Real-world acute toxicity and 90-day mortality in patients with stage I non-small cell lung cancer treated with stereotactic body radiotherapy.

Non-small cell lung cancer SBRT mortality stereotactic radiotherapy toxicity

Journal

Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer
ISSN: 1556-1380
Titre abrégé: J Thorac Oncol
Pays: United States
ID NLM: 101274235

Informations de publication

Date de publication:
25 Jul 2024
Historique:
received: 18 04 2024
revised: 30 06 2024
accepted: 21 07 2024
medline: 28 7 2024
pubmed: 28 7 2024
entrez: 27 7 2024
Statut: aheadofprint

Résumé

Stereotactic body radiotherapy (SBRT) has firmly established its role in stage I non-small cell lung cancer (NSCLC). Clinical trial results may not fully apply to real-world scenarios. This study aimed to uncover the real-world incidence of acute toxicity and 90-day mortality in SBRT-treated stage I NSCLC patients and develop prediction models for these outcomes. Prospective data from the Dutch Lung Cancer Audit for Radiotherapy (DLCA-R) were collected nationally. Patients with stage I NSCLC (cT1-2aN0M0) treated with SBRT in 2017-2021 were included. Acute toxicity was assessed, defined as grade ≥2 radiation-pneumonitis or grade ≥3 non-hematologic toxicity ≤90 days after SBRT. Prediction models for acute toxicity and 90-day mortality were developed and internally validated. Among 7,279 patients, the mean age was 72.5 years, with 21.6% being >80 years. Most were female (50.7%), had WHO scores 0-1 (73.3%), and cT1a-b tumors (64.6%), predominantly in upper lobes (65.2%). Acute toxicity was observed in 280 (3.8%) of patients and 90-day mortality in 122 (1.7%). Predictors for acute toxicity included WHO ≥2, lower FEV1 and DLCO, no pathology confirmation, middle/lower lobe tumor location, cT1c-cT2a stage, and higher mean lung dose (c-statistic 0.68). Female gender, WHO ≥2, and acute toxicity predicted higher 90-day mortality (c-statistic 0.73). This nationwide study revealed a low rate of acute toxicity and an acceptable 90-day mortality rate in SBRT-treated stage I NSCLC patients. Notably, advanced age did not increase acute toxicity or mortality risk. Our predictive models, with satisfactory performance, offer valuable tools for identifying high-risk patients.

Identifiants

pubmed: 39067700
pii: S1556-0864(24)00684-1
doi: 10.1016/j.jtho.2024.07.016
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024 International Association for the Study of Lung Cancer. Published by Elsevier Inc. All rights reserved.

Auteurs

Peter S N van Rossum (PSN)

Department of Radiation Oncology, The Netherlands Cancer Institute-Antoni van Leeuwenhoek, Amsterdam, The Netherlands; Department of Radiation Oncology, Amsterdam UMC, Amsterdam, The Netherlands. Electronic address: p.s.n.vanrossum@amsterdamumc.nl.

Nienke Wolfhagen (N)

Dutch Institute for Clinical Auditing, Leiden, The Netherlands; Department of Cardiothoracic Surgery, Radboud University Medical Center, Nijmegen, The Netherlands.

Liselotte W van Bockel (LW)

Department of Radiation Oncology, Haga Hospital, The Hague, The Netherlands.

Ida E M Coremans (IEM)

Department of Radiation Oncology, Leiden University Medical Center, Leiden, The Netherlands.

Corine A van Es (CA)

Department of Radiation Oncology, University Medical Center Utrecht, Utrecht, The Netherlands.

Annelies M van der Geest (AM)

Radiotherapy Institute Friesland, Leeuwarden, The Netherlands.

Katrien E A De Jaeger (KEA)

Department of Radiation Oncology, Catharina Hospital, Eindhoven, The Netherlands.

Barbara Wachters (B)

Southwest Radiotherapy Institute, Vlissingen and Roosendaal, The Netherlands.

Hans P Knol (HP)

Department of Radiation Oncology, Northwest Hospital Group, Alkmaar, The Netherlands.

Friederike L A Koppe (FLA)

Department of Radiation Oncology, Institute Verbeeten, Tilburg, The Netherlands.

Jacqueline Pomp (J)

Department of Radiation Oncology, University Medical Center Utrecht, Utrecht, The Netherlands.

Bart J T Reymen (BJT)

Department of Radiation Oncology (MAASTRO), GROW School for Oncology and Developmental Biology, Maastricht University Medical Centre+, Maastricht, The Netherlands.

Dominic A X Schinagl (DAX)

Department of Radiation Oncology, Radboud University Medical Center, Nijmegen, The Netherlands.

Femke O B Spoelstra (FOB)

Department of Radiation Oncology, Amsterdam UMC, Amsterdam, The Netherlands.

Caroline J A Tissing-Tan (CJA)

Radiotherapy Group, Institute for Radiation Oncology, Arnhem, The Netherlands.

Max Peters (M)

Radiotherapy Group, Institute for Radiation Oncology, Deventer, The Netherlands.

Noëlle C M G van der Voort van Zijp (NCMG)

Department of Radiation Oncology, Haaglanden Medical Center, The Hague, The Netherlands.

Antoinet M van der Wel (AM)

Department of Radiation Oncology, Amsterdam UMC, Amsterdam, The Netherlands.

Erwin M Wiegman (EM)

Department of Radiation Oncology, Isala Oncology Center, Zwolle, The Netherlands.

Robin Wijsman (R)

Department of Radiation Oncology, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.

Ronald A M Damhuis (RAM)

Department of Research, Netherlands Comprehensive Cancer Organization, Utrecht, The Netherlands.

José S A Belderbos (JSA)

Department of Radiation Oncology, The Netherlands Cancer Institute-Antoni van Leeuwenhoek, Amsterdam, The Netherlands.

Classifications MeSH