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De-escalation strategies with targeted therapies in non-small cell lung cancer

  • Martina Bortolot
  • , Jordi Remon*
  • , Paolo Bironzo
  • , Francesco Cortiula
  • , Jessica Menis
  • , Sze Wai Chan
  • , Robin van Geel
  • , Noemi Reguart
  • , Oscar Arrieta
  • , Giannis Mountzios
  • , Anne Marie C. Dingemans
  • , Benjamin Besse
  • , Lizza E.L. Hendriks
  • *Corresponding author for this work

Research output: Contribution to journal › (Systematic) Review article › peer-review

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Abstract

Targeted therapies (TT) for non-small cell lung cancer (NSCLC) with actionable genomic alterations (AGA), particularly EGFR-mutant and ALK-rearranged tumors, have become the standard of care across nearly all stages of the disease. However, the arbitrarily defined dose and treatment duration of TT, as well as the financial cost of these drugs, reduce their availability worldwide. Pharmacokinetic and pharmacodynamic properties of TT suggest that doses of some TT are overestimated as there is limited evidence supporting a direct relationship between therapeutic intensity and outcomes. This can lead to overtreatment of patients, resulting in an increased risk of toxicity without enhanced efficacy. Some academic initiatives have been launched aiming to explore de-escalating strategies with TT, either reducing the dose or the duration of these drugs. These approaches can decrease the risk of adverse events positively impacting patients’ quality of life, without compromising efficacy, while reducing economic impact. In this review, we summarize current data regarding de-escalating strategies with TT, ongoing trials and challenges of this approach.
Original languageEnglish
Article number102995
Number of pages7
JournalCancer Treatment Reviews
Volume139
DOIs
Publication statusPublished - 1 Sept 2025

Keywords

  • Actionable genomic alterations
  • De-escalation strategies
  • NSCLC
  • Targeted therapies
  • Treatment dose
  • Treatment duration

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