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Radiogenomics for predicting p53 status, PD-L1 expression, and prognosis with machine learning in pancreatic cancer

BACKGROUND: Radiogenomics is an emerging field that integrates “Radiomics” and “Genomics”. In the current study, we aimed to predict the genetic information of pancreatic tumours in a simple, inexpensive, and non-invasive manner, using cancer imaging analysis and radiogenomics. We focused on p53 mut...

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Autores principales: Iwatate, Yosuke, Hoshino, Isamu, Yokota, Hajime, Ishige, Fumitaka, Itami, Makiko, Mori, Yasukuni, Chiba, Satoshi, Arimitsu, Hidehito, Yanagibashi, Hiroo, Nagase, Hiroki, Takayama, Wataru
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7555500/
https://www.ncbi.nlm.nih.gov/pubmed/32690867
http://dx.doi.org/10.1038/s41416-020-0997-1
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author Iwatate, Yosuke
Hoshino, Isamu
Yokota, Hajime
Ishige, Fumitaka
Itami, Makiko
Mori, Yasukuni
Chiba, Satoshi
Arimitsu, Hidehito
Yanagibashi, Hiroo
Nagase, Hiroki
Takayama, Wataru
author_facet Iwatate, Yosuke
Hoshino, Isamu
Yokota, Hajime
Ishige, Fumitaka
Itami, Makiko
Mori, Yasukuni
Chiba, Satoshi
Arimitsu, Hidehito
Yanagibashi, Hiroo
Nagase, Hiroki
Takayama, Wataru
author_sort Iwatate, Yosuke
collection PubMed
description BACKGROUND: Radiogenomics is an emerging field that integrates “Radiomics” and “Genomics”. In the current study, we aimed to predict the genetic information of pancreatic tumours in a simple, inexpensive, and non-invasive manner, using cancer imaging analysis and radiogenomics. We focused on p53 mutations, which are highly implicated in pancreatic ductal adenocarcinoma (PDAC), and PD-L1, a biomarker for immune checkpoint inhibitor-based therapies. METHODS: Overall, 107 patients diagnosed with PDAC were retrospectively examined. The relationship between p53 mutations as well as PD-L1 abnormal expression and clinicopathological factors was investigated using immunohistochemistry. Imaging features (IFs) were extracted from CT scans and were used to create prediction models of p53 and PD-L1 status. RESULTS: We found that p53 and PD-L1 are significant independent prognostic factors (P = 0.008, 0.013, respectively). The area under the curve for p53 and PD-L1 predictive models was 0.795 and 0.683, respectively. Radiogenomics-predicted p53 mutations were significantly associated with poor prognosis (P = 0.015), whereas the predicted abnormal expression of PD-L1 was not significant (P = 0.096). CONCLUSIONS: Radiogenomics could predict p53 mutations and in turn the prognosis of PDAC patients. Hence, prediction of genetic information using radiogenomic analysis may aid in the development of precision medicine.
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spelling pubmed-75555002021-07-21 Radiogenomics for predicting p53 status, PD-L1 expression, and prognosis with machine learning in pancreatic cancer Iwatate, Yosuke Hoshino, Isamu Yokota, Hajime Ishige, Fumitaka Itami, Makiko Mori, Yasukuni Chiba, Satoshi Arimitsu, Hidehito Yanagibashi, Hiroo Nagase, Hiroki Takayama, Wataru Br J Cancer Article BACKGROUND: Radiogenomics is an emerging field that integrates “Radiomics” and “Genomics”. In the current study, we aimed to predict the genetic information of pancreatic tumours in a simple, inexpensive, and non-invasive manner, using cancer imaging analysis and radiogenomics. We focused on p53 mutations, which are highly implicated in pancreatic ductal adenocarcinoma (PDAC), and PD-L1, a biomarker for immune checkpoint inhibitor-based therapies. METHODS: Overall, 107 patients diagnosed with PDAC were retrospectively examined. The relationship between p53 mutations as well as PD-L1 abnormal expression and clinicopathological factors was investigated using immunohistochemistry. Imaging features (IFs) were extracted from CT scans and were used to create prediction models of p53 and PD-L1 status. RESULTS: We found that p53 and PD-L1 are significant independent prognostic factors (P = 0.008, 0.013, respectively). The area under the curve for p53 and PD-L1 predictive models was 0.795 and 0.683, respectively. Radiogenomics-predicted p53 mutations were significantly associated with poor prognosis (P = 0.015), whereas the predicted abnormal expression of PD-L1 was not significant (P = 0.096). CONCLUSIONS: Radiogenomics could predict p53 mutations and in turn the prognosis of PDAC patients. Hence, prediction of genetic information using radiogenomic analysis may aid in the development of precision medicine. Nature Publishing Group UK 2020-07-21 2020-10-13 /pmc/articles/PMC7555500/ /pubmed/32690867 http://dx.doi.org/10.1038/s41416-020-0997-1 Text en © The Author(s), under exclusive licence to Cancer Research UK 2020 https://creativecommons.org/licenses/by/4.0/Note This work is published under the standard license to publish agreement. After 12 months the work will become freely available and the license terms will switch to a Creative Commons Attribution 4.0 International (CC BY 4.0).
spellingShingle Article
Iwatate, Yosuke
Hoshino, Isamu
Yokota, Hajime
Ishige, Fumitaka
Itami, Makiko
Mori, Yasukuni
Chiba, Satoshi
Arimitsu, Hidehito
Yanagibashi, Hiroo
Nagase, Hiroki
Takayama, Wataru
Radiogenomics for predicting p53 status, PD-L1 expression, and prognosis with machine learning in pancreatic cancer
title Radiogenomics for predicting p53 status, PD-L1 expression, and prognosis with machine learning in pancreatic cancer
title_full Radiogenomics for predicting p53 status, PD-L1 expression, and prognosis with machine learning in pancreatic cancer
title_fullStr Radiogenomics for predicting p53 status, PD-L1 expression, and prognosis with machine learning in pancreatic cancer
title_full_unstemmed Radiogenomics for predicting p53 status, PD-L1 expression, and prognosis with machine learning in pancreatic cancer
title_short Radiogenomics for predicting p53 status, PD-L1 expression, and prognosis with machine learning in pancreatic cancer
title_sort radiogenomics for predicting p53 status, pd-l1 expression, and prognosis with machine learning in pancreatic cancer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7555500/
https://www.ncbi.nlm.nih.gov/pubmed/32690867
http://dx.doi.org/10.1038/s41416-020-0997-1
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