Stereotactic radiotherapy to oligoprogressive lesions detected with Ga-68-PSMA-PET/CT in castration-resistant prostate cancer patients

dc.contributor.authorOnal, Cem
dc.contributor.authorOzyigit, Gokhan
dc.contributor.authorOymak, Ezgi
dc.contributor.authorGuler, Ozan Cem
dc.contributor.authorTilki, Burak
dc.contributor.authorHurmuz, Pervin
dc.contributor.authorAkyol, Fadil
dc.contributor.orcID0000-0002-2742-9021en_US
dc.contributor.pubmedID33693965en_US
dc.contributor.researcherIDD-5195-2014en_US
dc.date.accessioned2022-08-08T06:41:04Z
dc.date.available2022-08-08T06:41:04Z
dc.date.issued2021
dc.description.abstractPurpose We assessed the outcomes of stereotactic body radiotherapy (SBRT) to treat oligoprogressive castration-resistant prostate cancer (CRPC) patients with <= 5 lesions using gallium prostate-specific membrane antigen-positron emission tomography (Ga-68-PSMA-PET/CT). Methods The clinical data of 67 CRPC patients with 133 lesions treated with Ga-68-PSMA-PET/CT-based SBRT were retrospectively analyzed. All of the patients had oligoprogressive disease during androgen-deprivation therapy (ADT). The prognostic factors for overall- (OS) and progression-free survival (PFS) and the predictive factors for switching to next-line systemic treatment (NEST) and NEST-free survival (NEST-FS) were analyzed. Results With a median follow-up of 17.5 months, the 2-year overall survival (OS) and PFS rates were 86.9% and 34.4%, respectively. The PSA response was observed in 49 patients (73.1%). Progression was observed in 37 patients (55.2%) at a median of 11.0 months following SBRT. A total of 45 patients (67.2%) remained on ADT after SBRT, and 22 patients (32.8%) had a NEST change at a median of 16.4 months after metastasis-directed treatment (MDT). Patients with a NEST change had higher post-SBRT PSA values and fewer PSA nadirs after MDT than their counterparts. In multivariate analysis, higher pre-SBRT PSA values were the only significant predictor for worse OS and NEST-FS, and no significant factor was found for PFS. No serious acute or late toxicities were observed. Conclusion This study demonstrated the feasibility of MDT using SBRT to treat oligoprogressive lesions by Ga-68-PSMA-PET/CT in CRPC patients is efficient and well-tolerated, prolonging the effectiveness of ADT by delaying NEST.en_US
dc.identifier.endpage3692en_US
dc.identifier.issn1619-7070en_US
dc.identifier.issue11en_US
dc.identifier.scopus2-s2.0-85102436914en_US
dc.identifier.startpage3683en_US
dc.identifier.urihttp://hdl.handle.net/11727/7248
dc.identifier.volume48en_US
dc.identifier.wos000627192800001en_US
dc.language.isoengen_US
dc.relation.isversionof10.1007/s00259-021-05298-zen_US
dc.relation.journalEUROPEAN JOURNAL OF NUCLEAR MEDICINE AND MOLECULAR IMAGINGen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergien_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectProstate canceren_US
dc.subjectCastration-resistanten_US
dc.subjectOligometastasisen_US
dc.subjectOligoprogressionen_US
dc.subjectStereotactic body radiotherapyen_US
dc.titleStereotactic radiotherapy to oligoprogressive lesions detected with Ga-68-PSMA-PET/CT in castration-resistant prostate cancer patientsen_US
dc.typearticleen_US

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