Biodistribution and radiation dosimetry in cancer patients of the ascorbic acid analogue 6-Deoxy-6-[<sup>18</sup>F] fluoro-L-ascorbic acid PET imaging: first-in-human study.
prospective_cohort · Level II
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- Record sourced from PubMed, PMID 37191679.
- Also identified by DOI 10.1007/s00259-023-06262-9.
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Abstract
Clinical studies on the use of ascorbic acid (AA) have become a hot spot in cancer research. There remains an unmet need to assess AA utilization in normal tissues and tumors. 6-Deoxy-6-[<sup>18</sup>F]fluoro-L-ascorbic acid ([<sup>18</sup>F]DFA) displayed distinctive tumor localization and similar distribution as AA in mice. In this study, to evaluate the distribution, tumor detecting ability and radiation dosimetry of [<sup>18</sup>F]DFA in humans, we performed the first-in-human PET imaging study. Six patients with a variety of cancers underwent whole-body PET/CT scans after injection of 313-634 MBq of [<sup>18</sup>F]DFA. Five sequential dynamic emission scans in each patient were acquired at 5-60 min. Regions of interest (ROI) were delineated along the edge of the source-organ and tumor on the transverse PET slice. Tumor-to-background ratio (TBR) was obtained using the tumor SUVmax to background SUVmean. Organ residence times were calculated via time-activity curves, and human absorbed doses were estimated from organ residence time using the medical internal radiation dosimetry method. [<sup>18</sup>F]DFA was well tolerated in all subjects without serious adverse event. The high uptake was found in the liver, adrenal glands, kidneys, choroid plexus, and pituitary gland. [<sup>18</sup>F]DFA accumulated in tumor rapidly and the TBR increased over time. The average SUVmax of [<sup>18</sup>F]DFA in tumor lesions was 6.94 ± 3.92 (range 1.62-22.85, median 5.94). The organs with the highest absorbed doses were the liver, spleen, adrenal glands, and kidneys. The mean effective dose was estimated to be 1.68 ± 0.36 E<sup>-02</sup> mSv/MBq. [<sup>18</sup>F]DFA is safe to be used in humans. It showed a similar distribution pattern as AA, and displayed high uptake and retention in tumors with appropriate kinetics. [<sup>18</sup>F]DFA might be a promising radiopharmaceutical in identifying tumors with high affinity for SVCT2 and monitoring AA distribution in both normal tissues and tumors. Chinese Clinical Trial Registry; Registered Number: ChiCTR2200057842 (registered 19 March 2022).
Medical subject headings
- Positron Emission Tomography Computed Tomography
- Neoplasms