Is There a Role for Hypofractionated Thoracic Radiation Therapy in Limited-Stage Small Cell Lung Cancer? A Propensity Score Matched Analysis.


Journal

International journal of radiation oncology, biology, physics
ISSN: 1879-355X
Titre abrégé: Int J Radiat Oncol Biol Phys
Pays: United States
ID NLM: 7603616

Informations de publication

Date de publication:
01 11 2020
Historique:
received: 19 02 2020
revised: 07 06 2020
accepted: 08 06 2020
pubmed: 17 6 2020
medline: 10 4 2021
entrez: 17 6 2020
Statut: ppublish

Résumé

Various radiation schedules are used in concurrent chemoradiation therapy for limited-stage small cell lung cancer (LS-SCLC). Since there is currently no randomized evidence comparing hypofractionated radiation therapy (HFRT) and conventionally fractionated radiation therapy (CFRT), the aim of this study was to compare overall survival (OS), progression-free survival (PFS), and toxicity of HFRT and CFRT in LS-SCLC. Patients with LS-SCLC treated between 2000 and 2013 with HFRT (40 Gy/15 fractions, 45 Gy/15 fractions, 45 Gy/20 fractions) or CFRT (60 Gy/30 or 66 Gy/33 fractions) were included. Propensity scores were generated using a multivariable logistic regression model. Patients were matched on a 1:1 ratio with a caliper distance of 0.20. OS and PFS were estimated by the Kaplan-Meier method and compared using log-rank tests. As a sensitivity analysis, univariable and multivariable Cox regression was performed including all patients without matching. Logistic regression was performed to identify predictors of pulmonary and esophageal adverse events. In the overall group of 117 patients, there were significant baseline differences between the HFRT and CFRT cohorts. Patients who received CFRT were older, more often smoked concurrently with treatment, had higher Eastern Cooperative Oncology Group performance status, different T and N stage patterns, and more commonly received concurrent chemoradiation therapy and prophylactic cranial irradiation. After propensity score matching for these differences, 72 patients were included, 36 in the HFRT and CFRT cohorts, respectively. There was no difference in OS (P = .724), PFS (P = .862), or any pulmonary (P = .350) or esophageal (P = .097) adverse events between cohorts. Skin adverse events were significantly higher for CFRT (41.7%) compared with HFRT (16.7%, P = .020). Multivariable Cox regression also revealed no differences in OS (P = .886) or PFS (P = .717) between all HFRT and CFRT patients, without matching. No grade 5 adverse events were observed. In LS-SCLC patients, HFRT was associated with comparable survival and toxicity outcomes and may be considered as an alternative to CFRT, should its efficacy be confirmed in prospective studies.

Identifiants

pubmed: 32544575
pii: S0360-3016(20)31249-9
doi: 10.1016/j.ijrobp.2020.06.008
pmc: PMC7293491
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

575-586

Commentaires et corrections

Type : CommentIn

Informations de copyright

Crown Copyright © 2020. Published by Elsevier Inc. All rights reserved.

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Auteurs

Sondos Zayed (S)

Department of Radiation Oncology, London Health Sciences Centre, London, ON, Canada.

Hanbo Chen (H)

Department of Radiation Oncology, London Health Sciences Centre, London, ON, Canada.

Emma Ali (E)

Department of Internal Medicine, University of Toronto, Toronto, ON, Canada.

George B Rodrigues (GB)

Department of Radiation Oncology, London Health Sciences Centre, London, ON, Canada.

Andrew Warner (A)

Department of Radiation Oncology, London Health Sciences Centre, London, ON, Canada.

David A Palma (DA)

Department of Radiation Oncology, London Health Sciences Centre, London, ON, Canada.

Alexander V Louie (AV)

Odette Cancer Centre, Sunnybrook Health Sciences Centre, Toronto, ON, Canada. Electronic address: dr.alexlouie@gmail.com.

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