medicine, 6273 - Seoul/KR

Resources

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Abstract 4774

Background

Recent studies demonstrated profound clinical activity of osimertinib in epidermal growth factor receptor (EGFR)-mutant non-small cell lung cancer (NSCLC) patients. However, the emergence of resistance limits the clinical benefit inevitably, demanding dissection of its underlying mechanisms. Here, we provide the molecular landscape of osimertinib resistance investigated by clinical sample sequencing and patient-derived cancer models.

Methods

The paired tumor tissue (n = 10) and plasma samples (n = 8) were collected from 12 EGFR-mutant NSCLC patients before and after osimertinib treatment in the ASTRIS trial (NCT02474355). The tissue and plasma DNAs were analyzed by targeted next-generation sequencing (NGS) of 112 cancer-related genes (AZ100 panel). The patient-derived cancer cell lines (PDC) and tumor xenografts (PDTX) were established from osimertinib-treated patients. Osimertinib resistant cell line (PC9-GR/AR) was also established by chronic drug administration. The preclinical resistance models were investigated by whole-exome sequencing (WES) and RNA-seq.

Results

The paired baseline and progression sample analysis identified the emergence of acquired mutations, EGFR C797S (n = 1), KRAS G12D (n = 1), and PIK3CA E545K mutations (n = 2), in the progression samples. One of these progression tissue samples with an acquired PIK3CA mutation also lost EGFR. A preexisting KRAS G12D mutation and PTEN loss were also identified in two patients who showed primary resistance to osimertinib. The WES of osimertinib-resistant PDC revealed amplification of GLI1, CDK4, and CCND1. The osimertinib-resistant PDTXs harboring PIK3CA H1047R mutation and MET amplification were established, and PI3K inhibitors and MET inhibitors will be tested. The RNA-seq analysis showed upregulation of epithelial-mesenchymal transition signatures in PC9-GR/AR cells compared to PC9-GR cells that are potentially related to epigenetic resistance mechanisms.

Conclusions

Our multi-layered molecular analysis of osimertinib-resistant patients’ clinical samples and patient-derived cancer models demonstrates a diverse spectrum of osimertinib resistance mechanisms.

Clinical trial identification

Legal entity responsible for the study

Byoung Chul Cho.

Funding

AstraZeneca.

Editorial Acknowledgement

Disclosure

J.C. Barrett, D. Stetson, J. Chmielecki, A. Markovets: Employee: AstraZeneca. All other authors have declared no conflicts of interest.

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