Home > Publications database > Impact of long-term androgen deprivation therapy on PSMA ligand PET/CT in patients with castration-sensitive prostate cancer.060 > print |
001 | 141171 | ||
005 | 20240229105121.0 | ||
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024 | 7 | _ | |a 1619-7089 |2 ISSN |
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100 | 1 | _ | |a Afshar-Oromieh, Ali |b 0 |
245 | _ | _ | |a Impact of long-term androgen deprivation therapy on PSMA ligand PET/CT in patients with castration-sensitive prostate cancer.060 |
260 | _ | _ | |a Heidelberg [u.a.] |c 2018 |b Springer-Verl. |
336 | 7 | _ | |a article |2 DRIVER |
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520 | _ | _ | |a 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. |
536 | _ | _ | |a 315 - Imaging and radiooncology (POF3-315) |0 G:(DE-HGF)POF3-315 |c POF3-315 |f POF III |x 0 |
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700 | 1 | _ | |a Debus, Nils |b 1 |
700 | 1 | _ | |a Uhrig, Monika |0 P:(DE-He78)1fb1300fe0ab9b45defcb93300ea3299 |b 2 |u dkfz |
700 | 1 | _ | |a Hope, Thomas A |b 3 |
700 | 1 | _ | |a Evans, Michael J |b 4 |
700 | 1 | _ | |a Holland-Letz, Tim |0 P:(DE-He78)457c042884c901eb0a02c18bb1d30103 |b 5 |u dkfz |
700 | 1 | _ | |a Giesel, Frederik L |b 6 |
700 | 1 | _ | |a Kopka, Klaus |0 P:(DE-He78)9793347ba83f527b81a22ab75af9378a |b 7 |u dkfz |
700 | 1 | _ | |a Hadaschik, Boris |b 8 |
700 | 1 | _ | |a Kratochwil, Clemens |b 9 |
700 | 1 | _ | |a Haberkorn, Uwe |0 P:(DE-He78)13a0afba029f5f64dc18b25ef7499558 |b 10 |e Last author |u dkfz |
773 | _ | _ | |a 10.1007/s00259-018-4079-z |g Vol. 45, no. 12, p. 2045 - 2054 |0 PERI:(DE-600)2098375-X |n 12 |p 2045 - 2054 |t European journal of nuclear medicine and molecular imaging |v 45 |y 2018 |x 1619-7089 |
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