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Does acute pancreatitis herald pancreatic ductal adenocarcinoma? A multicenter electronic health research network study

BACKGROUND AND OBJECTIVES: High mortality in pancreas ductal adenocarcinoma (PDAC) is related to delayed diagnosis and lack of cost‐effective early detection strategies. Retrospective studies have demonstrated an association between PDAC and acute pancreatitis (AP). Herein, we explore the incidence...

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Autores principales: Singh, Ritu R., Klein, Alison P., Sharma, Neil R., O'Reilly, Eileen M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9939170/
https://www.ncbi.nlm.nih.gov/pubmed/35909243
http://dx.doi.org/10.1002/cam4.5094
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author Singh, Ritu R.
Klein, Alison P.
Sharma, Neil R.
O'Reilly, Eileen M.
author_facet Singh, Ritu R.
Klein, Alison P.
Sharma, Neil R.
O'Reilly, Eileen M.
author_sort Singh, Ritu R.
collection PubMed
description BACKGROUND AND OBJECTIVES: High mortality in pancreas ductal adenocarcinoma (PDAC) is related to delayed diagnosis and lack of cost‐effective early detection strategies. Retrospective studies have demonstrated an association between PDAC and acute pancreatitis (AP). Herein, we explore the incidence of PDAC in patients with non‐biliary and non‐alcoholic AP. METHODS: A population‐based, retrospective cohort study was conducted utilizing TriNetX (Cambridge, MA). Patients ≥40 years with AP (ICD‐10‐CM code: K85) and without biliary AP (K85.1), alcohol‐induced AP (K85.2) or chronic pancreatitis (K86.0, K86.1), were identified. The primary outcome was incidence of PDAC (C25) in patients at defined intervals following AP. We compared the rate of early‐stage diagnosis (stage 1–2) and surgical resection among patients with and without preceding AP. RESULTS: The incidence of PDAC ranged from 2.16% (1 year) to 3.43% (5 years). Patients with PDAC and AP in preceding year were more likely to undergo surgical resection relative to those without AP (10.1% vs. 6.3%, risk ratio 1.62: 95% confidence interval, CI 1.47–1.79). Early‐stage diagnosis of PDAC was more frequent in patients with preceding AP; however, difference was insignificant (p = 0.48; 95% CI 0.64–2.58). CONCLUSION: AP is infrequently associated with PDAC and can precede a diagnosis of PDAC in a minority of patients without another known etiology of pancreatitis. Patients with a recent AP are more likely to undergo surgical resection of PDAC and a trend toward diagnosis at an earlier stage compared to patients with PDAC and without AP. The impact of AP‐related PDAC on survival is unknown.
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spelling pubmed-99391702023-02-20 Does acute pancreatitis herald pancreatic ductal adenocarcinoma? A multicenter electronic health research network study Singh, Ritu R. Klein, Alison P. Sharma, Neil R. O'Reilly, Eileen M. Cancer Med RESEARCH ARTICLES BACKGROUND AND OBJECTIVES: High mortality in pancreas ductal adenocarcinoma (PDAC) is related to delayed diagnosis and lack of cost‐effective early detection strategies. Retrospective studies have demonstrated an association between PDAC and acute pancreatitis (AP). Herein, we explore the incidence of PDAC in patients with non‐biliary and non‐alcoholic AP. METHODS: A population‐based, retrospective cohort study was conducted utilizing TriNetX (Cambridge, MA). Patients ≥40 years with AP (ICD‐10‐CM code: K85) and without biliary AP (K85.1), alcohol‐induced AP (K85.2) or chronic pancreatitis (K86.0, K86.1), were identified. The primary outcome was incidence of PDAC (C25) in patients at defined intervals following AP. We compared the rate of early‐stage diagnosis (stage 1–2) and surgical resection among patients with and without preceding AP. RESULTS: The incidence of PDAC ranged from 2.16% (1 year) to 3.43% (5 years). Patients with PDAC and AP in preceding year were more likely to undergo surgical resection relative to those without AP (10.1% vs. 6.3%, risk ratio 1.62: 95% confidence interval, CI 1.47–1.79). Early‐stage diagnosis of PDAC was more frequent in patients with preceding AP; however, difference was insignificant (p = 0.48; 95% CI 0.64–2.58). CONCLUSION: AP is infrequently associated with PDAC and can precede a diagnosis of PDAC in a minority of patients without another known etiology of pancreatitis. Patients with a recent AP are more likely to undergo surgical resection of PDAC and a trend toward diagnosis at an earlier stage compared to patients with PDAC and without AP. The impact of AP‐related PDAC on survival is unknown. John Wiley and Sons Inc. 2022-07-31 /pmc/articles/PMC9939170/ /pubmed/35909243 http://dx.doi.org/10.1002/cam4.5094 Text en © 2022 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle RESEARCH ARTICLES
Singh, Ritu R.
Klein, Alison P.
Sharma, Neil R.
O'Reilly, Eileen M.
Does acute pancreatitis herald pancreatic ductal adenocarcinoma? A multicenter electronic health research network study
title Does acute pancreatitis herald pancreatic ductal adenocarcinoma? A multicenter electronic health research network study
title_full Does acute pancreatitis herald pancreatic ductal adenocarcinoma? A multicenter electronic health research network study
title_fullStr Does acute pancreatitis herald pancreatic ductal adenocarcinoma? A multicenter electronic health research network study
title_full_unstemmed Does acute pancreatitis herald pancreatic ductal adenocarcinoma? A multicenter electronic health research network study
title_short Does acute pancreatitis herald pancreatic ductal adenocarcinoma? A multicenter electronic health research network study
title_sort does acute pancreatitis herald pancreatic ductal adenocarcinoma? a multicenter electronic health research network study
topic RESEARCH ARTICLES
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9939170/
https://www.ncbi.nlm.nih.gov/pubmed/35909243
http://dx.doi.org/10.1002/cam4.5094
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