Table 1 Clinical characteristics according to cohort

From: Analysis of the prognostic utility of the cell cycle progression (CCP) score generated from needle biopsy in men treated with definitive therapy

 

Ochsner Clinic (N = 646)

Bishoff Cohort (N = 416)

 

Characteristic

N

Median (IQR) or frequency

N

Median (IQR) or frequency

p-value

Age at diagnosis (years)

646

64 (58, 70)

416

62 (58, 66)

2.0 × 10−5

Ancestry

  African-American

241

37.3%

67

16.1%

2.8 × 10−14

  Non African-American

405

62.7%

349

83.9%

Pre-biopsy PSA (ng/μL)

646

5.8 (4.5, 8.3)

416

6.0 (4.6, 9.0)

0.49

Biopsy Gleason Scorea

  <7

333

51.5%

159

54.3%

3.2 × 10−3

  3 + 4 = 7

156

24.1%

86

29.4%

  4 + 3 = 7

61

9.4%

28

9.6%

  >7

96

14.9%

28

6.8%

Clinical T stage

  T1

471

72.9%

261

62.7%

1.4 × 10−8

  T2

151

23.4%

154

37.0%

  T3

24

3.7%

1

0.2%

Percent positive cores

646

42.9 (28.6, 66.7)

416

33.3 (20.0, 50.0)

1.3 × 10−7

CAPRA risk category

  Low (0–2)

288

44.6%

202

48.6%

3.2 × 10−5

  Intermediate (3–5)

258

39.9%

187

45.0%

  High (6–10)

100

15.5%

27

6.5%

CCP score

646

0.3 (−0.2, 0.9)

416

−0.1 (−0.6, 0.5)

1.5 × 10−12

Treatment

  Surgery

384

59.4%

416

100%

<2.2 × 10−16

  XRT

262

40.6%

0

0%

Progression to metastatic disease

  Events

28

4.3%

7

1.7%

<2.2 × 10−16c

  Years to last follow-upb

646

5.5 (4.0, 6.8)

416

7.1 (5.4, 10.0)

Events by AUA Risk Categoryd

  Low

2/285

0.7%

0/189

0.0%

n/a

 Intermediate

9/200

4.5%

4/184

2.2%

  High

17/161

10.6%

3/43

7.0%

  1. PSA prostate-specific antigen, CAPRA cancer of the prostate risk assessment, CCP cell cycle progression, XRT external radiation therapy
  2. aIHC cohort excluded from Bishoff cohort due to some patients missing secondary Gleason
  3. bFollow-up time for men who had not experienced an event and were alive at the end of follow-up
  4. cWilcoxon rank sum p-value for follow-up time
  5. dN shown as number of events over total number of patients within that risk category