Breast cancer: initial workup and staging with FDG PET/CT.

Breast cancer FDG Initial workup PET/CT Staging

Journal

Clinical and translational imaging
ISSN: 2281-5872
Titre abrégé: Clin Transl Imaging
Pays: Italy
ID NLM: 101616225

Informations de publication

Date de publication:
2021
Historique:
received: 07 02 2021
accepted: 13 04 2021
pubmed: 4 5 2021
medline: 4 5 2021
entrez: 3 5 2021
Statut: ppublish

Résumé

Precise staging is needed to plan optimal management in breast cancer. 18F-fluorodeoxyglucose positron emission tomography coupled with computed tomography (FDG-PET/CT) offers high sensitivity in detecting extra axillary lymph nodes and distant metastases. This review aims to clarify in which groups of patients staging with FDG-PET/CT would be beneficial and should be offered. We also discuss how tumor biology and breast cancer subtypes should be taken into account when interpreting FDG-PET/CT scans. We performed a comprehensive literature review and rigorous appraisal of research studies assessing indications for FDG-PET/CT in breast cancer. This assessment regarding breast cancer served as a basis for the recommendations set by a working group of the French Society of Nuclear Medicine, in collaboration with oncological societies, for developing good clinical practice recommendations on the use of FDG-PET/CT in oncology. FDG-PET/CT is useful for initial staging of breast cancer, independently of tumor phenotype (triple negative, luminal or HER2 +) and regardless of tumor grade. Considering histological subtype, FDG-PET/CT performs better for staging invasive ductal carcinoma, although it is also helpful for staging invasive lobular carcinomas. Based on the available data, FDG-PET/CT becomes useful for staging starting from clinical stage IIB. FDG-PET/CT is possibly useful in patients with clinical stage IIA (T1N1 or T2N0), but there is not enough strong data to recommend routine use in this subgroup. For clinical stage I (T1N0) patients, staging with FDG-PET/CT offers no added value. FDG-PET/CT is useful for staging patients with breast cancer, starting from clinical stage IIB.

Identifiants

pubmed: 33937141
doi: 10.1007/s40336-021-00426-z
pii: 426
pmc: PMC8075837
doi:

Types de publication

Journal Article Review

Langues

eng

Pagination

221-231

Informations de copyright

© Italian Association of Nuclear Medicine and Molecular Imaging 2021.

Déclaration de conflit d'intérêts

Conflict of interestAll the authors (David Groheux and Elif Hindié) declare no conflict of interest.

Auteurs

David Groheux (D)

Department of Nuclear Medicine, Saint-Louis Hospital, Paris, France.
University Paris-Diderot, INSERM U976, HIPI, Paris, France.

Elif Hindie (E)

Department of Nuclear Medicine, Bordeaux University Hospital, Bordeaux, France.

Classifications MeSH