Evidence map›Paper›PMID 34905131›Full record

ArticleEJNMMI physics2021

A population-based method to determine the time-integrated activity in molecular radiotherapy.

Deni Hardiansyah, Ade Riana, Peter Kletting, Nouran R R Zaid, Matthias Eiber, Supriyanto A Pawiro, Ambros J Beer, Gerhard Glatting

Abstract read
In one paragraph

Article in EJNMMI physics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. Review
  2. EJNMMI physics · 2025
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  8. Impact of the Reference Multiple-Time-Point Dosimetry Protocol on the Validity of Single-Time-Point Dosimetry for [Journal of nuclear medicine : official publication, Society of Nuclear Medicine · 2024
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  11. Metabolic kinetic modeling of [European journal of nuclear medicine and molecular imaging · 2023
    Article
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4 · The record

Corrections and comments

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

8 authors.

Deni HardiansyahMedical Physics and Biophysics Division, Physics Department, Faculty of Mathematics and Natural Sciences, Universitas Indonesia, 16424, Depok, Indonesia.
Ade RianaMedical Physics and Biophysics Division, Physics Department, Faculty of Mathematics and Natural Sciences, Universitas Indonesia, 16424, Depok, Indonesia.
Peter KlettingMedical Radiation Physics, Department of Nuclear Medicine, Ulm University, Albert-Einstein-Allee 23, 89081, Ulm, Germany.
Nouran R R ZaidMedical Radiation Physics, Department of Nuclear Medicine, Ulm University, Albert-Einstein-Allee 23, 89081, Ulm, Germany.
Matthias EiberDepartment of Nuclear Medicine, Klinikum rechts der Isar, Technische Universität München, 81675, Munich, Germany.
Supriyanto A PawiroMedical Physics and Biophysics Division, Physics Department, Faculty of Mathematics and Natural Sciences, Universitas Indonesia, 16424, Depok, Indonesia.
Ambros J BeerDepartment of Nuclear Medicine, Ulm University, 89081, Ulm, Germany.
Gerhard GlattingMedical Radiation Physics, Department of Nuclear Medicine, Ulm University, Albert-Einstein-Allee 23, 89081, Ulm, Germany. gerhard.glatting@uni-ulm.de.ORCID http://orcid.org/0000-0001-7916-1576

Funding

deutscher akademischer austauschdienst 2018/19-57381412universitas indonesia NKB-1947/UN2.R3.1/HKP.05.00/2019
6 · The paper itself

Abstract

backgroundThe calculation of time-integrated activities (TIAs) for tumours and organs is required for dosimetry in molecular radiotherapy. The accuracy of the calculated TIAs is highly dependent on the chosen fit function. Selection of an adequate function is therefore of high importance. However, model (i.e. function) selection works more accurately when more biokinetic data are available than are usually obtained in a single patient. In this retrospective analysis, we therefore developed a method for population-based model selection that can be used for the determination of individual time-integrated activities (TIAs). The method is demonstrated at an example of [

methodsRenal biokinetics of [

resultsThe function [Formula: see text] with shared parameter [Formula: see text] was selected as the function most supported by the data with an Akaike weight of 97%. Parameters [Formula: see text] and [Formula: see text] were fitted individually for every patient while parameter [Formula: see text] was fitted as a shared parameter in the population yielding a value of 0.9632 ± 0.0037.

conclusionsThe presented population-based model selection allows for a higher number of parameters of investigated fit functions which leads to better fits. It also reduces the uncertainty of the obtained Akaike weights and the selected best fit function based on them. The use of the population-determined shared parameter for future patients allows the fitting of more appropriate functions also for patients for whom only a low number of individual data are available.

Indexed as

Absorbed doseModel selectionTIAs

Identifiers

PMID34905131
PMCPMC8671591

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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.