Routine first-line detection of breast cancer therapy-related cardiotoxicity by serial, fast and ultra-low-dose equilibrium radionuclide angiography.


Journal

Journal of nuclear cardiology : official publication of the American Society of Nuclear Cardiology
ISSN: 1532-6551
Titre abrégé: J Nucl Cardiol
Pays: United States
ID NLM: 9423534

Informations de publication

Date de publication:
06 2023
Historique:
received: 08 07 2022
accepted: 28 09 2022
medline: 14 6 2023
pubmed: 27 10 2022
entrez: 26 10 2022
Statut: ppublish

Résumé

This study assesses a first-line left ventricular ejection fraction (LVEF) monitoring provided by an ultra-low-dose equilibrium radionuclide angiography (ERNA) in breast cancer women treated with potentially cardiotoxic drugs and analyzes patient outcome based on the ERNA results. Breast cancer women treated with anthracyclines, followed or not by trastuzumab, were monitored using ERNA with a high-sensitivity CZT-camera. Calibrated LVEF measurements were obtained with an almost threefold reduction of radiation doses and 10-min recording times. During a mean 24 ± 6 months follow-up, 552 ERNAs with a mean effective dose of 2.3 ± 0.6 mSv were performed in 195 women, among whom 22 (11%) presented both ERNA criteria of cardiotoxicity (LVEF < 50% and > 10% drop from baseline; Tox + group), 35 (18%) only one criterion (Tox ± group), and 138 (71%) neither (Tox - group). This ERNA-based classification correlated with trastuzumab-anthracycline treatment (p = 0.001), prior cardiovascular disease (p = 0.018), and cardiac outcome, with a 30-month survival with no cardiotoxicity-driven drug regimen changes of 97 ± 2% in Tox -, 60 ± 13% in Tox ± and 36 ± 13% in Tox + (p < 0.001) groups. First-line detection of breast cancer therapy-related cardiotoxicity by ultra-low-dose ERNA provides consistent results, confirming the excellent cardiac outcome for the greatest majority of women with no ERNA cardiotoxicity criteria.

Sections du résumé

BACKGROUND
This study assesses a first-line left ventricular ejection fraction (LVEF) monitoring provided by an ultra-low-dose equilibrium radionuclide angiography (ERNA) in breast cancer women treated with potentially cardiotoxic drugs and analyzes patient outcome based on the ERNA results.
METHODS
Breast cancer women treated with anthracyclines, followed or not by trastuzumab, were monitored using ERNA with a high-sensitivity CZT-camera. Calibrated LVEF measurements were obtained with an almost threefold reduction of radiation doses and 10-min recording times.
RESULTS
During a mean 24 ± 6 months follow-up, 552 ERNAs with a mean effective dose of 2.3 ± 0.6 mSv were performed in 195 women, among whom 22 (11%) presented both ERNA criteria of cardiotoxicity (LVEF < 50% and > 10% drop from baseline; Tox + group), 35 (18%) only one criterion (Tox ± group), and 138 (71%) neither (Tox - group). This ERNA-based classification correlated with trastuzumab-anthracycline treatment (p = 0.001), prior cardiovascular disease (p = 0.018), and cardiac outcome, with a 30-month survival with no cardiotoxicity-driven drug regimen changes of 97 ± 2% in Tox -, 60 ± 13% in Tox ± and 36 ± 13% in Tox + (p < 0.001) groups.
CONCLUSION
First-line detection of breast cancer therapy-related cardiotoxicity by ultra-low-dose ERNA provides consistent results, confirming the excellent cardiac outcome for the greatest majority of women with no ERNA cardiotoxicity criteria.

Identifiants

pubmed: 36289164
doi: 10.1007/s12350-022-03124-z
pii: 10.1007/s12350-022-03124-z
doi:

Substances chimiques

Trastuzumab P188ANX8CK
Antibiotics, Antineoplastic 0
Anthracyclines 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

1202-1209

Informations de copyright

© 2022. The Author(s) under exclusive licence to American Society of Nuclear Cardiology.

Références

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Auteurs

Charles-Edouard Decorads (CE)

Université de Lorraine, Department of Nuclear Medicine and Nancyclotep Imaging Platform, CHRU Nancy, 54000, Nancy, France.

Aurélien Lambert (A)

Institut de Cancérologie de Lorraine, Department of Medical Oncology, 54500, Vandœuvre-Lès-Nancy, France.

Véronique Roch (V)

Université de Lorraine, Department of Nuclear Medicine and Nancyclotep Imaging Platform, CHRU Nancy, 54000, Nancy, France.

Laetitia Imbert (L)

Université de Lorraine, Department of Nuclear Medicine and Nancyclotep Imaging Platform, CHRU Nancy, 54000, Nancy, France.
Université de Lorraine, INSERM, UMR1254, 54000, Nancy, France.

Mathieu Perrin (M)

Université de Lorraine, Department of Nuclear Medicine and Nancyclotep Imaging Platform, CHRU Nancy, 54000, Nancy, France.

Marine Claudin (M)

Université de Lorraine, Department of Nuclear Medicine and Nancyclotep Imaging Platform, CHRU Nancy, 54000, Nancy, France.

Julia Salleron (J)

Institut de Cancérologie de Lorraine, Biostatistics Unit, 54500, Vandœuvre-Lès-Nancy, France.

Nicolas Veran (N)

Université de Lorraine, Department of Nuclear Medicine and Nancyclotep Imaging Platform, CHRU Nancy, 54000, Nancy, France.

Zohra Lamiral (Z)

Université de Lorraine, CHRU-Nancy, INSERM, CIC, 1433, Nancy, France.

Catherine Henneton (C)

Institut de Cancérologie de Lorraine, Department of Medical Oncology, 54500, Vandœuvre-Lès-Nancy, France.

Pierre-Yves Marie (PY)

Université de Lorraine, Department of Nuclear Medicine and Nancyclotep Imaging Platform, CHRU Nancy, 54000, Nancy, France. py.marie@chru-nancy.fr.
Université de Lorraine, INSERM, UMR 1116, 54000, Nancy, France. py.marie@chru-nancy.fr.

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