Effect of hypofractionation on the incidental axilla dose during tangential field radiotherapy in breast cancer.


Journal

Strahlentherapie und Onkologie : Organ der Deutschen Rontgengesellschaft ... [et al]
ISSN: 1439-099X
Titre abrégé: Strahlenther Onkol
Pays: Germany
ID NLM: 8603469

Informations de publication

Date de publication:
Sep 2020
Historique:
received: 19 12 2019
accepted: 09 05 2020
pubmed: 4 6 2020
medline: 15 12 2020
entrez: 4 6 2020
Statut: ppublish

Résumé

Tangential field irradiation in breast cancer potentially treats residual tumor cells in the axilla after sentinel lymph node biopsy (SLNB). In recent years, hypofractionated radiotherapy has gained importance and currently represents the recommended standard in adjuvant breast cancer treatment for many patients. So far, the impact of hypofractionation on the effect of incidental lymph node irradiation has not be addressed. Biological effective dose (BED) and tumor control probability (TCP) were estimated for four different hypofractionated radiation schemes (42.50 Gy in 16 fractions [Fx]; 40.05 Gy in 15 Fx; 27 Gy in 5 Fx; and 26 in 5 Fx) and compared to conventional fractionation (50 Gy in 25 Fx). For calculation of BED and TCP, a previously published radiobiological model with an α/β ratio of 4 Gy was used. The theoretical BED and TCP for incidental irradiation between 0 and 100% of the prescribed dose were evaluated. Subsequently, we assessed BED and TCP in 431 axillary lymph node metastases. The extent of incidental lymph node irradiation and the fractionation scheme have a direct impact on BED and TCP. The estimated mean TCP in the axillary nodes ranged from 1.5 ± 6.4% to 57.5 ± 22.9%, depending on the patient's anatomy and the fractionation scheme. Hypofractionation led to a significant reduction of mean TCP of lymph node metastases for all schedules. Our data indicate that hypofractionation might affect the effectiveness of incidental radiotherapy in the axilla. This is particularly relevant for patients with positive sentinel lymph nodes who receive SLNB only.

Identifiants

pubmed: 32488292
doi: 10.1007/s00066-020-01636-6
pii: 10.1007/s00066-020-01636-6
pmc: PMC7450000
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

771-778

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Auteurs

Kai J Borm (KJ)

Department of RadiationOncology, Technical University Munich, Medical School, Klinikum rechts der Isar, Munich, Germany.

Markus Oechsner (M)

Department of RadiationOncology, Technical University Munich, Medical School, Klinikum rechts der Isar, Munich, Germany.

Mathias Düsberg (M)

Department of RadiationOncology, Technical University Munich, Medical School, Klinikum rechts der Isar, Munich, Germany.

Gabriel Buschner (G)

Department of Nuclear Medicine, Technical University Munich, Medical School, Klinikum rechts der Isar, Munich, Germany.

Weber Wolfgang (W)

Department of Nuclear Medicine, Technical University Munich, Medical School, Klinikum rechts der Isar, Munich, Germany.

Stephanie E Combs (SE)

Department of RadiationOncology, Technical University Munich, Medical School, Klinikum rechts der Isar, Munich, Germany.
Deutsches Konsortium für Translationale Krebsforschung (DKTK)-Partner Site Munich, Munich, Germany.
Institute of Radiation Medicine, Helmholtzzentrum München, Ingolstaedter Landstr. 1, 85764, Neuherberg, Germany.

Marciana N Duma (MN)

Department of RadiationOncology, Technical University Munich, Medical School, Klinikum rechts der Isar, Munich, Germany. Marciana-Nona.Duma@med.uni-jena.de.
Department of Radiotherapy and Radiation Oncology, Friedrich Schiller University Hospital, Bachstraße 18, 07743, Jena, Germany. Marciana-Nona.Duma@med.uni-jena.de.

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Classifications MeSH