Medication guide for dose adjustment and management of cardiotoxicity and lipid metabolic adverse events of oral antineoplastic therapy

ObjectiveThe management of cardiotoxicity concerning the use of oral antineoplastic agents (OAAs) is a challenge for healthcare professionals. Our objective was to create a comprehensive medication management guide with dose adjustment recommendations on OAAs concerning cardiotoxic and lipid metabol...

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Main Authors: Elena Ramos-Ruperez, Vicente Escudero-Vilaplana, Paula Ruiz-Briones, Roberto Collado-Borrell, Cristina Villanueva-Bueno, José Luis Revuelta-Herrero, Eva González-Haba, Xandra Garcia-Gonzalez, Sara Ibañez-Garcia, Sara Perez-Ramirez, Eduardo Zatarain-Nicolás, Ana Herranz, María Sanjurjo
Format: Article
Language:English
Published: Frontiers Media S.A. 2023-08-01
Series:Frontiers in Oncology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fonc.2023.1220305/full
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author Elena Ramos-Ruperez
Vicente Escudero-Vilaplana
Vicente Escudero-Vilaplana
Paula Ruiz-Briones
Paula Ruiz-Briones
Roberto Collado-Borrell
Roberto Collado-Borrell
Cristina Villanueva-Bueno
Cristina Villanueva-Bueno
José Luis Revuelta-Herrero
José Luis Revuelta-Herrero
Eva González-Haba
Eva González-Haba
Xandra Garcia-Gonzalez
Xandra Garcia-Gonzalez
Sara Ibañez-Garcia
Sara Ibañez-Garcia
Sara Perez-Ramirez
Sara Perez-Ramirez
Eduardo Zatarain-Nicolás
Eduardo Zatarain-Nicolás
Eduardo Zatarain-Nicolás
Eduardo Zatarain-Nicolás
Ana Herranz
Ana Herranz
María Sanjurjo
María Sanjurjo
author_facet Elena Ramos-Ruperez
Vicente Escudero-Vilaplana
Vicente Escudero-Vilaplana
Paula Ruiz-Briones
Paula Ruiz-Briones
Roberto Collado-Borrell
Roberto Collado-Borrell
Cristina Villanueva-Bueno
Cristina Villanueva-Bueno
José Luis Revuelta-Herrero
José Luis Revuelta-Herrero
Eva González-Haba
Eva González-Haba
Xandra Garcia-Gonzalez
Xandra Garcia-Gonzalez
Sara Ibañez-Garcia
Sara Ibañez-Garcia
Sara Perez-Ramirez
Sara Perez-Ramirez
Eduardo Zatarain-Nicolás
Eduardo Zatarain-Nicolás
Eduardo Zatarain-Nicolás
Eduardo Zatarain-Nicolás
Ana Herranz
Ana Herranz
María Sanjurjo
María Sanjurjo
author_sort Elena Ramos-Ruperez
collection DOAJ
description ObjectiveThe management of cardiotoxicity concerning the use of oral antineoplastic agents (OAAs) is a challenge for healthcare professionals. Our objective was to create a comprehensive medication management guide with dose adjustment recommendations on OAAs concerning cardiotoxic and lipid metabolic adverse events (AEs) to assist healthcare professionals when prescribing OAAs.Materials and methodsA review of the available information on all dose adjustments necessary to safely prescribe and dispense OAAs concerning cardiotoxicity was conducted. In January 2023, we identified all OAAs authorized by the European Medicines Agency (EMA). For each drug, the latest summary of product characteristics (SPC) approved by the EMA and the tertiary data source Lexicomp® were reviewed. Cardiotoxic AEs were recorded, namely, QT interval prolongation, decrease in left ventricular ejection fraction (LVEF), imbalances in blood pressure (hypertension and hypotension), alterations in heart rate (tachycardia and bradycardia), and thrombosis. Any available dose adjustment recommendations in case of an occurrence of these adverse events were collected.ResultsIn all, 93 different OAAs had been approved by the EMA and were reviewed. Among them, 51.6% have recognized cardiotoxic AEs and 10.8% can cause alterations in lipid metabolism. A total of 27 (29.0%) OAAs had specific recommendations regarding QT prolongation; 88.9% were listed in the SPC and 59.3% in Lexicomp®. Eight OAAs (9.68%) have reported a decrease in LVEF, and four of these drugs, namely, encorafenib, lorlatinib, ripretinib, and sunitinib, have specific management recommendations. Almost half (49.5%) of currently approved OAAs can potentially alter blood pressure; 34 (36.6%) of them have been reported to cause hypertension and 12 (12.9%) are related to hypotension. Tachycardia and/or bradycardia are associated with 22.6% and 8.6% of the evaluated drugs, respectively. Regarding thrombosis, 30 (32.3%) of the drugs analyzed included the appearance of a thrombus as a possible AE.ConclusionsMore than half of the OAAs can produce cardiotoxic effects, with the most frequent being blood pressure alteration and QT interval prolongation with a non-depreciable incidence of LV dysfunction or thrombosis. Before starting the treatment, it is necessary to stratify baseline cardiovascular risk, plan a surveillance schedule, and consider referral to cardio-oncology units.
