The role of online MR-guided multi-fraction stereotactic ablative radiotherapy in lung tumours.

Lung cancer MR-Linac, SBRT, SABR, lung metastases MR-guided SABR MR-guided SBRT MR-guided radiotherapy Radiation oncology

Journal

Clinical and translational radiation oncology
ISSN: 2405-6308
Titre abrégé: Clin Transl Radiat Oncol
Pays: Ireland
ID NLM: 101713416

Informations de publication

Date de publication:
Mar 2024
Historique:
received: 01 09 2023
revised: 18 01 2024
accepted: 21 01 2024
medline: 4 3 2024
pubmed: 4 3 2024
entrez: 4 3 2024
Statut: epublish

Résumé

The aim of this prospective observational study was to evaluate the dosimetry benefits, changes in pulmonary function, and clinical outcome of online adaptive MR-guided SBRT. From 11/2020-07/2022, 45 consecutive patients with 59 lesions underwent multi-fraction SBRT (3-8 fractions) at our institution. Patients were eligible if they had biopsy-proven NSCLC or lung cancer/metastases diagnosed via clinical imaging. Endpoints were local control (LC) and overall survival (OS). We evaluated PTV/GTV dose coverage, organs at risk exposure, and changes in pulmonary function (PF). Acute toxicity was classified per the National Cancer Institute-Common Terminology Criteria for Adverse Events version 5.0. The median PTV was 14.4 cm Online adaptive MR-guided SBRT is an effective, safe and generally well tolerated treatment option for lung tumours achieving encouraging local control rates with significantly improved target volume coverage.

Sections du résumé

Background UNASSIGNED
The aim of this prospective observational study was to evaluate the dosimetry benefits, changes in pulmonary function, and clinical outcome of online adaptive MR-guided SBRT.
Methods UNASSIGNED
From 11/2020-07/2022, 45 consecutive patients with 59 lesions underwent multi-fraction SBRT (3-8 fractions) at our institution. Patients were eligible if they had biopsy-proven NSCLC or lung cancer/metastases diagnosed via clinical imaging. Endpoints were local control (LC) and overall survival (OS). We evaluated PTV/GTV dose coverage, organs at risk exposure, and changes in pulmonary function (PF). Acute toxicity was classified per the National Cancer Institute-Common Terminology Criteria for Adverse Events version 5.0.
Results UNASSIGNED
The median PTV was 14.4 cm
Conclusions UNASSIGNED
Online adaptive MR-guided SBRT is an effective, safe and generally well tolerated treatment option for lung tumours achieving encouraging local control rates with significantly improved target volume coverage.

Identifiants

pubmed: 38433949
doi: 10.1016/j.ctro.2024.100736
pii: S2405-6308(24)00013-2
pmc: PMC10909605
doi:

Types de publication

Journal Article

Langues

eng

Pagination

100736

Informations de copyright

© 2024 The Author(s).

Déclaration de conflit d'intérêts

The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: The Department of Radiation Oncology of the LMU University Hospital, LMU Munich has research agreements with ViewRay Inc., Elekta, Brainlab, and C-RAD. ViewRay Inc. did not fund this study and was not involved and had no influence on the study design, the collection or analysis of data, or on the writing of the manuscript. MN reports research grants and speaker fees/travel support from Brainlab, ViewRay, AstraZeneca. FM reports a research grant from AstraZeneca and honoraria from AstraZeneca, Novartis, Roche, Lilly, Elekta and Brainlab. FM serves on the advisory board of AstraZeneca, Novartis. CB reports receiving grants or contracts from ViewRay, Brainlab, and Elekta; payment or honoraria from Bristol-Myers Squibb, Roche, Merck, AstraZeneca, Opasca, C-RAD, Elekta, and ViewRay; receiving support for attending meetings or travel from Bristol-Myers Squibb, Roche, Merck, AstraZeneca, Elekta, and View Ray; and having a leadership or fiduciary role with ESTRO, all outside the submitted work. SC reports research grants and speaker fees/travel support from Elekta, Viewray and Brainlab. CE reports consulting fees from Novartis outside the submitted work.

Auteurs

Svenja Hering (S)

Department of Radiation Oncology, LMU University Hospital, LMU Munich, Munich, Germany.

Alexander Nieto (A)

Department of Radiation Oncology, LMU University Hospital, LMU Munich, Munich, Germany.

Sebastian Marschner (S)

Department of Radiation Oncology, LMU University Hospital, LMU Munich, Munich, Germany.

Jan Hofmaier (J)

Department of Radiation Oncology, LMU University Hospital, LMU Munich, Munich, Germany.

Nina-Sophie Schmidt-Hegemann (NS)

Department of Radiation Oncology, LMU University Hospital, LMU Munich, Munich, Germany.

Vanessa da Silva Mendes (V)

Department of Radiation Oncology, LMU University Hospital, LMU Munich, Munich, Germany.

Guillaume Landry (G)

Department of Radiation Oncology, LMU University Hospital, LMU Munich, Munich, Germany.

Maximilian Niyazi (M)

Department of Radiation Oncology, LMU University Hospital, LMU Munich, Munich, Germany.
Department of Radiation Oncology, University of Tübingen, Tübingen, Germany.

Farkhad Manapov (F)

Department of Radiation Oncology, LMU University Hospital, LMU Munich, Munich, Germany.
Comprehensive Pneumology Center Munich (CPC-M), Member of the German Center for Lung Research (DZL), Munich, Germany.

Claus Belka (C)

Department of Radiation Oncology, LMU University Hospital, LMU Munich, Munich, Germany.
German Cancer Consortium (DKTK), partner site Munich; and German Cancer Research Center (DKFZ), Heidelberg, Germany.
Comprehensive Pneumology Center Munich (CPC-M), Member of the German Center for Lung Research (DZL), Munich, Germany.
Bavarian Cancer Research Center (BZKF), Munich, Germany.

Stefanie Corradini (S)

Department of Radiation Oncology, LMU University Hospital, LMU Munich, Munich, Germany.

Chukwuka Eze (C)

Department of Radiation Oncology, LMU University Hospital, LMU Munich, Munich, Germany.

Classifications MeSH