Abstract 360P
Background
Osimertinib – a 3rd-generation EGFR-TKI – is the preferred 1L treatment for EGFRm advanced NSCLC; however, pts can eventually develop progressive disease (PD). ELIOS (NCT03239340) characterised resistance mechanisms to 1L osimertinib. To our knowledge, this is the first prospective study with a primary objective comparing paired baseline and post-PD tumour tissue biopsies.
Methods
Pts with EGFR-TKI naïve advanced NSCLC with an EGFR-TKI-sensitising mutation received osimertinib 80 mg QD. Mandatory tumour biopsies were taken pre-treatment and post-PD; samples were analysed by next-generation sequencing. 1º endpoint: proportion of pts with a given tumour genetic and proteomic marker (including, but not limited to, EGFR mutations, HER2 and MET expression and/or amplification [amp]) at PD. 2º endpoints included investigator-assessed PFS (RECIST 1.1) and safety.
Results
154 pts were enrolled (full analysis set; FAS): median age 62 yrs (range 35–87), 77% Asian, Ex19Del/L858R/atypical EGFR mutations 55/38/7%. At data cutoff, 119 pts had PD (24 not progressed; 11 censored for other reasons); of these, 46 (39%) had evaluable paired biopsies. Median PFS (FAS) was 16.4 months (95% CI, 12.7, 20.3). AEs/SAEs occurred in 97/31% of pts. Key genetic alterations (Table) included acquired amp in MET (17%) and NKX2.1 (11%) and acquired EGFR C797S (15%). High frequency mutations at baseline (CDKN2A loss, EGFR amp, EGFR and TP53 mutations) did not differ significantly at PD.
Conclusions
Efficacy and safety of 1L osimertinib were consistent with FLAURA. MET amp was the main acquired resistance mechanism to osimertinib, consistent with previous data. NKX2.1 amp was identified as a potential new resistance marker. Paired biopsies were obtained in only 39% of pts, highlighting the challenges of obtaining post-PD tissue biopsies and the need for more comprehensive non-invasive testing methods. Table: 360P
N (%) | Baseline (N=46) | Progression (N=46) | Acquired* (N=46) |
MET amp | 2 (4) | 9 (20) | 8 (17) |
CDKN2A del | 10 (22) | 11 (24) | 7 (15) |
CDKN2B del | 9 (20) | 11 (24) | 7 (15) |
MTAP del | 7 (15) | 10 (22) | 7 (15) |
EGFR C797S | 0 (0) | 7 (15) | 7 (15) |
NKX2.1 amp | 4 (9) | 9 (20) | 5 (11) |
EGFR amp | 13 (28) | 11 (24) | 5 (11) |
CCNE1 amp | 3 (7) | 6 (13) | 3 (7) |
ARAF amp | 0 (0) | 2 (4) | 2 (4) |
ALK fusion | 0 (0) | 1 (2) | 1 (2) |
*Defined as mutations detectable at PD that were not detectable at baseline (for an individual patient) Genetic alterations shown were selected based on high-frequency of detection and/or prior knowledge of involvement in osimertinib resistance.
Clinical trial identification
NCT03239340.
Editorial acknowledgement
The authors would like to acknowledge Caroline Allinson, BSc, of Ashfield MedComms, an Inizio Company, for medical writing support that was funded by AstraZeneca in accordance with Good Publications Practice (GPP3) guidelines (http://www.ismpp.org/gpp3).
Legal entity responsible for the study
AstraZeneca.
Funding
AstraZeneca.
Disclosure
Z. Piotrowska: Financial Interests, Personal, Advisory Board: Takeda, AstraZeneca, Janssen, Eli Lilly, C4 Therapeutics, Cullinan, Blueprint, Eli Lilly, Daiichi, Janssen; Non-Financial Interests, Institutional, Principal Investigator: Cullinan; Financial Interests, Institutional, Principal Investigator: AstraZeneca; Financial Interests, Institutional, Research Grant: Blueprint, Janssen, AbbVie, Daiichi, Cullinan, GSK, Tesaro, AstraZeneca, Spectrum, Takeda, Novartis. M. Ahn: Financial Interests, Personal, Advisory Board: AstraZeneca, Bristol Myers Squibb, MSD, Ono Pharmaceutical, Roche, Takeda, Alpha Pharmaceutical; Other, Personal, Other: AstraZeneca, Bristol Myers Squibb, MSD, Ono Pharmaceutical, Roche. Y. Pang: Financial Interests, Personal, Principal Investigator: AstraZeneca. S.H. How: Financial Interests, Personal, Invited Speaker: AstraZeneca, MSD, Boehringer Ingelheim; Financial Interests, Personal, Advisory Board: AstraZeneca, Pfizer, Novartis, Roche, MSD, Boehringer Ingelheim, Takeda; Financial Interests, Personal, Research Grant: AstraZeneca, Pfizer, Novartis, Roche, MSD, Boehringer Ingelheim. K. Sang-We: Financial Interests, Personal, Research Grant: AstraZeneca, Boehringer Ingelheim, Novartis, Eli Lilly, Yuhan; Financial Interests, Personal, Other: Novartis, BMS, Roche, Eli Lilly, Boehringer Ingelheim, AstraZeneca. P.J. Voon: Financial Interests, Personal, Advisory Board: AstraZeneca, MSD, Novartis, Pfizer, Ipsen. D.L. Cortinovis: Financial