Evidence map›Paper›PMID 37099047›Full record

ArticleEJNMMI research2023

Detecting localised prostate cancer using radiomic features in PSMA PET and multiparametric MRI for biologically targeted radiation therapy.

Tsz Him Chan, Annette Haworth, Alan Wang, Mahyar Osanlouy, Scott Williams, Catherine Mitchell, Michael S Hofman, Rodney J Hicks, Declan G Murphy, Hayley M Reynolds

Open access · goldAbstract read
In one paragraph

Article in EJNMMI research, 2023. 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
5.2field-weighted citation impact, top 4% of its field
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, 20 citations in OpenAlex.

  1. Review
  2. An interpretableEuropean journal of nuclear medicine and molecular imaging · 2026
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  13. [Bioengineering (Basel, Switzerland) · 2023
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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

10 authors at 4 institutions in 2 countries.

Tsz Him ChanAuckland Bioengineering Institute, The University of Auckland, Auckland, New Zealand.
Annette HaworthInstitute of Medical Physics, School of Physics, The University of Sydney, Sydney, NSW, Australia.
Alan WangAuckland Bioengineering Institute, The University of Auckland, Auckland, New Zealand.
Mahyar OsanlouyAuckland Bioengineering Institute, The University of Auckland, Auckland, New Zealand.
Scott WilliamsSir Peter MacCallum Department of Oncology, The University of Melbourne, Melbourne, VIC, Australia.
Catherine MitchellDepartment of Pathology, Peter MacCallum Cancer Centre, Melbourne, VIC, Australia.
Michael S HofmanSir Peter MacCallum Department of Oncology, The University of Melbourne, Melbourne, VIC, Australia.
Rodney J HicksDepartment of Medicine, St Vincent's Hospital Medical School, The University of Melbourne, Melbourne, VIC, Australia.
Declan G MurphyDivision of Cancer Surgery, Peter MacCallum Cancer Centre, Melbourne, VIC, Australia.
Hayley M ReynoldsAuckland Bioengineering Institute, The University of Auckland, Auckland, New Zealand. Hayley.Reynolds@auckland.ac.nz.ORCID http://orcid.org/0000-0001-8146-1113
University of Auckland · NZThe University of Melbourne · AUPeter MacCallum Cancer Centre · AUThe University of Sydney · AU

Funding

Health Research Council of New Zealand 20/017National Health and Medical Research Council 1126955Prostate Cancer Foundation of Australia YI 0513
6 · The paper itself

Abstract

backgroundProstate-Specific Membrane Antigen (PSMA) PET/CT and multiparametric MRI (mpMRI) are well-established modalities for identifying intra-prostatic lesions (IPLs) in localised prostate cancer. This study aimed to investigate the use of PSMA PET/CT and mpMRI for biologically targeted radiation therapy treatment planning by: (1) analysing the relationship between imaging parameters at a voxel-wise level and (2) assessing the performance of radiomic-based machine learning models to predict tumour location and grade.

methodsPSMA PET/CT and mpMRI data from 19 prostate cancer patients were co-registered with whole-mount histopathology using an established registration framework. Apparent Diffusion Coefficient (ADC) maps were computed from DWI and semi-quantitative and quantitative parameters from DCE MRI. Voxel-wise correlation analysis was conducted between mpMRI parameters and PET Standardised Uptake Value (SUV) for all tumour voxels. Classification models were built using radiomic and clinical features to predict IPLs at a voxel level and then classified further into high-grade or low-grade voxels.

resultsPerfusion parameters from DCE MRI were more highly correlated with PET SUV than ADC or T2w. IPLs were best detected with a Random Forest Classifier using radiomic features from PET and mpMRI rather than either modality alone (sensitivity, specificity and area under the curve of 0.842, 0.804 and 0.890, respectively). The tumour grading model had an overall accuracy ranging from 0.671 to 0.992.

conclusionsMachine learning classifiers using radiomic features from PSMA PET and mpMRI show promise for predicting IPLs and differentiating between high-grade and low-grade disease, which could be used to inform biologically targeted radiation therapy planning.

Indexed as

Multiparametric MRIProstate cancerPSMA PET/CTRadiation therapyRadiomics

Identifiers

PMID37099047
PMCPMC10133419
OpenAlexW4367047690

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.