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QTc prolongation risk among patients receiving oral targeted antineoplastic medications: A real-world community-based oncology analysis

INTRODUCTION: Thirty oral targeted antineoplastic agents are associated with prolongation of the QT interval. However, limited data exists regarding QTc prolongation and associated risk factors in the ambulatory oncology setting. METHODS: This retrospective study was completed to describe QTc prolon...

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Autores principales: Reeves, David J., Russell, Molly, Rao, Vijay U.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10036778/
https://www.ncbi.nlm.nih.gov/pubmed/36969042
http://dx.doi.org/10.3389/fonc.2023.1098333
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author Reeves, David J.
Russell, Molly
Rao, Vijay U.
author_facet Reeves, David J.
Russell, Molly
Rao, Vijay U.
author_sort Reeves, David J.
collection PubMed
description INTRODUCTION: Thirty oral targeted antineoplastic agents are associated with prolongation of the QT interval. However, limited data exists regarding QTc prolongation and associated risk factors in the ambulatory oncology setting. METHODS: This retrospective study was completed to describe QTc prolongation incidence among patients receiving oral targeted tyrosine kinase inhibitors (TKI) and identify potential risk factors in the ambulatory community-based oncology clinic. RESULTS: Of the 341 patients identified as receiving oral TKI, 49 with a baseline and follow-up ECG were included. The incidence of QTc prolongation (QTc > 470 ms in males, QTc > 480 ms in females, or >20 ms increase in QTc from baseline) was 24%. Three patients developed significant QTc prolongation (QTc >500 ms or >60 ms increase in QTc from baseline). No patients discontinued therapy primarily due to QTc prolongation or experienced symptomatic torsades de pointes. Analysis of risk factors demonstrated that patients with QTc prolongation were more likely to receive concomitant therapy with a loop diuretic (41% vs 11%, respectively, p=0.029). DISCUSSION: The frequency of QTc prolongation may be higher in the real-world setting than that observed in clinical trials; however, continuation of therapy may be possible. Patients receiving concomitant loop diuretics should be monitored more closely for QTc prolongation and electrolyte abnormalities.
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spelling pubmed-100367782023-03-25 QTc prolongation risk among patients receiving oral targeted antineoplastic medications: A real-world community-based oncology analysis Reeves, David J. Russell, Molly Rao, Vijay U. Front Oncol Oncology INTRODUCTION: Thirty oral targeted antineoplastic agents are associated with prolongation of the QT interval. However, limited data exists regarding QTc prolongation and associated risk factors in the ambulatory oncology setting. METHODS: This retrospective study was completed to describe QTc prolongation incidence among patients receiving oral targeted tyrosine kinase inhibitors (TKI) and identify potential risk factors in the ambulatory community-based oncology clinic. RESULTS: Of the 341 patients identified as receiving oral TKI, 49 with a baseline and follow-up ECG were included. The incidence of QTc prolongation (QTc > 470 ms in males, QTc > 480 ms in females, or >20 ms increase in QTc from baseline) was 24%. Three patients developed significant QTc prolongation (QTc >500 ms or >60 ms increase in QTc from baseline). No patients discontinued therapy primarily due to QTc prolongation or experienced symptomatic torsades de pointes. Analysis of risk factors demonstrated that patients with QTc prolongation were more likely to receive concomitant therapy with a loop diuretic (41% vs 11%, respectively, p=0.029). DISCUSSION: The frequency of QTc prolongation may be higher in the real-world setting than that observed in clinical trials; however, continuation of therapy may be possible. Patients receiving concomitant loop diuretics should be monitored more closely for QTc prolongation and electrolyte abnormalities. Frontiers Media S.A. 2023-03-10 /pmc/articles/PMC10036778/ /pubmed/36969042 http://dx.doi.org/10.3389/fonc.2023.1098333 Text en Copyright © 2023 Reeves, Russell and Rao https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Reeves, David J.
Russell, Molly
Rao, Vijay U.
QTc prolongation risk among patients receiving oral targeted antineoplastic medications: A real-world community-based oncology analysis
title QTc prolongation risk among patients receiving oral targeted antineoplastic medications: A real-world community-based oncology analysis
title_full QTc prolongation risk among patients receiving oral targeted antineoplastic medications: A real-world community-based oncology analysis
title_fullStr QTc prolongation risk among patients receiving oral targeted antineoplastic medications: A real-world community-based oncology analysis
title_full_unstemmed QTc prolongation risk among patients receiving oral targeted antineoplastic medications: A real-world community-based oncology analysis
title_short QTc prolongation risk among patients receiving oral targeted antineoplastic medications: A real-world community-based oncology analysis
title_sort qtc prolongation risk among patients receiving oral targeted antineoplastic medications: a real-world community-based oncology analysis
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10036778/
https://www.ncbi.nlm.nih.gov/pubmed/36969042
http://dx.doi.org/10.3389/fonc.2023.1098333
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