Pervin Hurmuz1, Cem Onal2, Gokhan Ozyigit3,4, Sefik Igdem5, Banu Atalar6, Haluk Sayan7, Zuleyha Akgun8, Meral Kurt9, Hale Basak Ozkok10, Ugur Selek11, Ezgi Oymak12, Burak Tilki1, Ozan Cem Guler2, Teuto Zoto Mustafayev6, Irem Saricanbaz7, Rashad Rzazade10, Fadıl Akyol1. 1. Faculty of Medicine, Department of Radiation Oncology, Hacettepe University, Ankara, Turkey. 2. Faculty of Medicine, Adana Dr Turgut Noyan Research and Treatment Center, Department of Radiation Oncology, Baskent University, Adana, Turkey. 3. Faculty of Medicine, Department of Radiation Oncology, Hacettepe University, Ankara, Turkey. gozyigit@hacettepe.edu.tr. 4. Turkish Society for Radiation Oncology, Istanbul, Turkey. gozyigit@hacettepe.edu.tr. 5. Department of Radiation Oncology, Istanbul Bilim University, Istanbul, Turkey. 6. Maslak Hospital, Department of Radiation Oncology, Acıbadem MAA University, Istanbul, Turkey. 7. Department of Radiation Oncology, Ankara Bilkent City Hospital, Ankara, Turkey. 8. Division of Radiation Oncology, Memorial Sisli Hospital, Istanbul, Turkey. 9. Faculty of Medicine, Department of Radiation Oncology, Uludag University, Bursa, Turkey. 10. Division of Radiation Oncology, ASM Hospital, Istanbul, Turkey. 11. Faculty of Medicine, Department of Radiation Oncology, Koc University, Istanbul, Turkey. 12. Division of Radiation Oncology, Iskenderun Gelisim Hospital, Hatay, Turkey.
Abstract
PURPOSE: The aim of this study was to evaluate the outcomes of 68Ga prostate-specific membrane antigen (68Ga-PSMA) positron-emission tomography (PET)/CT-based metastasis-directed treatment (MDT) for oligometastatic prostate cancer (PC). METHODS: In this multi-institutional study, clinical data of 176 PC patients with 353 lesions receiving MDT between 2014 and 2019 were retrospectively evaluated. All patients had biopsy proven PC with ≤5 metastases detected with 68Ga-PSMA-PET/CT. MDT was delivered with conventional fractionation or stereotactic body radiotherapy (SBRT) techniques. CTCAE v4.0 was used for acute and RTOG/EORTC Late Radiation Morbidity Scoring Schema was used for late toxicity evaluation. RESULTS: At the time of MDT, 59 patients (33.5%) had synchronous and 117 patients (66.5%) had metachronous metastases. Median number of metastases was one and the MDT technique was SBRT in 73.3% patients. The 2‑year overall survival (OS) and progression-free survival (PFS) rates were 87.6% and 63.1%, respectively. With a median follow-up of 22.9 months, 9 patients had local recurrence at the irradiated site. The 2‑year local control rate at the treated oligometastatic site per patient was 93.2%. In multivariate analysis, an increased number of oligometastases and untreated primary PC were negative predictors for OS; advanced clinical tumor stage, untreated primary PC, BED3 value of ≤108 Gy, and MDT with conventional fractionation were negative predictors for PFS. No patient experienced grade ≥3 acute toxicity, but one patient had a late grade 3 toxicity of compression fracture after spinal SBRT. CONCLUSION: 68Ga-PSMA-PET/CT-based MDT is an efficient and safe treatment for oligometastatic PC patients. Proper patient selection might improve treatment outcomes.
PURPOSE: The aim of this study was to evaluate the outcomes of 68Ga prostate-specific membrane antigen (68Ga-PSMA) positron-emission tomography (PET)/CT-based metastasis-directed treatment (MDT) for oligometastatic prostate cancer (PC). METHODS: In this multi-institutional study, clinical data of 176 PC patients with 353 lesions receiving MDT between 2014 and 2019 were retrospectively evaluated. All patients had biopsy proven PC with ≤5 metastases detected with 68Ga-PSMA-PET/CT. MDT was delivered with conventional fractionation or stereotactic body radiotherapy (SBRT) techniques. CTCAE v4.0 was used for acute and RTOG/EORTC Late Radiation Morbidity Scoring Schema was used for late toxicity evaluation. RESULTS: At the time of MDT, 59 patients (33.5%) had synchronous and 117 patients (66.5%) had metachronous metastases. Median number of metastases was one and the MDT technique was SBRT in 73.3% patients. The 2‑year overall survival (OS) and progression-free survival (PFS) rates were 87.6% and 63.1%, respectively. With a median follow-up of 22.9 months, 9 patients had local recurrence at the irradiated site. The 2‑year local control rate at the treated oligometastatic site per patient was 93.2%. In multivariate analysis, an increased number of oligometastases and untreated primary PC were negative predictors for OS; advanced clinical tumor stage, untreated primary PC, BED3 value of ≤108 Gy, and MDT with conventional fractionation were negative predictors for PFS. No patient experienced grade ≥3 acute toxicity, but one patient had a late grade 3 toxicity of compression fracture after spinal SBRT. CONCLUSION: 68Ga-PSMA-PET/CT-based MDT is an efficient and safe treatment for oligometastatic PC patients. Proper patient selection might improve treatment outcomes.
Entities:
Keywords:
Oligometastasis; PSMA PET; Prostate adenocarcinoma; Stereotactic body radiotherapy; Survival
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