Single-isocenter versus multiple-isocenters for multiple lung metastases: Evaluation of lung dose.


Journal

Radiotherapy and oncology : journal of the European Society for Therapeutic Radiology and Oncology
ISSN: 1879-0887
Titre abrégé: Radiother Oncol
Pays: Ireland
ID NLM: 8407192

Informations de publication

Date de publication:
01 2022
Historique:
received: 24 07 2021
revised: 22 11 2021
accepted: 25 11 2021
pubmed: 6 12 2021
medline: 20 4 2022
entrez: 5 12 2021
Statut: ppublish

Résumé

A potential challenge in single-isocenter multi-lesion lung stereotactic body radiotherapy (SBRT) is that patient positioning is not based on each lesion individually, but on the average position of all lesions. This may lead to larger margins compared to treating with one isocenter per lesion, but increases workflow efficiency. The aim of this study was to investigate whether a single-isocenter technique leads to increased normal lung dose compared to a conventional multiple-isocenters technique. A cohort of 15 NSCLC patients with two or three lesions previously treated with SBRT was subjected to treatment planning with a multiple-isocenter technique and a single-isocenter technique. For the latter, two margin approaches were evaluated: (1) identical margins for each internal target volume (ITV), assuming an average registration for all lesions in cone-beam CT (CBCT) positioning verification and (2) a smaller margin for the largest lesion, assuming an optimal registration for that lesion. For all 45 treatment plans, mean lung dose (MLD) and lungs-V The MLD was 4.9 ± 1.9 Gy (mean ± SD) for multiple-isocenters and 5.4 ± 2.1 Gy and 5.3 ± 2.2 Gy for single-isocenter approach 1 and 2, respectively. V A single-isocenter SBRT technique for lung patients with multiple targets results in clinically acceptable increases in normal lung dose.

Sections du résumé

BACKGROUND AND PURPOSE
A potential challenge in single-isocenter multi-lesion lung stereotactic body radiotherapy (SBRT) is that patient positioning is not based on each lesion individually, but on the average position of all lesions. This may lead to larger margins compared to treating with one isocenter per lesion, but increases workflow efficiency. The aim of this study was to investigate whether a single-isocenter technique leads to increased normal lung dose compared to a conventional multiple-isocenters technique.
MATERIALS AND METHODS
A cohort of 15 NSCLC patients with two or three lesions previously treated with SBRT was subjected to treatment planning with a multiple-isocenter technique and a single-isocenter technique. For the latter, two margin approaches were evaluated: (1) identical margins for each internal target volume (ITV), assuming an average registration for all lesions in cone-beam CT (CBCT) positioning verification and (2) a smaller margin for the largest lesion, assuming an optimal registration for that lesion. For all 45 treatment plans, mean lung dose (MLD) and lungs-V
RESULTS
The MLD was 4.9 ± 1.9 Gy (mean ± SD) for multiple-isocenters and 5.4 ± 2.1 Gy and 5.3 ± 2.2 Gy for single-isocenter approach 1 and 2, respectively. V
CONCLUSION
A single-isocenter SBRT technique for lung patients with multiple targets results in clinically acceptable increases in normal lung dose.

Identifiants

pubmed: 34864135
pii: S0167-8140(21)09026-5
doi: 10.1016/j.radonc.2021.11.030
pii:
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

189-194

Informations de copyright

Copyright © 2021 The Author(s). Published by Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Conflict of interest statement Dr. Hoogeman reports grants from Elekta, grants from Accuray, grants from Varian, other from Accuray, outside the submitted work. Dr. Tanadini-Lang reports that her husband works at Varian Medical Systems. Dr. van Timmeren, dr. Ehrbar, miss Chamberlain, dr. Mayinger, dr. Andratschke and dr. Guckenberger report no conflict of interest.

Auteurs

Janita E van Timmeren (JE)

Department of Radiation Oncology, University Hospital Zürich and University of Zürich, Switzerland. Electronic address: janita.vantimmeren@usz.ch.

Stefanie Ehrbar (S)

Department of Radiation Oncology, University Hospital Zürich and University of Zürich, Switzerland.

Madalyne Chamberlain (M)

Department of Radiation Oncology, University Hospital Zürich and University of Zürich, Switzerland.

Michael Mayinger (M)

Department of Radiation Oncology, University Hospital Zürich and University of Zürich, Switzerland.

Mischa S Hoogeman (MS)

Erasmus MC Cancer Institute, University Medical Center Rotterdam, Department of Radiotherapy, Rotterdam, The Netherlands.

Nicolaus Andratschke (N)

Department of Radiation Oncology, University Hospital Zürich and University of Zürich, Switzerland.

Matthias Guckenberger (M)

Department of Radiation Oncology, University Hospital Zürich and University of Zürich, Switzerland.

Stephanie Tanadini-Lang (S)

Department of Radiation Oncology, University Hospital Zürich and University of Zürich, Switzerland.

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