Literature DB >> 25220626

Diabetes mellitus and ovarian cancer: more complex than just increasing risk.

Monjri M Shah1, Britt K Erickson2, Tasnia Matin3, Gerald McGwin4, Jovana Y Martin5, Laura Becca Daily5, Daniel Pasko5, Christen W Haygood2, Janelle M Fauci2, Charles A Leath2.   

Abstract

OBJECTIVE: Diabetes mellitus (DM) is a risk factor for endometrial cancer and is associated with poorer outcomes in breast and colon cancers. This association is less clear in epithelial ovarian cancer (EOC). We sought to examine the effect of DM on progression-free (PFS) and overall survival (OS) in women with EOC.
METHODS: A retrospective cohort study of EOC patients diagnosed between 2004 and 2009 at a single institution was performed. Demographic, pathologic and DM diagnosis data were abstracted. Pearson chi-square test and t test were used to compare variables. The Kaplan-Meier method and the log rank test were used to compare PFS and OS between non-diabetic (ND) and DM patients.
RESULTS: 62 (17%) of 367 patients had a diagnosis of DM. No differences in age, histology, debulking status, or administration of intraperitoneal chemotherapy between ND and DM patients were present, although there were more stage I and IV patients in the ND group (p=0.04). BMI was significantly different between the two groups (ND vs. DM, 27.5 vs. 30.7kg/m(2), p<0.001). While there were no differences in survival based on BMI, diabetic patients had a poorer PFS (10.3 vs. 16.3months, p=0.024) and OS (26.1 vs. 42.2months, p=0.005) compared to ND patients. Metformin use among diabetic patients did not appear to affect PFS or OS.
CONCLUSIONS: EOC patients with DM have poorer survival than patients without diabetes; this association is independent of obesity. Metformin use did not affect outcomes. The pathophysiology of this observation requires more inquiry.
Copyright © 2014 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Body mass index; Diabetes; Outcomes; Ovarian cancer

Mesh:

Substances:

Year:  2014        PMID: 25220626      PMCID: PMC4252660          DOI: 10.1016/j.ygyno.2014.09.004

Source DB:  PubMed          Journal:  Gynecol Oncol        ISSN: 0090-8258            Impact factor:   5.482


  39 in total

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