Colette A Whitney1, Lauren E Howard1,2, Christopher L Amling3, William J Aronson4,5, Matthew R Cooperberg6, Christopher J Kane7, Martha K Terris8, Stephen J Freedland1,9. 1. Urology Section, Veterans Affairs Medical Center, Durham, North Carolina. 2. Department of Biostatistics and Bioinformatics, Duke University School of Medicine, Durham, North Carolina. 3. Division of Urology, Department of Surgery, Oregon Health and Science University, Portland, Oregon. 4. Urology Section, Department of Surgery, Veterans Affairs Medical Center, Greater Los Angeles, Los Angeles, California. 5. Department of Urology, University of California at Los Angeles Medical Center, Los Angeles, California. 6. Department of Urology, University of California at San Francisco Helen Diller Family Comprehensive Cancer Center, San Francisco, California. 7. Division of Urology, Department of Surgery, University of California at San Diego Medical Center, San Diego, California. 8. Urology Section, Division of Surgery, Veterans Affairs Medical Center and Division of Urologic Surgery, Department of Surgery, Medical College of Georgia, Augusta, Georgia. 9. Department of Surgery, Division of Urology and Samuel Oschin Comprehensive Cancer Institute, Cedars-Sinai Medical Center, Los Angeles, California.
Abstract
BACKGROUND: Although race is associated with prostate cancer progression in early stage disease, once men have advanced disease, it is unclear whether race continues to predict a poor outcome. The authors hypothesized that, in an equal-access setting among patients with castration-resistant prostate cancer (CRPC) and no known metastases (M0/Mx), black men would receive imaging tests at similar rates as nonblack men (ie, there would be an equal opportunity to detect metastases) but would have a higher risk of metastatic disease. METHODS: In total, 837 men who were diagnosed with M0/Mx CRPC during 2000 through 2014 from 5 Veterans Affairs hospitals in the SEARCH (Shared Equal Access Regional Cancer Hospital) database were analyzed. Data on all imaging tests after CRPC diagnosis were collected, including date, type, and outcome. Multivariable Cox models were used to test associations between race and the time to first metastasis, first bone metastasis, first bone scan, second bone scan among men who had a negative first bone scan, and overall survival. RESULTS: Black men (n = 306) were equally as likely as nonblack men (n = 531) to receive a first and second bone scan after a diagnosis of CRPC. There were no significant differences in the risk of developing any metastases, bone metastases, time to bone scans, or overall survival between black men and nonblack men (all P > .2). CONCLUSIONS: The lack of racial differences in the development of metastases and scanning practices observed in this study suggests that, once men have a diagnosis of M0/Mx CRPC, race may not be a prognostic factor. Efforts to understand prostate cancer racial disparities may derive greater benefit by focusing on the risk of developing prostate cancer and on the outcomes of men who have early stage disease. Cancer 2016;122:3848-3855.
BACKGROUND: Although race is associated with prostate cancer progression in early stage disease, once men have advanced disease, it is unclear whether race continues to predict a poor outcome. The authors hypothesized that, in an equal-access setting among patients with castration-resistant prostate cancer (CRPC) and no known metastases (M0/Mx), black men would receive imaging tests at similar rates as nonblack men (ie, there would be an equal opportunity to detect metastases) but would have a higher risk of metastatic disease. METHODS: In total, 837 men who were diagnosed with M0/Mx CRPC during 2000 through 2014 from 5 Veterans Affairs hospitals in the SEARCH (Shared Equal Access Regional Cancer Hospital) database were analyzed. Data on all imaging tests after CRPC diagnosis were collected, including date, type, and outcome. Multivariable Cox models were used to test associations between race and the time to first metastasis, first bone metastasis, first bone scan, second bone scan among men who had a negative first bone scan, and overall survival. RESULTS: Black men (n = 306) were equally as likely as nonblack men (n = 531) to receive a first and second bone scan after a diagnosis of CRPC. There were no significant differences in the risk of developing any metastases, bone metastases, time to bone scans, or overall survival between black men and nonblack men (all P > .2). CONCLUSIONS: The lack of racial differences in the development of metastases and scanning practices observed in this study suggests that, once men have a diagnosis of M0/Mx CRPC, race may not be a prognostic factor. Efforts to understand prostate cancer racial disparities may derive greater benefit by focusing on the risk of developing prostate cancer and on the outcomes of men who have early stage disease. Cancer 2016;122:3848-3855.
Authors: Adriana C Vidal; Lauren E Howard; Amanda De Hoedt; Christopher J Kane; Martha K Terris; William J Aronson; Matthew R Cooperberg; Christopher L Amling; Stanislav Lechpammer; Scott C Flanders; Stephen J Freedland Journal: Cancer Date: 2018-11-14 Impact factor: 6.860
Authors: Brian T Hanyok; Mary M Everist; Lauren E Howard; Amanda M De Hoedt; William J Aronson; Matthew R Cooperberg; Christopher J Kane; Christopher L Amling; Martha K Terris; Stephen J Freedland Journal: Asian J Urol Date: 2019-01-18
Authors: Ashley W Johnston; Thomas A Longo; Leah Gerber Davis; Daniel Zapata; Stephen J Freedland; Jonathan C Routh Journal: Int Braz J Urol Date: 2020 Jan-Feb Impact factor: 1.541