Literature DB >> 15963115

Racial differences in serum prostate-specific antigen (PSA) doubling time, histopathological variables and long-term PSA recurrence between African-American and white American men undergoing radical prostatectomy for clinically localized prostate cancer.

Ashutosh Tewari1, Wolfgang Horninger, Ketan K Badani, Mazen Hasan, Steven Coon, E David Crawford, Eduard J Gamito, John Wei, David Taub, James Montie, Chris Porter, George W Divine, Georg Bartsch, Mani Menon.   

Abstract

OBJECTIVE: To determine if there are significant differences in biochemical characteristics, biopsy variables, histopathological data, and rates of prostate-specific antigen (PSA) recurrence between African-American (AA) and white American (WA) men undergoing radical prostatectomy (RP), as AA men are twice as likely to die from prostate cancer than their white counterparts. PATIENTS AND METHODS: We established a cohort of 1058 patients (402 AA, 646 WA) who had RP and were followed for PSA recurrence. Age, race, serum PSA, biopsy Gleason score, clinical stage, pathological stage, and PSA recurrence data were available for the cohort. The chi-square test of proportions and t-tests were used to assess basic associations with race, and log-rank tests and Cox regression models for time to PSA recurrence. Forward stepwise variable selection was used to assess the effect on the risk of PSA recurrence for race, adjusted by the other variables added one at a time.
RESULTS: The AA men had higher baseline PSA levels, more high-grade prostatic intraepithelial neoplasia (HGPIN) in the biopsy, and more HGPIN in the pathology specimen than WA men. The AA men also had a shorter mean (sd) PSA doubling time before RP, at 4.2 (4.7) vs 5.2 (5.9) years. However, race was not an independent predictor of PSA recurrence (P = 0.225). Important predictors for PSA recurrence in a multivariable model were biopsy HGPIN (P < 0.014), unilateral vs bilateral cancer (P < 0.006), pathology Gleason score and positive margin status (both P < 0.001).
CONCLUSIONS: This study indicates that while there are racial differences in baseline serum PSA and incidence of HGPIN, race is not an independent risk factor for PSA recurrence. Rather, other variables such as pathology Gleason score, bilateral cancers, HGPIN and margin positivity are independently associated with PSA recurrence. The PSA doubling time after recurrence may also be important, leading to the increased mortality of AA men with prostate cancer.

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Year:  2005        PMID: 15963115     DOI: 10.1111/j.1464-410X.2005.05561.x

Source DB:  PubMed          Journal:  BJU Int        ISSN: 1464-4096            Impact factor:   5.588


  12 in total

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2.  Potential effect of anti-inflammatory drug use on PSA kinetics and subsequent prostate cancer diagnosis: Risk stratification in black and white men with benign prostate biopsy.

Authors:  Oleksandr N Kryvenko; Yun Wang; Sudha Sadasivan; Nilesh S Gupta; Craig Rogers; Kevin Bobbitt; Dhananjay A Chitale; Andrew Rundle; Deliang Tang; Benjamin A Rybicki
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3.  Association of Anthropometric Measures with Prostate Cancer among African American Men in the NCI-Maryland Prostate Cancer Case-Control Study.

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Review 4.  Interactions among genes, tumor biology and the environment in cancer health disparities: examining the evidence on a national and global scale.

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5.  Impact of race on survival in patients with clinically nonmetastatic prostate cancer who deferred primary treatment.

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8.  Racial differences in clinical and pathological associations with PhIP-DNA adducts in prostate.

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9.  Clinical and biochemical outcomes of men undergoing radical prostatectomy or radiation therapy for localized prostate cancer.

Authors:  David Schreiber; Justin Rineer; Jeffrey P Weiss; Joseph Safdieh; Joseph Weiner; Marvin Rotman; David Schwartz
Journal:  Radiat Oncol J       Date:  2015-03-31

Review 10.  Genetic and molecular differences in prostate carcinogenesis between African American and Caucasian American men.

Authors:  James Farrell; Gyorgy Petrovics; David G McLeod; Shiv Srivastava
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