Real-World Treatment Patterns of Metastatic Epidermal Growth Factor Receptor (EGFR)-Mutated Non-small Cell Lung

Tao Ran1, Iris Lin1, Cindy Chen2

  • 1Oncology, Real World Value and Evidence, Johnson and Johnson, Titusville, USA.

Cureus
|December 23, 2025
PubMed

Insights

Real-world data shows that despite guidelines, immunotherapy is used in first- and second-line treatments for metastatic non-small cell lung cancer with EGFR mutations, indicating unmet needs for targeted therapies.

Area of Science:

  • Oncology
  • Medical Informatics
  • Clinical Research

Background:

  • Targeted therapies are standard for EGFR-mutated metastatic non-small cell lung cancer (mNSCLC).
  • Limited real-world data exists on patient characteristics and treatment patterns for this specific mNSCLC population.
  • Understanding current treatment trends is crucial for identifying unmet needs.

Purpose of the Study:

  • To describe real-world treatment patterns in patients with EGFR-mutated (exon 19 deletion [Ex19del]/L858R) mNSCLC.
  • To analyze the use of immunotherapy in first-line (1L) and second-line (2L) settings for this patient group.

Main Methods:

  • Retrospective analysis of deidentified Integra Connect data.
  • Inclusion of patients with EGFR-mutated (Ex19del/L858R) mNSCLC initiating 1L treatment on or after January 1, 2018.
  • Descriptive analysis of patient demographics, testing, treatment patterns, and outcomes.

Main Results:

  • Osimertinib monotherapy (74.7%) and combination therapies (10.9%) were the most common 1L treatments.
  • Immunotherapy was used in 9.4% of 1L treatments and 31.4% of 2L treatments.
  • Most patients (72.7%) had next-generation sequencing, and median time to 1L treatment was short (1.1 months).

Conclusions:

  • Real-world data reveals immunotherapy use in 1L and 2L settings for EGFR-mutated mNSCLC, contrary to guidelines.
  • This observed pattern highlights significant unmet needs in mNSCLC treatment.
  • There is a continued need for more effective targeted therapies for patients with EGFR-mutated mNSCLC.