Interests, Personal, Invited Speaker: AstraZeneca, Roche; Financial Interests, Personal, Advisory Board: MSD, BMS, Novartis, Boehringer Ingelheim, Amgen, Roche, Sanofi Genzyme, Takeda. J. De Castro Carpeno: Financial Interests, Personal, Invited Speaker: AstraZeneca, Bristol Myers Squibb, Gilead, Roche, MSD, Pfizer, Takeda; Financial Interests, Personal, Advisory Board: AstraZeneca, Bayer, Boehringer Ingelheim, Bristol Myers Squibb, GSK, Janssen, Eli Lilly, MSD, Novartis, Pfizer, Roche, Sanofi, Takeda. M. Tiseo: Financial Interests, Personal, Speaker’s Bureau: AstraZeneca, MSD, Novartis, Roche, BMS, Boehringer Ingelheim, Amgen, Takeda, Sanofi, Otsuka, Eli Lilly, Pfizer, Sanofi, Pierre Fabre; Financial Interests, Institutional, Research Grant: AstraZeneca, Boehringer Ingelheim. D. Rodriguez Abreu: Financial Interests, Personal, Speaker’s Bureau: AstraZeneca, Roche, Pfizer, BMS, MSD, Eli Lilly, Novartis; Financial Interests, Personal, Other: BMS, MSD, Roche, Novartis. S.S. Ramalingam: Financial Interests, Personal, Research Grant: AstraZeneca, BMS, MSD, Takeda, Genmab, Tesaro, Amgen, Advaxis; Financial Interests, Personal, Other: BMS, Amgen, Genentech, MSD, Tesaro, Takeda, GSK, AstraZeneca. J. Li, L. Servidio, S. Sadow: Financial Interests, Personal, Full or part-time Employment: AstraZeneca; Financial Interests, Personal, Stocks/Shares: AstraZeneca. R.J. Hartmaier: Financial Interests, Personal, Full or part-time Employment: AstraZeneca; Financial Interests, Personal, Stocks/Shares: AstraZeneca; Non-Financial Interests, Personal, Other, Inventor on a patent without royalties for US11066709B2: Genentech, Foundation Medicine. B.C. Cho: Financial Interests, Personal, Advisory Board: KANAPH Therapeutic Inc, Brigebio therapeutics, Cyrus therapeutics, Guardant Health, Oscotec Inc; Financial Interests, Personal, Member of the Board of Directors: Interpark Bio Convergence Corp., J INTS BIO; Financial Interests, Personal, Stocks/Shares: TheraCanVac Inc, Gencurix Inc, Bridgebio therapeutics, KANAPH Therapeutic Inc, Cyrus therapeutics, Interpark Bio Convergence Corp., J INTS BIO; Financial Interests, Personal, Royalties: Champions Oncology; Financial Interests, Personal, Research Grant: Novartis, Bayer, AstraZeneca, MOGAM Institute, Dong-A ST, Champions Oncology, Janssen, Yuhan, Ono, Dizal Pharma, MSD, AbbVie, Medpacto, GIInnovation, Eli Lilly, Blueprint medicines, Interpark Bio Convergence Corp.; Financial Interests, Personal, Advisory Role: Blueprint medicines, Medpacto, Janssen, Novartis, MSD, Takeda, Eli Lilly, AstraZeneca, Pfizer, Yuhan, Ono, BMS, Boehringer Ingelheim, Roche; Financial Interests, Personal, Other: DAAN Biotherapeutics.
Resources from the same session
374P - NX-019, a brain penetrant, mutation selective EGFR inhibitor with broad mutant EGFR activity
Presenter: Keith Wilson
Session: Poster viewing 05.
375P - Stereotactic radiotherapy (SRT) in combination with aumolertinib to treat intracranial oligometastatic non-small cell lung cancer (NSCLC): A phase II, prospective study
Presenter: Jiayan Chen
Session: Poster viewing 05.
377P - Aumolertinib as second-line therapy in T790M-positive or-negative patients with EGFR-mutated non-small cell lung cancer (NSCLC): A retrospective study
Presenter: Hongying Lv
Session: Poster viewing 05.
378P - Could the model of EGFR-TKIs plus antiangiogenesis as first-line treatments in patients with EGFR-mutated non-small cell lung cancer take a step further: A updated meta-analysis
Presenter: Yuexiao Qi
Session: Poster viewing 05.
380P - Survival outcome and cost-effectiveness of tyrosine kinase inhibitor in EGFR sensitive mutation advanced-stage NSCLC in Thammasat university hospital
Presenter: Chayanid Rungtivasuwan
Session: Poster viewing 05.
381P - Real-world experience of treatment with afatinib in advanced non-small cell lung cancer (NSCLC) in Vietnam
Presenter: Hiep Dong
Session: Poster viewing 05.
382P - Real-world data on treatment outcome of ALK positive non-small cell lung cancer from an Indian multi-centric cancer registry
Presenter: Soumya Surath Panda
Session: Poster viewing 05.
383P - Treatment outcomes with BRAF inhibitors with or without MEK inhibitors in advanced non-small cell lung cancer with positive BRAF mutation: A systematic review
Presenter: Animesh Saha
Session: Poster viewing 05.
384P - Prevalence of fibroblast growth factor receptor 2b (FGFR2b) protein overexpression in squamous non-small cell lung cancer (sqNSCLC)
Presenter: Hiroaki Akamatsu
Session: Poster viewing 05.