Toxicity of internal mammary irradiation in breast cancer. Are concerns still justified in times of modern treatment techniques?


Journal

Acta oncologica (Stockholm, Sweden)
ISSN: 1651-226X
Titre abrégé: Acta Oncol
Pays: England
ID NLM: 8709065

Informations de publication

Date de publication:
Oct 2020
Historique:
pubmed: 4 7 2020
medline: 27 7 2021
entrez: 4 7 2020
Statut: ppublish

Résumé

The purpose of this study was to estimate the additional risk of side effects attributed to internal mammary node irradiation (IMNI) as part of regional lymph node irradiation (RNI) in breast cancer patients and to compare it with estimated overall survival (OS) benefit from IMNI. Treatment plans ( IMNI notably increased the mean OAR doses. The mean heart dose increased upon IMNI by 0.2-3.4 Gy (median: 1.9 Gy) in FB and 0.0-1.5 Gy (median 0.4 Gy) in DIBH. However, the estimated absolute additional 10-year cardiac mortality caused by IMNI was <0.5% for all patients studied except 70-year-old high risk patients (0.2-2.4% in FB and 0.0-1.1% in DIBH). In comparison to this, the published oncological benefit of IMNI ranges between 3.3% and 4.7%. The estimated additional 10-year risk of secondary cancer of the lung or contralateral breast ranged from 0-1.5% and 0-2.8%, respectively, depending on age and risk levels. IMNI increased the pneumonitis risk in all groups (0-2.2%). According to our analyses, the published oncological benefit of IMNI outweighs the estimated risk of cardiac mortality even in case of (e.g., cardiac) risk factors during VMAT. The estimated risk of secondary cancer or pneumonitis attributed to IMNI is low. DIBH reduces the estimated additional risk of IMNI even further and should be strongly considered especially in patients with a high baseline risk.

Sections du résumé

BACKGROUND BACKGROUND
The purpose of this study was to estimate the additional risk of side effects attributed to internal mammary node irradiation (IMNI) as part of regional lymph node irradiation (RNI) in breast cancer patients and to compare it with estimated overall survival (OS) benefit from IMNI.
MATERIAL AND METHODS METHODS
Treatment plans (
RESULTS RESULTS
IMNI notably increased the mean OAR doses. The mean heart dose increased upon IMNI by 0.2-3.4 Gy (median: 1.9 Gy) in FB and 0.0-1.5 Gy (median 0.4 Gy) in DIBH. However, the estimated absolute additional 10-year cardiac mortality caused by IMNI was <0.5% for all patients studied except 70-year-old high risk patients (0.2-2.4% in FB and 0.0-1.1% in DIBH). In comparison to this, the published oncological benefit of IMNI ranges between 3.3% and 4.7%. The estimated additional 10-year risk of secondary cancer of the lung or contralateral breast ranged from 0-1.5% and 0-2.8%, respectively, depending on age and risk levels. IMNI increased the pneumonitis risk in all groups (0-2.2%).
CONCLUSION CONCLUSIONS
According to our analyses, the published oncological benefit of IMNI outweighs the estimated risk of cardiac mortality even in case of (e.g., cardiac) risk factors during VMAT. The estimated risk of secondary cancer or pneumonitis attributed to IMNI is low. DIBH reduces the estimated additional risk of IMNI even further and should be strongly considered especially in patients with a high baseline risk.

Identifiants

pubmed: 32619381
doi: 10.1080/0284186X.2020.1787509
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1201-1209

Auteurs

Kai Joachim Borm (KJ)

Department of Radiation Oncology, Technical University of Munich (TUM), München, Germany.

Cristoforo Simonetto (C)

Institute of Radiation Medicine, Helmholtz Zentrum München, Neuherberg, Germany.

Pavel Kundrát (P)

Institute of Radiation Medicine, Helmholtz Zentrum München, Neuherberg, Germany.
Department of Radiation Dosimetry, Nuclear Physics Institute of the Czech Academy of Sciences, Prague, Czech Republic.

Markus Eidemüller (M)

Institute of Radiation Medicine, Helmholtz Zentrum München, Neuherberg, Germany.

Markus Oechsner (M)

Department of Radiation Oncology, Technical University of Munich (TUM), München, Germany.

Mathias Düsberg (M)

Department of Radiation Oncology, Technical University of Munich (TUM), München, Germany.

Stephanie Elisabeth Combs (SE)

Department of Radiation Oncology, Technical University of Munich (TUM), München, Germany.
Institute of Radiation Medicine, Helmholtz Zentrum München, Neuherberg, Germany.
Deutsches Konsortium für Translationale Krebsforschung, (DKTK)-Partner Site Munich, München, Germany.

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Classifications MeSH