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A Randomized Study Comparing Digital Imaging to Traditional Glass Slide Microscopy for Breast Biopsy and Cancer Diagnosis

BACKGROUND: Digital whole slide imaging may be useful for obtaining second opinions and is used in many countries. However, the U.S. Food and Drug Administration requires verification studies. METHODS: Pathologists were randomized to interpret one of four sets of breast biopsy cases during two phase...

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Autores principales: Elmore, Joann G., Longton, Gary M., Pepe, Margaret S., Carney, Patricia A., Nelson, Heidi D., Allison, Kimberly H., Geller, Berta M., Onega, Tracy, Tosteson, Anna N. A., Mercan, Ezgi, Shapiro, Linda G., Brunyé, Tad T., Morgan, Thomas R., Weaver, Donald L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5364740/
https://www.ncbi.nlm.nih.gov/pubmed/28382226
http://dx.doi.org/10.4103/2153-3539.201920
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author Elmore, Joann G.
Longton, Gary M.
Pepe, Margaret S.
Carney, Patricia A.
Nelson, Heidi D.
Allison, Kimberly H.
Geller, Berta M.
Onega, Tracy
Tosteson, Anna N. A.
Mercan, Ezgi
Shapiro, Linda G.
Brunyé, Tad T.
Morgan, Thomas R.
Weaver, Donald L.
author_facet Elmore, Joann G.
Longton, Gary M.
Pepe, Margaret S.
Carney, Patricia A.
Nelson, Heidi D.
Allison, Kimberly H.
Geller, Berta M.
Onega, Tracy
Tosteson, Anna N. A.
Mercan, Ezgi
Shapiro, Linda G.
Brunyé, Tad T.
Morgan, Thomas R.
Weaver, Donald L.
author_sort Elmore, Joann G.
collection PubMed
description BACKGROUND: Digital whole slide imaging may be useful for obtaining second opinions and is used in many countries. However, the U.S. Food and Drug Administration requires verification studies. METHODS: Pathologists were randomized to interpret one of four sets of breast biopsy cases during two phases, separated by ≥9 months, using glass slides or digital format (sixty cases per set, one slide per case, n = 240 cases). Accuracy was assessed by comparing interpretations to a consensus reference standard. Intraobserver reproducibility was assessed by comparing the agreement of interpretations on the same cases between two phases. Estimated probabilities of confirmation by a reference panel (i.e., predictive values) were obtained by incorporating data on the population prevalence of diagnoses. RESULTS: Sixty-five percent of responding pathologists were eligible, and 252 consented to randomization; 208 completed Phase I (115 glass, 93 digital); and 172 completed Phase II (86 glass, 86 digital). Accuracy was slightly higher using glass compared to digital format and varied by category: invasive carcinoma, 96% versus 93% (P = 0.04); ductal carcinoma in situ (DCIS), 84% versus 79% (P < 0.01); atypia, 48% versus 43% (P = 0.08); and benign without atypia, 87% versus 82% (P < 0.01). There was a small decrease in intraobserver agreement when the format changed compared to when glass slides were used in both phases (P = 0.08). Predictive values for confirmation by a reference panel using glass versus digital were: invasive carcinoma, 98% and 97% (not significant [NS]); DCIS, 70% and 57% (P = 0.007); atypia, 38% and 28% (P = 0.002); and benign without atypia, 97% and 96% (NS). CONCLUSIONS: In this large randomized study, digital format interpretations were similar to glass slide interpretations of benign and invasive cancer cases. However, cases in the middle of the spectrum, where more inherent variability exists, may be more problematic in digital format. Future studies evaluating the effect these findings exert on clinical practice and patient outcomes are required.
