Evidence map›Paper›PMID 30887194›Full record

ArticleEuropean radiology2019

Assessment of the extracellular volume fraction for the grading of clear cell renal cell carcinoma: first results and histopathological findings.

Lisa C Adams, Philipp Jurmeister, Bernhard Ralla, Keno K Bressem, Ute L Fahlenkamp, Guenther Engel, Stefan Siepmann, Moritz Wagner, Bernd Hamm, Jonas Busch and 1 more

Abstract read
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In one paragraph

Article in European radiology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
1.0field-weighted citation impact, top 22% 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

35 citing papers in PubMed, 43 citations in OpenAlex.

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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

11 authors at 1 institution in 1 country.

Lisa C AdamsDepartment of Radiology, Charité, Charitéplatz 1, 10117, Berlin, Germany. Lisa.adams@charite.de.ORCID http://orcid.org/0000-0001-5836-4542
Philipp JurmeisterDepartment of Pathology, Charité, Charitéplatz 1, 10117, Berlin, Germany.
Bernhard RallaDepartment of Urology, Charité, Charitéplatz 1, 10117, Berlin, Germany.
Keno K BressemDepartment of Radiology, Charité, Hindenburgdamm 30, 12203, Berlin, Germany.
Ute L FahlenkampDepartment of Radiology, Charité, Charitéplatz 1, 10117, Berlin, Germany.
Guenther EngelDepartment of Radiology, Charité, Charitéplatz 1, 10117, Berlin, Germany.
Stefan SiepmannDepartment of Radiology, Charité, Charitéplatz 1, 10117, Berlin, Germany.
Moritz WagnerDepartment of Radiology, Charité, Charitéplatz 1, 10117, Berlin, Germany.
Bernd HammDepartment of Radiology, Charité, Charitéplatz 1, 10117, Berlin, Germany.
Jonas BuschDepartment of Urology, Charité, Charitéplatz 1, 10117, Berlin, Germany.
Marcus R MakowskiDepartment of Radiology, Charité, Charitéplatz 1, 10117, Berlin, Germany.
Charité - Universitätsmedizin Berlin · DE

Funding

Deutsche Forschungsgemeinschaft SFB 1340/1 2018, 5943/31/41
6 · The paper itself

Abstract

objectivesTo assess the potential of T1 mapping-based extracellular volume fraction (ECV) for the identification of higher grade clear cell renal cell carcinoma (cRCC), based on histopathology as the reference standard.

methodsFor this single-center, institutional review board-approved prospective study, 27 patients (17 men, median age 62 ± 12.4 years) with pathologic diagnosis of cRCC (nucleolar International Society of Urological Pathology (ISUP) grading) received abdominal MRI scans at 1.5 T using a modified Look-Locker inversion recovery (MOLLI) sequence between January 2017 and June 2018. Quantitative T1 values were measured at different time points (pre- and postcontrast agent administration) and quantification of the ECV was performed on MRI and histological sections (H&E staining).

resultsReduction in T1 value after contrast agent administration and MR-derived ECV were reliable predictors for differentiating higher from lower grade cRCC. Postcontrast T1

conclusionsT1 mapping with ECV measurement could represent a novel in vivo biomarker for the classification of cRCC regarding their nucleolar grade, providing incremental diagnostic value as a quantitative MR marker. KEY POINTS: • Reduction in MRI T1 relaxation times after contrast agent administration and MR-derived extracellular volume fraction are useful parameters for grading of clear cell renal cell carcinoma (cRCC). • T1 differences between the native and the nephrogenic phase are higher for higher grade cRCC compared with lower grade cRCC and MRI-derived extracellular volume fraction (ECV) and histological ECV show a strong correlation. • T1 mapping with ECV measurement may be helpful for the noninvasive assessment of cRCC pathology, being a safe and feasible method, and it has potential to optimize individualized treatment options, e.g., in the decision of active surveillance.

Indexed as

Carcinoma, Renal CellFemaleHumansKidneyKidney NeoplasmsMagnetic Resonance ImagingMaleMiddle AgedNeoplasm StagingProspective StudiesReproducibility of ResultsROC CurveExtracellular matrixExtracellular spaceMagnetic resonance imagingNeoplasm gradingRenal cell carcinoma

Identifiers

PMID30887194
OpenAlexW2921207121

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.