Elsevier

Human Pathology

Volume 32, Issue 4, April 2001, Pages 417-427
Human Pathology

Original Contributions
Web-based tissue microarray image data analysis: Initial validation testing through prostate cancer Gleason grading*,**

https://doi.org/10.1053/hupa.2001.23517Get rights and content

Abstract

Tissue microarray technology promises to enhance tissue-based molecular research by allowing improved conservation of tissue resources and experimental reagents, improved internal experimental control, and increased sample numbers per experiment. Organized, well-validated collection and analysis of the voluminous image data produced by tissue microarray technology is critical to maximize its value. Web-based technology for visual analysis and searchable storage of microarray image data could provide optimal flexibility for research groups in meeting this goal, but this approach has not been examined scientifically. Toward this goal, a prostate tissue microarray block containing 432 tissue cores (0.6 mm diameter) was constructed. Moderately compressed (200 kb).jpg images of each tissue spot were acquired and were saved using a naming convention developed by the SPORE Prostate Tissue Microarray Collaborative Group. Four hundred three tissue array spot images were uploaded into a database developed for this study and were converted to.fpx format to decrease Internet transmission times for high-resolution image data. In phase I of the image analysis portion of the study, testing and preliminary analysis of the Web technology was performed by 2 pathologists (M.A.R. and G.S.B.). In phase II, 2 pathologists (J.I.E. and T.M.W.) with no previous exposure to this technology and no knowledge of the structure of the study were presented a set of 130 sequential tissue spot images via the Web on their office computers. In phase III, the same pathologists were presented a set of 193 images, including all 130 from phase II and 63 others, with image presentation order randomized. With each zoomable tissue spot image, each pathologist was presented with a nested set of questions regarding overall interpretability of the image, presence or absence of cancer, and predominant and second most frequent Gleason grade. In phases II and III of the study, 319 of 323 (99%) image presentations using this Web technology were rated interpretable. Comparing the 2 pathologists' readings in phases II and III, Gleason grade determinations by each pathologist were identical in 179 of 221 (81%) determinations and were within 1 point of each other in 221 of 221 (100%) determinations, a performance rate similar to if not better than that previously reported for direct microscopic Gleason grading. Interobserver comparison of Gleason score determinations and intraobserver comparisons for Gleason grade and score also showed a pattern of uniformity similar to those reported in direct microscope-based Gleason grading studies. Interobserver (7.5%) and intraobserver (5% and 3%) variability in determining whether diagnosable cancer was present point out the existence of a “threshold effect” that has rarely been studied but may provide a basis for identification of features that are most amenable to improved diagnostic standardization. In summary, storage and analysis of tissue microarray spot images using Web-based technology is feasible and practical, and the quality of images obtained using the techniques described here appears adequate for most tissue-based pathology research applications. HUM PATHOL 32:417-427. Copyright © 2001 by W.B. Saunders Company

Section snippets

Tissue microarray construction

A prostate tissue microarray block containing 432 tissue cores (each core 0.6 mm in diameter) was constructed from formalin-fixed, paraffin-embedded radical prostatectomy tissues from men with clinically localized, previously untreated prostate cancer. Specific representative regions of cancer and noncancerous prostate tissue for tissue microarray biopsy were circled on face sections of donor blocks from these cases by 1 pathologist (M.A.R.). Array construction was performed using a manual

Image download and interpretation time

Transmission time from our Baltimore-based server for single flashpix images during the analysis sessions varied from 2 to 3 seconds in Baltimore to 3 to 5 seconds on 1 day in Houston and 10 seconds on another day in Houston. Download times in Ann Arbor similarly were usually in the 2- to 3-second range but also were much longer (up to 15 seconds) on another occasion. Individual image interpretation time was not specifically measured but in general varied between <5 seconds and 30 seconds per

Discussion

Recent improvements in the ability to study multiple tissues on single glass slides has cracked open the door for high-throughput tissue-based research.1, 2, 3, 4 Tissue microarray technology is similar in name to complementary DNA (cDNA) array technology but has many requirements that are unique to tissue analysis, and its limitations have not been studied in depth. The work described here is a test of a novel Web-based approach to tissue microarray image data storage and analysis. To test

Acknowledgements

The authors thank Radhakrishnan Balu for computer programming.

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*

Supported by grants NCI 1P50 CA58236 and ACS TPRN-98-286-01-CCE (to G.S.B.), NIH 5P30 CA06973-35 (to G.P.), NCI 1P50 CA58236 (to J.I.E.), NCI 1P50 CA 58204-01 CF2 (to T.W.), and NCI 1P50 CA69568 (to M.R. and N.M.).

**

Address correspondence and reprint requests to G. Steven Bova, MD, Johns Hopkins Department of Pathology, PELICAN Informatics Laboratory, Pathology Building Rm 301, 600 North Wolfe St, Baltimore, MD 21287-6417.

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