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. 2021 Jun 7;23(6):634–641. doi: 10.1016/j.neo.2021.05.012

Table 1.

Clinicopathological and molecular characteristics for patients stratified by high and low expression of SCHLAP1.

Expression of SCHLAP1 (Summarized Per Patient)
High (n = 42) Low (n = 102) P
Age at surgery 0.1
<60 13 (31%) 24 (24%)
60–70 28 (67%) 64 (63%)
> 70 1 (2%) 14 (14%)
Preoperative PSA 0.2
<10 ng/ml 19 (45%) 46 (45%)
10 ng/ml–20 ng/ml 12 (29%) 41 (40%)
> 20 ng/ml 11 (26%) 15 (15%)
Grade group 0.02*
1–2 12 (29%) 47 (46%)
3 10 (24%) 31 (30%)
4–5 20 (48%) 24 (24%)
pT stage 0.006*
pT2 6 (14%) 42 (41%)
pT3a 26 (62%) 46 (45%)
pT3b 10 (24%) 13 (13%)
NA 0 (0 %) 1 (1%)
Lymph node status 0.1
NX 22 (52%) 72 (71%)
N0 14 (33%) 27 (26%)
N1 6 (14%) 3 (3%)
Surgical margin 0.3
Positive 11 (26%) 17 (17%)
Negative 31 (74%) 85 (83%)
ERG overexpression < 0.001*
Yes 36 (86%) 33 (32%)
No 6 (14%) 69 (68%)
Invasive cribriform growth/IDCP < 0.001*
Yes 34 (81%) 49 (48%)
No 8 (19%) 53 (52%)
Reactive stroma 0.001*
Yes 25 (60%) 30 (29%)
No 17 (40%) 72 (71%)
Biochemical recurrence < 0.001*
Yes 23 (55%) 21 (21%)
No 19 (45%) 81 (79%)
Clinical recurrence 0.1
Yes 6 (14%) 7 (7%)
No 36 (86%) 95 (93%)
Death (overall survival) 0.01*
Yes 10 (24%) 8 (8%)
No 32 (76%) 94 (92%)

Patients were classified as having high expression of SCHLAP1 when at least one malignant sample displayed expression levels above the threshold. A χ2 test of independence or Fisher's exact test was applied to investigate associations between categorical variables. Univariable Cox regression was used to assess association with BCR, clinical recurrence and death (overall survival).

IDCP = intraductal carcinoma of the prostate; PSA = prostate-specific antigen; pT stage = pathological tumor stage.

indicate statistical significance, P < 0.05.