| Literature DB >> 35266063 |
Rosario Mazzola1, Francesco Cuccia2, Edoardo Pastorello1, Matteo Salgarello3, Giulio Francolini4,5, Lorenzo Livi4,5, Luca Triggiani6, Stefano Maria Magrini6, Gianluca Ingrosso7, Cynthia Aristei7, Ciro Franzese8,9, Marta Scorsetti8,9, Filippo Alongi1,10.
Abstract
To assess the outcomes of a cohort of bone oligometastatic prostate cancer patients treated with PSMA-PET guided stereotactic body radiotherapy (SBRT). From April 2017 to January 2021, 40 patients with oligorecurrent prostate cancer detected by PSMA-PET were treated with SBRT for bone oligometastases. Concurrent androgen deprivation therapy was an exclusion criterion. A total of 56 prostate cancer bone oligometastases were included in the present analysis. In 28 patients (70%), oligometastatic disease presented as a single lesion, two lesions in 22.5%, three lesions in 5%, four lesions in 2.5%. 30.3% were spine-metastases, while 69.7% were non-spine metastases. SBRT was delivered for a median dose of 30 Gy (24-40 Gy) in 3-5 fractions, with a median EQD2 = 85 Gy2 (64.3-138.9Gy2). With a median follow-up of 22 months (range 2-48 months), local control (LC) 1- and 2-years rates were 96.3% and 93.9%, while distant progression-free survival (DPFS) rates were 45.3% and 27%. At multivariate analysis, the lower PSA nadir value after SBRT remained significantly related to better DPFS rates (p = 0.03). In 7 patients, a second SBRT course was proposed with concurrent ADT, while 11 patients, due to polymetastatic spread, received ADT alone, resulting in 1- and 2-years ADT-free survival rates of 67.5% and 61.8%. At multivariate analysis, a lower number of treated oligometastases maintained a correlation with higher ADT-free survival rates (p = 0.04). In our experience, PSMA-PET guided SBRT resulted in excellent results in terms of clinical outcomes, representing a helpful tool with the aim to delay the start of ADT.Entities:
Keywords: Oligometastases; PSMA-PET; Stereotactic body radiotherapy
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Year: 2022 PMID: 35266063 DOI: 10.1007/s10585-022-10157-8
Source DB: PubMed Journal: Clin Exp Metastasis ISSN: 0262-0898 Impact factor: 4.510