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Multicenter Study
. 2023 Feb;12(3):2505-2513.
doi: 10.1002/cam4.5094. Epub 2022 Jul 31.

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

Affiliations
Multicenter Study

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

Ritu R Singh et al. Cancer Med. 2023 Feb.

Abstract

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.

Keywords: acute pancreatitis; database; pancreas ductal adenocarcinoma; pancreatic neoplasm.

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Conflict of interest statement

Ritu R. Singh: None; Neil R. Sharma: Consultant for Boston Scientific, Medtronic, Mauna Kea, Steris medical; Eileen M. O'Reilly: Research Funding to MSK: Genentech/Roche, Celgene/BMS, BioNTech, AstraZeneca, Arcus, Elicio, Parker Institute; Consulting/DSMB: Cytomx Therapeutics (DSMB), Rafael Therapeutics (DSMB), Seagen, Boehringer Ingelheim, BioNTech, Ipsen, Merck, IDEAYA, Novartis, AstraZeneca, Noxxon, BioSapien, Novartis, Cend Therapeutics, Thetis, Autem, Agios (spouse), Genentech‐Roche (spouse), Eisai (spouse).

Figures

FIGURE 1
FIGURE 1
Consort flow diagram of database search and results.
FIGURE 2
FIGURE 2
(A) Incidence of pancreatic adenocarcinoma in patients with acute pancreatitis. (B) Probability of developing pancreatic adenocarcinoma each year after acute pancreatitis.
FIGURE 3
FIGURE 3
Image depicting location of pancreatic adenocarcinoma within the pancreas in patients with acute pancreatitis.

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