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Incidence of Bone Metastases and Skeletal-Related Events in Patients With EGFR-Mutated NSCLC Treated With Osimertinib

  • Anita J.W.M. Brouns
  • , Ard van Veelen
  • , G. D.Marijn Veerman
  • , Christi Steendam
  • , Safiye Dursun
  • , Cor van der Leest
  • , Sander Croes
  • , Anne Marie C. Dingemans
  • , Lizza E.L. Hendriks*
  • *Corresponding author for this work
  • Alfred Health
  • Maastricht University Medical Centre
  • GROW - School for Oncology and Reproduction
  • Maastricht University
  • Erasmus University Rotterdam
  • Amphia Hospital

Research output: Contribution to journalArticleAcademicpeer-review

10 Citations (Scopus)
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Abstract

Introduction: Bone metastases are frequent in patients with EGFR-mutated (EGFR+) NSCLC. Skeletal-related events (SREs) are common in these patients; however, no data on SRE in osimertinib-treated patients are reported. We investigated the development of bone metastases and SREs in patients with EGFR+ NSCLC treated with osimertinib. Methods: This is a retrospective multicenter cohort study that included patients with metastatic EGFR+ NSCLC who were treated with osimertinib between February 2016 and September 2021. Demographics, bone metastases-related outcomes, SREs, treatment efficacy, and overall survival (OS) were collected. Results: In total, 250 patients treated with osimertinib (43% first line) were included. Of the patients, 51% had bone metastases at initiation of osimertinib. Furthermore, 16% of the patients with bone metastases used bone-targeted agents. Median follow-up from initiation of osimertinib was 23.4 months (95% confidence interval [CI]: 19.9–26.9 mo). During osimertinib treatment, 10% developed new bone metastases or bone progression. Of the patients with bone metastases, 39% had more than or equal to one SREs: 28% developed first SRE before osimertinib treatment, 1% after, and 11% during. Median OS post-bone metastasis was 30.8 months (95% CI: 21.9–39.7). Median OS after first SRE was 31.1 months (95% CI: 15.8–46.5). Conclusions: Bone metastases and SREs are frequent before and during treatment with osimertinib in EGFR+ NSCLC. Because of these findings and the long OS post-bone metastases, we advocate prescription of bone-targeted agents in these patients and recommend adding bone-specific end points in clinical trials.

Original languageEnglish
Article number100513
JournalJTO Clinical and Research Reports
Volume4
Issue number5
DOIs
Publication statusPublished - May 2023

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Publisher Copyright: © 2023 The Authors

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