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Table 1 Baseline and clinical characteristics of 404 participants with prostate cancer from the PHS and HPFS

From: The role of tumor metabolism as a driver of prostate cancer progression and lethal disease: results from a nested case-control study

Characteristic

Non-lethal (n = 291)

Lethal (n = 113)

Cohort, N (%)

 PHS

120 (41.2%)

30 (26.5%)

 HPFS

171 (58.8%)

83 (73.5%)

Age at diagnosis, mean (SD)

64.9 (6.2)

67.5 (6.7)

Clinical tumor stage, N (%)a

 T1/T2 N0/Nx M0/Mx

271 (94.1%)

79 (72.5%)

 T3 N0/Nx M0/Mx

16 (5.6%)

11 (10.1%)

 T4/N1/M1

1 (0.3%)

19 (17.4%)

Gleason grade, N (%)

 2–6

56 (19.2%)

1 (0.9%)

 3 + 4

126 (43.3%)

13 (11.5%)

 4 + 3

67 (23.0%)

35 (31.0%)

 8–10

42 (14.4%)

64 (56.6%)

PSA at diagnosis, ng/ml, N (%)b

  

 0–3.9

29 (10.7%)

4 (5.7%)

 4–10

163 (60.1%)

35 (50.0%)

 10–19.9

54 (19.9%)

15 (21.4%)

 >20

25 (9.2%)

16 (22.9%)

Tissue from RP, N (%)

283 (97.3%)

86 (76.1%)

BMI at diagnosis, mean (SD)

25.1 (2.8)

25.9 (3.3)

BMI at baseline, mean (SD)

24.6 (2.5)

25.6 (3.2)

Matched normal tissue available

140 (48.1%)

62 (54.9)

  1. aClinical tumor stage was unknown for 3 (1%) non-lethal cases and 4 (3.5%) lethal cases
  2. bPSA was unknown for 20 (6.9%) non-lethal cases and 43 (38.1%) lethal cases