Discontinuous stereotactic body radiotherapy schedule increases overall survival in early-stage non-small cell lung cancer.


Journal

Lung cancer (Amsterdam, Netherlands)
ISSN: 1872-8332
Titre abrégé: Lung Cancer
Pays: Ireland
ID NLM: 8800805

Informations de publication

Date de publication:
07 2021
Historique:
received: 06 04 2021
revised: 07 05 2021
accepted: 10 05 2021
pubmed: 22 5 2021
medline: 25 6 2021
entrez: 21 5 2021
Statut: ppublish

Résumé

The duration of stereotactic body radiotherapy (SBRT) for early-stage non-small cell lung cancer (NSCLC) may affect patient outcomes. We aimed to determine the impact of a continuous versus discontinuous SBRT schedule on local control (LC) and overall survival (OS) in NSCLC patients. Consecutive NSCLC stage I patients (475) treated with SBRT in four centers were retrospectively analyzed. The delivered dose ranged from 48 to 75 Gy in 3-10 fractions. Based on the ratio between the treatment duration (TD) and number of fractions (n), patients were divided into two groups: continuous schedule (CS) (TD ≤ 1.6n; 239 patients) and discontinuous schedule (DS) (TD > 1.6n; 236 patients). LC and OS were compared using Cox regression analyses after propensity score matching (216 pairs). The median follow-up period was 41 months. Multivariate analysis showed that the DS (hazard ratio (HR): 0.42; 95 % confidence interval (CI): 0.22-0.78) and number of fractions (HR: 1.24; 95 % CI: 1.07-1.43) were significantly associated with LC. The DS (HR: 0.67; 95 % CI: 0.51-0.89), age (HR: 1.02; 95 % CI: 1-1.03), WHO performance status (HR: 2.27; 95 % CI: 1.39-3.7), and T stage (HR: 1.4; 95 % CI: 1.03-1.87) were significantly associated with OS. The 3-year LC and OS were 92 % and 64 % and 81 % and 53 % for DS and CS treatments, respectively (p < 0.01). Cox analysis confirmed that the discontinuous SBRT schedule significantly increased LC and OS. DS is associated with significantly improved LC and OS in early-stage NSCLC patients treated with SBRT.

Identifiants

pubmed: 34016489
pii: S0169-5002(21)00195-1
doi: 10.1016/j.lungcan.2021.05.016
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

100-108

Informations de copyright

Copyright © 2021. Published by Elsevier B.V.

Auteurs

L Duvergé (L)

Radiation Oncology Department, Centre Eugène Marquis, Avenue Flandres Dunkerque, 35000 Rennes, France. Electronic address: l.duverge@rennes.unicancer.fr.

P-Y Bondiau (PY)

Radiation Oncology Department, Centre Antoine Lacassagne, 06000 Nice, France.

L Claude (L)

Radiation Oncology Department, Centre Léon-Bérard, 28, rue Laennec, 69008 Lyon, France.

S Supiot (S)

Radiation Oncology Department, Institut de Cancérologie de l'Ouest- René Gauducheau, Bd J Monod, 44800 Nantes, St-Herblain, France.

L Vaugier (L)

Radiation Oncology Department, Institut de Cancérologie de l'Ouest- René Gauducheau, Bd J Monod, 44800 Nantes, St-Herblain, France.

F Thillays (F)

Radiation Oncology Department, Institut de Cancérologie de l'Ouest- René Gauducheau, Bd J Monod, 44800 Nantes, St-Herblain, France.

J Doyen (J)

Radiation Oncology Department, Centre Antoine Lacassagne, 06000 Nice, France.

C Ricordel (C)

Pneumology Department, Centre Hospitalier Universitaire de Rennes, 2 rue Henri Le Guilloux, 35000 Rennes, France.

H Léna (H)

Pneumology Department, Centre Hospitalier Universitaire de Rennes, 2 rue Henri Le Guilloux, 35000 Rennes, France.

J Bellec (J)

Radiation Oncology Department, Centre Eugène Marquis, Avenue Flandres Dunkerque, 35000 Rennes, France.

E Chajon (E)

Radiation Oncology Department, Centre Eugène Marquis, Avenue Flandres Dunkerque, 35000 Rennes, France.

R de Crevoisier (R)

Radiation Oncology Department, Centre Eugène Marquis, Avenue Flandres Dunkerque, 35000 Rennes, France.

J Castelli (J)

Radiation Oncology Department, Centre Eugène Marquis, Avenue Flandres Dunkerque, 35000 Rennes, France.

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Classifications MeSH