TABLE 1.

Demographic and Clinical Patient Data

VariablehsPC (n = 74)CRPC (n = 74)
Age at inclusion (y)69.9 ± 7.8 (50.0–85.0)71.5 ± 7.5 (49.0–85.0)
Tracer dose (MBq)185.6 ± 20.7 (134.0–300.0)184.3 ± 17.1 (149.0–263.0)
cfDNA (ng/μL)0.745 ± 0.654 (0.0009–4.25)1.04 ± 1.42 (0.0818–9.49)
PSMA-TV (cm3)14.2 ± 76.7 (0.0–659.1)175.5 ± 369.2 (0.0–1,597.7)
PSMA-positive lesion
 Any lesion51 (68.9%)64 (86.5%)
 Prostate lesion25 (33.8%)19 (25.7%)
 Lymph node lesion26 (35.1%)37 (50.0%)
 Bone lesion14 (18.9%)48 (64.9%)
 Organ lesion4 (5.4%)13 (17.6%)
Dominant fraction
 Prostate19 (25.7%)5 (6.8%)
 Lymph node22 (29.7%)19 (25.7%)
 Bone8 (10.8%)39 (52.7%)
 Organ2 (2.7%)1 (1.4%)
PSA (ng/dL)*24.98 ± 105.34 (0.09–761.0)186.42 ± 618.29 (0.01–3,689.0)
Hemoglobin (g/dL)14.06 ± 1.64 (12.1–17.8)11.96 ± 1.84 (7.8–15.4)
Lactate dehydrogenase (U/L)201.21 ± 47.37 (149.0–312.0)250.05 ± 229.26 (130.0–1,573.0)
Systemic therapies while PET
 Antihormonal therapies4 (5.41%)55 (78.57%)
 Cytotoxic therapies1 (1.35%)3 (16.67%)
Systemic therapies after PET
 Local24 (55.8%)10 (23.3%)
 Local + ADT6 (14.0%)
 ADT9 (20.9%)14 (32.6%)
 CHT1 (2.3%)2 (4.7%)
 CHT + ADT1 (2.3%)
 177Lu-PSMA1 (2.3%)16 (37.2%)
 Study1 (2.3%)1 (2.3%)
Mean follow-up (mo)19.8 ± 13.5 (0.0–47.9)16.0 ± 14.0 (0.0–49.0)
  • * n = 14 and 11 data missing in hsPC and CRPC groups, respectively.

  • n = 59 and 35 data missing in hsPC and CRPC groups, respectively.

  • n = 60 and 36 data missing in hsPC and CRPC groups, respectively.

  • ADT = androgen deprivation therapy; CHT = concurrent hormone therapy.

  • Qualitative data are number and percentage; continuous data are mean ± SD and range. Local disease comprised prostate and seminal vesicle lesions.