Concomitant medication effects on patients with lung cancer taking immune checkpoint inhibitors a review

Med Oncol. 2025 Jan 7;42(2):40. doi: 10.1007/s12032-024-02591-3.

Abstract

In the past decade, a variety of immune checkpoint inhibitors (ICIs) are currently approved for lung cancer in the world. As a new therapeutic approach, ICIs have shown significant clinical benefits in the first-line or second-line treatment for advanced lung cancer, improving the survival and quality of life of patients. Patients need to take multiple drugs in the meantime due to their own disease or side effects during treatment. In view of drug interactions, concomitant medications have a positive or negative impact on the prognosis of lung cancer patients. In this review, we reviewed the effects of multiple drugs on the prognosis of patients with lung cancer taking ICIs. Several studies indicate that antibiotics, proton pump inhibitors (PPIs), corticosteroids, and opioid analgesics can decrease the efficacy of ICIs. Aspirin and bone-targeting drugs can enhance the efficacy of ICIs and improve the survival rate. The effects of metformin (MET), renin-angiotensin-aldosterone system inhibitors (RASI), nonsteroidal anti-inflammatory drug (NSAIDS) (except aspirin), and statins on ICIs are controversial. Future research should further explore the effects of these concomitant medications on ICIs and develop personalized prescriptions based on the specific needs of patients.

Keywords: Biologic mechanism; Clinical efficacy; Concomitant medications; Immune checkpoint inhibitors; Lung cancer.

Publication types

  • Review

MeSH terms

  • Anti-Inflammatory Agents, Non-Steroidal / therapeutic use
  • Drug Interactions*
  • Humans
  • Immune Checkpoint Inhibitors* / adverse effects
  • Immune Checkpoint Inhibitors* / therapeutic use
  • Lung Neoplasms* / drug therapy
  • Prognosis
  • Proton Pump Inhibitors / adverse effects
  • Proton Pump Inhibitors / therapeutic use

Substances

  • Immune Checkpoint Inhibitors
  • Anti-Inflammatory Agents, Non-Steroidal
  • Proton Pump Inhibitors