Validation of the Enriching New-Onset Diabetes for Pancreatic Cancer Model; A Retrospective Cohort Study Using Real-World Data

Ben Boursi, Tal Patalon, Muriel Webb, Ofer Margalit, Tamar Beller, Yu Xiao Yang, Gabriel Chodick

Research output: Contribution to journalArticlepeer-review

Abstract

Objectives: The Enriching New-onset Diabetes for Pancreatic Cancer (END-PAC) model identified patients at high-risk for pancreatic ductal adenocarcinoma (PDAC) more than 6 months before diagnosis. The current study aimed to validate the END-PAC model using a large, state-mandated health care provider database. Methods: A retrospective cohort study of patients older than 50 years that had a diagnosis of new-onset diabetes (NOD) between 2006 and 2015. A risk score was assigned according to the END-PAC model. Patients who developed PDAC over the 3-year period after NOD diagnosis were identified using the Israeli National Cancer Registry. Results: Twenty-three percent (1245/5408) of NOD patients were classified as high-risk, of them 32 (2.6%) developed PDAC. Median follow-up time from NOD detection to PDAC diagnosis was 609 days (interquartile range, 367–997). The hazard ratio for PDAC diagnosis among individuals at the high-risk group compared with the low-risk group was 5.70 (95% confidence interval, 2.93–11.06). Using the high-risk group as the screening threshold, the sensitivity, specificity, positive predictive value and negative predictive value of the model were 54.2%, 76.98%, 2.57%, and 99.4%, respectively. Area under the curve of the model was 0.69. Conclusions: Our findings support the robustness, generalizability and clinical applicability of the END-PAC model.

Original languageEnglish
Pages (from-to)196-199
Number of pages4
JournalPancreas
Volume51
Issue number2
DOIs
StatePublished - 1 Feb 2022

Keywords

  • END-PAC
  • new-onset diabetes
  • pancreatic cancer
  • validation (Pancreas 2022;51: 196–199)

All Science Journal Classification (ASJC) codes

  • Internal Medicine
  • Endocrinology, Diabetes and Metabolism
  • Hepatology
  • Endocrinology

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