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1
Summary: The correct interpretation of
biochemical
recurrence
is crucial to treatment decision-making.
2
Kaplan-Meier estimates of freedom from
biochemical
recurrence
were compared among the groups.
3
The PSA bounce phenomenon was not predictive of time to
biochemical
recurrence
.
4
SSEA-4 expression in post-NHT tissues was significantly associated with
biochemical
recurrence
-
free
survival.
5
Conclusions: cPSA has high validity for the diagnosis of
biochemical
recurrence
after RP.
6
Kaplan-Meier analysis was used to evaluate the likelihood of
biochemical
recurrence
.
7
We also examined whether the
biochemical
recurrence
rates after RP have changed with time.
8
Cutpoints were identified to define patients with differing risk of
biochemical
recurrence
after RP.
9
Recent findings: There is a disconnection between
biochemical
recurrence
and progression to clinical disease.
10
The risk of
biochemical
recurrence
was not increased for those who received cell-salvaged blood.
11
Subsequently, we examined the relationship between LMW-PTP expression levels and clinicopathological factors including
biochemical
recurrence
.
12
Cox proportional hazard regression models were used to analyse clinicopathological variables associated with
biochemical
recurrence
.
13
Objectives: To evaluate the risk of long-term
biochemical
recurrence
for patients who receive cell-salvaged blood.
14
It also evaluates the array of diagnostic tests frequently employed when
biochemical
recurrence
has occurred.
15
Current imaging modalities are rarely useful in localizing disease when
biochemical
recurrence
is first detected.
16
Conclusions: Preoperative p27 expression is an independent predictor of time to
biochemical
recurrence
following radical prostatectomy.
biochemical
recurrence
biochemical