Evidence map›Paper›PMID 36908585›Full record

ArticleJournal of clinical imaging science2023

Multiparametric magnetic resonance imaging for characterizing renal tumors: A validation study of the algorithm presented by Cornelis

Pia Iben Pietersen, Janni Lynggård Bo Madsen, Jon Asmussen, Lars Lund, Tommy Kjærgaard Nielsen, Michael Pedersen, Birte Engvad, Ole Graumann

Abstract read
In one paragraph

Article in Journal of clinical imaging science, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Innovative studies in the Journal of Clinical Imaging Science.Journal of clinical imaging science · 2024
    Article
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.

Pia Iben PietersenDepartment of Radiology, Odense University Hospital, Odense, Denmark.ORCID https://orcid.org/0000-0001-5718-3635
Janni Lynggård Bo MadsenResearch and Innovation Unit, Department of Clinical Research, University of Southern Denmark, Odense, Denmark.
Jon AsmussenDepartment of Radiology, Odense University Hospital, Odense, Denmark.
Lars LundDepartment of Urology, Odense University Hospital, Odense, Denmark.
Tommy Kjærgaard NielsenDepartment of Urology, Aarhus University Hospital, Aarhus, Denmark.ORCID https://orcid.org/0000-0002-4379-1979
Michael PedersenDepartment of Clinical Medicine - Comparative Medicine Lab, Aarhus University Hospital, Aarhus, Denmark.
Birte EngvadDepartment of Pathology, Odense University Hospital, Odense, Denmark.
Ole GraumannDepartment of Radiology, Odense University Hospital, Odense, Denmark.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objectives: In the last decade, the incidence of renal cell carcinoma (RCC) has been rising, with the greatest increase observed for solid tumors. Magnetic resonance imaging (MRI) protocols and algorithms have recently been available for classifying RCC subtypes and benign subtypes. The objective of this study was to prospectively validate the MRI algorithm presented by Cornelis Material and Methods: Over a 7-month period, 38 patients with 44 renal tumors were prospectively included in the study and received an MRI examination in addition to the conventional investigation program. The MRI sequences were: T2-weighted, dual chemical shift MRI, diffusion-weighted imaging (DWI), and dynamic contrast-enhanced T1-weighted in wash-in and wash-out phases. The images were evaluated according to the algorithm by two experienced, blinded radiologists, and the histopathological diagnosis served as the gold standard. Results: Of 44 tumors in 38 patients, only 8 tumors (18.2%) received the same MRI diagnosis according to the algorithm as the histopathological diagnosis. MRI diagnosed 16 angiomyolipoma, 14 clear cell RCC (ccRCC), 12 chromophobe RCC (chRCC), and two papillary RCC (pRCC), while histopathological examination diagnosed 24 ccRCC, four pRCC, one chRCC, and one mixed tumor of both pRCC and chRCC. Malignant tumors were statistically significantly larger than the benign (3.16 ± 1.34 cm vs. 2.00 ± 1.04 cm, Conclusion: This prospective study could not reproduce Cornelis

Indexed as

Imaging sequencesKidneyMagnetic resonance imagingNeoplasms-primaryUrinary

Identifiers

PMID36908585
PMCPMC9992978

What OpenQuestion holds

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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.