Enhancing mitosis quantification and detection in meningiomas with computational digital pathology
Mitosis is a critical criterion for meningioma grading. However, pathologists’ assessment of mitoses is subject to significant inter-observer variation due to challenges in locating mitosis hotspots and accurately detecting mitotic figures. To address this issue, we leverage digital pathology and pr...
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Published in | Acta neuropathologica communications Vol. 12; no. 1; pp. 7 - 15 |
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Main Authors | , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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England
BioMed Central
11.01.2024
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Abstract | Mitosis is a critical criterion for meningioma grading. However, pathologists’ assessment of mitoses is subject to significant inter-observer variation due to challenges in locating mitosis hotspots and accurately detecting mitotic figures. To address this issue, we leverage digital pathology and propose a computational strategy to enhance pathologists’ mitosis assessment. The strategy has two components: (1) A depth-first search algorithm that quantifies the mathematically maximum mitotic count in 10 consecutive high-power fields, which can enhance the preciseness, especially in cases with borderline mitotic count. (2) Implementing a collaborative sphere to group a set of pathologists to detect mitoses under each high-power field, which can mitigate subjective random errors in mitosis detection originating from individual detection errors. By depth-first search algorithm (1) , we analyzed 19 meningioma slides and discovered that the proposed algorithm upgraded two borderline cases verified at consensus conferences. This improvement is attributed to the algorithm’s ability to quantify the mitotic count more comprehensively compared to other conventional methods of counting mitoses. In implementing a collaborative sphere (2) , we evaluated the correctness of mitosis detection from grouped pathologists and/or pathology residents, where each member of the group annotated a set of 48 high-power field images for mitotic figures independently. We report that groups with sizes of three can achieve an average precision of 0.897 and sensitivity of 0.699 in mitosis detection, which is higher than an average pathologist in this study (precision: 0.750, sensitivity: 0.667). The proposed computational strategy can be integrated with artificial intelligence workflow, which envisions the future of achieving a rapid and robust mitosis assessment by interactive assisting algorithms that can ultimately benefit patient management. |
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AbstractList | Abstract Mitosis is a critical criterion for meningioma grading. However, pathologists’ assessment of mitoses is subject to significant inter-observer variation due to challenges in locating mitosis hotspots and accurately detecting mitotic figures. To address this issue, we leverage digital pathology and propose a computational strategy to enhance pathologists’ mitosis assessment. The strategy has two components: (1) A depth-first search algorithm that quantifies the mathematically maximum mitotic count in 10 consecutive high-power fields, which can enhance the preciseness, especially in cases with borderline mitotic count. (2) Implementing a collaborative sphere to group a set of pathologists to detect mitoses under each high-power field, which can mitigate subjective random errors in mitosis detection originating from individual detection errors. By depth-first search algorithm (1) , we analyzed 19 meningioma slides and discovered that the proposed algorithm upgraded two borderline cases verified at consensus conferences. This improvement is attributed to the algorithm’s ability to quantify the mitotic count more comprehensively compared to other conventional methods of counting mitoses. In implementing a collaborative sphere (2) , we evaluated the correctness of mitosis detection from grouped pathologists and/or pathology residents, where each member of the group annotated a set of 48 high-power field images for mitotic figures independently. We report that groups with sizes of three can achieve an average precision of 0.897 and sensitivity of 0.699 in mitosis detection, which is higher than an average pathologist in this study (precision: 0.750, sensitivity: 0.667). The proposed computational strategy can be integrated with artificial intelligence workflow, which envisions the future of achieving a rapid and robust mitosis assessment by interactive assisting algorithms that can ultimately benefit patient management. Mitosis is a critical criterion for meningioma grading. However, pathologists’ assessment of mitoses is subject to significant inter-observer variation due to challenges in locating mitosis hotspots and accurately detecting mitotic figures. To address this issue, we leverage digital pathology and propose a computational strategy to enhance pathologists’ mitosis assessment. The strategy has two components: (1) A depth-first search algorithm that quantifies the mathematically maximum mitotic count in 10 consecutive high-power fields, which can enhance the preciseness, especially in cases with borderline mitotic count. (2) Implementing a collaborative sphere to group a set of pathologists to detect mitoses under each high-power field, which can mitigate subjective random errors in mitosis detection originating from individual detection errors. By depth-first search algorithm (1) , we analyzed 19 meningioma slides and discovered that the proposed algorithm upgraded two borderline cases verified at consensus conferences. This improvement is attributed to the algorithm’s ability to quantify the mitotic count more comprehensively compared to other conventional methods of counting mitoses. In implementing a collaborative sphere (2) , we evaluated the correctness of mitosis detection from grouped pathologists and/or pathology residents, where each member of the group annotated a set of 48 high-power field images for mitotic figures independently. We report that groups with sizes of three can achieve an average precision of 0.897 and sensitivity of 0.699 in mitosis detection, which is higher than an average pathologist in this study (precision: 0.750, sensitivity: 0.667). The proposed computational strategy can be integrated with artificial intelligence workflow, which envisions the future of achieving a rapid and robust mitosis assessment by interactive assisting algorithms that can ultimately benefit patient management. Mitosis is a critical criterion for meningioma grading. However, pathologists’ assessment of mitoses is subject to significant inter-observer variation due to challenges in locating mitosis hotspots and accurately detecting mitotic figures. To address this issue, we leverage digital pathology and propose a computational strategy to enhance pathologists’ mitosis assessment. The strategy has two components: (1) A depth-first search algorithm that quantifies the mathematically maximum mitotic count in 10 consecutive high-power fields, which can enhance the preciseness, especially in cases with borderline mitotic count. (2) Implementing a collaborative sphere to group a set of pathologists to detect mitoses under each high-power field, which can mitigate subjective random errors in mitosis detection originating from individual detection errors. By depth-first search algorithm (1) , we analyzed 19 meningioma slides and discovered that the proposed algorithm upgraded two borderline cases verified at consensus conferences. This improvement is attributed to the algorithm’s ability to quantify the mitotic count more comprehensively compared to other conventional methods of counting mitoses. In implementing a collaborative sphere (2) , we evaluated the correctness of mitosis detection from grouped pathologists and/or pathology residents, where each member of the group annotated a set of 48 high-power field images for mitotic figures independently. We report that groups with sizes of three can achieve an average precision of 0.897 and sensitivity of 0.699 in mitosis detection, which is higher than an average pathologist in this study (precision: 0.750, sensitivity: 0.667). The proposed computational strategy can be integrated with artificial intelligence workflow, which envisions the future of achieving a rapid and robust mitosis assessment by interactive assisting algorithms that can ultimately benefit patient management. Mitosis is a critical criterion for meningioma grading. However, pathologists' assessment of mitoses is subject to significant inter-observer variation due to challenges in locating mitosis hotspots and accurately detecting mitotic figures. To address this issue, we leverage digital pathology