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Enhanced diagnostic accuracy for quantitative bone scan using an artificial neural network system: a Japanese multi-center database project

BACKGROUND: Artificial neural network (ANN)-based bone scan index (BSI), a marker of the amount of bone metastasis, has been shown to enhance diagnostic accuracy and reproducibility but is potentially affected by training databases. The aims of this study were to revise the software using a large nu...

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Autores principales: Nakajima, Kenichi, Nakajima, Yasuo, Horikoshi, Hiroyuki, Ueno, Munehisa, Wakabayashi, Hiroshi, Shiga, Tohru, Yoshimura, Mana, Ohtake, Eiji, Sugawara, Yoshifumi, Matsuyama, Hideyasu, Edenbrandt, Lars
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3877947/
https://www.ncbi.nlm.nih.gov/pubmed/24369784
http://dx.doi.org/10.1186/2191-219X-3-83
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author Nakajima, Kenichi
Nakajima, Yasuo
Horikoshi, Hiroyuki
Ueno, Munehisa
Wakabayashi, Hiroshi
Shiga, Tohru
Yoshimura, Mana
Ohtake, Eiji
Sugawara, Yoshifumi
Matsuyama, Hideyasu
Edenbrandt, Lars
author_facet Nakajima, Kenichi
Nakajima, Yasuo
Horikoshi, Hiroyuki
Ueno, Munehisa
Wakabayashi, Hiroshi
Shiga, Tohru
Yoshimura, Mana
Ohtake, Eiji
Sugawara, Yoshifumi
Matsuyama, Hideyasu
Edenbrandt, Lars
author_sort Nakajima, Kenichi
collection PubMed
description BACKGROUND: Artificial neural network (ANN)-based bone scan index (BSI), a marker of the amount of bone metastasis, has been shown to enhance diagnostic accuracy and reproducibility but is potentially affected by training databases. The aims of this study were to revise the software using a large number of Japanese databases and to validate its diagnostic accuracy compared with the original Swedish training database. METHODS: The BSI was calculated with EXINIbone (EB; EXINI Diagnostics) using the Swedish training database (n = 789). The software using Japanese training databases from a single institution (BONENAVI version 1, BN1, n = 904) and the revised version from nine institutions (version 2, BN2, n = 1,532) were compared. The diagnostic accuracy was validated with another 503 multi-center bone scans including patients with prostate (n = 207), breast (n = 166), and other cancer types. The ANN value (probability of abnormality) and BSI were calculated. Receiver operating characteristic (ROC) and net reclassification improvement (NRI) analyses were performed. RESULTS: The ROC analysis based on the ANN value showed significant improvement from EB to BN1 and BN2. In men (n = 296), the area under the curve (AUC) was 0.877 for EB, 0.912 for BN1 (p = not significant (ns) vs. EB) and 0.934 for BN2 (p = 0.007 vs. EB). In women (n = 207), the AUC was 0.831 for EB, 0.910 for BN1 (p = 0.016 vs. EB), and 0.932 for BN2 (p < 0.0001 vs. EB). The optimum sensitivity and specificity based on BN2 was 90% and 84% for men and 93% and 85% for women. In patients with prostate cancer, the AUC was equally high with EB, BN1, and BN2 (0.939, 0.949, and 0.957, p = ns). In patients with breast cancer, the AUC was improved from EB (0.847) to BN1 (0.910, p = ns) and BN2 (0.924, p = 0.039). The NRI using ANN between EB and BN1 was 17.7% (p = 0.0042), and that between EB and BN2 was 29.6% (p < 0.0001). With respect to BSI, the NRI analysis showed downward reclassification with total NRI of 31.9% ( p < 0.0001). CONCLUSION: In the software for calculating BSI, the multi-institutional database significantly improved identification of bone metastasis compared with the original database, indicating the importance of a sufficient number of training databases including various types of cancers.
