Evidence map›Paper›PMID 37351769›Full record

ArticleMolecular imaging and biology2023

Evaluating Receptor-Specific Fresh Specimen Staining for Tumor Margin Detection in Clinical Breast Specimens.

Brook K Byrd, Wendy A Wells, Rendall R Strawbridge, Connor W Barth, Kimberley S Samkoe, Summer L Gibbs, Scott C Davis

Open access · hybridAbstract read
In one paragraph

Article in Molecular imaging and biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 31% of its field
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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Article
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

7 authors at 3 institutions in 1 country.

Brook K ByrdThayer School of Engineering, Dartmouth College, Hanover, NH, 03755, USA.
Wendy A WellsDepartment of Pathology and Laboratory Medicine, Dartmouth Hitchcock Medical Center, Lebanon, NH, 03766, USA.
Rendall R StrawbridgeThayer School of Engineering, Dartmouth College, Hanover, NH, 03755, USA.
Connor W BarthBiomedical Engineering Department, Oregon Health & Science University, Portland, OR, 97201, USA.
Kimberley S SamkoeThayer School of Engineering, Dartmouth College, Hanover, NH, 03755, USA.
Summer L GibbsBiomedical Engineering Department, Oregon Health & Science University, Portland, OR, 97201, USA.
Scott C DavisThayer School of Engineering, Dartmouth College, Hanover, NH, 03755, USA. Scott.C.Davis@dartmouth.edu.
Dartmouth College · USOregon Health & Science University · USDartmouth–Hitchcock Medical Center · US

Funding

Multi-probe fluorescence imaging for rapid intra-operative tumor margin assessmentR01CA188491 · NCI · DARTMOUTH COLLEGE · PI DAVIS, SCOTT C · 2015 to 2019
$2.9M
Training in Surgical InnovationT32EB021966 · NIBIB · DARTMOUTH COLLEGE · PI Eric R Fossum, Sohail K Mirza · 2017 to 2026
$1.7M
NCI NIH HHS R01 CA188491NIBIB NIH HHS T32 EB021966
6 · The paper itself

Abstract

purposeReliable and rapid identification of tumor in the margins of breast specimens during breast-conserving surgery to reduce repeat surgery rates is an active area of investigation. Dual-stain difference imaging (DDSI) is one of many approaches under evaluation for this application. This technique aims to topically apply fluorescent stain pairs (one targeted to a receptor-of-interest and the other a spectrally distinct isotype), image both stains, and compute a normalized difference image between the two channels. Prior evaluation and optimization in a variety of preclinical models produced encouraging diagnostic performance. Herein, we report on a pilot clinical study which evaluated HER2-targeted DDSI on 11 human breast specimens. PROCEDURES: Gross sections from 11 freshly excised mastectomy specimens were processed using a HER2-receptor-targeted DDSI protocol shortly after resection. After staining with the dual-probe protocol, specimens were imaged on a fluorescence scanner, followed by tissue fixation for hematoxylin and eosin and anti-HER2 immunohistochemical staining. Receiver operator characteristic curves and area under the curve (AUC) analysis were used to assess diagnostic performance of the resulting images. Performance values were also compared to expression level determined from IHC staining.

resultsEight of the 11 specimens presented with distinguishable invasive ductal carcinoma and/or were not affected by an imaging artifact. In these specimens, the DDSI technique provided an AUC = 0.90 ± 0.07 for tumor-to-adipose tissue and 0.81 ± 0.15 for tumor-to-glandular tissue, which was significantly higher than AUC values recovered from images of the targeted probe alone. DDSI values and diagnostic performance did not correlate with HER2 expression level, and tumors with low HER2 expression often produced high AUC, suggesting that even the low expression levels were enough to help distinguish tumor.

conclusionsThe results from this preliminary study of rapid receptor-specific staining in human specimens were consistent with prior preclinical results and demonstrated promising diagnostic potential.

Indexed as

Breast NeoplasmsMastectomyColoring AgentsFemaleHumansMastectomy, SegmentalStaining and LabelingColoring AgentsBreast cancer surgeryFluorescence-guided surgery (FGS)Fluorescence imagingHER2Molecular imagingTumor margins

Identifiers

PMID37351769
PMCPMC10598096
OpenAlexW4381715132

What OpenQuestion holds

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LicenceCC BY
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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.