and propose a computational strategy to enhance pathologists' mitosis assessment. The strategy has two components: (1) A depth-first search algorithm that quantifies the mathematically maximum mitotic count in 10 consecutive high-power fields, which can enhance the preciseness, especially in cases with borderline mitotic count. (2) Implementing a collaborative sphere to group a set of pathologists to detect mitoses under each high-power field, which can mitigate subjective random errors in mitosis detection originating from individual detection errors. By depth-first search algorithm (1) , we analyzed 19 meningioma slides and discovered that the proposed algorithm upgraded two borderline cases verified at consensus conferences. This improvement is attributed to the algorithm's ability to quantify the mitotic count more comprehensively compared to other conventional methods of counting mitoses. In implementing a collaborative sphere (2) , we evaluated the correctness of mitosis detection from grouped pathologists and/or pathology residents, where each member of the group annotated a set of 48 high-power field images for mitotic figures independently. We report that groups with sizes of three can achieve an average precision of 0.897 and sensitivity of 0.699 in mitosis detection, which is higher than an average pathologist in this study (precision: 0.750, sensitivity: 0.667). The proposed computational strategy can be integrated with artificial intelligence workflow, which envisions the future of achieving a rapid and robust mitosis assessment by interactive assisting algorithms that can ultimately benefit patient management.Mitosis is a critical criterion for meningioma grading. However, pathologists' assessment of mitoses is subject to significant inter-observer variation due to challenges in locating mitosis hotspots and accurately detecting mitotic figures. To address this issue, we leverage digital pathology and propose a computational strategy to enhance pathologists' mitosis assessment. The strategy has two components: (1) A depth-first search algorithm that quantifies the mathematically maximum mitotic count in 10 consecutive high-power fields, which can enhance the preciseness, especially in cases with borderline mitotic count. (2) Implementing a collaborative sphere to group a set of pathologists to detect mitoses under each high-power field, which can mitigate subjective random errors in mitosis detection originating from individual detection errors. By depth-first search algorithm (1) , we analyzed 19 meningioma slides and discovered that the proposed algorithm upgraded two borderline cases verified at consensus conferences. This improvement is attributed to the algorithm's ability to quantify the mitotic count more comprehensively compared to other conventional methods of counting mitoses. In implementing a collaborative sphere (2) , we evaluated the correctness of mitosis detection from grouped pathologists and/or pathology residents, where each member of the group annotated a set of 48 high-power field images for mitotic figures independently. We report that groups with sizes of three can achieve an average precision of 0.897 and sensitivity of 0.699 in mitosis detection, which is higher than an average pathologist in this study (precision: 0.750, sensitivity: 0.667). The proposed computational strategy can be integrated with artificial intelligence workflow, which envisions the future of achieving a rapid and robust mitosis assessment by interactive assisting algorithms that can ultimately benefit patient management. |
ArticleNumber | 7 |
Author | Magaki, Shino Vinters, Harry V. Haeri, Mohammad Zhang, Xinhai Robert Chen, Xiang Anthony Khanlou, Negar Williams, Christopher Kazu Cobos, Inma Lakis, Nelli Onstott, Ellie Kate Yang, Chunxu Al-kharouf, Issa Yan, Wenzhong Gu, Hongyan Zarrin-Khameh, Neda Alrosan, Sallam Mohammad |
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CitedBy_id | crossref_primary_10_1038_s41598_024_77244_6 crossref_primary_10_3390_cancers16111976 crossref_primary_10_1016_j_labinv_2024_102130 crossref_primary_10_1016_j_ijhcs_2024_103315 |
