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A case of torsades de pointes induced by the third-generation EGFR-TKI, osimertinib combined with moxifloxacin

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 s...

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Autores principales: Bian, Shuang, Tang, Xiaomiao, Lei, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7313192/
https://www.ncbi.nlm.nih.gov/pubmed/32580784
http://dx.doi.org/10.1186/s12890-020-01217-4
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author Bian, Shuang
Tang, Xiaomiao
Lei, Wei
author_facet Bian, Shuang
Tang, Xiaomiao
Lei, Wei
author_sort Bian, Shuang
collection PubMed
description 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.
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spelling pubmed-73131922020-06-24 A case of torsades de pointes induced by the third-generation EGFR-TKI, osimertinib combined with moxifloxacin Bian, Shuang Tang, Xiaomiao Lei, Wei BMC Pulm Med Case Report 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. BioMed Central 2020-06-24 /pmc/articles/PMC7313192/ /pubmed/32580784 http://dx.doi.org/10.1186/s12890-020-01217-4 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Case Report
Bian, Shuang
Tang, Xiaomiao
Lei, Wei
A case of torsades de pointes induced by the third-generation EGFR-TKI, osimertinib combined with moxifloxacin
title A case of torsades de pointes induced by the third-generation EGFR-TKI, osimertinib combined with moxifloxacin
title_full A case of torsades de pointes induced by the third-generation EGFR-TKI, osimertinib combined with moxifloxacin
title_fullStr A case of torsades de pointes induced by the third-generation EGFR-TKI, osimertinib combined with moxifloxacin
title_full_unstemmed A case of torsades de pointes induced by the third-generation EGFR-TKI, osimertinib combined with moxifloxacin
title_short A case of torsades de pointes induced by the third-generation EGFR-TKI, osimertinib combined with moxifloxacin
title_sort case of torsades de pointes induced by the third-generation egfr-tki, osimertinib combined with moxifloxacin
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7313192/
https://www.ncbi.nlm.nih.gov/pubmed/32580784
http://dx.doi.org/10.1186/s12890-020-01217-4
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