Lembessis Peter, Msaouel Pavlos, Halapas Antonis, Sourla Antigone, Panteleakou Zacharoula, Pissimissis Nikolaos, Milathianakis Constantine, Bogdanos John, Papaioannou Andreas, Maragoudakis Evangelos, Dardoufas Constantine, Dimopoulos Theodoros, Koutsilieris Michael
Department of Experimental Physiology, National and Kapodistrian University of Athens, Athens, Greece.
Clin Chem Lab Med. 2007;45(11):1488-94. doi: 10.1515/CCLM.2007.301.
The clinical relevance of positive molecular staging as defined by reverse transcriptase-polymerase chain reaction (RT-PCR) detections of both prostate-specific antigen (PSA) and prostate-specific membrane antigen (PSMA) transcripts in the peripheral blood (PB) of patients with prostate cancer is still debatable.
We analyzed the biochemical failure-free survival (bFFS) of prostate cancer patients with positive molecular staging who underwent immediate curative therapy (Group I, n=39) compared to prostate cancer patients who did convert their positive molecular staging by the administration of combined androgen blockade (CAB) for 12 months prior to curative treatment (Group II, n=15).
The median bFFS for Group I was 9 months (95% CI 5-13 months) and was significantly lower compared to Group II (>36 months, p<0.001). In Group I, the median time for PSA values of >2.0 ng/mL was 18 months (95% CI 12-21 months, range 12-36 months). Notably, only one patient from Group II reached PSA values>2.0 ng/mL at 36 months post-curative treatment.
In patients with clinically localized prostate cancer and positive RT-PCR detection of PSA and PSMA transcripts in PB, CAB can convert positive molecular staging status to negative and by doing so it modifies the post-curative therapy bFFS of patients with clinically localized prostate cancer.