4 research outputs found
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IMPACT OF RACE AND ETHNICITY UPON MALNUTRITION INFLAMMATION SCORE AND MORTALITY RISK IN A PROSPECTIVE HEMODIALYSIS COHORT
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BODY COMPOSITION MARKERS AND MORTALITY RISK IN A PROSPECTIVE HEMODIALYSIS COHORT
Prostate-specific antigen 10–20 ng/mL: A predictor of degree of upgrading to ≥8 among patients with biopsy Gleason score 6
Purpose: This study aimed to identify the predictors of upgrading and degree of upgrading among patients who have initial Gleason
score (GS) 6 treated with robot-assisted radical prostatectomy (RARP).
Materials and Methods: A retrospective review of the data of 359 men with an initial biopsy GS 6, localized prostate cancer who
underwent RARP between July 2005 to June 2010 was performed. They were grouped into group 1 (nonupgrade) and group 2 (upgraded)
based on their prostatectomy specimen GS. Logistic regression analysis of studied cases identified significant predictors of
upgrading and the degree of upgrading after RARP.
Results: The mean age and prostate-specific antigen (PSA) was 63±7.5 years, 8.9±8.77 ng/mL, respectively. Median follow-up
was 59 months (interquartile range, 47–70 months). On multivariable analysis, age, PSA, PSA density and ≥2 cores positive were
predictors of upgrading with (odds ratio [OR], 1.03; 95% confidence interval [CI], 1.01–1.06; p=0.003; OR, 1.006; 95% CI, 1.01–1.11;
p=0.018; OR, 0.65; 95% CI, 0.43–0.98, p=0.04), respectively. On subanalysis, only PSA level of 10–20 ng/mL is associated with upgrading
into GS ≥8. They also had lower biochemical recurrence free survival, cancer specific survival, and overall survival (p≤0.001,
p=0.003, and p=0.01, respectively).
Conclusions: Gleason score 6 patients with PSA (10–20 ng/mL) have an increased risk of upgrading to pathologic GS (≥8), subsequently
poorer oncological outcome thus require a stricter follow-up. These patients should be carefully counseled in making an
optimal treatment decision