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Pixelwise H-score: a novel digital image analysis-based metric to quantify membrane biomarker expression from immunohistochemistry images

View ORCID ProfileSripad Ram, Pamela Vizcarra, Pamela Whalen, Shibing Deng, CL Painter, Amy Jackson-Fisher, Steven Pirie-Shepherd, Xiaoling Xia, Eric L. Powell
doi: https://doi.org/10.1101/2021.01.06.425539
Sripad Ram
1Drug-Safety Research and Development, Pfizer Inc., La Jolla, CA 92121
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  • ORCID record for Sripad Ram
  • For correspondence: Sripad.ram@pfizer.com
Pamela Vizcarra
2Tumor Morphology Group, Oncology Research and Development, Pfizer Inc., La Jolla, CA 92121
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Pamela Whalen
2Tumor Morphology Group, Oncology Research and Development, Pfizer Inc., La Jolla, CA 92121
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Shibing Deng
3Biostatistics Unit, Oncology Research and Development, Pfizer Inc., La Jolla, CA 92121
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CL Painter
2Tumor Morphology Group, Oncology Research and Development, Pfizer Inc., La Jolla, CA 92121
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Amy Jackson-Fisher
2Tumor Morphology Group, Oncology Research and Development, Pfizer Inc., La Jolla, CA 92121
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Steven Pirie-Shepherd
2Tumor Morphology Group, Oncology Research and Development, Pfizer Inc., La Jolla, CA 92121
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Xiaoling Xia
2Tumor Morphology Group, Oncology Research and Development, Pfizer Inc., La Jolla, CA 92121
4Ventana Medical Systems, Tucson, AZ 85755
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Eric L. Powell
2Tumor Morphology Group, Oncology Research and Development, Pfizer Inc., La Jolla, CA 92121
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ABSTRACT

Immunohistochemistry (IHC) assays play a central role in evaluating biomarker expression in tissue sections for diagnostic and research applications. Manual scoring of IHC images, which is the current standard of practice, is known to have several shortcomings in terms of reproducibility and scalability to large scale studies. Here, by using a digital image analysis-based approach, we introduce a new metric called the pixelwise H-score (pix H-score) that quantifies biomarker expression from whole-slide scanned IHC images. The pix H-score is an unsupervised algorithm that only requires the specification of intensity thresholds for the biomarker and the nuclear-counterstain channels. We present the detailed implementation of the pix H-score in two different whole-slide image analysis software packages Visiopharm and HALO. We consider three biomarkers P-cadherin, PD-L1, and 5T4, and show how the pix H-score exhibits tight concordance to multiple orthogonal measurements of biomarker abundance such as the biomarker mRNA transcript and the pathologist H-score. We also compare the pix H-score to existing automated image analysis algorithms and demonstrate that the pix H-score provides either comparable or significantly better performance over these methodologies. We also present results of an empirical resampling approach to assess the performance of the pix H-score in estimating biomarker abundance from select regions within the tumor tissue relative to the whole tumor resection. We anticipate that the new metric will be broadly applicable to quantify biomarker expression from a wide variety of IHC images. Moreover, these results underscore the benefit of digital image analysis-based approaches which offer an objective, reproducible, and highly scalable strategy to quantitatively analyze IHC images.

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The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY 4.0 International license.
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Posted January 06, 2021.
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Pixelwise H-score: a novel digital image analysis-based metric to quantify membrane biomarker expression from immunohistochemistry images
Sripad Ram, Pamela Vizcarra, Pamela Whalen, Shibing Deng, CL Painter, Amy Jackson-Fisher, Steven Pirie-Shepherd, Xiaoling Xia, Eric L. Powell
bioRxiv 2021.01.06.425539; doi: https://doi.org/10.1101/2021.01.06.425539
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Pixelwise H-score: a novel digital image analysis-based metric to quantify membrane biomarker expression from immunohistochemistry images
Sripad Ram, Pamela Vizcarra, Pamela Whalen, Shibing Deng, CL Painter, Amy Jackson-Fisher, Steven Pirie-Shepherd, Xiaoling Xia, Eric L. Powell
bioRxiv 2021.01.06.425539; doi: https://doi.org/10.1101/2021.01.06.425539

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