Efficacy, safety, and feasibility of volumetric modulated arc therapy for synchronous bilateral breast cancer management.

VMAT bilateral breast cancer cancer care dosimetric analysis radiotherapy treatment outcome treatment planning

Journal

Frontiers in oncology
ISSN: 2234-943X
Titre abrégé: Front Oncol
Pays: Switzerland
ID NLM: 101568867

Informations de publication

Date de publication:
2022
Historique:
received: 12 06 2022
accepted: 02 08 2022
entrez: 5 9 2022
pubmed: 6 9 2022
medline: 6 9 2022
Statut: epublish

Résumé

Volumetric Modulated Arc Therapy (VMAT) exhibits potent advantages regarding target volume coverage and protection of organs at risk, notably in the context of anatomical constraints. Nevertheless, reports concerning VMAT for the treatment of synchronous bilateral breast cancers (SBBC) have been scarce to date. As such, we conducted this observational study to assess efficacy, safety and feasibility of VMAT in SBBC. From August 2011 to December 2017, 54 consecutive patients with SBBC with or without axillary nodes involvement underwent a treatment protocol containing radiotherapy using VMAT. A total dose (TD) of 52.2Gy in 29 fractions was delivered to breast and internal mammary chain (IMC) nodes Planning Target Volume (PTV) plus, if applicable, a TD of 49.3Gy in 29 fractions to the supra- and infra-clavicular nodes PTV and a TD of 63.22Gy in 29 fractions to tumor boost PTV. Lungs, heart, esophagus, trachea, liver, thyroid and spinal cord were considered as organs at risk. VMAT feasibility and organ at risk sparing were evaluated by treatments planning of the 20 first enrolled patients. Tolerance and patients' outcome were prospectively monitored by acute/late toxicities records and by the analysis of overall survival (OS), locoregional recurrence-free survival (LRFS) and recurrence-free survival (RFS). Breast, supraclavicular nodes and boost PTV coverage was adequate with at least 98% of PTV encompassed by more than 95% of the prescribed dose. Less than 90% of IMC PTV was encompassed by 95% of the prescribed dose. Mean lung dose was 12.3Gy (range: 7.7 - 18.7); mean heart dose was 10.7Gy (range: 6.2 - 22.3). Concerning acute toxicities, only 2 patients experienced grade 3 skin toxicity (3.7%) and only 1 patient developed grade 1 pneumonitis. After a median follow-up of 5.3 years, grade 2 fibrosis and/or shrinking was observed in 5 patients (10%), and grade 3 fibrosis in 1 patients (2%). The 5-year LRFS-rate, RFS-rate and OS were 98% [95% CI= 86.12-99.70%], 96% [95% CI= 84.63-98.96%] and 100%, respectively.

Identifiants

pubmed: 36059658
doi: 10.3389/fonc.2022.967479
pmc: PMC9436014
doi:

Types de publication

Journal Article

Langues

eng

Pagination

967479

Informations de copyright

Copyright © 2022 Quesada, Fenoglietto, Gourgou, Lemanski, Draghici, Ailleres, Prunaretty, Azria and Bourgier.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Stanislas Quesada (S)

Faculty of Medicine, University of Montpellier, Montpellier, France.
Department of Radiation Oncology, Montpellier Cancer Institute (ICM), Montpellier, France.

Pascal Fenoglietto (P)

Department of Radiation Oncology, Montpellier Cancer Institute (ICM), Montpellier, France.

Sophie Gourgou (S)

Institute of Cancer Research of Montpellier (IRCM), Montpellier, France.

Claire Lemanski (C)

Department of Radiation Oncology, Montpellier Cancer Institute (ICM), Montpellier, France.

Roxana Draghici (R)

Department of Radiation Oncology, Montpellier Cancer Institute (ICM), Montpellier, France.

Norbert Ailleres (N)

Department of Radiation Oncology, Montpellier Cancer Institute (ICM), Montpellier, France.

Jessica Prunaretty (J)

Department of Radiation Oncology, Montpellier Cancer Institute (ICM), Montpellier, France.

David Azria (D)

Faculty of Medicine, University of Montpellier, Montpellier, France.
Department of Radiation Oncology, Montpellier Cancer Institute (ICM), Montpellier, France.
Institute of Cancer Research of Montpellier (IRCM), Montpellier, France.

Céline Bourgier (C)

Faculty of Medicine, University of Montpellier, Montpellier, France.
Department of Radiation Oncology, Montpellier Cancer Institute (ICM), Montpellier, France.
Institute of Cancer Research of Montpellier (IRCM), Montpellier, France.

Classifications MeSH