Oligometastatic Bone Disease in Castration-Sensitive Prostate Cancer Patients Treated With Stereotactic Body Radiotherapy Using Ga-68-PSMA PET/CT TROD 09-004 Study

dc.contributor.authorOnal, Cem
dc.contributor.authorOzyigit, Gokhan
dc.contributor.authorAkgun, Zuleyha
dc.contributor.authorAtalar, Banu
dc.contributor.authorIgdem, Sefik
dc.contributor.authorOymak, Ezgi
dc.contributor.authorAgaoglu, Fulya
dc.contributor.authorSelek, Ugur
dc.contributor.authorGuler, Ozan Cem
dc.contributor.authorHurmuz, Pervin
dc.contributor.pubmedID33661210en_US
dc.date.accessioned2022-09-08T12:27:24Z
dc.date.available2022-09-08T12:27:24Z
dc.date.issued2021
dc.description.abstractPurpose To evaluate the outcomes of metastasis-directed treatment (MDT) using stereotactic body radiotherapy (SBRT) for bone-only oligometastasis (OM) detected with gallium prostate-specific membrane antigen (Ga-68-PSMA) PET/CT in castration-sensitive prostate cancer (PC) patients. Methods In this multi-institutional study, clinical data of 74 PC patients with 153 bone lesions who were undergoing MDT were retrospectively evaluated. Twenty-seven patients (36.5%) had synchronous, and 47 (63.5%) had metachronous OM. All patients had PC with 5 metastases or fewer detected by Ga-68-PSMA PET/CT and treated using SBRT with a median dose of 20 Gy. The prognostic factors for PC-specific survival (PCSS) and progression-free survival (PFS) were analyzed. Results The median follow-up was 27.3 months. Patients with synchronous OM were older and received higher rates of androgen deprivation therapy after SBRT compared with patients with metachronous OM. The 2-year PCSS and PFS rates were 92.0% and 72.0%, respectively. A prostate-specific antigen (PSA) decline was observed in 56 patients (75.7%), and 48 (64.9%) had a PSA response defined as at least 25% decrease of PSA after MDT. The 2-year local control rate per lesion was 95.4%. In multivariate analysis, single OM and PSA response after MDT were significant predictors for better PCSS and PFS. In-field recurrence was observed in 4 patients (6.5%) with 10 lesions at a median of 13.1 months after MDT completion. No serious late toxicity was observed. Conclusions We demonstrated that SBRT is an efficient and well-tolerated treatment option for PC patients with 5 bone-only oligometastases or fewer detected with Ga-68-PSMA PET/CT.en_US
dc.identifier.endpage470en_US
dc.identifier.issn0363-9762en_US
dc.identifier.issue6en_US
dc.identifier.scopus2-s2.0-85106069551en_US
dc.identifier.startpage465en_US
dc.identifier.urihttp://hdl.handle.net/11727/7623
dc.identifier.volume46en_US
dc.identifier.wos000651397900015en_US
dc.language.isoengen_US
dc.relation.isversionof10.1097/RLU.0000000000003558en_US
dc.relation.journalCLINICAL NUCLEAR MEDICINEen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergien_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectmetastases directed treatmenten_US
dc.subjectoligometastasesen_US
dc.subjectprostate canceren_US
dc.subjectradiotherapyen_US
dc.subjectstereotactic body radiotherapyen_US
dc.titleOligometastatic Bone Disease in Castration-Sensitive Prostate Cancer Patients Treated With Stereotactic Body Radiotherapy Using Ga-68-PSMA PET/CT TROD 09-004 Studyen_US
dc.typearticleen_US

Files

License bundle

Now showing 1 - 1 of 1
No Thumbnail Available
Name:
license.txt
Size:
1.71 KB
Format:
Item-specific license agreed upon to submission
Description: