Evidence map›Paper›PMID 38837087›Full record

ArticleBreast cancer research and treatment2024

Therapeutic impact of

Chloé François, Audrey Mailliez, Sebastian Chretien, Clémence Leguillette, Aurore Oudoux, Luc Ceugnart, Maël Barthoulot, Olivier Cougnenc, Anaïs Olivier

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In one paragraph

Article in Breast cancer research and treatment, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Chloé FrançoisDepartment of Nuclear Medicine, Centre Oscar Lambret, 3 rue Combemale, 59020, Lille Cedex, France. chloe@francois.nom.fr.
Audrey MailliezDepartment of Medical Oncology, Centre Oscar Lambret, Lille, France.ORCID http://orcid.org/0000-0002-0475-8631
Sebastian ChretienDepartment of Medical Oncology, Centre Oscar Lambret, Lille, France.
Clémence LeguilletteMethodology and Biostatistic Unit, Centre Oscar Lambret, Lille, France.
Aurore OudouxDepartment of Nuclear Medicine, Centre Oscar Lambret, 3 rue Combemale, 59020, Lille Cedex, France.
Luc CeugnartDepartment of Radiology, Centre Oscar Lambret, Lille, France.
Maël BarthoulotMethodology and Biostatistic Unit, Centre Oscar Lambret, Lille, France.
Olivier CougnencDepartment of Clinical Pharmacy, Centre Oscar Lambret, Lille, France.
Anaïs OlivierDepartment of Nuclear Medicine, Centre Oscar Lambret, 3 rue Combemale, 59020, Lille Cedex, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeWhile

methodsPatients who underwent FDG-PET/CT staging before any treatment between January 2015 and December 2020 at Oscar Lambret Center were included. EXCLUSIONS: patients with symptoms or conventional imaging suggestive of metastatic dissemination, or with prior malignancies. Initial stage was determined from mammography, breast ultrasound, breast MRI, and clinical examination. Staging and therapeutic impact based on FDG-PET/CT findings collected, including intra- (modification of dose/site/strategy in a type of management previously indicated) and inter-modality (modification of planned treatment strategy) changes.

resultsThe cohort included 287 female patients with clinical stage I or IIA, HER2+ , or TNBC. Therapeutic impact observed for 18% of patients (n = 52), with 2% (n = 7) undergoing inter-modality change with omission of planned surgery. The impact on patient management was higher for stage IIA patients (20%, 47/237) than for stage I patients (10%, 5/50). Among stage IIA disease, changes in management were more important for T2N0 patients (22%, 44/205) than for T1N1 patients (9%, 3/32). While not statistically significant, trends suggest usefulness of FDG-PET/CT for T2N0 patients.

conclusionConsidering substantial therapeutic implications, our study suggests the usefulness of FDG-PET/CT for patients with stage IIA, HER2-positive, or Triple-Negative BC with tumor size > 2 cm (T2N0).

Indexed as

Erb-b2 Receptor Tyrosine KinasesFluorodeoxyglucose F18Neoplasm StagingPositron Emission Tomography Computed TomographyTriple Negative Breast NeoplasmsAdultAgedAged, 80 and overBreast NeoplasmsFemaleHumansMiddle AgedRadiopharmaceuticalsRetrospective StudiesERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesFluorodeoxyglucose F18RadiopharmaceuticalsEarly breast cancerFDG PET/CTHER2-positive breast cancerPrimary stagingTriple-negative breast cancer

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.