Treatment Patterns and Resource Use After Osimertinib Discontinuation in Patients with EGFR + Metastatic NSCLC

Elizabeth Marrett1, Winghan Jacqueline Kwong2, Jinlin Song3

  • 1Health Economic and Outcomes Research, Daiichi Sankyo, Inc., 211 Mount Airy Road, Basking Ridge, NJ, 07920, USA. elizabeth.marrett@daiichisankyo.com.

Oncology and Therapy
|July 30, 2024
PubMed
Abstract

Insights

Subsequent therapies for EGFR-mutated non-small cell lung cancer after osimertinib are often short-lived. Most patients receive platinum-based chemotherapy, highlighting an unmet need for more effective treatments against EGFR tyrosine kinase inhibitor resistance.

Area of Science:

  • Oncology
  • Pharmacology
  • Clinical Research

Background:

  • Current guidelines recommend EGFR tyrosine kinase inhibitors (TKIs), particularly osimertinib, for first-line treatment of EGFR-mutated metastatic non-small cell lung cancer (mNSCLC).
  • Acquired resistance to targeted therapies like osimertinib is common, necessitating subsequent treatment lines.
  • Systemic chemotherapy is typically recommended after progression on targeted therapy.

Purpose of the Study:

  • To characterize the subsequent line of therapy (LOT) following osimertinib discontinuation in patients with EGFR-mutated mNSCLC.
  • To evaluate treatment patterns and duration of subsequent therapies.
  • To identify unmet needs in managing EGFR TKI resistance.

Main Methods:

  • Retrospective analysis of medical and pharmacy claims data.
  • Inclusion of adult patients who initiated a subsequent LOT after discontinuing osimertinib between November 2015 and September 2019.
  • Characterization of treatment regimens, duration, and healthcare utilization.

Main Results:

  • 135 patients met the inclusion criteria.
  • Most patients (57%) received platinum-based chemotherapy in the subsequent LOT, with 40.3% including immuno-oncology therapy.
  • EGFR TKI reuse or continuation was observed in 24% of patients.
  • The median time to treatment discontinuation for the subsequent LOT was short (2.4 months).
  • Significant proportions of patients experienced inpatient (31.9%) or emergency department (35.6%) visits.

Conclusions:

  • The subsequent line of therapy following osimertinib in EGFR-mNSCLC is often of short duration.
  • Tolerability issues appear to be a significant factor contributing to treatment discontinuation.
  • There is a high unmet need for novel therapeutic strategies to overcome EGFR TKI resistance.

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