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024 7 _ |a pmid:32405735
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024 7 _ |a 0340-6997
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024 7 _ |a 1432-105X
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024 7 _ |a 1619-7070
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024 7 _ |a 1619-7089
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037 _ _ |a DKFZ-2020-01038
041 _ _ |a eng
082 _ _ |a 610
100 1 _ |a Koerber, Stefan A
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245 _ _ |a Clinical outcome of PSMA-guided radiotherapy for patients with oligorecurrent prostate cancer.
260 _ _ |a Heidelberg [u.a.]
|c 2021
|b Springer-Verl.
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500 _ _ |a 2021 Jan;48(1):143-151
520 _ _ |a First-line treatment of patients with recurrent, metastatic prostate cancer involves hormone therapy with or without additional systemic therapies. Prostate-specific membrane antigen (PSMA) positron emission tomography (PET)/computed tomography (CT) allows the detection of oligometastatic disease that may be amenable to image-guided radiotherapy. The current study classifies the type and localization of metastases and the clinical outcome of PSMA-PET/CT-guided radiotherapy to selected metastases.Between 2011 and 2019, 86 patients with recurrent, oligometastatic prostate carcinoma were identified by PSMA-PET/CT and were treated with image-guided radiotherapy of their metastases. Sites of relapse were characterized, and the primary endpoint overall survival (OS), biochemical progression-free survival (bPFS), and androgen deprivation therapy (ADT)-free survival were tabulated.In total, 37% of the metastases were bone metastases, 48% were pelvic nodal metastases, and 15% were nodal metastases outside of the pelvis. After PSMA-guided radiotherapy, a biochemical response was detected in 83% of the cohort. A statistically significant decrease in the standard uptake value (SUV) was seen in irradiated metastases. After a median follow-up of 26 months, the 3-year OS and bPFS were 84% and 55%, respectively. The median time of ADT-free survival was 13.5 months. A better clinical outcome was observed for patients receiving concomitant ADT or more than 24 fractions of radiation.PSMA-guided radiotherapy is a promising therapeutic approach with excellent infield control for men with oligorecurrent prostate carcinoma. However, prospective, randomized trials are necessary to determine if this approach confers a survival advantage.
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700 1 _ |a Sprute, Katharina
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700 1 _ |a Kratochwil, Clemens
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700 1 _ |a Winter, Erik
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700 1 _ |a Haefner, Matthias F
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700 1 _ |a Katayama, Sonja
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700 1 _ |a Schlampp, Ingmar
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700 1 _ |a Herfarth, Klaus
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700 1 _ |a Kopka, Klaus
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700 1 _ |a Afshar-Oromieh, Ali
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700 1 _ |a Zschaebitz, Stefanie
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700 1 _ |a Holland-Letz, Tim
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700 1 _ |a Choyke, Peter L
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700 1 _ |a Jaeger, Dirk
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700 1 _ |a Hohenfellner, Markus
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700 1 _ |a Haberkorn, Uwe
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700 1 _ |a Giesel, Frederik
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773 _ _ |a 10.1007/s00259-020-04777-z
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