Undetectable ultrasensitive PSA after radical prostatectomy for prostate cancer predicts relapse-free survival
Adult
Male
ANTIGEN
Predictive Value of Test
Sensitivity and Specificity
Disease-Free Survival
SERUM
Decision Support Techniques
Decision Support Technique
03 medical and health sciences
0302 clinical medicine
Predictive Value of Tests
Humans
PRESERVATION
Oncology & Carcinogenesis
RECURRENCE
COMBINATION
Multivariate Analysi
radical retropubic prostatectomy
Aged
Neoplasm Staging
Proportional Hazards Models
Prostatectomy
Salvage Therapy
RETROPUBIC PROSTATECTOMY
SURGICAL MARGINS
Science & Technology
Settore MED/24 - UROLOGIA
PATHOLOGICAL FINDINGS
Prostatic Neoplasms
Regular Article
Middle Aged
Prostate-Specific Antigen
ONCOLOGY
prostate cancer
PSA nadir
Sensitivity and Specificity; Disease-Free Survival; Neoplasm Staging; Prostatectomy; Humans; Prostate-Specific Antigen; Salvage Therapy; Aged; Predictive Value of Tests; Multivariate Analysis; Adult; Middle Aged; Prostatic Neoplasms; Male; Decision Support Techniques; Proportional Hazards Models
TIME
3. Good health
Oncology
Prostatic Neoplasm
Multivariate Analysis
RESOLVED IMMUNOFLUOROMETRIC ASSAY
Life Sciences & Biomedicine
1112 Oncology And Carcinogenesis
Human
DOI:
10.1054/bjoc.2000.1474
Publication Date:
2002-07-26T11:27:09Z
AUTHORS (7)
ABSTRACT
Radical retropubic prostatectomy is considered by many centres to be the treatment of choice for men aged less than 70 years with localized prostate cancer. A rise in serum prostate-specific antigen after radical prostatectomy occurs in 10-40% of cases. This study evaluates the usefulness of novel ultrasensitive PSA assays in the early detection of biochemical relapse. 200 patients of mean age 61. 2 years underwent radical retropubic prostatectomy. Levels < or = 0.01 ng ml-1 were considered undetectable. Mean pre-operative prostate-specific antigen was 13.3 ng ml-1. Biochemical relapse was defined as 3 consecutive rises. The 2-year biochemical disease-free survival for the 134 patients with evaluable prostate-specific antigen nadir data was 61.1% (95% CI: 51.6-70.6%). Only 2 patients with an undetectable prostate-specific antigen after radical retropubic prostatectomy biochemically relapsed (3%), compared to 47 relapses out of 61 patients (75%) who did not reach this level. Cox multivariate analysis confirms prostate-specific antigen nadir < or = 0.01 ng ml-1 to be a superb independent variable predicting a favourable biochemical disease-free survival (P < 0.0001). Early diagnosis of biochemical relapse is feasible with sensitive prostate-specific antigen assays. These assays more accurately measure the prostate-specific antigen nadir, which is an excellent predictor of biochemical disease-free survival. Thus, sensitive prostate-specific antigen assays offer accurate prognostic information and expedite decision-making regarding the use of salvage prostate-bed radiotherapy or hormone therapy.
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