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   <subfield code="a">10.1007/s10147-014-0681-7</subfield>
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   <subfield code="a">Prostate-specific antigen measured 3months after radical prostatectomy as a new predictor of biochemical recurrence</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Hitoshi Inoue, Kensaku Nishimura, Seiji Yamaguchi, Norio Nonomura, Tsuneo Hara]</subfield>
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   <subfield code="a">Background: This study was undertaken to investigate if the prostate-specific antigen (PSA) level measured 3months after radical prostatectomy (RP) is a predictor of biochemical recurrence (BCR)-free survival. Methods: We retrospectively reviewed the clinicopathologic data of 174 patients with a follow-up of at least 3years after RP for clinically localized prostate cancer. None of the patients received neoadjuvant/adjuvant therapy. Subjects were categorized according to PSA level 3months after RP (3M-PSA): &lt;0.010ng/mL (group 1; n=119) or 0.010-0.100ng/mL (group 2; n=55). BCR was defined as two consecutive rises in PSA level ≥0.2ng/mL. Results: At a median follow-up of 69.5months (range 36-113months), 32 (18.4%) patients experienced BCR. The median time to BCR was 16months (range 4-98months) after RP. The 5-year BCR-free survival rate was 92.6 and 57.4% in groups 1 and 2, respectively. Patients in group 1 had a significantly higher BCR-free survival rate than those in group 2 (log-rank P&lt;0.001). According to the Cox proportional hazards model, patients with a 3M-PSA level of &lt;0.010ng/mL were at lower risk for BCR (P&lt;0.001), along with pathologic Gleason sum 6 (P=0.028). PSA nadir level after RP was also a risk factor for BCR (log-rank P&lt;0.001). Area under the receiver operating characteristic curve for 3M-PSA to predict BCR was almost equivalent to that for the PSA nadir level (0.855 vs. 0.849). Conclusions: 3M-PSA is an independent predictor of BCR-free survival. Our findings might be used for a risk-adjusted follow-up protocol.</subfield>
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   <subfield code="a">Japan Society of Clinical Oncology, 2014</subfield>
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   <subfield code="a">Prostate cancer</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">Prostate-specific antigen</subfield>
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   <subfield code="a">Radical prostatectomy</subfield>
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   <subfield code="a">Predictor</subfield>
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   <subfield code="a">Biochemical recurrence</subfield>
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   <subfield code="a">Inoue</subfield>
   <subfield code="D">Hitoshi</subfield>
   <subfield code="u">Department of Urology, Ikeda Municipal Hospital, 3-1-18 Jonan, 563-8510, Ikeda, Osaka, Japan</subfield>
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   <subfield code="a">Nishimura</subfield>
   <subfield code="D">Kensaku</subfield>
   <subfield code="u">Department of Urology, Ikeda Municipal Hospital, 3-1-18 Jonan, 563-8510, Ikeda, Osaka, Japan</subfield>
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   <subfield code="a">Yamaguchi</subfield>
   <subfield code="D">Seiji</subfield>
   <subfield code="u">Department of Urology, Osaka General Medical Center, Osaka, Japan</subfield>
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   <subfield code="a">Nonomura</subfield>
   <subfield code="D">Norio</subfield>
   <subfield code="u">Department of Urology, Osaka University Graduate School of Medicine, Osaka, Japan</subfield>
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   <subfield code="a">Hara</subfield>
   <subfield code="D">Tsuneo</subfield>
   <subfield code="u">Department of Urology, Ikeda Municipal Hospital, 3-1-18 Jonan, 563-8510, Ikeda, Osaka, Japan</subfield>
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  <datafield tag="773" ind1="0" ind2=" ">
   <subfield code="t">International Journal of Clinical Oncology</subfield>
   <subfield code="d">Springer Japan</subfield>
   <subfield code="g">20/1(2015-02-01), 171-175</subfield>
   <subfield code="x">1341-9625</subfield>
   <subfield code="q">20:1&lt;171</subfield>
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   <subfield code="a">Metadata rights reserved</subfield>
   <subfield code="b">Springer special CC-BY-NC licence</subfield>
   <subfield code="2">nationallicence</subfield>
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