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spelling pubmed-53647402017-04-05 A Randomized Study Comparing Digital Imaging to Traditional Glass Slide Microscopy for Breast Biopsy and Cancer Diagnosis Elmore, Joann G. Longton, Gary M. Pepe, Margaret S. Carney, Patricia A. Nelson, Heidi D. Allison, Kimberly H. Geller, Berta M. Onega, Tracy Tosteson, Anna N. A. Mercan, Ezgi Shapiro, Linda G. Brunyé, Tad T. Morgan, Thomas R. Weaver, Donald L. J Pathol Inform Research Article BACKGROUND: Digital whole slide imaging may be useful for obtaining second opinions and is used in many countries. However, the U.S. Food and Drug Administration requires verification studies. METHODS: Pathologists were randomized to interpret one of four sets of breast biopsy cases during two phases, separated by ≥9 months, using glass slides or digital format (sixty cases per set, one slide per case, n = 240 cases). Accuracy was assessed by comparing interpretations to a consensus reference standard. Intraobserver reproducibility was assessed by comparing the agreement of interpretations on the same cases between two phases. Estimated probabilities of confirmation by a reference panel (i.e., predictive values) were obtained by incorporating data on the population prevalence of diagnoses. RESULTS: Sixty-five percent of responding pathologists were eligible, and 252 consented to randomization; 208 completed Phase I (115 glass, 93 digital); and 172 completed Phase II (86 glass, 86 digital). Accuracy was slightly higher using glass compared to digital format and varied by category: invasive carcinoma, 96% versus 93% (P = 0.04); ductal carcinoma in situ (DCIS), 84% versus 79% (P < 0.01); atypia, 48% versus 43% (P = 0.08); and benign without atypia, 87% versus 82% (P < 0.01). There was a small decrease in intraobserver agreement when the format changed compared to when glass slides were used in both phases (P = 0.08). Predictive values for confirmation by a reference panel using glass versus digital were: invasive carcinoma, 98% and 97% (not significant [NS]); DCIS, 70% and 57% (P = 0.007); atypia, 38% and 28% (P = 0.002); and benign without atypia, 97% and 96% (NS). CONCLUSIONS: In this large randomized study, digital format interpretations were similar to glass slide interpretations of benign and invasive cancer cases. However, cases in the middle of the spectrum, where more inherent variability exists, may be more problematic in digital format. Future studies evaluating the effect these findings exert on clinical practice and patient outcomes are required. Medknow Publications & Media Pvt Ltd 2017-03-10 /pmc/articles/PMC5364740/ /pubmed/28382226 http://dx.doi.org/10.4103/2153-3539.201920 Text en Copyright: © 2017 Journal of Pathology Informatics http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Research Article
Elmore, Joann G.
Longton, Gary M.
Pepe, Margaret S.
Carney, Patricia A.
Nelson, Heidi D.
Allison, Kimberly H.
Geller, Berta M.
Onega, Tracy
Tosteson, Anna N. A.
Mercan, Ezgi
Shapiro, Linda G.
Brunyé, Tad T.
Morgan, Thomas R.
Weaver, Donald L.
A Randomized Study Comparing Digital Imaging to Traditional Glass Slide Microscopy for Breast Biopsy and Cancer Diagnosis
title A Randomized Study Comparing Digital Imaging to Traditional Glass Slide Microscopy for Breast Biopsy and Cancer Diagnosis
title_full A Randomized Study Comparing Digital Imaging to Traditional Glass Slide Microscopy for Breast Biopsy and Cancer Diagnosis
title_fullStr A Randomized Study Comparing Digital Imaging to Traditional Glass Slide Microscopy for Breast Biopsy and Cancer Diagnosis
title_full_unstemmed A Randomized Study Comparing Digital Imaging to Traditional Glass Slide Microscopy for Breast Biopsy and Cancer Diagnosis
title_short A Randomized Study Comparing Digital Imaging to Traditional Glass Slide Microscopy for Breast Biopsy and Cancer Diagnosis
title_sort randomized study comparing digital imaging to traditional glass slide microscopy for breast biopsy and cancer diagnosis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5364740/
https://www.ncbi.nlm.nih.gov/pubmed/28382226
http://dx.doi.org/10.4103/2153-3539.201920
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