JTO Clinical and Research Reports (Mar 2024)

Initial Safety and Feasibility Results From a Phase 1, Diagnose-and-Treat Trial of Neoadjuvant Intratumoral Cisplatin for Stage IV NSCLC

  • Farrah B. Khan, MD,
  • Pamela C. Gibson, MD,
  • Scott Anderson, MD,
  • Sarah Wagner, BS,
  • Bernard F. Cole, PhD,
  • Peter Kaufman, MD,
  • C. Matthew Kinsey, MD, MPH

Journal volume & issue
Vol. 5, no. 3
p. 100634

Abstract

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Neoadjuvant intratumoral cisplatin has the potential to generate substantial cytotoxicity and immune priming within the tumor environment, while minimizing systemic, off-target, adverse events. We initiated a phase 1A, 3+3 dose-ranging study of neoadjuvant, intratumoral cisplatin, delivered through endobronchial ultrasound bronchoscopy, in the same procedure as the initial diagnosis. There were no dose-limiting toxicity identified at the 20mg level

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