Evidence map›Paper›PMID 25653133›Full record

ArticleCancer medicine2015

Detection of tumor ALK status in neuroblastoma patients using peripheral blood.

Valérie Combaret, Isabelle Iacono, Angela Bellini, Stéphanie Bréjon, Virginie Bernard, Aurélien Marabelle, Carole Coze, Gaelle Pierron, Eve Lapouble, Gudrun Schleiermacher and 1 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Cancer medicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
5.5field-weighted citation impact, top 4% 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

47 citing papers in PubMed, 75 citations in OpenAlex.

  1. Article
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  7. Sequential Analysis of cfDNA Reveals Clonal Evolution in Patients with Neuroblastoma Receiving ALK-Targeted Therapy.Clinical cancer research : an official journal of the American Association for Cancer Research · 2024
    Article
  8. Article
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  10. Article
  11. Article
  12. Review
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  15. Review
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  17. Advancing therapy for neuroblastoma.Nature reviews. Clinical oncology · 2022
    Review
  18. Article
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  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 5 institutions in 1 country.

Valérie CombaretCentre Léon-Bérard, Laboratoire de Recherche Translationnelle, 28 rue Laennec, 69373, Lyon Cedex 08, France.
Isabelle Iacono
Angela Bellini
Stéphanie Bréjon
Virginie Bernard
Aurélien Marabelle
Carole Coze
Gaelle Pierron
Eve Lapouble
Gudrun Schleiermacher
Jean Yves Blay
Centre Léon Bérard · FRInstitut Curie · FRInserm · FRAix-Marseille Université · FRInstitut d’Hématologie et d’Oncologie Pédiatrique · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

New protocols based on ALK-targeted therapy by crizotinib or other ALK-targeting molecules have opened for the treatment of patients with neuroblastoma (NB) if their tumors showed mutation and/or amplification of the ALK gene. However, tumor samples are not always available for analysis of ALK mutational status in particular at relapse. Here, we evaluated the ALK mutational status of NB samples by analysis of circulating DNA, using the droplet digital PCR (ddPCR) system. ddPCR assays was developed for the detection of ALK mutations at F1174 and R1275 hotspots found in NB tumors and was applied for the analysis of circulating DNA obtained from 200 μL of serum or plasma samples collected from 114 patients with NB. The mutations F1174L (exon 23 position 3520, T>C and position 3522, C>A) and the mutation R1275Q (exon 25 position 3824, G>A) were detected in circulating DNA. The sensitivity of our test was 100%, 85%, and 92%, respectively, and the specificity was 100%, 91%, and 98%, respectively. In conclusion, the assay that we have developed offers a reliable, noninvasive blood test to assess ALK mutational status at F1174 and R1275 hotspots and should help clinicians to identify patients showing an ALK mutation in particular when no tumor tissue is available.

Indexed as

Case-Control StudiesChildDNA Mutational AnalysisDNA, NeoplasmExonsHumansMutationNeuroblastomaPolymerase Chain ReactionReceptor Protein-Tyrosine KinasesDNA, NeoplasmReceptor Protein-Tyrosine KinasesALK mutationcell-free DNAddPCRneuroblastoma

Identifiers

PMID25653133
PMCPMC4402069
OpenAlexW2074987529

What OpenQuestion holds

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Registered trials

None linked

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.