A case of torsades de pointes induced by the third-generation EGFR-TKI, osimertinib combined with moxifloxacin
- PMID: 32580784
- PMCID: PMC7313192
- DOI: 10.1186/s12890-020-01217-4
A case of torsades de pointes induced by the third-generation EGFR-TKI, osimertinib combined with moxifloxacin
Abstract
Background: Torsade de pointes (TdP) is a malignant arrhythmia that can be induced by QT internal prolongation due to a variety of factors. Here we report an elderly patient with advanced non-small cell lung cancer (NSCLC) had sudden TdP during hospitalization, which was caused by multiple factors such as osimertinib, moxifloxacin and patient self-factors.
Case presentation: An 85-year-old man with advanced NSCLC with brain andbone metastasis was initially treated with gefitinib targeted therapy. After 4 months treatment, the patient developed drug resistance and a second genetic testing revealed that the T790M mutation was positive. And the patient was then changed to targeted therapy with osimertinib, followed by adverse reactions of varying severity such as diarrhea, electrolyte imbalance, decreased cardiac function, leukopenia, and prolonged QTc interval. Six months after the administration of osimertinib, the patient was admitted to the hospital, chest CT showed the lesion progressed again, and during which hospital-acquired infection occurred. After concomitant use of moxifloxacin, the patient had sudden TdP, and finally died of this cardiac event.
Conclusions: It is suggested that clinicians need to identify patients with high risk factors of TdP, and consider comprehensively in concomitant medication to avoid such events to the greatest extent.
Keywords: Adverse events; EGFR-TKIs; Moxifloxacin; Osimertinib; QT interval; TdP.
Conflict of interest statement
The authors declare that they have no competing interests.
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References
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- Drew BJ, Ackerman MJ, Funk M, Gibler WB, Kligfield P, Menon V, et al. Prevention of torsade de pointes in hospital settings: a scientific statement from the American Heart Association and the American College of Cardiology Foundation. Circulation. 2010;121(8):1047–1060. doi: 10.1161/CIRCULATIONAHA.109.192704. - DOI - PMC - PubMed
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