Cites_doi | 10.3390/biology5010003 10.1002/1097-0142(19941215)74:12<3176::AID-CNCR2820741217>3.0.CO;2-N 10.1016/j.media.2022.102699 10.3390/jcm9030749 10.1038/s41374-019-0275-0 10.1371/journal.pone.0161286 10.1097/01.pas.0000141389.06925.d5 10.1016/j.prp.2010.09.002 10.1177/0300985819890686 10.1007/s10014-009-0249-9 10.1007/s11060-022-04220-3 10.1007/s11060-019-03218-8 10.1177/03009858211067478 10.1007/978-3-031-29750-2_13 10.1007/s00401-018-1879-y 10.1038/s41597-023-02327-4 10.1093/neuonc/noz061 10.4103/2153-3539.112693 10.1056/NEJM198506203122504 10.1038/s41379-021-00825-7 10.1093/neuonc/noab150 10.21037/cco.2017.05.02 10.1038/s41598-020-73246-2 10.1093/neuonc/noac202 10.1016/S1470-2045(17)30155-9 10.1145/3577011 10.1016/j.media.2019.02.012 10.1038/nrn1518 10.1016/S0344-0338(96)80075-6 10.1109/JBHI.2020.3032060 10.1007/978-3-031-33658-4_21 10.1145/3544548.3580694 10.1007/s004120050256 10.1016/j.jpi.2023.100316 10.1038/s41597-020-00756-z 10.1038/modpathol.3800388 10.1309/HXUNAG34B3CEFDU8 10.1038/s41597-019-0290-4 10.3171/jns.1978.49.5.0689 10.1007/s00401-015-1519-8 10.1038/s41598-021-85652-1 10.1093/neuonc/noab106 10.1093/neuonc/nov002 10.1097/MD.0000000000018644 |
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Keywords | Digital pathology Mitosis Meningioma Depth-first search Pathologist group decision |
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References | CR Garcia (1707_CR6) 2019; 144 K Stacke (1707_CR35) 2021; 25 JS Meyer (1707_CR4) 2005; 18 E Duregon (1707_CR14) 2015; 17 S Fukushima (1707_CR17) 2009; 26 AR Feinstein (1707_CR41) 1985; 312 CA Bertram (1707_CR30) 2019; 6 Z Wang (1707_CR37) 2020 YUI Collan (1707_CR5) 1996; 192 N Liu (1707_CR11) 2020; 99 M Aubreville (1707_CR31) 2020; 7 F Sahm (1707_CR43) 2016; 131 CA Bertram (1707_CR3) 2020; 57 M Aubreville (1707_CR45) 2023; 10 M Ohta (1707_CR9) 1994; 74 JZ Wang (1707_CR22) 2023; 1416 1707_CR25 M Veta (1707_CR24) 2016; 11 H Gu (1707_CR26) 2023 DN Louis (1707_CR2) 2021; 23 YJ Kim (1707_CR16) 2007; 128 PS Mischel (1707_CR42) 2004; 5 L Roux (1707_CR32) 2013; 4 IA Cree (1707_CR7) 2021; 34 J Singh (1707_CR18) 2023; 161 M Veta (1707_CR33) 2019; 54 CA Bertram (1707_CR27) 2022; 59 MJ Hendzel (1707_CR13) 1997; 106 F Sahm (1707_CR21) 2017; 18 MCA Balkenhol (1707_CR29) 2019; 99 D Capper (1707_CR20) 2018; 136 T Mahmood (1707_CR47) 2020; 9 PN Harter (1707_CR12) 2017; 6 BW Scheithauer (1707_CR40) 1978; 49 A Sohail (1707_CR46) 2021; 11 F Nassiri (1707_CR19) 2019; 21 S Kurdyukov (1707_CR44) 2016 SA Van Bergeijk (1707_CR28) 2023; 14 R Goldbrunner (1707_CR8) 2021; 23 E Abry (1707_CR10) 2010; 206 T Ribalta (1707_CR15) 2004; 28 1707_CR1 1707_CR36 M Aubreville (1707_CR34) 2023; 84 1707_CR39 M Aubreville (1707_CR23) 2020; 10 1707_CR38 |
References_xml | – year: 2016 ident: 1707_CR44 publication-title: Biology doi: 10.3390/biology5010003 – volume: 74 start-page: 3176 issue: 12 year: 1994 ident: 1707_CR9 publication-title: Cancer doi: 10.1002/1097-0142(19941215)74:12<3176::AID-CNCR2820741217>3.0.CO;2-N – volume: 84 year: 2023 ident: 1707_CR34 publication-title: Med Image Anal doi: 10.1016/j.media.2022.102699 – volume: 9 start-page: 749 issue: 3 year: 2020 ident: 1707_CR47 publication-title: J Clin Med doi: 10.3390/jcm9030749 – volume: 99 start-page: 1596 issue: 11 year: 2019 ident: 1707_CR29 publication-title: Lab Invest doi: 10.1038/s41374-019-0275-0 – volume: 11 issue: 8 year: 2016 ident: 1707_CR24 publication-title: PLoS ONE doi: 10.1371/journal.pone.0161286 – volume: 28 start-page: 1532 issue: 11 year: 2004 ident: 1707_CR15 publication-title: Am J Surg Pathol doi: 10.1097/01.pas.0000141389.06925.d5 – volume: 206 start-page: 810 issue: 12 year: 2010 ident: 1707_CR10 publication-title: Pathol Res Pract doi: 10.1016/j.prp.2010.09.002 – volume: 57 start-page: 214 issue: 2 year: 2020 ident: 1707_CR3 publication-title: Vet Pathol doi: 10.1177/0300985819890686 – volume: 26 start-page: 51 year: 2009 ident: 1707_CR17 publication-title: Brain Tumor Pathol doi: 10.1007/s10014-009-0249-9 – volume: 161 start-page: 339 issue: 2 year: 2023 ident: 1707_CR18 publication-title: J Neurooncol doi: 10.1007/s11060-022-04220-3 – volume: 144 start-page: 179 issue: 1 year: 2019 ident: 1707_CR6 publication-title: J Neurooncol doi: 10.1007/s11060-019-03218-8 – volume: 59 start-page: 211 issue: 2 year: 2022 ident: 1707_CR27 publication-title: Vet Pathol doi: 10.1177/03009858211067478 – volume: 1416 start-page: 175 year: 2023 ident: 1707_CR22 publication-title: Adv Exp Med Biol doi: 10.1007/978-3-031-29750-2_13 – volume: 136 start-page: 181 issue: 2 year: 2018 ident: 1707_CR20 publication-title: Acta Neuropathol doi: 10.1007/s00401-018-1879-y – volume: 10 start-page: 484 issue: 1 year: 2023 ident: 1707_CR45 publication-title: Sci Data doi: 10.1038/s41597-023-02327-4 – volume: 21 start-page: 901 issue: 7 