Family History of Cancer in Benign Brain Tumor Subtypes Versus Gliomas

Quinn T. Ostrom(Case Comprehensive Cancer Center), Christopher J. McCulloh(Case Western Reserve University), Yanwen Chen(Case Comprehensive Cancer Center), Karen Devine(Case Comprehensive Cancer Center), Yingli Wolinsky(Case Comprehensive Cancer Center), Perica Davitkov(Case Comprehensive Cancer Center), Sarah Robbins(Case Western Reserve University), Rajesh Cherukuri(Case Comprehensive Cancer Center), Ashokkumar A. Patel(Case Comprehensive Cancer Center), Rajnish A. Gupta(Case Western Reserve University), Mark L. Cohen(Case Western Reserve University), Jaime Vengoechea Barrios(University Hospitals Case Medical Center), Cathy Brewer(Cleveland Clinic), Cathy Schilero(Cleveland Clinic), Kathy Smolenski(Cleveland Clinic), Mary McGraw(Cleveland Clinic), B. Denk(Cleveland Clinic), Theresa Naska(Cleveland Clinic), Frances Laube(University of Cincinnati Medical Center), Ruth Steele(University of Cincinnati Medical Center), Dale Greene(University of Cincinnati Medical Center), Alison Kastl(University of Cincinnati Medical Center), Susan D. Bell(The Ohio State University), Dina Aziz(The Ohio State University), E. Antonio Chiocca(The Ohio State University), Christopher McPherson(University of Cincinnati Medical Center), Ronald E. Warnick(University of Cincinnati Medical Center), Gene H. Barnett(Cleveland Clinic), Andrew E. Sloan(Case Western Reserve University), Jill S. Barnholtz‐Sloan(Case Comprehensive Cancer Center)
Frontiers in Oncology
January 1, 2012
Cited by 28Open Access
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Abstract

Purpose: Family history is associated with gliomas, but this association has not ben established for benign brain tumors. Using information from newly diagnosed primary brain tumor patients, we describe patterns of family cancer histories in patients with benign brain tumors and compare those to patients with gliomas. Methods: Newly diagnosed primary brain tumor patients were identified as part of the Ohio Brain Tumor Study (OBTS). Each patient was asked to participate in a telephone interview about personal medical history, family history of cancer, and other exposures. Information was available from 33 acoustic neuroma (65%), 78 meningioma (65%), 49 pituitary adenoma (73.1%) and 152 glioma patients (58.2%). The association between family history of cancer and each subtype was compared with gliomas using unconditional logistic regression models generating odds ratios (ORs) and 95% confidence intervals (95% CI). Results: There was no significant difference in family history of cancer between patients with glioma and benign subtypes. Conclusions: The results suggest that benign brain tumor may have an association with family history of cancer. More studies are warranted to disentangle the potential genetic and/or environmental causes for these diseases.


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