PT - JOURNAL ARTICLE AU - Le, Hoa AU - Ziogas, Argyrios AU - Rhee, Jessica M. AU - Lee, John G. AU - Lipkin, Steven M. AU - Zell, Jason A. TI - A Population-Based, Descriptive Analysis of Malignant Intraductal Papillary Mucinous Neoplasms of the Pancreas AID - 10.1158/1055-9965.EPI-08-0417 DP - 2008 Oct 01 TA - Cancer Epidemiology Biomarkers & Prevention PG - 2737--2741 VI - 17 IP - 10 4099 - http://cebp.aacrjournals.org/content/17/10/2737.short 4100 - http://cebp.aacrjournals.org/content/17/10/2737.full SO - Cancer Epidemiol Biomarkers Prev2008 Oct 01; 17 AB - Background: Intraductal papillary mucinous neoplasms (IPMN) are distinct precursor lesions that can progress to pancreatic adenocarcinoma; thus, it has been of particular interest to cancer prevention researchers. We set out to do a population-based analysis of malignant IPMNs compared with other pancreatic subtypes to better delineate its characteristics and explore implications for prevention and management. Methods: We conducted a case-only analysis of California Cancer Registry data (2000-2007), including descriptive analysis of relevant clinical variables. Overall survival univariate analyses were conducted using the Kaplan-Meier method. Multivariate survival analyses were done using Cox proportional hazards ratios. Results: Overall, 15,296 pancreatic cancer cases were identified, including incident cases of 10,186 adenocarcinomas, 880 mucinous tumors, 568 endocrine tumors, 3,619 carcinoma not otherwise specified tumors, and 43 malignant IPMNs. Thirty-three (80.5%) IPMN cases had localized disease at presentation, eight had regional disease (19.5%), and no IPMNs were identified with distant disease (two were unstaged). Five-year overall survival was better for malignant IPMN cases (65%) compared with pancreatic endocrine tumors (30%), mucinous tumors (5%), carcinoma not otherwise specified (2%), and adenocarcinoma cases (2%). Compared with adenocarcinoma cases, malignant IPMN cases (hazard ratio = 0.19; 95% CI, 0.10-0.35), endocrine tumors (hazard ratio = 0.28; 95% CI, 0.25-0.32), and mucinous tumors (hazard ratio = 0.84; 95% CI, 0.77-0.90) had higher overall survival in a multivariate survival analysis after adjustment for age, gender, stage, race, socioeconomic status, surgery, chemotherapy, and radiation therapy. Conclusions: Pancreatic malignant IPMNs represent an uncommon pancreatic tumor subtype, uniquely characterized by early stage at presentation and better survival. (Cancer Epidemiol Biomarkers Prev 2008;17(10):2737–41)