TABLE 3.

Clinical, Imaging, and Treatment Characteristics of Patients Undergoing [18F]F-PSMA-1007 or [68Ga]Ga-PSMA-11 PET/CT–Guided MDT After Propensity Score Matching

ParameterOverall (n = 88)[18F]F-PSMA-1007–guided MDT (n = 44)[68Ga]Ga-PSMA-11–guided MDT (n = 44)P
Preimaging clinical characteristics
 Age (y)73.07 ± 6.4273.2 ± 7.2372.94 ± 5.560.850
 Initial AJCC stage
  I4 (4.55%)3 (6.82%)1 (2.27%)0.308
  II22 (25.00%)9 (20.45%)13 (29.55%)0.327
  III54 (61.36%)26 (59.09%)28 (63.64%)0.663
  IV8 (9.09%)6 (13.64%)2 (4.54%)0.140
 ISUP grade
  110 (11.36%)4 (9.09%)6 (13.64%)0.504
  219 (21.59%)10 (22.73%)9 (20.45%)0.796
  325 (28.41%)12 (27.27%)13 (29.55%)0.814
  419 (21.59%)10 (22.73%)9 (20.45%)0.796
  515 (17.05%)8 (18.18%)7 (15.91%)0.778
 Primary treatment
  Surgery74 (84.09%)34 (77.27%)40 (90.91%)0.082
  Radiotherapy (±ADT)14 (15.91%)10 (22.73%)4 (9.09%)0.082
 CRPC at time of MDT15 (17.05%)7 (15.91%)8 (18.18%)0.778
 PSA at time of MDT (ng/mL)2.42 ± 5.012.27 ± 3.802.58 ± 6.050.769
Imaging findings
 Number of metastatic lesions
  169 (78.41%)34 (77.27%)35 (79.55%)0.796
  213 (14.77%)6 (13.54%)7 (15.91%)0.755
  3–56 (6.82%)4 (9.09%)2 (4.54%)0.400
 Site of metastases
  Lymph node59 (67.04%)27 (61.36%)32 (72.73%)0.259
  Bone28 (31.82%)16 (36.36%)12 (27.27%)0.367
  Visceral1 (1.14%)1 (2.27%)0 (0.00%)0.318
MDT parameters and clinical follow-up
 MDT total dose (per lesion)34.02 ± 4.8633.84 ± 5.2234.20 ± 4.510.731
 MDT BED (per lesion)117.89 ± 20.18115.40 ± 11.77120.11 ± 25.640.492
 Concurrent systemic treatment in addition to MDT29 (32.96%)14 (31.82%)15 (34.09%)0.822
 PSA nadir after MDT (ng/mL)1.093 ± 1.771.70 ± 2.240.53 ± 0.910.003
Propensity score matching0.52 ± 0.150.52 ± 0.150.52 ± 0.150.988
  • AJCC = American Joint Committee on Cancer; ISUP = International Society of Urological Pathology; BED = biologically effective dose.

  • Qualitative data are number and percentage; continuous data are mean ± SD.