Evidence map›Paper›PMID 37692846›Full record

ArticleFrontiers in oncology2023

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

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 and 3 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.1field-weighted citation impact, top 20% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors at 2 institutions in 1 country.

Elena Ramos-RuperezSan Pablo Centro de Estudios Universitarios (CEU), University, Madrid, Spain.
Vicente Escudero-VilaplanaPharmacy Department, Hospital General Universitario Gregorio Marañón, Madrid, Spain.
Paula Ruiz-BrionesPharmacy Department, Hospital General Universitario Gregorio Marañón, Madrid, Spain.
Roberto Collado-BorrellPharmacy Department, Hospital General Universitario Gregorio Marañón, Madrid, Spain.
Cristina Villanueva-BuenoPharmacy Department, Hospital General Universitario Gregorio Marañón, Madrid, Spain.
José Luis Revuelta-HerreroPharmacy Department, Hospital General Universitario Gregorio Marañón, Madrid, Spain.
Eva González-HabaPharmacy Department, Hospital General Universitario Gregorio Marañón, Madrid, Spain.
Xandra Garcia-GonzalezPharmacy Department, Hospital General Universitario Gregorio Marañón, Madrid, Spain.
Sara Ibañez-GarciaPharmacy Department, Hospital General Universitario Gregorio Marañón, Madrid, Spain.
Sara Perez-RamirezInstituto de Investigación Sanitaria Gregorio Marañón, Madrid, Spain.
Eduardo Zatarain-NicolásInstituto de Investigación Sanitaria Gregorio Marañón, Madrid, Spain.
Ana HerranzPharmacy Department, Hospital General Universitario Gregorio Marañón, Madrid, Spain.
María SanjurjoPharmacy Department, Hospital General Universitario Gregorio Marañón, Madrid, Spain.
Hospital General Universitario Gregorio Marañón · ESUniversidad San Pablo CEU · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: The 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 methods: A 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 Results: In 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 Conclusions: More 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.

Indexed as

adverse eventcancercardiologycardiotoxicityoral antineoplastic therapysafety

Identifiers

PMID37692846
PMCPMC10485602
OpenAlexW4386157917

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.