year: 2019 ident: 1707_CR19 publication-title: Neuro Oncol doi: 10.1093/neuonc/noz061 – volume: 4 start-page: 8 issue: 1 year: 2013 ident: 1707_CR32 publication-title: J Pathol Inform doi: 10.4103/2153-3539.112693 – ident: 1707_CR36 – volume: 312 start-page: 1604 issue: 25 year: 1985 ident: 1707_CR41 publication-title: N Engl J Med doi: 10.1056/NEJM198506203122504 – volume: 34 start-page: 1651 issue: 9 year: 2021 ident: 1707_CR7 publication-title: Mod Pathol doi: 10.1038/s41379-021-00825-7 – volume: 23 start-page: 1821 issue: 11 year: 2021 ident: 1707_CR8 publication-title: Neuro Oncol doi: 10.1093/neuonc/noab150 – volume: 6 start-page: S2 issue: S1 year: 2017 ident: 1707_CR12 publication-title: Chin Clin Oncol doi: 10.21037/cco.2017.05.02 – volume: 10 start-page: 16447 issue: 1 year: 2020 ident: 1707_CR23 publication-title: Sci Rep doi: 10.1038/s41598-020-73246-2 – ident: 1707_CR1 doi: 10.1093/neuonc/noac202 – volume: 18 start-page: 682 issue: 5 year: 2017 ident: 1707_CR21 publication-title: Lancet Oncol doi: 10.1016/S1470-2045(17)30155-9 – year: 2023 ident: 1707_CR26 publication-title: ACM Trans Comput-Hum Interact doi: 10.1145/3577011 – volume: 54 start-page: 111 year: 2019 ident: 1707_CR33 publication-title: Med Image Anal doi: 10.1016/j.media.2019.02.012 – volume: 5 start-page: 782 issue: 10 year: 2004 ident: 1707_CR42 publication-title: Nat Rev Neurosci doi: 10.1038/nrn1518 – ident: 1707_CR39 – volume: 192 start-page: 931 issue: 9 year: 1996 ident: 1707_CR5 publication-title: Pathol Res Pract doi: 10.1016/S0344-0338(96)80075-6 – volume: 25 start-page: 325 issue: 2 year: 2021 ident: 1707_CR35 publication-title: IEEE J Biomed Health Inform doi: 10.1109/JBHI.2020.3032060 – ident: 1707_CR38 doi: 10.1007/978-3-031-33658-4_21 – ident: 1707_CR25 doi: 10.1145/3544548.3580694 – volume: 106 start-page: 348 issue: 6 year: 1997 ident: 1707_CR13 publication-title: Chromosoma doi: 10.1007/s004120050256 – volume: 14 year: 2023 ident: 1707_CR28 publication-title: J Pathol Inform doi: 10.1016/j.jpi.2023.100316 – volume: 7 start-page: 417 issue: 1 year: 2020 ident: 1707_CR31 publication-title: Sci Data doi: 10.1038/s41597-020-00756-z – volume: 18 start-page: 1067 issue: 8 year: 2005 ident: 1707_CR4 publication-title: Mod Pathol doi: 10.1038/modpathol.3800388 – volume: 128 start-page: 118 issue: 1 year: 2007 ident: 1707_CR16 publication-title: Am J Clin Pathol doi: 10.1309/HXUNAG34B3CEFDU8 – volume-title: Medical image computing and computer assisted intervention - MICCAI 2020 year: 2020 ident: 1707_CR37 – volume: 6 start-page: 274 issue: 1 year: 2019 ident: 1707_CR30 publication-title: Sci Data doi: 10.1038/s41597-019-0290-4 – volume: 49 start-page: 689 issue: 5 year: 1978 ident: 1707_CR40 publication-title: J Neurosurg doi: 10.3171/jns.1978.49.5.0689 – volume: 131 start-page: 903 issue: 6 year: 2016 ident: 1707_CR43 publication-title: Acta Neuropathol doi: 10.1007/s00401-015-1519-8 – volume: 11 start-page: 6215 issue: 1 year: 2021 ident: 1707_CR46 publication-title: Sci Rep doi: 10.1038/s41598-021-85652-1 – volume: 23 start-page: 1231 issue: 8 year: 2021 ident: 1707_CR2 publication-title: Neuro Oncol doi: 10.1093/neuonc/noab106 – volume: 17 start-page: 663 issue: 5 year: 2015 ident: 1707_CR14 publication-title: Neuro Oncol doi: 10.1093/neuonc/nov002 – volume: 99 issue: 9 year: 2020 ident: 1707_CR11 publication-title: Medicine doi: 10.1097/MD.0000000000018644 |
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Snippet | Mitosis is a critical criterion for meningioma grading. However, pathologists’ assessment of mitoses is subject to significant inter-observer variation due to... Mitosis is a critical criterion for meningioma grading. However, pathologists' assessment of mitoses is subject to significant inter-observer variation due to... Abstract Mitosis is a critical criterion for meningioma grading. However, pathologists’ assessment of mitoses is subject to significant inter-observer... |
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SubjectTerms | Algorithms Annotations Artificial Intelligence Brain cancer Depth-first search Digital pathology Humans Meningeal Neoplasms - pathology Meningioma Meningioma - pathology Mitosis Mitotic Index - methods Pathologist group decision Pathology Tumors |
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Title | Enhancing mitosis quantification and detection in meningiomas with computational digital pathology |
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