International journal of radiation oncology, biology, physics · 2025
PSMA-PET-Guided Intraprostatic Boost in Prostate SBRT (PROBE): A Phase 2 Trial.
СтатьяКлиническое исследование II фазыПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод в очереди
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Singh Maneesh, Katdare Aparna, Ghosh Suchismita, Choudhury Sayak, Phurailatpam Reena, Patil Divya, Tiwari Mahima, Anaz Muhammed, Chougle Nazneen Husain, Sable Nilesh, Agrawal Archi, Pawar Akash, Rangarajan Venkatesh, Maitre Priyamvada, Murthy Vedang
Аннотация
PURPOSE: To assess the safety of using combined Gallium68-prostate-specific membrane antigen (PSMA)-positron emission tomography (PET)/computed tomography (CT) (68Ga-PSMA-PET/CT) and multiparametric magnetic resonance imaging (mpMRI) for planning dominant intraprostatic lesion (DIL) boost in prostate stereotactic radiation therapy (SBRT) for dose escalation (PROBE).
METHODS AND MATERIALS: Patients with intermediate- or high-risk prostate adenocarcinoma with DIL identified on mpMRI and 68Ga-PSMA-PET/CT and suitable for SBRT were enrolled in this phase 2 trial. 68Ga-PSMA-PET/CT was fused with mpMRI for gross tumor volume (GTV) delineation. Semiautomatic contouring of DIL was performed using 20% to 90% of the maximum standardized uptake value (SUVmax) (DILx%). Concordance metrics were used to select the DILx% matching closest to GTVMRI (GTVPET). Prostate (36.25 Gy), pelvic nodes (25 Gy), GTVunion: GTVPET ∪ GTVMRI (40 Gy), and GTVoverlap: GTVPET ∩ GTVMRI (42.5 Gy) were planned for 5-fraction SBRT. All patients received androgen deprivation therapy (ADT) for 6 months. The primary endpoint for the present analysis was concordance (volumetric and spatial) between GTVMRI and GTVPET. Secondary endpoints included the percentage SUVmax threshold for GTVPET contouring (%SUVGTV-PET) and cumulative acute (≤90 days) urinary and gastrointestinal toxicity using Common Terminology Criteria for Adverse Event (CTCAE) v5.0.
RESULTS: Thirty patients (54% intermediate risk, 46% high risk) were enrolled. GTVMRI and GTVPET showed strong volumetric correlation (Spearman correlation coefficient ρ = 0.817, 95% CI, 0.64-0.91; P < .001). The median Dice similarity coefficient, Jaccard index, and the mean Hausdorff distance for PET and magnetic resonance imaging boost volumes were 0.56, 0.37, and 2.2, respectively. The median %SUVGTV-PET was 48% (IQR, 40%-58%). There was an inverse correlation between DIL SUVmax and %SUVGTV-PET (Spearman correlation coefficient ρ = -0.598, 95% CI lower -0.79, upper -0.29; P < 0.001). Cumulative grade 2 acute urinary and GI toxicity were 13.3% and 6.6%, respectively, with no grade ≥3 toxicities.
CONCLUSION: Boost volumes on 68Ga-PSMA-PET/CT and mpMRI were volumetrically similar, however, with poor spatial concordance. The %SUVmax threshold for GTVPET contouring correlated inversely with DIL SUVmax and was a median of 48%. Based on the favorable acute toxicity profile, PSMA-PET-guided intraprostatic boost is likely to be safe for dose escalation in prostate SBRT.
METHODS AND MATERIALS: Patients with intermediate- or high-risk prostate adenocarcinoma with DIL identified on mpMRI and 68Ga-PSMA-PET/CT and suitable for SBRT were enrolled in this phase 2 trial. 68Ga-PSMA-PET/CT was fused with mpMRI for gross tumor volume (GTV) delineation. Semiautomatic contouring of DIL was performed using 20% to 90% of the maximum standardized uptake value (SUVmax) (DILx%). Concordance metrics were used to select the DILx% matching closest to GTVMRI (GTVPET). Prostate (36.25 Gy), pelvic nodes (25 Gy), GTVunion: GTVPET ∪ GTVMRI (40 Gy), and GTVoverlap: GTVPET ∩ GTVMRI (42.5 Gy) were planned for 5-fraction SBRT. All patients received androgen deprivation therapy (ADT) for 6 months. The primary endpoint for the present analysis was concordance (volumetric and spatial) between GTVMRI and GTVPET. Secondary endpoints included the percentage SUVmax threshold for GTVPET contouring (%SUVGTV-PET) and cumulative acute (≤90 days) urinary and gastrointestinal toxicity using Common Terminology Criteria for Adverse Event (CTCAE) v5.0.
RESULTS: Thirty patients (54% intermediate risk, 46% high risk) were enrolled. GTVMRI and GTVPET showed strong volumetric correlation (Spearman correlation coefficient ρ = 0.817, 95% CI, 0.64-0.91; P < .001). The median Dice similarity coefficient, Jaccard index, and the mean Hausdorff distance for PET and magnetic resonance imaging boost volumes were 0.56, 0.37, and 2.2, respectively. The median %SUVGTV-PET was 48% (IQR, 40%-58%). There was an inverse correlation between DIL SUVmax and %SUVGTV-PET (Spearman correlation coefficient ρ = -0.598, 95% CI lower -0.79, upper -0.29; P < 0.001). Cumulative grade 2 acute urinary and GI toxicity were 13.3% and 6.6%, respectively, with no grade ≥3 toxicities.
CONCLUSION: Boost volumes on 68Ga-PSMA-PET/CT and mpMRI were volumetrically similar, however, with poor spatial concordance. The %SUVmax threshold for GTVPET contouring correlated inversely with DIL SUVmax and was a median of 48%. Based on the favorable acute toxicity profile, PSMA-PET-guided intraprostatic boost is likely to be safe for dose escalation in prostate SBRT.
Предметные рубрики MeSH
HumansMaleProstatic NeoplasmsRadiosurgeryPositron Emission Tomography Computed TomographyAgedGallium RadioisotopesMiddle AgedMultiparametric Magnetic Resonance ImagingAdenocarcinomaRadiotherapy, Image-GuidedGallium IsotopesRadiopharmaceuticalsTumor BurdenGlutamate Carboxypeptidase IIAged, 80 and over