Evidence map›Paper›PMID 34694452›Full record

ArticleEuropean radiology2022

Autofluorescence imaging within the liver: a promising tool for the detection and characterization of primary liver tumors.

Charlotte Benoit, Aurélie Rodrigues, Julien Calderaro, Cécile Charpy, Sylvie Simonin, Jean-Charles Deybach, Laurent Gouya, Hervé Puy, Caroline Schmitt, René Farcy and 7 more

Abstract read
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In one paragraph

Article in European radiology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.2field-weighted citation impact, top 45% 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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. 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

17 authors at 6 institutions in 1 country.

Charlotte BenoitNodea Medical, 1 mail du Pr Georges Mathé, 94800, Villejuif, France.
Aurélie RodriguesNodea Medical, 1 mail du Pr Georges Mathé, 94800, Villejuif, France.
Julien CalderaroFaculté de Santé de Créteil, UPEC, Créteil, France.
Cécile CharpyDépartement de Pathologie, Hôpitaux Universitaires Henri Mondor, AP-HP, 51 Avenue du Marechal de Lattre de Tassigny, 94010, Créteil Cedex, France.
Sylvie SimoninCentre Français Des Porphyries, Hôpital Louis Mourier, Assistance Publique-Hôpitaux de Paris, Colombes, France.
Jean-Charles DeybachCentre Français Des Porphyries, Hôpital Louis Mourier, Assistance Publique-Hôpitaux de Paris, Colombes, France.
Laurent GouyaCentre Français Des Porphyries, Hôpital Louis Mourier, Assistance Publique-Hôpitaux de Paris, Colombes, France.
Hervé PuyCentre Français Des Porphyries, Hôpital Louis Mourier, Assistance Publique-Hôpitaux de Paris, Colombes, France.
Caroline SchmittCentre Français Des Porphyries, Hôpital Louis Mourier, Assistance Publique-Hôpitaux de Paris, Colombes, France.
René FarcyLaboratoire Aimé Cotton, Université Paris-Sud, ENS Cachan, CNRS, Université Paris-Saclay, 91405, Orsay Cedex, France.
Valérie VilgrainRadiologie, Hôpital Beaujon, APHP, Clichy, France.
Valérie ParadisAnatomopathologie, Hôpital Beaujon, APHP, Clichy, France.
Nicolas PoteAnatomopathologie, Hôpital Beaujon, APHP, Clichy, France.
Fouad LafdilINSERM IMRB U955, Equipe 18, Créteil, France.
Sébastien MuleINSERM IMRB U955, Equipe 18, Créteil, France.
Emmanuel IttiFaculté de Santé de Créteil, UPEC, Créteil, France.
Alain LucianiINSERM IMRB U955, Equipe 18, Créteil, France. alain.luciani@aphp.fr.ORCID http://orcid.org/0000-0003-0331-9474
Inserm · FRHôpital Beaujon · FRUniversité Paris-Est Créteil · FRAssistance Publique – Hôpitaux de Paris · FRHôpital Louis-Mourier · FRUniversité Paris-Sud · FR

Funding

ANR ANR CE19 0007 ALIVE
6 · The paper itself

Abstract

objectivesTo assess the performance of 405 nm-induced autofluorescence for the characterization of primary liver nodules on ex vivo resected specimens. MATERIALS AND

methodsForty resected liver specimens bearing 53 primary liver nodules were included in this IRB-approved prospective study. Intratissular spectroscopic measurements were performed using a 25-G fibered-needle on all ex vivo specimens: 5 autofluorescence measurements were performed in both nodules and adjacent parenchyma. The spectra derivatives of the 635 and 670 nm autofluorescence peaks observed in nodules and in adjacent liver parenchyma were compared (Kruskal-Wallis and Mann-Whitney when appropriate).

resultsA total of 42 potentially evolutive primary liver nodules-34 hepatocellular carcinomas, 4 intrahepatic cholangiocarcinomas, 4 hepatocellular adenomas-and 11 benign nodules-5 focal nodular hyperplasias, 6 regenerative nodules-were included. Both 635 and 670 nm Δderivatives were significantly higher in benign as compared to potentially evolutive (PEV) nodules (respectively 32.9 ± 4.5 vs 15.3 ± 1.4; p < 0.0001 and 5.7 ± 0.6 vs 2.5 ± 0.1; p < 0.0001) with respective sensitivity and specificity of 78% and 91% for distinguishing PEV from benign nodules.

conclusion405 nm-induced autofluorescence enables the discrimination of benign from PEV primary liver nodules, suggesting that autofluorescence imaging could be used to optimize US targeted liver biopsies. KEY POINTS: • 405 nm-induced autofluorescence can distinguish liver tumors from the adjacent liver parenchyma. • The analysis of autofluorescence imaging observed within primary liver tumors can discriminate benign tumors from those requiring follow-up or targeted liver biopsy. • In current practice, autofluorescence imaging could be embedded within biopsy needle, to enable, in addition to ultrasound guidance, optimal targeting of liver nodules which could optimize tissue sampling.

Indexed as

Bile Duct NeoplasmsCarcinoma, HepatocellularLiver NeoplasmsBile Ducts, IntrahepaticHumansLiverOptical ImagingProspective StudiesSensitivity and SpecificityBiopsyDiagnosisFluorescenceLiver neoplasmsOptical imaging

Identifiers

PMID34694452
OpenAlexW3210106104

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.