Evidence map›Paper›PMID 28805805›Full record

ArticleLaboratory investigation; a journal of technical methods and pathology2017

Whole tumor section quantitative image analysis maximizes between-pathologists' reproducibility for clinical immunohistochemistry-based biomarkers.

Michael Barnes, Chukka Srinivas, Isaac Bai, Judith Frederick, Wendy Liu, Anindya Sarkar, Xiuzhong Wang, Yao Nie, Bryce Portier, Monesh Kapadia and 4 more

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Article in Laboratory investigation; a journal of technical methods and pathology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

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17citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

Who cites it

17 citing papers in PubMed.

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  16. Intertumoral Heterogeneity of CD3Clinical cancer research : an official journal of the American Association for Cancer Research · 2019
    Article
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4 · The record

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5 · Who and what money

Authors and funding

14 authors.

Michael BarnesRoche Diagnostics, Medical Innovation, Tucson, AZ, USA.
Chukka SrinivasRoche Diagnostics, Imaging Group, Mountain View, CA, USA.
Isaac BaiRoche Diagnostics, Imaging Group, Mountain View, CA, USA.
Judith FrederickRoche Diagnostics, Imaging Group, Mountain View, CA, USA.
Wendy LiuRoche Diagnostics, Imaging Group, Mountain View, CA, USA.
Anindya SarkarRoche Diagnostics, Imaging Group, Mountain View, CA, USA.
Xiuzhong WangRoche Diagnostics, Imaging Group, Mountain View, CA, USA.
Yao NieRoche Diagnostics, Imaging Group, Mountain View, CA, USA.
Bryce PortierRoche Diagnostics, Medical Innovation, Tucson, AZ, USA.
Monesh KapadiaRoche Diagnostics, Medical Innovation, Tucson, AZ, USA.
Olcay SertelRoche Diagnostics, Imaging Group, Mountain View, CA, USA.
Elizabeth LittleRoche Diagnostics, Imaging Group, Mountain View, CA, USA.
Bikash SabataRoche Diagnostics, Imaging Group, Mountain View, CA, USA.
Jim Ranger-MooreRoche Diagnostics, Medical Innovation, Tucson, AZ, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pathologists have had increasing responsibility for quantitating immunohistochemistry (IHC) biomarkers with the expectation of high between-reader reproducibility due to clinical decision-making especially for patient therapy. Digital imaging-based quantitation of IHC clinical slides offers a potential aid for improvement; however, its clinical adoption is limited potentially due to a conventional field-of-view annotation approach. In this study, we implemented a novel solely morphology-based whole tumor section annotation strategy to maximize image analysis quantitation results between readers. We first compare the field-of-view image analysis annotation approach to digital and manual-based modalities across multiple clinical studies (~120 cases per study) and biomarkers (ER, PR, HER2, Ki-67, and p53 IHC) and then compare a subset of the same cases (~40 cases each from the ER, PR, HER2, and Ki-67 studies) using whole tumor section annotation approach to understand incremental value of all modalities. Between-reader results for each biomarker in relation to conventional scoring modalities showed similar concordance as manual read: ER field-of-view image analysis: 95.3% (95% CI 92.0-98.2%) vs digital read: 92.0% (87.8-95.8%) vs manual read: 94.9% (91.4-97.8%); PR field-of-view image analysis: 94.1% (90.3-97.2%) vs digital read: 94.0% (90.2-97.1%) vs manual read: 94.4% (90.9-97.2%); Ki-67 field-of-view image analysis: 86.8% (82.1-91.4%) vs digital read: 76.6% (70.9-82.2%) vs manual read: 85.6% (80.4-90.4%); p53 field-of-view image analysis: 81.7% (76.4-86.8%) vs digital read: 80.6% (75.0-86.0%) vs manual read: 78.8% (72.2-83.3%); and HER2 field-of-view image analysis: 93.8% (90.0-97.2%) vs digital read: 91.0 (86.6-94.9%) vs manual read: 87.2% (82.1-91.9%). Subset implementation and analysis on the same cases using whole tumor section image analysis approach showed significant improvement between pathologists over field-of-view image analysis and manual read (HER2 100% (97-100%), P=0.013 field-of-view image analysis and 0.013 manual read; Ki-67 100% (96.9-100%), P=0.040 and 0.012; ER 98.3% (94.1-99.5%), p=0.232 and 0.181; and PR 96.6% (91.5-98.7%), p=0.012 and 0.257). Overall, whole tumor section image analysis significantly improves between-pathologist's reproducibility and is the optimal approach for clinical-based image analysis algorithms.

Indexed as

Biomarkers, TumorBreast NeoplasmsFemaleHumansImage Interpretation, Computer-AssistedImmunohistochemistryKi-67 AntigenTumor Suppressor Protein p53Biomarkers, TumorKi-67 AntigenTP53 protein, humanTumor Suppressor Protein p53

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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.