Sensitizing and T790M mutant EGFR tyrosine kinase inhibition

CompoundOsimertinib

Area under investigation

EGFRm NSCLC

Scientific PillarTumor Drivers & Resistance Mechanisms

Target Overview

Targeted inhibition of tumors harboring activating mutations in epidermal growth factor receptor (EGFR) has helped to advance the treatment approach for advanced non-small cell lung carcinoma (NSCLC).

While the majority of these activating mutations also sensitize EGFR (EGFRm) to effective targeting by early-generation EGFR-tyrosine kinase inhibitors (TKIs), the emergence of a secondary resistance mutation (EGFR T790M) results in treatment-refractory NSCLC disease progression. Approximately 51%-68% of tumors that progress on a first- and second-generation EGFR TKI are EGFR T790M mutation positive.1-7

Compound Overview

Osimertinib is a third-generation, irreversible, CNS-active EGFR-TKI designed to selectively target both EGFR-sensitizing (ie, T790M, L858R and exon 19 deletion) and EGFR T790M-resistance mutations.1,8

Osimertinib is being clinically evaluated in EGFRm-containing NSCLC.

Mechanism of Action

  • Mechanism of Action

References

Clinical trial information


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Abbreviations

  • 1L

    first line

  • 2L

    second line

  • ADC

    antibody drug conjugate

  • AE

    adverse event

  • AUC

    area under the curve

  • BICR

    blinded independent central review

  • CNS

    central nervous system

  • CPR

    complete pathological response

  • CRC

    colorectal cancer

  • CRT

    chemoradiotherapy

  • CT

    chemotherapy

  • CTCAE

    Common Terminology Criteria for Adverse Events

  • ctDNA

    circulating tumor DNA

  • DCR

    disease control rate

  • DFS

    disease-free survival

  • DoR

    duration of response

  • ECG

    electrocardiogram

  • ECOG PS

    Eastern Cooperative Oncology Group Performance Score

  • EFS

    event-free survival

  • EGFR

    epidermal growth factor receptor

  • EGFRm

    epidermal growth factor receptor mutation

  • EGFRwt

    epidermal growth factor receptor wild type

  • EORTC QLQ-C30

    European Organization for the Research and Treatment of Cancer Quality of Life Questionnaire

  • Ex19del

    exon 19 deletion

  • FISH

    fluorescence in situ hybridization

  • FISH10+

    fluorescence in situ hybridization (MET copy ≥10)

  • Gy

    gray

  • HBV

    hepatitis B virus

  • HCV

    hepatitis C virus

  • HIV

    human immunodeficiency virus

  • HNSCC

    head and neck squamous cell carcinoma

  • HRQoL

    health-related quality of life

  • IASLC

    International Association For The Study Of Lung Cancer

  • ICR

    independent central review

  • IHC3+/≥90%

    3+ immunohistochemistry overexpression in 90% of tumor cells

  • ILD

    interstitial lung disease

  • IV

    intravenous

  • L858R

    exon 21 L858R point mutation

  • MET

    hepatocyte growth factor receptor

  • NEC

    large cell neuroendocrine carcinoma

  • NSCLC

    non-small cell lung cancer

  • OD

    once daily

  • ORR

    overall or objective response rate

  • OS

    overall survival

  • PD

    progressive disease

  • PFS

    progression-free survival

  • PFS2

    time to second progression or death

  • PFS24

    PFS at 24 months from randomization

  • PK

    pharmacokinetics

  • PO

    per oral

  • PS

    phosphatidylserine

  • PtCh

    platinum-based chemotherapy

  • Q*W

    every * weeks

  • Q3W

    every 3 weeks

  • QD

    once daily

  • R

    randomization

  • RECIST

    Response Evaluation Criteria in Solid Tumors

  • RECIST v1.1

    Response Evaluation Criteria in Solid Tumors version 1.1

  • RT

    radiotherapy

  • SBRT

    stereotactic body radiation therapy

  • SCLC

    small cell lung cancer

  • SoC

    standard of care

  • TDT

    time to discontinuation or death

  • TFST

    time to first subsequent therapy

  • TKI

    tyrosine kinase inhibitor

  • TNM

    tumor node metastasis staging

  • TNM8

    Tumor Node Metastasis 8th edition

  • tSCLC

    transformed small cell lung cancer

  • TSST

    time to start of second subsequent therapy

  • TTD

    time to treatment discontinuation

  • TTDM

    time to death or distant metastases

  • TTP

    time to progression

  • WHO

    World Health Organization

  • WHO PS

    World Health Organization performance status

  • WT

    wild type