Evidence map›Paper›PMID 41432893›Full record

ArticleEJNMMI physics2025

Morphological versus spherical cellular geometry models: impact on dose-response of CA20948 cells to

Kaat Spoormans, Melissa Crabbé, Lara Struelens, Michel Koole

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

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0citing papers in PubMed
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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

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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

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Kaat SpoormansNuclear Medical Applications, Belgian Nuclear Research Centre (SCK CEN), Mol, 2400, Belgium.
Melissa CrabbéNuclear Medical Applications, Belgian Nuclear Research Centre (SCK CEN), Mol, 2400, Belgium. Melissa.Crabbe@sckcen.be.ORCID http://orcid.org/0000-0002-3706-6914
Lara StruelensNuclear Medical Applications, Belgian Nuclear Research Centre (SCK CEN), Mol, 2400, Belgium.
Michel KooleNuclear Medicine and Molecular Imaging, Department of Imaging and Pathology, KU Leuven, Leuven, 3000, Belgium.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAccurate cellular dosimetry is essential to investigate fundamental mechanisms of targeted radionuclide therapy. The aim of this study was to assess how morphological cellular geometry models influence cellular dosimetry estimates, in comparison to simplified spherical models that do not properly represent an adherent cell geometry.

methodsVirtual cell models of the CA20948 cell line were generated by confocal microscopy of SSTR2 and DAPI staining and served as input to derive morphological S-values for

resultsThirty-four cell geometries were modeled and a spherical model with equivalent volume was generated with a radius for the cell and nucleus of 8.6(7) µm and 5.5(6) µm, respectively. Compared to spherical cell models, morphological cell models significantly changed the S-value with an increase of 13% (

conclusionThese findings validate the use of simplified spherical models for CA20948 cells but highlight the importance of a correct estimation of the cell dimensions.

Indexed as

Cell dosimetryDOTA-LM3DOTA-TATELutetium-177Morphological cell modelPRRTSSTR2Terbium-161

Identifiers

PMID41432893
PMCPMC12847496

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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.