Kinetics of serum prostate-specific antigen after external beam radiation for clinically localized prostate cancer

1997 ◽  
Vol 44 (3) ◽  
pp. 213-221 ◽  
Author(s):  
Gunar K. Zagars ◽  
Alan Pollack
2002 ◽  
pp. 2001-2005 ◽  
Author(s):  
CHARLES J. ROSSER ◽  
DEBORAH A. KUBAN ◽  
LAWRENCE B. LEVY ◽  
RAMSEY CHICHAKLI ◽  
ALAN POLLACK ◽  
...  

2002 ◽  
Vol 168 (5) ◽  
pp. 2001-2005 ◽  
Author(s):  
CHARLES J. ROSSER ◽  
DEBORAH A. KUBAN ◽  
LAWRENCE B. LEVY ◽  
RAMSEY CHICHAKLI ◽  
ALAN POLLACK ◽  
...  

2021 ◽  
Vol 11 (3) ◽  
pp. 205-212
Author(s):  
Alexey Yu. Kneev ◽  
Michail I. Shkolnik ◽  
Oleg A. Bogomolov ◽  
Julia G. Vershinskaya ◽  
Gennady M. Zharinov

BACKGROUND:The most important task in the field of improving the results of treatment of patients with prostate cancer (PCa) is their correct stratification by risk groups. Modern stratification systems do not fully provide an adequate risk assessment for all patients with prostate cancer. Further development of algorithms for predicting the clinical course of prostate cancer for a particular patient can positively affect the course and outcome of the disease. AIM:Determination of the clinical and prognostic value of the density of prostate-specific antigen (PSAD) in patients with localized prostate cancer who underwent combined external beam radiation with androgen deprivation therapy. MATERIALS AND METHODS:The effect of the PSAD parameter on the tumor-specific survival rates, as well as the clinical and morphological parameters of the tumor process, was assessed in 272 patients with localized prostate cancer who underwent combined external beam radiation with androgen deprivation therapy from January 1996 to July 2007. RESULTS:The high clinical significance of the PSAD indicator has been demonstrated. An increase in PSAD correlated with an increase in serum PSA concentration, a decrease in PSA doubling time, and a decrease in tumor differentiation. The prognostic value of PSAD was confirmed in patients with localized prostate cancer who received combined hormone-radiation therapy. Using ROC-analysis, the threshold value of the PSAD index was determined 0.36 ng / ml / cm3, the excess of which was associated with a statistically significant decrease in the level of tumor-specific survival. The area under the curve was 0.703 (95% CI 0.2360.434;p 0.001). The risk of tumor-specific mortality and recurrence increased as the PSAD value increased. CONCLUSION:The PSAD parameter is a reliable biomarker of prostate cancer with high rates of clinical and prognostic significance, the use of which is not associated with the introduction of costly and cumbersome methods of laboratory and instrumental diagnostics.


2000 ◽  
pp. 1085-1089 ◽  
Author(s):  
FRANK A. CRITZ ◽  
W. HAMILTON WILLIAMS ◽  
JAMES B. BENTON ◽  
A. KEITH LEVINSON ◽  
CLINTON T. HOLLADAY ◽  
...  

2000 ◽  
Vol 163 (4) ◽  
pp. 1085-1089 ◽  
Author(s):  
FRANK A. CRITZ ◽  
W. HAMILTON WILLIAMS ◽  
JAMES B. BENTON ◽  
A. KEITH LEVINSON ◽  
CLINTON T. HOLLADAY ◽  
...  

1992 ◽  
Vol 10 (8) ◽  
pp. 1208-1217 ◽  
Author(s):  
M A Ritter ◽  
E M Messing ◽  
T G Shanahan ◽  
S Potts ◽  
R J Chappell ◽  
...  

PURPOSE A study of preradiation and postradiation, serial serum prostate-specific antigen (PSA) levels was performed in patients who had clinically localized prostate cancer. The prognostic value of the PSA in pretreatment evaluation and posttreatment follow-up was assessed. PATIENTS AND METHODS Sixty-three patients who presented with clinically localized prostate cancer and who were treated with external-beam radiation therapy were followed-up for a median of 25 months. A serum PSA and physical examination were performed at 3-month intervals, and a bone scan was done yearly. An increase in PSA triggered an additional metastatic workup. Prostate rebiopsy was performed for new, palpable nodules or for a serial increase in PSA in the context of a negative metastatic workup. RESULTS Forty-one patients remained recurrence-free and 22 recurred clinically, 15 distantly and seven locally. The PSA was the strongest, independent, pretreatment prognostic indicator (P = .019) among pretreatment PSA, stage, and grade, but lost significance when the serum prostatic acid phosphatase (PAP) status was included. The initial rate of the PSA decrease after radiation (median half-life, 2.6 months) failed to predict outcome. Recurrence-free patients reached postradiation PSA levels that were equivalent to those reported in disease-free male populations; failure of the PSA to reach such normal levels was a multivariate predictor of subsequent failure (P less than .037). All clinicopathologic documentations of failure were preceded by an increase in PSA levels during follow-up. Delayed versus early PSA increase was associated with clinically localized versus metastatic first recurrence. CONCLUSIONS The serum PSA is an independent pretreatment and posttreatment predictor of outcome. Additionally, for a median follow-up of 25 months, delayed PSA failure is associated with clinically localized rather than metastatic recurrence, a relationship that may help in selection for local salvage therapy.


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