Pharmacokinetic studies of [68 Ga]Ga-PSMA-11 in patients with biochemical recurrence of prostate cancer: detection, differences in temporal distribution and kinetic modelling by tissue type

• Published in: European journal of nuclear medicine and molecular imaging 2021-12, Vol.48 (13), p.4472-4482
• Main Authors: Strauss, Dimitrios S., Sachpekidis, C., Kopka, K., Pan, L., Haberkorn, U., Dimitrakopoulou-Strauss, A.
• Format: Article
• Language: English
• Subjects: Bladder; Cardiology; Computed tomography; Edetic Acid; Fractal geometry; Heterogeneity; Humans; Imaging; Kinetics; Lesions; Lymph nodes; Male; Medicine; Medicine & Public Health; Metastases; Metastasis; Modelling; Neoplasm Recurrence, Local - diagnostic imaging; Nuclear Medicine; Oncology; Oncology – Genitourinary; Original; Original Article; Orthopedics; Pharmaceuticals; Pharmacokinetics; Pharmacology; Positron Emission Tomography Computed Tomography; Prostate cancer; Prostatic Neoplasms - diagnostic imaging; Radiochemical analysis; Radioisotopes; Radiology; Retrospective Studies; Temporal distribution; Transport rate; Tumors; Windows (intervals)
• ISSN: 1619-7070; 1619-7089
• DOI: 10.1007/s00259-021-05420-1

Purpose [ 68  Ga]Ga-PSMA-11 is a promising radiopharmaceutical for detecting tumour lesions in prostate cancer, but knowledge of the pharmacokinetics is limited. Dynamic PET-CT was performed to investigate the tumour detection and differences in temporal distribution, as well as in kinetic modelling of [ 68  Ga]Ga-PSMA-11 by tissue type. Methods Dynamic PET-CT over the lower abdomen and static whole-body PET-CT 80–90 min p.i. from 142 patients with biochemical recurrence were retrospectively analysed. Detection rates were compared to PSA levels. Average time-activity curves were calculated from tumour lesions and normal tissue. A three-compartment model and non-compartment model were used to calculate tumour kinetics. Results Overall detection rate was 70.42%, and in patients with PSA > 0.4 ng/mL 76.67%. All tumour lesions presented the steepest standardised uptake value (SUV) incline in the first 7–8 min before decreasing to different degrees. Normal tissue presented with a low uptake, except for the bladder, which accumulated activity the steepest 15–16 min. p.i.. While all tumour lesions continuously increased, bone metastases showed the steepest decline, resulting in a significantly lower SUV than lymph node metastases (60 and 80–90 min). Transport rate from the blood and tracer binding and internalisation rate were lower in bone metastases. Heterogeneity (fractal dimension) and vascular density were significantly lower in bone metastases. Conclusion Even at low PSA between 0.51 and 0.99 ng/mL, detection rate was 57%. Dynamic imaging showed a time window in the first 10 min where tumour uptake is high, but no bladder activity is measured, aiding accuracy in distinction of local recurrence. Kinetic modelling provided additional information for tumour characterisation by tissue type.