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spelling doaj.art-53a5cf4d22e14290a294cade5ade37332023-08-25T17:48:01ZengFrontiers Media S.A.Frontiers in Oncology2234-943X2023-08-011310.3389/fonc.2023.12203051220305Medication guide for dose adjustment and management of cardiotoxicity and lipid metabolic adverse events of oral antineoplastic therapyElena Ramos-Ruperez0Vicente Escudero-Vilaplana1Vicente Escudero-Vilaplana2Paula Ruiz-Briones3Paula Ruiz-Briones4Roberto Collado-Borrell5Roberto Collado-Borrell6Cristina Villanueva-Bueno7Cristina Villanueva-Bueno8José Luis Revuelta-Herrero9José Luis Revuelta-Herrero10Eva González-Haba11Eva González-Haba12Xandra Garcia-Gonzalez13Xandra Garcia-Gonzalez14Sara Ibañez-Garcia15Sara Ibañez-Garcia16Sara Perez-Ramirez17Sara Perez-Ramirez18Eduardo Zatarain-Nicolás19Eduardo Zatarain-Nicolás20Eduardo Zatarain-Nicolás21Eduardo Zatarain-Nicolás22Ana Herranz23Ana Herranz24María Sanjurjo25María Sanjurjo26San Pablo Centro de Estudios Universitarios (CEU), University, Madrid, SpainPharmacy Department, Hospital General Universitario Gregorio Marañón, Madrid, SpainInstituto de Investigación Sanitaria Gregorio Marañón, Madrid, SpainPharmacy Department, Hospital General Universitario Gregorio Marañón, Madrid, SpainInstituto de Investigación Sanitaria Gregorio Marañón, Madrid, SpainPharmacy Department, Hospital General Universitario Gregorio Marañón, Madrid, SpainInstituto de Investigación Sanitaria Gregorio Marañón, Madrid, SpainPharmacy Department, Hospital General Universitario Gregorio Marañón, Madrid, SpainInstituto de Investigación Sanitaria Gregorio Marañón, Madrid, SpainPharmacy Department, Hospital General Universitario Gregorio Marañón, Madrid, SpainInstituto de Investigación Sanitaria Gregorio Marañón, Madrid, SpainPharmacy Department, Hospital General Universitario Gregorio Marañón, Madrid, SpainInstituto de Investigación Sanitaria Gregorio Marañón, Madrid, SpainPharmacy Department, Hospital General Universitario Gregorio Marañón, Madrid, SpainInstituto de Investigación Sanitaria Gregorio Marañón, Madrid, SpainPharmacy Department, Hospital General Universitario Gregorio Marañón, Madrid, SpainInstituto de Investigación Sanitaria Gregorio Marañón, Madrid, SpainInstituto de Investigación Sanitaria Gregorio Marañón, Madrid, SpainMedical Oncology Department, Hospital General Universitario Gregorio Marañón, Madrid, SpainInstituto de Investigación Sanitaria Gregorio Marañón, Madrid, SpainCardiology Department, Hospital General Universitario Gregorio Marañón, Madrid, SpainCentro de Investigación Biomédica en Red de Enfermedades Cardiovasculares (CIBER-CV), Madrid, SpainComplutense University, Madrid, SpainPharmacy Department, Hospital General Universitario Gregorio Marañón, Madrid, SpainInstituto de Investigación Sanitaria Gregorio Marañón, Madrid, SpainPharmacy Department, Hospital General Universitario Gregorio Marañón, Madrid, SpainInstituto de Investigación Sanitaria Gregorio Marañón, Madrid, SpainObjectiveThe management of cardiotoxicity concerning the use of oral antineoplastic agents (OAAs) is a challenge for healthcare professionals. Our objective was to create a comprehensive medication management guide with dose adjustment recommendations on OAAs concerning cardiotoxic and lipid metabolic adverse events (AEs) to assist healthcare professionals when prescribing OAAs.Materials and methodsA review of the available information on all dose adjustments necessary to safely prescribe and dispense OAAs concerning cardiotoxicity was conducted. In January 2023, we identified all OAAs authorized by the European Medicines Agency (EMA). For each drug, the latest summary of product characteristics (SPC) approved by the EMA and the tertiary data source Lexicomp® were