Baseline Cardiac Parameters as Biomarkers of Radiation Cardiotoxicity in Lung Cancer: An NI-HEART Analysis.
biomarkers
cardiac events
cardiac substructures
lung cancer
radiation therapy
survival
Journal
JACC. CardioOncology
ISSN: 2666-0873
Titre abrégé: JACC CardioOncol
Pays: United States
ID NLM: 101761697
Informations de publication
Date de publication:
Aug 2024
Aug 2024
Historique:
received:
23
11
2023
revised:
02
05
2024
accepted:
05
05
2024
medline:
6
9
2024
pubmed:
6
9
2024
entrez:
6
9
2024
Statut:
epublish
Résumé
Radiation-induced cardiotoxicity poses a significant challenge in lung cancer management because of the close anatomical proximity of the heart to the lungs, compounded by a high prevalence of cardiovascular risk factors among patients. The aim of this study was to assess the predictive value of routinely available clinical and imaging-based cardiac parameters in identifying "high risk" patients for major adverse cardiac events (MACE) and mortality following radiation therapy (RT). The medical records of patients who underwent definitive RT for non-small cell lung cancer using modern planning techniques at a single center between 2015 and 2020 were retrospectively reviewed. Cardiac events were verified by cardiologists, and mortality data were confirmed with the national registry. Cardiac substructures were autosegmented on RT planning scans for retrospective structure and dose analysis, and their correlation with clinical factors was examined. Fine-Gray models were used to analyze relationships while considering the competing risk for death. Among 478 patients included in the study, 77 (16%) developed 88 MACE, with a median time to event of 16.3 months. A higher burden of pre-existing cardiac diseases was associated with an increased cumulative incidence of MACE (55% [95% CI: 12%-20%] vs 16% [95% CI: 35%-71%]; The present findings suggest that cardiac history and RT planning scan parameters may offer potential utility in prospectively evaluating cardiotoxicity risk following RT for patients with lung cancer.
Sections du résumé
Background
UNASSIGNED
Radiation-induced cardiotoxicity poses a significant challenge in lung cancer management because of the close anatomical proximity of the heart to the lungs, compounded by a high prevalence of cardiovascular risk factors among patients.
Objectives
UNASSIGNED
The aim of this study was to assess the predictive value of routinely available clinical and imaging-based cardiac parameters in identifying "high risk" patients for major adverse cardiac events (MACE) and mortality following radiation therapy (RT).
Methods
UNASSIGNED
The medical records of patients who underwent definitive RT for non-small cell lung cancer using modern planning techniques at a single center between 2015 and 2020 were retrospectively reviewed. Cardiac events were verified by cardiologists, and mortality data were confirmed with the national registry. Cardiac substructures were autosegmented on RT planning scans for retrospective structure and dose analysis, and their correlation with clinical factors was examined. Fine-Gray models were used to analyze relationships while considering the competing risk for death.
Results
UNASSIGNED
Among 478 patients included in the study, 77 (16%) developed 88 MACE, with a median time to event of 16.3 months. A higher burden of pre-existing cardiac diseases was associated with an increased cumulative incidence of MACE (55% [95% CI: 12%-20%] vs 16% [95% CI: 35%-71%];
Conclusions
UNASSIGNED
The present findings suggest that cardiac history and RT planning scan parameters may offer potential utility in prospectively evaluating cardiotoxicity risk following RT for patients with lung cancer.
Identifiants
pubmed: 39239328
doi: 10.1016/j.jaccao.2024.05.009
pii: S2666-0873(24)00197-2
pmc: PMC11372030
doi:
Types de publication
Journal Article
Langues
eng
Pagination
529-540Informations de copyright
© 2024 The Authors.
Déclaration de conflit d'intérêts
This analysis was funded by an Irish Clinical Academic Training Programme Fellowship held by Dr Walls, which is supported by the Wellcome Trust and the Health Research Board (203930/B/16/Z), the Health Service Executive National Doctors Training and Planning, and the Health and Social Care, Research and Development Division. The lead author currently holds a Cancer Research UK Post-Doctoral Bursary Award (RCCPOB-Nov22/100010). Dr Walls has received speaker fee from an education event organized by AstraZeneca. Prof Jain has received research support from Boston Scientific; has received consulting fees from Boston Scientific; has received honoraria from Janssen, Astellas, Bayer, Astra Zeneca, Pfizer, and Accord; and has received support for attending meetings and/or travel from Janssen and Bayer. All other authors have reported that they have no relationships relevant to the contents of this paper to disclose.