Evidence map›Paper›PMID 33280268›Full record

ArticleCancer medicine2021

Rapid HER2 cytologic fluorescence in situ hybridization for breast cancer using noncontact alternating current electric field mixing.

Shin-Nosuke Watanabe, Kazuhiro Imai, Hiroshi Nanjo, Yuki Wakamatsu, Yoshihiko Kimura, Yoshihisa Katayose, Shuichi Kamata, Kaori Terata, Eriko Takahashi, Ayano Ibonai and 11 more

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Article in Cancer medicine, 2021. 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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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

21 authors at 4 institutions in 1 country.

Shin-Nosuke WatanabeDepartment of Thoracic Surgery, Akita University Graduate School of Medicine, Akita, Japan.
Kazuhiro ImaiDepartment of Thoracic Surgery, Akita University Graduate School of Medicine, Akita, Japan.ORCID 0000-0003-4490-7862
Hiroshi NanjoDepartment of Pathology, Akita University Graduate School of Medicine, Akita, Japan.
Yuki WakamatsuDepartment of Thoracic Surgery, Akita University Graduate School of Medicine, Akita, Japan.
Yoshihiko KimuraAkita Kousei Medical Center, Akita, Japan.
Yoshihisa KatayoseAkita City Hospital, Akita, Japan.
Shuichi KamataJapanese Red Cross Akita Hospital, Akita, Japan.
Kaori TerataDepartment of Thoracic Surgery, Akita University Graduate School of Medicine, Akita, Japan.
Eriko TakahashiDepartment of Thoracic Surgery, Akita University Graduate School of Medicine, Akita, Japan.
Ayano IbonaiDepartment of Thoracic Surgery, Akita University Graduate School of Medicine, Akita, Japan.
Ayuko YamaguchiDepartment of Thoracic Surgery, Akita University Graduate School of Medicine, Akita, Japan.
Hikari KonnoDepartment of Thoracic Surgery, Akita University Graduate School of Medicine, Akita, Japan.
Misako YatsuyanagiDepartment of Thoracic Surgery, Akita University Graduate School of Medicine, Akita, Japan.
Chiaki KudoDepartment of Thoracic Surgery, Akita University Graduate School of Medicine, Akita, Japan.
Shinogu TakashimaDepartment of Thoracic Surgery, Akita University Graduate School of Medicine, Akita, Japan.
Yoichi AkagamiAkita Industrial Technology Center, Akita, Japan.
Ryuta NakamuraAkita Industrial Technology Center, Akita, Japan.
Yusuke SatoDepartment of Thoracic Surgery, Akita University Graduate School of Medicine, Akita, Japan.
Satoru MotoyamaDepartment of Thoracic Surgery, Akita University Graduate School of Medicine, Akita, Japan.ORCID 0000-0001-9191-2563
Kyoko NomuraDepartment of Environmental Health Science and Public Health, Akita University Graduate School of Medicine, Akita, Japan.
Yoshihiro MinamiyaDepartment of Thoracic Surgery, Akita University Graduate School of Medicine, Akita, Japan.
Akita University · JPAkita Industrial Technology Center · JPAkita Red Cross Hospital · JPAkita University Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHuman epidermal growth factor receptor 2-in situ hybridization (HER2-ISH) is widely approved for diagnostic, prognostic biomarker testing of formalin-fixed paraffin-embedded tissue blocks. However, cytologic ISH analysis has a potential advantage in tumor samples such as pleural effusion and ascites that are difficult to obtain the histological specimens. Our aim was to evaluate the clinical reliability of a novel rapid cytologic HER2 fluorescence ISH protocol (rapid-CytoFISH). MATERIALS AND

methodsUsing a new device, we applied a high-voltage/frequency, noncontact alternating current electric field to tissue imprints and needle rinses, which mixed the probe within microdroplets as the voltage was switched on and off (AC mixing). Cytologic samples (n = 143) were collected from patients with immunohistochemically identified HER2 breast cancers. The specimens were then tested using standard dual-color ISH using formalin-fixed paraffin-embedded tissue (FFPE-tissue DISH) for HER2-targeted therapies, CytoFISH, and rapid-CytoFISH (completed within 4 h).

resultsAll 143 collected cytologic specimens (50 imprinted cytology specimens from resected tumors and 93 liquid-based cytology specimens from needle rinses) were suitable for FISH analysis. The HER2/chromosome enumeration probe (CEP) 17 ratios did not significantly differ between FFPE-tissue DISH and either CytoFISH protocol. Based on HER2 scoring criteria, we found 95.1% agreement between FFPE-tissue DISH and CytoFISH (Cohen's kappa coefficient = 0.771 and 95% confidence interval (CI): 0.614-0.927).

conclusionCytoFISH could potentially serve as a clinical tool for prompt determination of HER2 status in breast cancer cytology. Rapid-CytoFISH with AC mixing will enable cancer diagnoses and HER2 status to be determined on the same day a patient comes to a clinic or hospital.

Indexed as

ElectricityAdultAgedAged, 80 and overBreast NeoplasmsCarcinoma, Ductal, BreastCarcinoma, LobularCytodiagnosisDiagnostic Tests, RoutineErb-b2 Receptor Tyrosine KinasesFemaleFollow-Up StudiesHumansIn Situ Hybridization, FluorescenceMiddle AgedPrognosisERBB2 protein, humanErb-b2 Receptor Tyrosine Kinasesbreast cancercytologyhuman epidermal growth factor receptor 2in situ hybridizationnoncontact alternating current electric field mixing

Identifiers

PMID33280268
PMCPMC7877363
OpenAlexW3111770678

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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.