Sahota Sandeep, Quirindongo Krystal A, Piccolo Joseph, Chhabra Anupriya, Zaid Nouran, Deveauxbray Simin, Charles-Obi Kenechukwu C, Miller Brian, Hobbs Robert F, Sgouros George, Bastiaannet Remco
Mallinckrodt Institute of Radiology, University of Washington in St. Louis School of Medicine, St. Louis, MO, USA.
Russell H. Morgan Department of Radiology and Radiological Science, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Sci Rep. 2025 Aug 14;15(1):29807. doi: 10.1038/s41598-025-09277-4.
Alpha-emitter radiopharmaceutical therapy delivers highly localized radiation, offering potent therapeutic effects. However, microscale heterogeneity remains poorly characterized in vivo and may affect efficacy. This underscores the critical need for sub-organ dosimetry to better understand αRPT radiobiology and guide treatment optimization. While autoradiography enables high-resolution activity mapping, conventional approaches lack anatomical context for accurate dose mapping. To address this, we propose a comprehensive workflow integrating quantitative autoradiography with histological imaging. Tissues from αRPT-treated mice bearing HER2 + breast tumors were snap-frozen, sectioned, and imaged using autoradiography. The same sections were histologically stained and used for precise autoradiography-histology integration. These anatomical contexts were then used to accurately stack multiple sections in a 3D volume, and were used for subsequent microscale dosimetry. Both tumor and kidney tissues were analyzed. Snap-freezing in isopentane preserved tissue morphology optimally. Our method enabled precise activity localization, revealing significant accumulation in the kidney cortex region close to glomeruli. Anatomical context improved 3D reconstructions needed for accurate dose estimations in tumor tissue. This methodology enhances αRPT dosimetry by precise spatial mapping of autoradiography unto the underlying tissue morphology. These advancements provide crucial insights into αRPT spatial radiobiology at the near-cellular level and will aid in optimizing radiopharmaceutical design and treatment planning.
α发射体放射性药物疗法可提供高度局部化的辐射,具有强大的治疗效果。然而,体内微观尺度的异质性仍未得到充分表征,可能会影响疗效。这凸显了对亚器官剂量测定的迫切需求,以便更好地理解αRPT放射生物学并指导治疗优化。虽然放射自显影能够实现高分辨率的活性图谱绘制,但传统方法缺乏用于精确剂量映射的解剖学背景。为了解决这一问题,我们提出了一种将定量放射自显影与组织学成像相结合的综合工作流程。对携带HER2 +乳腺癌肿瘤的αRPT治疗小鼠的组织进行速冻、切片,并使用放射自显影进行成像。对相同的切片进行组织学染色,并用于精确的放射自显影 - 组织学整合。然后利用这些解剖学背景在三维体积中精确堆叠多个切片,并用于后续的微观尺度剂量测定。对肿瘤和肾脏组织均进行了分析。在异戊烷中速冻能最佳地保存组织形态。我们的方法能够实现精确的活性定位,揭示出在靠近肾小球的肾皮质区域有大量积累。解剖学背景改善了肿瘤组织中精确剂量估计所需的三维重建。这种方法通过将放射自显影精确地空间映射到基础组织形态上,增强了αRPT剂量测定。这些进展为近细胞水平的αRPT空间放射生物学提供了关键见解,并将有助于优化放射性药物设计和治疗计划。