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
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

529-540

Informations 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.

Auteurs

Gerard M Walls (GM)

Cancer Centre Belfast City Hospital, Belfast, United Kingdom.
Patrick G. Johnston Centre for Cancer Research, Queen's University Belfast, Belfast, United Kingdom.

Nicola Hill (N)

Cancer Centre Belfast City Hospital, Belfast, United Kingdom.

Michael McMahon (M)

Cancer Centre Belfast City Hospital, Belfast, United Kingdom.

Brian Óg Kearney (BÓ)

Cancer Centre Belfast City Hospital, Belfast, United Kingdom.

Conor McCann (C)

Department of Cardiology, Belfast Health & Social Care Trust, Belfast, United Kingdom.

Peter McKavanagh (P)

Department of Cardiology, South Eastern Health & Social Care Trust, Dundonald, United Kingdom.

Valentina Giacometti (V)

Cancer Centre Belfast City Hospital, Belfast, United Kingdom.
Patrick G. Johnston Centre for Cancer Research, Queen's University Belfast, Belfast, United Kingdom.

Aidan J Cole (AJ)

Cancer Centre Belfast City Hospital, Belfast, United Kingdom.
Patrick G. Johnston Centre for Cancer Research, Queen's University Belfast, Belfast, United Kingdom.

Suneil Jain (S)

Cancer Centre Belfast City Hospital, Belfast, United Kingdom.
Patrick G. Johnston Centre for Cancer Research, Queen's University Belfast, Belfast, United Kingdom.

Conor K McGarry (CK)

Cancer Centre Belfast City Hospital, Belfast, United Kingdom.
Patrick G. Johnston Centre for Cancer Research, Queen's University Belfast, Belfast, United Kingdom.

Karl Butterworth (K)

Patrick G. Johnston Centre for Cancer Research, Queen's University Belfast, Belfast, United Kingdom.

Jonathan McAleese (J)

Cancer Centre Belfast City Hospital, Belfast, United Kingdom.
Patrick G. Johnston Centre for Cancer Research, Queen's University Belfast, Belfast, United Kingdom.

Mark Harbinson (M)

Department of Cardiology, South Eastern Health & Social Care Trust, Dundonald, United Kingdom.
School of Medicine, Dentistry & Biological Sciences, Queen's University Belfast, Belfast, United Kingdom.

Gerard G Hanna (GG)

Cancer Centre Belfast City Hospital, Belfast, United Kingdom.
Patrick G. Johnston Centre for Cancer Research, Queen's University Belfast, Belfast, United Kingdom.

Classifications MeSH