Five-Year Outcomes After Prostate-Specific Membrane Antigen PET/CT-Guided Salvage Radiotherapy Following Radical Prostatectomy.
[BACKGROUND] Salvage radiotherapy (sRT) is the standard of care for biochemical recurrence of prostate cancer following radical prostatectomy (RP).
- p-value P=.035
- p-value P=.024
- 95% CI 24.1-74.3
- 추적기간 59.4 months
APA
Nikitas J, Smith CP, et al. (2026). Five-Year Outcomes After Prostate-Specific Membrane Antigen PET/CT-Guided Salvage Radiotherapy Following Radical Prostatectomy.. Journal of the National Comprehensive Cancer Network : JNCCN, 24(2), 11-18. https://doi.org/10.6004/jnccn.2025.7102
MLA
Nikitas J, et al.. "Five-Year Outcomes After Prostate-Specific Membrane Antigen PET/CT-Guided Salvage Radiotherapy Following Radical Prostatectomy.." Journal of the National Comprehensive Cancer Network : JNCCN, vol. 24, no. 2, 2026, pp. 11-18.
PMID
41698328
Abstract
[BACKGROUND] Salvage radiotherapy (sRT) is the standard of care for biochemical recurrence of prostate cancer following radical prostatectomy (RP). In this context, prostate-specific membrane antigen (PSMA) PET/CT offers superior sensitivity and specificity for the detection of recurrent disease. We aimed to evaluate the impact of PSMA PET/CT-guided management on clinical outcomes following sRT.
[PATIENTS AND METHODS] We retrospectively screened 5 prospective PSMA PET/CT studies conducted between 2016 and 2021. Eligible patients underwent PSMA PET/CT for restaging at first biochemical recurrence after RP, received sRT, and had ≥24 months of follow-up. Progression-free survival (PFS), freedom from distant progression, and overall survival (OS) were calculated using the Kaplan-Meier method. Adjusted hazard ratios (aHRs) for PFS were derived using Cox proportional hazards regression, adjusting for age, pre-sRT prostate-specific antigen (PSA) level, use of androgen deprivation therapy (ADT), and receipt of whole-pelvis radiotherapy (WPRT).
[RESULTS] Of the total cohort, 113 patients met the inclusion criteria. Median follow-up was 59.4 months (IQR, 47.4-69.5). Median PSA was 0.4 ng/mL (IQR, 0.3-1.1), and the median time from RP was 19.9 months (IQR, 5.6-51.8). On PSMA PET/CT, 19 (16.8%) patients were staged as TrN0M0, 32 (28.3%) as N1M0, 16 (14.2%) as M1, and 46 (40.7%) as T0N0M0 (no visible disease). ADT was administered to 76 (67.3%) patients, and 63 (55.8%) patients received WPRT. Disease progression occurred in 57 (50.4%) patients. Median PFS was 49.2 months (95% CI, 24.1-74.3), and median freedom from distant progression was 76.4 months (95% CI, 62.9-89.9). The 5-year OS rate was 97.1% (95% CI, 94.1%-100%). Receipt of WPRT was significantly associated with improved PFS among patients staged as TrN0M0 (aHR, 0.12; P=.035), whereas ADT was significantly associated with improved PFS in patients staged as N1/M1 (aHR, 0.37; P=.024).
[CONCLUSIONS] In this 5-year follow-up study from an institution that was an early adopter of PSMA PET/CT, PSMA PET/CT-guided sRT was associated with favorable oncologic outcomes. Exploratory analyses suggest a potential benefit of WPRT following a positive PSMA PET/CT and of ADT in patients with N1/M1 disease.
[PATIENTS AND METHODS] We retrospectively screened 5 prospective PSMA PET/CT studies conducted between 2016 and 2021. Eligible patients underwent PSMA PET/CT for restaging at first biochemical recurrence after RP, received sRT, and had ≥24 months of follow-up. Progression-free survival (PFS), freedom from distant progression, and overall survival (OS) were calculated using the Kaplan-Meier method. Adjusted hazard ratios (aHRs) for PFS were derived using Cox proportional hazards regression, adjusting for age, pre-sRT prostate-specific antigen (PSA) level, use of androgen deprivation therapy (ADT), and receipt of whole-pelvis radiotherapy (WPRT).
[RESULTS] Of the total cohort, 113 patients met the inclusion criteria. Median follow-up was 59.4 months (IQR, 47.4-69.5). Median PSA was 0.4 ng/mL (IQR, 0.3-1.1), and the median time from RP was 19.9 months (IQR, 5.6-51.8). On PSMA PET/CT, 19 (16.8%) patients were staged as TrN0M0, 32 (28.3%) as N1M0, 16 (14.2%) as M1, and 46 (40.7%) as T0N0M0 (no visible disease). ADT was administered to 76 (67.3%) patients, and 63 (55.8%) patients received WPRT. Disease progression occurred in 57 (50.4%) patients. Median PFS was 49.2 months (95% CI, 24.1-74.3), and median freedom from distant progression was 76.4 months (95% CI, 62.9-89.9). The 5-year OS rate was 97.1% (95% CI, 94.1%-100%). Receipt of WPRT was significantly associated with improved PFS among patients staged as TrN0M0 (aHR, 0.12; P=.035), whereas ADT was significantly associated with improved PFS in patients staged as N1/M1 (aHR, 0.37; P=.024).
[CONCLUSIONS] In this 5-year follow-up study from an institution that was an early adopter of PSMA PET/CT, PSMA PET/CT-guided sRT was associated with favorable oncologic outcomes. Exploratory analyses suggest a potential benefit of WPRT following a positive PSMA PET/CT and of ADT in patients with N1/M1 disease.
MeSH Terms
Retrospective Studies; Salvage Therapy; Adenocarcinoma; Prostatic Neoplasms; Positron Emission Tomography Computed Tomography; Follow-Up Studies; Radiotherapy, Image-Guided; Survival Analysis; Humans; Male; Middle Aged; Aged; Prostatectomy; Neoplasm Recurrence, Local; Los Angeles; Gallium Radioisotopes
같은 제1저자의 인용 많은 논문 (3)
- Phase 2 Prospective Trial of Retreatment with [Lu]Lu-PSMA-617 Molecular Radiotherapy for Metastatic Castration-Resistant Prostate Cancer-RE-LuPSMA.
- Redefining Salvage Therapy for Localized Radiorecurrent Prostate Cancer-In More Ways Than One.
- Patient-Reported Outcomes With Stereotactic Intensity Modulated Radiotherapy After Radical Prostatectomy: A Nonrandomized Clinical Trial.