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spelling pubmed-38779472014-01-03 Enhanced diagnostic accuracy for quantitative bone scan using an artificial neural network system: a Japanese multi-center database project Nakajima, Kenichi Nakajima, Yasuo Horikoshi, Hiroyuki Ueno, Munehisa Wakabayashi, Hiroshi Shiga, Tohru Yoshimura, Mana Ohtake, Eiji Sugawara, Yoshifumi Matsuyama, Hideyasu Edenbrandt, Lars EJNMMI Res Original Research BACKGROUND: Artificial neural network (ANN)-based bone scan index (BSI), a marker of the amount of bone metastasis, has been shown to enhance diagnostic accuracy and reproducibility but is potentially affected by training databases. The aims of this study were to revise the software using a large number of Japanese databases and to validate its diagnostic accuracy compared with the original Swedish training database. METHODS: The BSI was calculated with EXINIbone (EB; EXINI Diagnostics) using the Swedish training database (n = 789). The software using Japanese training databases from a single institution (BONENAVI version 1, BN1, n = 904) and the revised version from nine institutions (version 2, BN2, n = 1,532) were compared. The diagnostic accuracy was validated with another 503 multi-center bone scans including patients with prostate (n = 207), breast (n = 166), and other cancer types. The ANN value (probability of abnormality) and BSI were calculated. Receiver operating characteristic (ROC) and net reclassification improvement (NRI) analyses were performed. RESULTS: The ROC analysis based on the ANN value showed significant improvement from EB to BN1 and BN2. In men (n = 296), the area under the curve (AUC) was 0.877 for EB, 0.912 for BN1 (p = not significant (ns) vs. EB) and 0.934 for BN2 (p = 0.007 vs. EB). In women (n = 207), the AUC was 0.831 for EB, 0.910 for BN1 (p = 0.016 vs. EB), and 0.932 for BN2 (p < 0.0001 vs. EB). The optimum sensitivity and specificity based on BN2 was 90% and 84% for men and 93% and 85% for women. In patients with prostate cancer, the AUC was equally high with EB, BN1, and BN2 (0.939, 0.949, and 0.957, p = ns). In patients with breast cancer, the AUC was improved from EB (0.847) to BN1 (0.910, p = ns) and BN2 (0.924, p = 0.039). The NRI using ANN between EB and BN1 was 17.7% (p = 0.0042), and that between EB and BN2 was 29.6% (p < 0.0001). With respect to BSI, the NRI analysis showed downward reclassification with total NRI of 31.9% ( p < 0.0001). CONCLUSION: In the software for calculating BSI, the multi-institutional database significantly improved identification of bone metastasis compared with the original database, indicating the importance of a sufficient number of training databases including various types of cancers. Springer 2013-12-26 /pmc/articles/PMC3877947/ /pubmed/24369784 http://dx.doi.org/10.1186/2191-219X-3-83 Text en Copyright © 2013 Nakajima et al.; licensee Springer. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Nakajima, Kenichi
Nakajima, Yasuo
Horikoshi, Hiroyuki
Ueno, Munehisa
Wakabayashi, Hiroshi
Shiga, Tohru
Yoshimura, Mana
Ohtake, Eiji
Sugawara, Yoshifumi
Matsuyama, Hideyasu
Edenbrandt, Lars
Enhanced diagnostic accuracy for quantitative bone scan using an artificial neural network system: a Japanese multi-center database project
title Enhanced diagnostic accuracy for quantitative bone scan using an artificial neural network system: a Japanese multi-center database project
title_full Enhanced diagnostic accuracy for quantitative bone scan using an artificial neural network system: a Japanese multi-center database project
title_fullStr Enhanced diagnostic accuracy for quantitative bone scan using an artificial neural network system: a Japanese multi-center database project
title_full_unstemmed Enhanced diagnostic accuracy for quantitative bone scan using an artificial neural network system: a Japanese multi-center database project
title_short Enhanced diagnostic accuracy for quantitative bone scan using an artificial neural network system: a Japanese multi-center database project
title_sort enhanced diagnostic accuracy for quantitative bone scan using an artificial neural network system: a japanese multi-center database project
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3877947/
https://www.ncbi.nlm.nih.gov/pubmed/24369784
http://dx.doi.org/10.1186/2191-219X-3-83
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