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Comparison of PSA value at last follow-up of patients who underwent low-dose rate brachytherapy and intensity-modulated radiation therapy for prostate cancer.

Authors :
Tanaka, Nobumichi
Asakawa, Isao
Nakai, Yasushi
Miyake, Makito
Anai, Satoshi
Fujii, Tomomi
Hasegawa, Masatoshi
Konishi, Noboru
Fujimoto, Kiyohide
Source :
BMC Cancer; 8/25/2017, Vol. 17, p1-8, 8p, 6 Charts, 4 Graphs
Publication Year :
2017

Abstract

<bold>Background: </bold>To compare the PSA value at the last follow-up of patients who underwent prostate low-dose rate brachytherapy (LDR-BT) with that of patients who underwent intensity-modulated radiation therapy (IMRT).<bold>Methods: </bold>A total of 610 prostate cancer patients (cT1c-3bN0M0) were enrolled, and 445 of them underwent LDR-BT, while 165 received IMRT (74-76 Gy). The median follow-up period of these two groups was 75 months (LDR-BT) and 78 months (IMRT), respectively. We also evaluated the biochemical recurrence (BCR)-free rate using two definitions (Phoenix definition and PSA ≥ 0.2 ng/mL).<bold>Results: </bold>The percentage of patients who achieved PSA < 0.2 ng/mL at the last follow-up was 77.5% in the LDR-BT group and 49.7% in the IMRT group (p < 0.001). Among patients with a normal testosterone level at the last follow-up, the percentage of those who achieved PSA < 0.2 ng/mL at the last follow-up was 79.2% in the LDR-BT group and 32.1% in the IMRT group (p < 0.001). The 5-year BCR-free rate by the Phoenix definition in the IMRT and LDR-BT groups was 89.5 and 95.0% (p < 0.001), respectively. On the other hand, the 5-year BCR-free rate using the definition of PSA ≥ 0.2 ng/mL was 59.1 and 80.1% in the IMRT and LDR-BT groups, respectively (p < 0.001).<bold>Conclusions: </bold>The PSA value at the last follow-up of LDR-BT was significantly lower than that of IMRT, and this result was particularly marked in patients with a normal testosterone level at the last follow-up. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
14712407
Volume :
17
Database :
Complementary Index
Journal :
BMC Cancer
Publication Type :
Academic Journal
Accession number :
124818888
Full Text :
https://doi.org/10.1186/s12885-017-3565-1