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Predictive performance of factors associated with malignancy in intraductal papillary mucinous neoplasia of the pancreas

BACKGROUND: Estimation of the risk of malignancy in intraductal papillary mucinous neoplasia (IPMN) of the pancreas is a clinical challenge. Several routinely used clinical factors form the basis of the current consensus guidelines. This study aimed to determine the predictive values of the most com...

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Autores principales: Heckler, M., Brieger, L., Heger, U., Pausch, T., Tjaden, C., Kaiser, J., Tanaka, M., Hackert, T., Michalski, C. W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Ltd 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5989990/
https://www.ncbi.nlm.nih.gov/pubmed/29951625
http://dx.doi.org/10.1002/bjs5.38
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author Heckler, M.
Brieger, L.
Heger, U.
Pausch, T.
Tjaden, C.
Kaiser, J.
Tanaka, M.
Hackert, T.
Michalski, C. W.
author_facet Heckler, M.
Brieger, L.
Heger, U.
Pausch, T.
Tjaden, C.
Kaiser, J.
Tanaka, M.
Hackert, T.
Michalski, C. W.
author_sort Heckler, M.
collection PubMed
description BACKGROUND: Estimation of the risk of malignancy in intraductal papillary mucinous neoplasia (IPMN) of the pancreas is a clinical challenge. Several routinely used clinical factors form the basis of the current consensus guidelines. This study aimed to determine the predictive values of the most commonly assessed risk factors. METHODS: A meta‐analysis of individual risk factors of malignancy in IPMN was performed. Contingency tables were derived from these data, and sensitivity, specificity, negative and positive predictive values, and diagnostic odds ratios (DOR) were determined. Hierarchical summary receiver operating characteristic (HSROC) curves for each factor were calculated and the respective area under the curve (AUC) was assessed. RESULTS: A total of 3443 studies were screened initially. Analysis of recent literature revealed 60 studies with 13 relevant risk factors including clinical, serological and radiological parameters. The largest area under the HSROC curve was found for weight loss (0·84) and jaundice/raised bilirubin level (0·80), followed by increased carcinoembryonic antigen (CEA) (0·79) or carbohydrate antigen (CA) 19‐9 (0·78) levels. The most sensitive factors were patient age (71 per cent) and mural nodules (65 per cent), and jaundice/raised bilirubin level (97 per cent) and increased CEA level (95 per cent) were most specific. None of the analysed factors reached a positive or negative level of prediction beyond 90 per cent. CONCLUSION: None of the established criteria safely distinguishes malignant from non‐malignant lesions.
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spelling pubmed-59899902018-06-27 Predictive performance of factors associated with malignancy in intraductal papillary mucinous neoplasia of the pancreas Heckler, M. Brieger, L. Heger, U. Pausch, T. Tjaden, C. Kaiser, J. Tanaka, M. Hackert, T. Michalski, C. W. BJS Open Systematic Reviews BACKGROUND: Estimation of the risk of malignancy in intraductal papillary mucinous neoplasia (IPMN) of the pancreas is a clinical challenge. Several routinely used clinical factors form the basis of the current consensus guidelines. This study aimed to determine the predictive values of the most commonly assessed risk factors. METHODS: A meta‐analysis of individual risk factors of malignancy in IPMN was performed. Contingency tables were derived from these data, and sensitivity, specificity, negative and positive predictive values, and diagnostic odds ratios (DOR) were determined. Hierarchical summary receiver operating characteristic (HSROC) curves for each factor were calculated and the respective area under the curve (AUC) was assessed. RESULTS: A total of 3443 studies were screened initially. Analysis of recent literature revealed 60 studies with 13 relevant risk factors including clinical, serological and radiological parameters. The largest area under the HSROC curve was found for weight loss (0·84) and jaundice/raised bilirubin level (0·80), followed by increased carcinoembryonic antigen (CEA) (0·79) or carbohydrate antigen (CA) 19‐9 (0·78) levels. The most sensitive factors were patient age (71 per cent) and mural nodules (65 per cent), and jaundice/raised bilirubin level (97 per cent) and increased CEA level (95 per cent) were most specific. None of the analysed factors reached a positive or negative level of prediction beyond 90 per cent. CONCLUSION: None of the established criteria safely distinguishes malignant from non‐malignant lesions. John Wiley & Sons, Ltd 2018-02-05 /pmc/articles/PMC5989990/ /pubmed/29951625 http://dx.doi.org/10.1002/bjs5.38 Text en © 2018 The Authors. BJS Open published by John Wiley & Sons Ltd on behalf of BJS Society Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Systematic Reviews
Heckler, M.
Brieger, L.
Heger, U.
Pausch, T.
Tjaden, C.
Kaiser, J.
Tanaka, M.
Hackert, T.
Michalski, C. W.
Predictive performance of factors associated with malignancy in intraductal papillary mucinous neoplasia of the pancreas
title Predictive performance of factors associated with malignancy in intraductal papillary mucinous neoplasia of the pancreas
title_full Predictive performance of factors associated with malignancy in intraductal papillary mucinous neoplasia of the pancreas
title_fullStr Predictive performance of factors associated with malignancy in intraductal papillary mucinous neoplasia of the pancreas
title_full_unstemmed Predictive performance of factors associated with malignancy in intraductal papillary mucinous neoplasia of the pancreas
title_short Predictive performance of factors associated with malignancy in intraductal papillary mucinous neoplasia of the pancreas
title_sort predictive performance of factors associated with malignancy in intraductal papillary mucinous neoplasia of the pancreas
topic Systematic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5989990/
https://www.ncbi.nlm.nih.gov/pubmed/29951625
http://dx.doi.org/10.1002/bjs5.38
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