Association of Long-Term, New-Onset, and Postsurgical Diabetes with Survival in Patients with Resectable Pancreatic Cancer: A Retrospective Cohort Study

Sarah Kanbour, Gayane Yenokyan, Mohammed Abusamaan, Daniel Laheru, Ayman Alam, Marie Line El Asmar, Zunaira Virk, Dylan Hardenbergh, Nestoras Mathioudakis

Research output: Contribution to journalArticlepeer-review

Abstract

Background Pancreatic ductal adenocarcinoma (PDAC) has a poor prognosis. Identifying modifiable risk factors, such as diabetes, is crucial. In the context of PDAC diagnosis, diabetes manifests as long-Term (LTD), new-onset (NOD), or postsurgical (PSD) phenotypes. The link between these diabetes phenotypes and PDAC survival is debated. Materials and Methods We performed a retrospective study on patients with resectable PDAC who underwent pancreatectomy at Johns Hopkins Hospital from 2003 to 2017. We utilized the National Death Index and electronic medical records to determine vital status. We categorized diabetes as LTD, NOD, or PSD based on the timing of diagnosis relative to pancreatic resection. Using multivariable Cox models, we assessed hazard ratios (HRs) for survival times associated with each phenotype, considering known PDAC prognostic factors. Results Of 1556 patients, the 5-year survival was 19% (95% CI, 17-21). No significant survival differences were observed between diabetes phenotypes and non-diabetic patients. NOD and PSD presented nonsignificant increased risks of death (aHR: 1.14 [95% CI, 0.8-1.19] and 1.05 [95% CI, 0.89-1.25], respectively). LTD showed no survival difference (aHR, 0.98; 95% CI, 0.99-1.31). Conclusions No link was found between diabetes phenotypes and survival in resectable PDAC patients. Comprehensive prospective studies are required to validate these results.

Original languageEnglish (US)
Pages (from-to)E309-E314
JournalPancreas
Volume52
Issue number6
DOIs
StatePublished - Jul 1 2023

Keywords

  • diabetes mellitus
  • resectable pancreatic ductal adenocarcinoma
  • survival analysis

ASJC Scopus subject areas

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

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