International journal of radiation oncology, biology, physics · 2025
Machine Learning-based Dose Prediction in [177Lu]Lu-PSMA-617 Therapy by Integrating Biomarkers and Radiomic Features from [68Ga]Ga-PSMA-11 Positron Emission Tomography/Computed Tomography.
СтатьяПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод в очереди
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Yazdani Elmira, Sadeghi Mahdi, Karamzade-Ziarati Najme, Jabari Parmida, Amini Payam, Vosoughi Habibeh, Akbari Malihe Shahbazi, Asadi Mahboobeh, Kheradpisheh Saeed Reza, Geramifar Parham
Аннотация
PURPOSE: The study aimed to develop machine learning (ML) models for pretherapy prediction of absorbed doses (ADs) in kidneys and tumoral lesions for patients with metastatic castration-resistant prostate cancer (mCRPC) undergoing [177Lu]Lu-PSMA-617 (Lu-PSMA) radioligand therapy (RLT). By leveraging radiomic features (RFs) from [68Ga]Ga-PSMA-11 (Ga-PSMA) positron emission tomography/computed tomography (PET/CT) scans and clinical biomarkers (CBs), the approach has the potential to improve patient selection and tailor dosimetry-guided therapy.
METHODS AND MATERIALS: Twenty patients with mCRPC underwent Ga-PSMA PET/CT scans before the administration of an initial 6.8 ± 0.4 GBq activity of the first Lu-PSMA RLT cycle. Posttherapy dosimetry involved sequential scintigraphy imaging at ∼4, 48, and 72 hours, along with a single photon emission computed tomography (SPECT)/CT image at around 48 hours, to calculate time-integrated activity coefficients. Monte Carlo (MC) simulations, leveraging the Geant4 application for tomographic emission toolkit, were employed to derive ADs. The ML models were trained using pretherapy RFs from Ga-PSMA PET/CT and CBs as input, whereas the ADs in kidneys and lesions (n = 130), determined using MC simulations from scintigraphy and SPECT imaging, served as the ground truth. Model performance was assessed through leave-one-out cross-validation, with evaluation metrics including R² and root mean squared error (RMSE).
RESULTS: The mean delivered ADs were 0.88 ± 0.34 Gy/GBq for kidneys and 2.36 ± 2.10 Gy/GBq for lesions. Combining CBs with the best RFs produced optimal results: the extra trees regressor was the best ML model for predicting kidney ADs, achieving an RMSE of 0.11 Gy/GBq and an R² of 0.87. For lesion ADs, the gradient-boosting regressor performed best, with an RMSE of 1.04 Gy/GBq and an R² of 0.77.
CONCLUSIONS: Integrating pretherapy Ga-PSMA PET/CT RFs with CBs shows potential in predicting ADs in RLT. To personalize treatment planning and enhance patient stratification, it is crucial to validate these preliminary findings with a larger sample size and an independent cohort.
METHODS AND MATERIALS: Twenty patients with mCRPC underwent Ga-PSMA PET/CT scans before the administration of an initial 6.8 ± 0.4 GBq activity of the first Lu-PSMA RLT cycle. Posttherapy dosimetry involved sequential scintigraphy imaging at ∼4, 48, and 72 hours, along with a single photon emission computed tomography (SPECT)/CT image at around 48 hours, to calculate time-integrated activity coefficients. Monte Carlo (MC) simulations, leveraging the Geant4 application for tomographic emission toolkit, were employed to derive ADs. The ML models were trained using pretherapy RFs from Ga-PSMA PET/CT and CBs as input, whereas the ADs in kidneys and lesions (n = 130), determined using MC simulations from scintigraphy and SPECT imaging, served as the ground truth. Model performance was assessed through leave-one-out cross-validation, with evaluation metrics including R² and root mean squared error (RMSE).
RESULTS: The mean delivered ADs were 0.88 ± 0.34 Gy/GBq for kidneys and 2.36 ± 2.10 Gy/GBq for lesions. Combining CBs with the best RFs produced optimal results: the extra trees regressor was the best ML model for predicting kidney ADs, achieving an RMSE of 0.11 Gy/GBq and an R² of 0.87. For lesion ADs, the gradient-boosting regressor performed best, with an RMSE of 1.04 Gy/GBq and an R² of 0.77.
CONCLUSIONS: Integrating pretherapy Ga-PSMA PET/CT RFs with CBs shows potential in predicting ADs in RLT. To personalize treatment planning and enhance patient stratification, it is crucial to validate these preliminary findings with a larger sample size and an independent cohort.
Предметные рубрики MeSH
HumansMalePositron Emission Tomography Computed TomographyMachine LearningGallium RadioisotopesProstatic Neoplasms, Castration-ResistantLutetiumDipeptidesGallium IsotopesHeterocyclic Compounds, 1-RingAgedKidneyRadiotherapy DosageOrganometallic CompoundsMiddle AgedRadiopharmaceuticalsRadioisotopesBiomarkers, TumorMonte Carlo MethodRadiomicsProstate-Specific Antigen