Impact of long-term androgen deprivation therapy on PSMA ligand PET/CT in patients with castration-sensitive prostate cancer
Creators
- 1. Bern University Hospital, Department of Nuclear Medicine, Bern (Switzerland)
- 2. Heidelberg University Hospital, Department of Nuclear Medicine, Heidelberg (Germany)
- 3. German Cancer Research Center, Department of Radiology, Heidelberg (Germany)
- 4. University of California, Department of Radiology and Biomedical Imaging, San Francisco, CA (United States)
- 5. University of California, Department of Pharmaceutical Chemistry, San Francisco, CA (United States)
- 6. German Cancer Research Center, Department of Biostatistics, Heidelberg (Germany)
- 7. German Cancer Consortium (DKTK), Heidelberg (Germany)
- 8. German Cancer Research Center, Division of Radiopharmaceutical Chemistry, Heidelberg (Germany)
- 9. University of Duisburg-Essen, Department of Urology, Essen University Hospital, Essen (Germany)
- 10. German Cancer Research Centre, Clinical Cooperation Unit Nuclear Medicine, Heidelberg (Germany)
Description
Since the introduction of PSMA PET/CT with 68Ga-PSMA-11, this modality for imaging prostate cancer (PC) has spread worldwide. Preclinical studies have demonstrated that short-term androgen deprivation therapy (ADT) can significantly increase PSMA expression on PC cells. Additionally, retrospective clinical data in large patient cohorts suggest a positive association between ongoing ADT and a pathological PSMA PET/CT scan. The present evaluation was conducted to further analyse the influence of long-term ADT on PSMA PET/CT findings. A retrospective analysis was performed of all 1,704 patients who underwent a 68Ga-PSMA-11 PET/CT scan at our institution from 2011 to 2017 to detect PC. Of 306 patients scanned at least twice, 10 had started and continued ADT with a continuous clinical response between the two PSMA PET/CT scans. These ten patients were included in the current analysis which compared the tracer uptake intensity and volume of PC lesions on PSMA PET/CT before and during ongoing ADT. Overall, 31 PC lesions were visible in all ten patients before initiation of ADT. However, during ongoing ADT (duration 42-369 days, median 230 days), only 14 lesions were visible in eight of the ten patients. The average tracer uptake values decreased in 71% and increased in 12.9% of the PC lesions. Of all lesions, 33.3% were still visible in six patients with a complete PSA response (≤0.1 ng/ml). Continuous long-term ADT significantly reduces the visibility of castration-sensitive PC on PSMA PET/CT. If the objective is visualization of the maximum possible extent of disease, we recommend referring patients for PSMA PET/CT before starting ADT. (orig.)
Availability note (English)
Available from: http://dx.doi.org/10.1007/s00259-018-4079-zAdditional details
Identifiers
Publishing Information
- Journal Title
- European Journal of Nuclear Medicine and Molecular Imaging
- Journal Volume
- 45
- Journal Issue
- 12
- Journal Page Range
- p. 2045-2054
- ISSN
- 1619-7070
- CODEN
- EJNMA6
INIS
- Country of Publication
- Germany
- Country of Input or Organization
- Germany
- INIS RN
- 50004264
- Subject category
- S62: RADIOLOGY AND NUCLEAR MEDICINE;
- Descriptors DEI
- ANDROGENS; ANTIGENS; BIOCHEMISTRY; CARCINOMAS; COMPUTERIZED TOMOGRAPHY; GALLIUM 68; LIGANDS; LYMPH NODES; METASTASES; PEPTIDES; POSITRON COMPUTED TOMOGRAPHY; PROSTATE; RADIOPHARMACEUTICALS; SKELETAL DISEASES; THERAPY; TRACER TECHNIQUES; UPTAKE
- Descriptors DEC
- ANDROSTANES; BETA DECAY RADIOISOTOPES; BETA-PLUS DECAY RADIOISOTOPES; BODY; CHEMISTRY; COMPUTERIZED TOMOGRAPHY; DIAGNOSTIC TECHNIQUES; DISEASES; DRUGS; ELECTRON CAPTURE RADIOISOTOPES; EMISSION COMPUTED TOMOGRAPHY; GALLIUM ISOTOPES; GLANDS; HORMONES; HOURS LIVING RADIOISOTOPES; INTERMEDIATE MASS NUCLEI; ISOTOPE APPLICATIONS; ISOTOPES; LABELLED COMPOUNDS; LYMPHATIC SYSTEM; MALE GENITALS; MATERIALS; MEDICINE; NEOPLASMS; NUCLEI; ODD-ODD NUCLEI; ORGANIC COMPOUNDS; ORGANS; PROTEINS; RADIOACTIVE MATERIALS; RADIOISOTOPES; STEROID HORMONES; STEROIDS; TOMOGRAPHY