The Impact of Serum Glucose in the Treatment of Locoregionally Advanced Pancreatic Cancer.


Journal

American journal of clinical oncology
ISSN: 1537-453X
Titre abrégé: Am J Clin Oncol
Pays: United States
ID NLM: 8207754

Informations de publication

Date de publication:
09 2019
Historique:
pubmed: 25 7 2019
medline: 21 3 2020
entrez: 24 7 2019
Statut: ppublish

Résumé

Studies have consistently identified an increased risk of pancreatic cancer in diabetics, yet the role hyperglycemia may play in predicting prognosis is less clear. This work aims to evaluate the impact of glycemic state and antidiabetics on outcomes after systemic and local treatment for locoregionally advanced pancreatic cancer. This retrospective study consisted of 303 patients with newly diagnosed advanced-stage pancreatic cancer treated from 2004 to 2014. Kaplan-Meier survival analysis method was used to estimate time to event for overall survival, distant metastasis, and locoregional control. Blood glucose values (n=8599) were assessed both as continuous and categorical variables in univariate and multivariable Cox proportional hazard regression models to estimate hazard ratios (HRs) and identify independent prognostic factors. A 6-month conditional landmark analysis excluding patients with <6 months follow-up or survival was conducted. Median follow-up and survival was 18.1 and 18.4 months, respectively. On univariate analysis, maximum pretreatment glucose value was associated with reduced overall survival (HR 1.005, P=0.023) and locoregional control (HR 1.001, P=0.001). A pretreatment glucose value ≥200 mg/dL was associated with increased mortality in multivariable analysis (adjusted HR 1.01, P=0.015). After conditional analysis, glucose ≥200 mg/dL before local treatment was associated with reduced overall survival (adjusted HR 1.562; 95% confidence interval [CI], 1.16-2.11; P=0.003). Elevated blood glucose before treatment of locoregionally advanced pancreatic cancer was associated with poorer outcomes. These findings should be incorporated in future clinical trial design.

Identifiants

pubmed: 31335348
doi: 10.1097/COC.0000000000000580
pmc: PMC6710125
mid: NIHMS1533224
doi:

Substances chimiques

Blood Glucose 0

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

692-697

Subventions

Organisme : NIDDK NIH HHS
ID : P30 DK079307
Pays : United States
Organisme : NIDDK NIH HHS
ID : T35 DK065521
Pays : United States

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Auteurs

Nick A Iarrobino (NA)

University of Pittsburgh School of Medicine.

Beant S Gill (BS)

Department of Radiation Oncology, University of Pittsburgh Medical Center, Pittsburgh, PA.

Rainer J Klement (RJ)

Department of Radiation Oncology, Leopoldina Hospital, Schweinfurt, Germany.

Mark E Bernard (ME)

Department of Radiation Medicine, University of Kentucky, Lexington, KY.

Colin E Champ (CE)

Department of Radiation Oncology, University of Pittsburgh Medical Center, Pittsburgh, PA.

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Classifications MeSH