Blood-based reverse transcriptase polymerase chain reaction assays for prostatic specific antigen: Long term follow-up confirms the potential utilityof this assay in identifying patients more likely to have biochemical recurrence (rising PSA) following radical prostatectomy
A. De La Taille et al., Blood-based reverse transcriptase polymerase chain reaction assays for prostatic specific antigen: Long term follow-up confirms the potential utilityof this assay in identifying patients more likely to have biochemical recurrence (rising PSA) following radical prostatectomy, INT J CANC, 84(4), 1999, pp. 360-364
Reverse transcriptase polymerase chain reaction (RT-PCR) assay is a sensiti
ve technique to detect circulating cells expressing prostate-specific antig
en (PSA) in blood or bone marrow from patients with prostate cancer. When a
pplied to prostate cancer patients at our institution, this technique ident
ifies those patients with a greater likelihood of extraprostatic disease. W
e evaluated RT-PCR PSA as a predictor of PSA recurrence and compared it wit
h pre-operative (serum PSA, digital rectal examination, Gleason score on bi
opsy) and post-operative parameters (pathological findings).
Three hundred nineteen men scheduled for radical prostatectomy had an enhan
ced RT-PCR PSA assay before surgery. The enhanced RT-PCR PSA protocol has b
een previously described. PSA recurrence was defined as any serum PSA value
above 0.2 mu g/l.
Forty-six patients had PSA recurrence. The mean follow-up was 25.4 months.
Recurrence free survival was 53% for patients with positive RT-PCR PSA vs.
84% if RT-PCR PSA was negative. By using multivariate analyses, RT-PCR PSA
status was not an independent predictor of PSA recurrence compared to patho
logical stage pT3, Gleason score on prostate specimen and serum PSA. If onl
y pre-operative parameters were studied, serum PSA and RT-PCR PSA status we
re 2 independent pre-operative predictors of PSA recurrence compared with G
leason score on biopsy and digital rectal examination. Int. J. Cancer (Pred
. Oncol.) 84:360-364, 1999. (C) 1999 Wiley-Liss, Inc.