TY - JOUR
T1 - Anatomic site-specific disparities in survival outcomes for penile squamous cell carcinoma
AU - Tyson, Mark D.
AU - Etzioni, David A.
AU - Wisenbaugh, Eric S.
AU - Andrews, Paul E.
AU - Humphreys, Mitchell R.
AU - Ferrigni, Robert G.
AU - Swanson, Scott K.
AU - Castle, Erik P.
N1 - Copyright:
Copyright 2012 Elsevier B.V., All rights reserved.
PY - 2012/4
Y1 - 2012/4
N2 - Objective: To identify the predictors of cancer-specific mortality of penile squamous cell carcinoma (PSCC) using a population-based database. Methods: Using data from the National Cancer Institute's Surveillance, Epidemiology, and End Results registry, we performed a time-to-event analysis to determine which clinical parameters were useful in predicting cancer-specific mortality. Results: Our cohort consisted of 2515 cases of PSCC diagnosed from 1973 to 2007. The patients were divided into 2 groups: primary tumors of the prepuce (n = 722) and primary tumors of the glans, body, and overlapping lesions of the skin (n = 1793). The median follow-up for the cohort was 39 months (range 1-411). Compared with tumors of the prepuce, tumors of the body (hazard ratio 1.61, 95% confidence interval 1.00-2.60, P =.05) and overlapping tumors of the skin (hazard ratio 1.79, 95% confidence interval 1.13-2.83, P =.01) had a greater risk of cancer-specific mortality, even when controlling for age, Surveillance, Epidemiology, and End Results stage, and tumor grade. Furthermore, the disease-specific 10-year survival rate of those with preputial tumors was 89.4% compared with 78.7% for the other 3 groups combined (P <.0001). Conclusion: Anatomic site-specific disparities for PSCC survival appear to exist. Patients diagnosed with PSCC of the prepuce have greater overall long-term disease-specific survival than patients with primary tumors elsewhere.
AB - Objective: To identify the predictors of cancer-specific mortality of penile squamous cell carcinoma (PSCC) using a population-based database. Methods: Using data from the National Cancer Institute's Surveillance, Epidemiology, and End Results registry, we performed a time-to-event analysis to determine which clinical parameters were useful in predicting cancer-specific mortality. Results: Our cohort consisted of 2515 cases of PSCC diagnosed from 1973 to 2007. The patients were divided into 2 groups: primary tumors of the prepuce (n = 722) and primary tumors of the glans, body, and overlapping lesions of the skin (n = 1793). The median follow-up for the cohort was 39 months (range 1-411). Compared with tumors of the prepuce, tumors of the body (hazard ratio 1.61, 95% confidence interval 1.00-2.60, P =.05) and overlapping tumors of the skin (hazard ratio 1.79, 95% confidence interval 1.13-2.83, P =.01) had a greater risk of cancer-specific mortality, even when controlling for age, Surveillance, Epidemiology, and End Results stage, and tumor grade. Furthermore, the disease-specific 10-year survival rate of those with preputial tumors was 89.4% compared with 78.7% for the other 3 groups combined (P <.0001). Conclusion: Anatomic site-specific disparities for PSCC survival appear to exist. Patients diagnosed with PSCC of the prepuce have greater overall long-term disease-specific survival than patients with primary tumors elsewhere.
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U2 - 10.1016/j.urology.2011.12.047
DO - 10.1016/j.urology.2011.12.047
M3 - Article
C2 - 22381248
AN - SCOPUS:84859422988
SN - 0090-4295
VL - 79
SP - 804
EP - 808
JO - Urology
JF - Urology
IS - 4
ER -