Evidence map›Paper›PMID 41001569›Full record

ArticleArXiv2025

Quantitative In Vivo Cherenkov Luminescence Imaging and Dosimetry of

Campbell D Haasch, Malick Bio Idrissou, Sydney Jupitz, Aubrey Parks, Reinier Hernandez, Brian W Pogue, Bryan P Bednarz

Abstract readPreprint
In one paragraph

Article in ArXiv, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

Campbell D HaaschDepartment of Medical Physics, University of Wisconsin School of Medicine and Public Health, University of Wisconsin-Madison, Madison, WI, United States.ORCID 0009-0002-7128-0129
Malick Bio IdrissouDepartment of Medical Physics, University of Wisconsin School of Medicine and Public Health, University of Wisconsin-Madison, Madison, WI, United States.ORCID 0009-0001-0437-6668
Sydney JupitzDepartment of Medical Physics, University of Wisconsin School of Medicine and Public Health, University of Wisconsin-Madison, Madison, WI, United States.ORCID 0000-0001-9104-8920
Aubrey ParksDepartment of Medical Physics, University of Wisconsin School of Medicine and Public Health, University of Wisconsin-Madison, Madison, WI, United States.ORCID 0009-0000-9382-0937
Reinier HernandezDepartment of Medical Physics, University of Wisconsin School of Medicine and Public Health, University of Wisconsin-Madison, Madison, WI, United States.ORCID 0000-0002-0729-2179
Brian W PogueDepartment of Medical Physics, University of Wisconsin School of Medicine and Public Health, University of Wisconsin-Madison, Madison, WI, United States.ORCID 0000-0002-9887-670X
Bryan P BednarzDepartment of Medical Physics, University of Wisconsin School of Medicine and Public Health, University of Wisconsin-Madison, Madison, WI, United States.ORCID 0000-0002-7467-9816

Funding

UW COMPREHENSIVE CANCER CENTER SUPPORTP30CA014520 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI Justine Yang Bruce · 1985 to 2026
$142.6M
Radionuclide Production and Radiochemistry Core Description CoreP01CA250972 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI KIM, KYUNGMANN · 2020 to 2024
$12.5M
UW SPECT/CT AcquisitionS10OD028670 · OD · UNIVERSITY OF WISCONSIN-MADISON · PI WEICHERT, JAMEY P · 2020 to 2020
$598k
NCI NIH HHS P01 CA250972NCI NIH HHS P30 CA014520NIH HHS S10 OD028670
6 · The paper itself

Abstract

Purpose: The rapid expansion of radiopharmaceutical therapy (RPT) development demands scalable preclinical dosimetry methods. While PET and SPECT remain the gold standards, their low throughput and high cost limit large-cohort studies. Cherenkov luminescence imaging (CLI) offers a high-throughput alternative but suffers from depth-dependent attenuation and photon scatter that compromise quantitative accuracy. This work develops and validates a quantitative CLI methodology incorporating attenuation and scatter corrections to enable accurate preclinical dosimetry. Methods: Depth-dependent attenuation was characterized using a tissue-mimicking phantom to derive calibration coefficients. Photon scatter was modeled using GEANT4-generated Cherenkov spread functions (CSFs), applied in a depth-weighted iterative Richardson-Lucy deconvolution/reconvolution framework. The method was evaluated in NU/NU mice (n=4) bearing MC38 tumors after injection of Results: CLI-PET activity quantification yielded mean errors of 15.4% (liver) and 10.3% (tumor) over the first three timepoints. Tumor absorbed doses from CLI-derived synthetic PET images (3.4 ± 0.3 Gy/MBq) were statistically indistinguishable from PET-based estimates (3.2 ± 0.2 Gy/MBq, p=0.31). Discrepancies increased at late timepoints due to low activity and background auto-luminescence. Conclusions: With appropriate depth-dependent attenuation calibration and Monte Carlo-derived scatter correction, CLI can provide quantitative biodistribution and dosimetry estimates comparable to PET. This approach enables high-throughput, low-cost in vivo dosimetry, expanding the feasibility of large-scale preclinical RPT studies and supporting translational radiopharmaceutical development.

Indexed as

Cherenkov Luminescence Imaging (CLI)Preclinical DosimetryRadiopharmaceutical Therapy (RPT)

Identifiers

PMID41001569
PMCPMC12458591

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.