Evidence map›Paper›PMID 38748758›Full record

ArticlePloS one2024

Novel approach to HER2 quantification using phosphor-integrated dots in human breast invasive cancer microarray.

Naoya Saito, Tsukasa Matsuo, Hitoshi Tsuda, Hiroyuki Yokota, Hisatake Okada

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Article in PloS one, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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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

5 authors.

Naoya SaitoTechnology Development Headquarters, Advanced Core Technology Center, Konica Minolta, Inc., Hachioji, Japan.ORCID 0009-0007-9560-7671
Tsukasa MatsuoTechnology Development Headquarters, Advanced Core Technology Center, Konica Minolta, Inc., Hachioji, Japan.
Hitoshi TsudaDepartment of Basic Pathology, National Defense Medical College, Saitama, Japan.
Hiroyuki YokotaTechnology Development Headquarters, Advanced Core Technology Center, Konica Minolta, Inc., Hachioji, Japan.
Hisatake OkadaTechnology Development Headquarters, Advanced Core Technology Center, Konica Minolta, Inc., Hachioji, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

HER2 expression in breast cancer is evaluated to select patients for anti-HER2 therapy. With the advent of newly approved HER2-targeted drugs for low HER2 expression breast cancer, more solid evidence on the whole spectrum of HER2 expression is needed. In this study, we quantitatively assessed HER2 expression from the whole core by combining high-intensity phosphor-integrated dot (PID) immunostaining and whole slide imaging (WSI) analysis. Two types of staining were performed using a 170-core tissue microarray of invasive breast cancer. First, HER2 was stained by immunohistochemistry (IHC), and IHC scores were determined by two practicing pathologists according to the ASCO/CAP HER2 guideline. Second, HER2 was stained with PID, and tentative PID scores were determined by quantitative analysis. The results show that PID can numerically classify HER2 expression status into scores 3+, 2+, 1+, and 0. The HER2 value quantified by PID strongly correlated with the 3, 3'-diaminobenzidine (DAB) IHC score determined by pathologists (R2 = 0.93). PID IHC score 1+ cases included both DAB IHC score 1+ and 0 cases, and low HER2 expression cases appeared to be often evaluated as DAB IHC score 0. Therefore, digital image analysis by PID and WSI can help stratify HER2 IHC. It may also help classify low HER2 expression.

Indexed as

Breast NeoplasmsErb-b2 Receptor Tyrosine KinasesQuantum DotsFemaleHumansImmunohistochemistryNeoplasm InvasivenessTissue Array AnalysisErb-b2 Receptor Tyrosine Kinases

Identifiers

PMID38748758
PMCPMC11095758

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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.