Skip to main navigation Skip to search Skip to main content

Pulmonary vein dose and risk of atrial fibrillation in patients with non-small cell lung cancer following definitive radiotherapy: an NI-HEART analysis

  • Gerard M Walls
  • , Conor McCann
  • , John O'Connor
  • , Anna O'Sullivan
  • , David I Johnston
  • , Jonathan McAleese
  • , Conor K McGarry
  • , Aidan J Cole
  • , Suneil Jain
  • , Karl T Butterworth
  • , Gerard G Hanna

Research output: Contribution to journalArticlepeer-review

32 Downloads (Pure)

Abstract

Symptomatic arrhythmia is common following radiotherapy for non-small cell lung cancer (NSCLC), frequently resulting in morbidity and hospitalization. Modern treatment planning technology theoretically allows sparing of cardiac substructures. Atrial fibrillation (AF) comprises the majority of post-radiotherapy arrhythmias, but efforts to prevent this cardiotoxicity have been limited as the causative cardiac substructure is not known. In this study we investigated if incidental radiation dose to the pulmonary veins (PVs) is associated with AF. A single-centre study of patients completing contemporary (chemo)radiation for NSCLC, with modern planning techniques. Oncology, cardiology and death records were examined, and AF events were verified by a cardiologist. Cardiac substructures were contoured on planning scans for retrospective dose analysis. In 420 eligible patients with NSCLC treated with intensity-modulated (70%) or 3D-conformal (30%) radiotherapy with a median OS of 21.8 months (IQR 10.8-35.1), there were 26 cases of new AF (6%). All cases were grade 3 except two cases of grade 4. Dose metrics for both the left (V55) and right (V10) PVs were associated with the incidence of new AF. Metrics remained statistically significant after accounting for the competing risk of death and cardiovascular covariables for both the left (HR 1.02, 95%CI 1.00-1.03, p=0.005) and right (HR 1.01 (95%CI 1.00-1.02, p=0.033) PVs. Radiation dose to the PVs during treatment of NSCLC was associated with the onset of AF. Actively sparing the PVs during treatment planning could reduce the incidence of AF during follow-up. [Abstract copyright: Copyright © 2024. Published by Elsevier B.V.]
Original languageEnglish
Article number110085
Pages (from-to)1-39
Number of pages40
JournalRadiotherapy and Oncology
Volume192
Early online date4 Jan 2024
DOIs
Publication statusPublished (in print/issue) - Mar 2024

Bibliographical note

Copyright © 2024. Published by Elsevier B.V.

Funding

The authors wish to thank Mrs Diane Hanna for her contribution to this work. The authors are also indebted to the Northern Ireland Cancer Research Consumer's Forum for their generous input at the design stage of this project. This data collection for this work was funded by an Irish Clinical Academic Training Programme Fellowship (GW), which is supported by the Wellcome Trust and the Health Research Board (Grant Number 203930/B/16/Z), the Health Service Executive National Doctors Training and Planning and the Health and Social Care, Research and Development Division, Northern Ireland. The lead author conducted this analysis during a Cancer Research UK Post-doctoral Fellowship (RCCPOB-Nov22/100010). This data collection for this work was funded by an Irish Clinical Academic Training Programme Fellowship (GW), which is supported by the Wellcome Trust and the Health Research Board (Grant Number 203930/B/16/Z), the Health Service Executive National Doctors Training and Planning and the Health and Social Care, Research and Development Division, Northern Ireland. The lead author conducted this analysis during a Cancer Research UK Post-doctoral Fellowship (RCCPOB-Nov22/100010).

FundersFunder number
Wellcome Trust
203930/B/16/Z
Cancer Research UKRCCPOB-Nov22/100010

    UN SDGs

    This output contributes to the following UN Sustainable Development Goals (SDGs)

    1. SDG 3 - Good Health and Well-being
      SDG 3 Good Health and Well-being

    Fingerprint

    Dive into the research topics of 'Pulmonary vein dose and risk of atrial fibrillation in patients with non-small cell lung cancer following definitive radiotherapy: an NI-HEART analysis'. Together they form a unique fingerprint.

    Cite this