Evidence map›Paper›PMID 41491739›Full record

ArticleJournal of imaging informatics in medicine2026

Multiphase CT-Based Tumor and Peritumoral Radiomics for Characterization of Clear Cell Renal Cell Carcinoma.

Matt Muellner, S J Pawan, Xiaomeng Lei, Manju Aron, Mihir Desai, Neha Gurram, Mansi Garg, Steven Y Cen, Vinay Duddalwar

Abstract read
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In one paragraph

Article in Journal of imaging informatics in medicine, 2026. 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

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

9 authors.

Matt MuellnerRadiomics Lab, Department of Radiology, University of Southern California, Los Angeles, CA, 90033, USA.
S J PawanRadiomics Lab, Department of Radiology, University of Southern California, Los Angeles, CA, 90033, USA. pawansnj03@gmail.com.ORCID http://orcid.org/0000-0002-2560-9213
Xiaomeng LeiRadiomics Lab, Department of Radiology, University of Southern California, Los Angeles, CA, 90033, USA.
Manju AronRadiomics Lab, Department of Radiology, University of Southern California, Los Angeles, CA, 90033, USA.
Mihir DesaiDepartment of Radiology, Los Angeles General Medical Center, Los Angeles, CA, 90033, USA.
Neha GurramRadiomics Lab, Department of Radiology, University of Southern California, Los Angeles, CA, 90033, USA.
Mansi GargRadiomics Lab, Department of Radiology, University of Southern California, Los Angeles, CA, 90033, USA.
Steven Y CenRadiomics Lab, Department of Radiology, University of Southern California, Los Angeles, CA, 90033, USA.
Vinay DuddalwarRadiomics Lab, Department of Radiology, University of Southern California, Los Angeles, CA, 90033, USA.

Funding

USC/CHLA Summer Oncology Research Fellowship (SORF) Program for Medical StudentsR25CA225513 · NCI · CHILDREN'S HOSPITAL OF LOS ANGELES · PI ANAT ERDREICH-EPSTEIN, WIJBE MARTIN KAST · 2019 to 2026
$1.7M
NCI NIH HHS R25 CA225513
6 · The paper itself

Abstract

Clear cell renal cell carcinoma (ccRCC) prognosis is guided by a tumor's pathological features. While radiomics shows promise for non-invasive tumor characterization, it remains unclear whether incorporating the peritumoral region and leveraging multiphase CT imaging improves model performance beyond standard tumor-region analysis. This study aimed to determine whether radiomic features derived from the peritumoral area in standard four-phase CT protocol improve the prediction of ccRCC stage, grade, and aggressiveness compared to intratumoral features alone. A retrospective cohort of 250 patients with ccRCC was analyzed. Using tumor and 5-mm peritumoral regions on four-phase CT, 1874 radiomic features were extracted per region per phase. Elastic Net and Random Forest models were trained with tenfold cross-validation to predict binarized stage, grade, and aggressiveness outcomes using three feature sets: tumor region, peritumoral region, and a combined region including both the tumor and peritumoral regions. Models using only tumor-region features consistently outperformed those using the peritumoral and combined regions. The best tumor-region model achieved area under the receiver operating characteristic curve (AUC) values of 0.875 for stage, 0.697 for grade, and 0.915 for aggressiveness. Multiphase analysis provided no benefit over a single-phase approach, with the nephrographic phase alone yielding equivalent or superior performance to multiphase models across all outcomes. A simplified radiomic approach using features from the tumor region in the nephrographic phase alone provides optimal performance for predicting key ccRCC characteristics. The added complexity of peritumoral and multiphase analysis did not enhance predictive accuracy, potentially streamlining future ccRCC radiomic research.

Indexed as

Clear cell renal cell carcinomaMachine learningMultiphase CTPeritumoral regionRadiomicsTumor characterization

Identifiers

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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.