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Jean-Mathieu Beauregard

Publications and source records attributed to Jean-Mathieu Beauregard.

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Towards Routine AI-Based PET/CT and SPECT/CT Lesion Segmentation and Tracking in PSMA Theranostics

Quantitative molecular imaging is central to treatment response assessment in oncology, yet clinical practice remains largely dominated by patient-level or limited target-lesion criteria that ignore inter-lesion heterogeneity. This limitation is particularly important in prostate cancer, where PSMA PET/CT can reveal extensive skeletal and nodal metastatic disease that often evolves heterogeneously under therapy. Accurate and scalable lesion segmentation and tracking across serial PSMA PET/CT and post-therapy SPECT/CT scans is therefore essential for implementing emerging PSMA-specific response frameworks, such as RECIP 1.0, and for enabling lesion-level dosimetry in 177Lu-PSMA radiopharmaceutical therapies (RPTs). This article examines clinical motivations, technical foundations, and future pathways for automated lesion tracking in prostate cancer imaging. We focus on the unique requirements introduced by PSMA PET/CT compared with FDG PET/CT and highlight the critical role of quantitative SPECT/CT in linking imaging-derived disease characterization with delivered therapeutic dose. Recent advances in AI-based segmentation and automated lesion matching now make scalable longitudinal lesion correspondence feasible, providing comprehensive infrastructure for standardized response assessment and personalized PSMA-based theranostics

physics.med-ph

Role of AI in Theranostics: Towards Routine Personalized Radiopharmaceutical Therapies

We highlight emerging uses of artificial intelligence (AI) in the field of theranostics, focusing on its significant potential to enable routine and reliable personalization of radiopharmaceutical therapies (RPTs). Personalized RPTs require patient-individual dosimetry calculations accompanying therapy. Image-based dosimetry needs: 1) quantitative imaging; 2) co-registration and organ/tumor identification on serial and multimodality images; 3) determination of the time-integrated activity; and 4) absorbed dose determination. AI models that facilitate these steps are reviewed. Additionally we discuss the potential to exploit biological information from diagnostic and therapeutic molecular images to derive biomarkers for absorbed dose and outcome prediction, towards personalization of therapies. We try to motivate the nuclear medicine community to expand and align efforts into making routine and reliable personalization of RPTs a reality.

physics.med-ph