Evidence map›Paper›PMID 34069662›Full record

ArticleCancers2021

Proof of Concept of a Binary Blood Assay for Predicting Radiosensitivity.

Sophie Deneuve, Céline Mirjolet, Thierry Bastogne, Mirlande Duclos, Paul Retif, Philippe Zrounba, Pierre-Eric Roux, Marc Poupart, Guillaume Vogin, Nicolas Foray and 1 more

Abstract read
In one paragraph

Article in Cancers, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Human Radiosensitivity and Radiosusceptibility: What Are the Differences?International journal of molecular sciences · 2021
    Review
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.

Sophie DeneuveCentre Léon Bérard, UNICANCER, 69008 Lyon, France.
Céline MirjoletCentre Georges François Leclerc, UNICANCER, 27877 Dijon, France.ORCID 0000-0003-0047-9421
Thierry BastogneCRAN CNRS UMR 7039, Université de Lorraine, 54505 Vandœuvre-lès-Nancy, France.
Mirlande DuclosNeolys Diagnostics, 67960 Strasbourg, France.
Paul RetifRadiation Therapy Department, Centre Hospitalier Régional Metz-Thionville, 57530 Ars-Laquenexy, France.ORCID 0000-0003-4997-2620
Philippe ZrounbaCentre Léon Bérard, UNICANCER, 69008 Lyon, France.
Pierre-Eric RouxCentre Léon Bérard, UNICANCER, 69008 Lyon, France.
Marc PoupartCentre Léon Bérard, UNICANCER, 69008 Lyon, France.
Guillaume VoginCentre François Baclesse, 4240 Ezch-sur-Alzette, Luxembourg.
Nicolas ForayRadiobiology Group, U1296 INSERM, 69008 Lyon, France.ORCID 0000-0002-1282-1303
Sandrine PereiraRadiobiology Group, U1296 INSERM, 69008 Lyon, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Radiation therapy (RT), either alone or in combination with surgery and/or chemotherapy is a keystone of cancers treatment. Early toxicity is common, sometimes leading to discontinuation of treatment. Recent studies stressed the role of the phosphorylated ATM (pATM) protein in RT-toxicity genesis and its ability in predicting individual radiosensitivity (IRS) in fibroblasts. Here we assessed the reliability of the pATM quantification in lymphocytes to predict IRS. A first retrospective study was performed on 150 blood lymphocytes of patients with several cancer types. Patients were divided into 2 groups, according to the grade of experienced toxicity. The global quantity of pATM molecules was assessed by ELISA on lymphocytes to determine the best threshold value. Then, the binary assay was assessed on a validation cohort of 36 patients with head and neck cancers. The quantity of pATM molecules in each sample of the training cohort was found in agreement with the observed Common Terminology Criteria for Adverse Events (CTCAE) grades with an AUC = 0.71 alone and of 0.77 combined to chemotherapy information. In the validation cohort, the same test was conducted with the following performances: sensitivity = 0.84, specificity = 0.54, AUC = 0.70 and 0.72 combined to chemotherapy. This study provides the basis of an easy to perform assay for clinical use.

Indexed as

biological markercancernormal tissue complication probabilitypATMradiation-induced toxicity prediction

Identifiers

PMID34069662
PMCPMC8160794

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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.