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1000 Titel
  • Efficacy of repeated PSMA PET-directed radiotherapy for oligorecurrent prostate cancer after initial curative therapy
1000 Autor/in
  1. Henkenberens, Christoph |
  2. Oehus, Ann-Kathrin |
  3. Derlin, Thorsten |
  4. Bengel, Frank |
  5. Ross, Tobias L. |
  6. Kuczyk, Markus A. |
  7. Janssen, Stefan |
  8. Christiansen, Hans |
  9. von Klot, Christoph A. J. |
1000 Erscheinungsjahr 2020
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2020-05-12
1000 Erschienen in
1000 Quellenangabe
  • 196(11):1006-1017
1000 Copyrightjahr
  • 2020
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1007/s00066-020-01629-5 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7581615/ |
1000 Publikationsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • Purpose!#!To assess the outcome of prostate cancer (PCa) patients diagnosed with oligorecurrent disease and treated with a first and a second PSMA (prostate-specific membrane antigen ligand) PET(positron-emission tomography)-directed radiotherapy (RT).!##!Patients and methods!#!Thirty-two patients with oligorecurrent relapse after curative therapy received a first PSMA PET-directed RT of all metastases. After biochemical progression, all patients received a second PSMA PET-directed RT of all metastases. The main outcome parameters were biochemical progression-free survival (bPFS) and androgen deprivation therapy-free survival (ADT-FS). The intervals of BPFS were analyzed separately as follows: the interval from the last day of PSMA PET-directed RT to the first biochemical progression was defined as bPFS_1 and the interval from second PSMA PET-directed RT to further biochemical progression was defined as bPFS_2.!##!Results!#!The median follow-up duration was 39.5 months (18-60). One out of 32 (3.1%) patients died after 47 months of progressive metastatic prostate cancer (mPCa). All patients showed biochemical responses after the first PSMA PET-directed RT and the median prostate-specific antigen (PSA) level before RT was 1.70 ng/mL (0.2-3.8), which decreased significantly to a median PSA nadir level of 0.39 ng/mL (range <0.07-3.8; p = 0.004). The median PSA level at biochemical progression after the first PSMA PET-directed RT was 2.9 ng/mL (range 0.12-12.80; p = 0.24). Furthermore, the PSA level after the second PSMA PET-directed RT at the last follow-up (0.52 ng/mL, range <0.07-154.0) was not significantly different (p = 0.36) from the median PSA level (1.70 ng/mL, range 0.2-3.8) before the first PSMA PET-directed RT. The median bPFS_1 was 16.0 months after the first PSMA PET-directed RT (95% CI 11.9-19.2) and the median bPFS_2 was significantly shorter at 8.0 months (95% CI 6.3-17.7) after the second PSMA PET-directed RT (p = 0.03; 95% CI 1.9-8.3). Multivariate analysis revealed no significant parameter for bPFS_1, whereas extrapelvic disease was the only significant parameter (p = 0.02, OR 2.3; 95% CI 0.81-4.19) in multivariate analysis for bPFS_2. The median ADT-FS was 31.0 months (95% CI 20.1-41.8) and multivariate analysis showed that patients with bone metastases, compared to patients with only lymph node metastases at first PSMA PET-directed RT, had a significantly higher chance (p = 0.007, OR 4.51; 95% CI 1.8-13.47) of needing ADT at the last follow-up visit.!##!Conclusion!#!If patients are followed up closely, including PSMA PET scans, a second PSMA PET-directed RT represents a viable treatment option for well-informed and well-selected patients.
1000 Sacherschließung
lokal Antigens, Surface/analysis [MeSH]
lokal Disease Progression [MeSH]
lokal Aged [MeSH]
lokal Radiotherapy, Image-Guided/adverse effects [MeSH]
lokal Prostatic Neoplasms/radiotherapy [MeSH]
lokal Original Article
lokal Radio-oncology
lokal Adenocarcinoma/secondary [MeSH]
lokal Antigens, Neoplasm/analysis [MeSH]
lokal Male [MeSH]
lokal Neoplasm Recurrence, Local/diagnostic imaging [MeSH]
lokal Adenocarcinoma/radiotherapy [MeSH]
lokal Positron-Emission Tomography [MeSH]
lokal Radiation Injuries/etiology [MeSH]
lokal Adenocarcinoma/diagnostic imaging [MeSH]
lokal Biomarkers, Tumor/analysis [MeSH]
lokal Prostatic Neoplasms/surgery [MeSH]
lokal Lymphatic Metastasis/radiotherapy [MeSH]
lokal Bone Neoplasms/radiotherapy [MeSH]
lokal Biochemical progression
lokal Glutamate Carboxypeptidase II/analysis [MeSH]
lokal Follow-Up Studies [MeSH]
lokal Kaplan-Meier Estimate [MeSH]
lokal Humans [MeSH]
lokal Metastatic Prostate cancer
lokal Middle Aged [MeSH]
lokal Prostatic Neoplasms/diagnostic imaging [MeSH]
lokal Oligometastases
lokal PSMA
lokal Bone Neoplasms/secondary [MeSH]
lokal Neoplasm Recurrence, Local/radiotherapy [MeSH]
lokal Lymphatic Irradiation [MeSH]
lokal Prostatic Neoplasms/chemistry [MeSH]
lokal Adenocarcinoma/surgery [MeSH]
lokal Radiotherapy, Image-Guided/methods [MeSH]
lokal Bone Neoplasms/diagnostic imaging [MeSH]
1000 Liste der Beteiligten
  1. https://orcid.org/0000-0002-0721-5683|https://frl.publisso.de/adhoc/uri/T2VodXMsIEFubi1LYXRocmlu|https://frl.publisso.de/adhoc/uri/RGVybGluLCBUaG9yc3Rlbg==|https://frl.publisso.de/adhoc/uri/QmVuZ2VsLCBGcmFuaw==|https://frl.publisso.de/adhoc/uri/Um9zcywgVG9iaWFzIEwu|https://frl.publisso.de/adhoc/uri/S3VjenlrLCBNYXJrdXMgQS4=|https://frl.publisso.de/adhoc/uri/SmFuc3NlbiwgU3RlZmFu|https://frl.publisso.de/adhoc/uri/Q2hyaXN0aWFuc2VuLCBIYW5z|https://frl.publisso.de/adhoc/uri/dm9uIEtsb3QsIENocmlzdG9waCBBLiBKLg==
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1000 Erstellt am 2023-04-25T18:36:25.822+0200
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1000 Zuletzt bearbeitet Thu Oct 19 11:13:16 CEST 2023
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