reviewed. Cardiotoxic AEs were recorded, namely, QT interval prolongation, decrease in left ventricular ejection fraction (LVEF), imbalances in blood pressure (hypertension and hypotension), alterations in heart rate (tachycardia and bradycardia), and thrombosis. Any available dose adjustment recommendations in case of an occurrence of these adverse events were collected.ResultsIn all, 93 different OAAs had been approved by the EMA and were reviewed. Among them, 51.6% have recognized cardiotoxic AEs and 10.8% can cause alterations in lipid metabolism. A total of 27 (29.0%) OAAs had specific recommendations regarding QT prolongation; 88.9% were listed in the SPC and 59.3% in Lexicomp®. Eight OAAs (9.68%) have reported a decrease in LVEF, and four of these drugs, namely, encorafenib, lorlatinib, ripretinib, and sunitinib, have specific management recommendations. Almost half (49.5%) of currently approved OAAs can potentially alter blood pressure; 34 (36.6%) of them have been reported to cause hypertension and 12 (12.9%) are related to hypotension. Tachycardia and/or bradycardia are associated with 22.6% and 8.6% of the evaluated drugs, respectively. Regarding thrombosis, 30 (32.3%) of the drugs analyzed included the appearance of a thrombus as a possible AE.ConclusionsMore than half of the OAAs can produce cardiotoxic effects, with the most frequent being blood pressure alteration and QT interval prolongation with a non-depreciable incidence of LV dysfunction or thrombosis. Before starting the treatment, it is necessary to stratify baseline cardiovascular risk, plan a surveillance schedule, and consider referral to cardio-oncology units.https://www.frontiersin.org/articles/10.3389/fonc.2023.1220305/fulladverse eventcancercardiologycardiotoxicityoral antineoplastic therapysafety
spellingShingle Elena Ramos-Ruperez
Vicente Escudero-Vilaplana
Vicente Escudero-Vilaplana
Paula Ruiz-Briones
Paula Ruiz-Briones
Roberto Collado-Borrell
Roberto Collado-Borrell
Cristina Villanueva-Bueno
Cristina Villanueva-Bueno
José Luis Revuelta-Herrero
José Luis Revuelta-Herrero
Eva González-Haba
Eva González-Haba
Xandra Garcia-Gonzalez
Xandra Garcia-Gonzalez
Sara Ibañez-Garcia
Sara Ibañez-Garcia
Sara Perez-Ramirez
Sara Perez-Ramirez
Eduardo Zatarain-Nicolás
Eduardo Zatarain-Nicolás
Eduardo Zatarain-Nicolás
Eduardo Zatarain-Nicolás
Ana Herranz
Ana Herranz
María Sanjurjo
María Sanjurjo
Medication guide for dose adjustment and management of cardiotoxicity and lipid metabolic adverse events of oral antineoplastic therapy
Frontiers in Oncology
adverse event
cancer
cardiology
cardiotoxicity
oral antineoplastic therapy
safety
title Medication guide for dose adjustment and management of cardiotoxicity and lipid metabolic adverse events of oral antineoplastic therapy
title_full Medication guide for dose adjustment and management of cardiotoxicity and lipid metabolic adverse events of oral antineoplastic therapy
title_fullStr Medication guide for dose adjustment and management of cardiotoxicity and lipid metabolic adverse events of oral antineoplastic therapy
title_full_unstemmed Medication guide for dose adjustment and management of cardiotoxicity and lipid metabolic adverse events of oral antineoplastic therapy
title_short Medication guide for dose adjustment and management of cardiotoxicity and lipid metabolic adverse events of oral antineoplastic therapy
title_sort medication guide for dose adjustment and management of cardiotoxicity and lipid metabolic adverse events of oral antineoplastic therapy
topic adverse event
cancer
cardiology
cardiotoxicity
oral antineoplastic therapy
safety
url https://www.frontiersin.org/articles/10.3389/fonc.2023.1220305/full
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