Review of real-world experience with lurbinectedin in relapsed/refractory small cell lung cancer

J Chemother. 2024 Nov;36(7):587-592. doi: 10.1080/1120009X.2024.2302736. Epub 2024 Jan 17.

Abstract

Lurbinectedin, a novel antineoplastic agent, was granted the orphan drug designation by the United States Food and Drug Administration (US FDA) and approved for use in relapsed/refractory small cell lung cancer in June 2020. The approval was granted after its efficacy was demonstrated in a multicenter open-label, multi-cohort study enrolling 105 participants. Since then, real-world studies have examined the efficacy and safety profiles of lurbinectedin in clinical practice. By examining these outcomes, this review aims to provide clinicians with the tools necessary to make informed clinical decisions.

Keywords: Lurbinectedin; chemotherapy; lung cancer; relapse; sclc; small cell lung cancer.

Publication types

  • Review

MeSH terms

  • Antineoplastic Agents* / adverse effects
  • Antineoplastic Agents* / therapeutic use
  • Carbolines* / adverse effects
  • Carbolines* / therapeutic use
  • Drug Resistance, Neoplasm
  • Heterocyclic Compounds, 4 or More Rings* / administration & dosage
  • Heterocyclic Compounds, 4 or More Rings* / adverse effects
  • Heterocyclic Compounds, 4 or More Rings* / therapeutic use
  • Humans
  • Lung Neoplasms* / drug therapy
  • Neoplasm Recurrence, Local / drug therapy
  • Small Cell Lung Carcinoma* / drug therapy

Substances

  • PM 01183
  • Carbolines
  • Heterocyclic Compounds, 4 or More Rings
  • Antineoplastic Agents