QT-Interval Prolongation, Torsades de Pointes, and Heart Failure With EGFR Tyrosine Kinase Inhibitors in Non-Small Cell Lung Cancer: Systematic Review

Clin Lung Cancer. 2024 Jun;25(4):285-318. doi: 10.1016/j.cllc.2024.02.005. Epub 2024 Feb 17.

Abstract

A systematic literature review was conducted to determine the incidence and mortality of QT-interval prolongation (QTp), torsades de pointes (TdP), and heart failure (HF) in patients with non-small cell lung cancer (NSCLC) who received epidermal growth factor receptor (EGFR) TKIs. Of 296 identified publications, 95 met eligibility criteria and were abstracted for QTp/TdP and HF outcomes (QTp/TdP: 83 publications, including 5 case study publications; HF: 79 publications, including 6 case study publications [involving 8 patients]). QTp incidence ranged from 0% to 27.8% in observational studies and from 0% to 11% in clinical trials, with no deaths due to QTp. There were no TdP events or deaths due to TdP. The incidence of HF ranged from 0% to 8%, and HF mortality rates ranged from 0% to 4%. Patients receiving treatment with EGFR TKIs should be monitored for signs of QTp, TdP, and HF per prescribing information. Standardized definitions and methods to improve monitoring of QTp, TdP, and HF-related events are needed in patients with NSCLC.

Keywords: Cardiac arrhythmia; Cardiovascular adverse event; Epidermal growth factor receptor; Sudden cardiac death.

Publication types

  • Systematic Review
  • Review

MeSH terms

  • Carcinoma, Non-Small-Cell Lung* / complications
  • Carcinoma, Non-Small-Cell Lung* / drug therapy
  • ErbB Receptors* / antagonists & inhibitors
  • ErbB Receptors* / genetics
  • Heart Failure* / drug therapy
  • Humans
  • Incidence
  • Long QT Syndrome* / chemically induced
  • Lung Neoplasms* / complications
  • Lung Neoplasms* / drug therapy
  • Protein Kinase Inhibitors* / adverse effects
  • Protein Kinase Inhibitors* / therapeutic use
  • Torsades de Pointes* / chemically induced
  • Tyrosine Kinase Inhibitors

Substances

  • ErbB Receptors
  • Protein Kinase Inhibitors
  • EGFR protein, human
  • Tyrosine Kinase Inhibitors