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A Phase II Trial on Osimertinib as a First-Line Treatment for EGFR Mutation-Positive Advanced NSCLC in Elderly Patients: The SPIRAL-0 Study

  • Yusuke Chihara
  • , Takayuki Takeda
  • , Yasuhiro Goto
  • , Yoichi Nakamura
  • , Yuko Tsuchiya-Kawano
  • , Akira Nakao
  • , Keisuke Onoi
  • , Makoto Hibino
  • , Minoru Fukuda
  • , Ryoichi Honda
  • , Takahiro Yamada
  • , Ryusuke Taniguchi
  • , Sinjiro Sakamoto
  • , Koji Date
  • , Seiji Nagashima
  • , Shigeru Tanzawa
  • , Koichi Minato
  • , Koichi Nakatani
  • , Miiru Izumi
  • , Takayuki Shimose
  • Junji Kishimoto, Junji Uchino, Koichi Takayama
  • Uji-Tokushukai Medical Center
  • Japanese Red Cross Kyoto Daini Hospital
  • Fujita Health University
  • Tochigi Cancer Center
  • Kitakyushu Municipal Medical Center
  • Fukuoka University
  • Kyoto Prefectural University of Medicine
  • Shonan Fujisawa Tokushukai Hospital
  • Nagasaki University
  • Asahi General Hospital
  • Matsushita Memorial Hospital
  • Otsu City Hospital
  • Hiroshima University
  • Kyoto Chubu Medical Center
  • National Hospital Organization Nagasaki Medical Center
  • Gunma Prefectural Cancer Center
  • National Hospital Organization Kyoto Medical Center
  • National Hospital Organization Omuta National Hospital
  • Clinical Research Support Center Kyushu
  • Kyushu University

Research output: Contribution to journalArticlepeer-review

13 Scopus citations

Abstract

Background: Osimertinib is one of the standard first-line treatments for advanced non-small cell lung cancer in patients with epidermal growth factor receptor (EGFR) mutations, because it achieves significantly longer progression-free survival (PFS) than conventional first-line treatments (hazard ratio: 0.46). However, the efficacy and safety of osimertinib as a first-line treatment for patients aged ≥75 years remain unclear. Methods: This phase II study was performed to prospectively investigate the efficacy and safety of osimertinib for elderly patients with EGFR mutation-positive advanced non-small cell lung cancer. The primary endpoint was 1-year PFS rate; secondary endpoints were overall response rate (ORR), PFS, overall survival (OS), and safety. Results: Thirty-eight patients were included in the analysis. The 1-year PFS rate was 59.4% (95% confidence interval [CI], 46.1%-72.7%), which did not meet the primary endpoint (the threshold 1-year PFS rate of 50% predicted using data from the NEJ003 study). The most common grade 3/4 adverse events were rash/dermatitis acneiform/ALT increased/hypokalemia (2 patients, 5%). Seven patients developed pneumonitis (17.5%). There were no other cases of treatment discontinuation due to adverse events other than pneumonitis. Conclusion: Although this study did not meet the primary endpoint, osimertinib was tolerable for elderly patients with EGFR mutation-positive advanced non-small cell lung cancer.

Original languageEnglish
JournalOncologist
Volume27
Issue number11
DOIs
StatePublished - Nov 2022

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • EGFR-TKI
  • elderly patients
  • non-small cell lung cancer
  • osimertinib

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