Evidence map›Paper›PMID 27473086›Full record

ArticleTumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine2016

Total and mutated EGFR quantification in cell-free DNA from non-small cell lung cancer patients detects tumor heterogeneity and presents prognostic value.

E Alegre, J P Fusco, P Restituto, D Salas-Benito, M E Rodríguez-Ruiz, M P Andueza, M J Pajares, A Patiño-García, R Pio, M D Lozano and 5 more

Abstract read
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In one paragraph

Article in Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing 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

27 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Plausible Role of Estrogens in Pathogenesis, Progression and Therapy of Lung Cancer.International journal of environmental research and public health · 2021
    Review
  8. Review
  9. Review
  10. Article
  11. Comparison of cobasAnnals of laboratory medicine · 2019
    Article
  12. Article
  13. Review
  14. Article
  15. Review
  16. Article
  17. The Dynamic Use ofDisease markers · 2019
    Article
  18. Molecular Composition of GenomicDisease markers · 2019
    Article
  19. Article
  20. 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

15 authors.

E AlegreClinical Chemistry Department, Clínica Universidad de Navarra, Av Pio XII 36, 31008, Pamplona, Spain.
J P FuscoDepartment of Oncology, Clínica Universidad de Navarra, Av Pio XII 36, 31008, Pamplona, Spain.
P RestitutoClinical Chemistry Department, Clínica Universidad de Navarra, Av Pio XII 36, 31008, Pamplona, Spain.
D Salas-BenitoIdiSNA, Navarra Institute for Health Research, Irunlarrea 3, 31008, Pamplona, Spain.
M E Rodríguez-RuizIdiSNA, Navarra Institute for Health Research, Irunlarrea 3, 31008, Pamplona, Spain.
M P AnduezaDepartment of Oncology, Clínica Universidad de Navarra, Av Pio XII 36, 31008, Pamplona, Spain.
M J PajaresIdiSNA, Navarra Institute for Health Research, Irunlarrea 3, 31008, Pamplona, Spain.
A Patiño-GarcíaIdiSNA, Navarra Institute for Health Research, Irunlarrea 3, 31008, Pamplona, Spain.
R PioDepartment of Biochemistry and Genetics, Universidad de Navarra, Irunlarrea 1, 31008, Pamplona, Spain.
M D LozanoIdiSNA, Navarra Institute for Health Research, Irunlarrea 3, 31008, Pamplona, Spain.
A GúrpideIdiSNA, Navarra Institute for Health Research, Irunlarrea 3, 31008, Pamplona, Spain.
J M Lopez-PicazoIdiSNA, Navarra Institute for Health Research, Irunlarrea 3, 31008, Pamplona, Spain.
I Gil-BazoIdiSNA, Navarra Institute for Health Research, Irunlarrea 3, 31008, Pamplona, Spain.
J L Perez-GraciaIdiSNA, Navarra Institute for Health Research, Irunlarrea 3, 31008, Pamplona, Spain.
A GonzalezClinical Chemistry Department, Clínica Universidad de Navarra, Av Pio XII 36, 31008, Pamplona, Spain. agonzaleh@unav.es.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mutation analysis of epidermal growth factor receptor (EGFR) gene is essential for treatment selection in non-small cell lung cancer (NSCLC). Analysis is usually performed in tumor samples. We evaluated the clinical utility of EGFR analysis in plasma cell-free DNA (cfDNA) from patients under treatment with EGFR inhibitors. We selected 36 patients with NSCLC and EGFR-activating mutations. Blood samples were collected at baseline and during treatment with EGFR inhibitors. Wild-type EGFR, L858R, delE746-A750, and T790M mutations were quantified in cfDNA by droplet digital PCR. Stage IV patients had higher total circulating EGFR copy levels than stage I (3523 vs. 1003 copies/mL; p < 0.01). There was high agreement for activating mutations between baseline cfDNA and tumor samples, especially for L858R mutation (kappa index = 0.679; p = 0.001). In 34 % of advanced NSCLC patients, we detected mutations in cfDNA not previously detected in tumor samples and double mutations in 17 %. Patients with baseline total EGFR copy levels above the median presented decreased overall survival (OS) (341 vs. 870 days, p < 0.05) and progression-free survival (PFS) (238 vs. 783 days; p < 0.05) compared with those with total EGFR copy levels below the median. Patients with baseline concentrations of activating mutations above the median (94 copies/mL) had lower OS (317 vs. 805 days; p < 0.05) and PFS (195 vs. 724 days; p < 0.05). During follow-up, T790M resistance mutation was detected in 53 % of patients. Total and mutated EGFR analysis in cfDNA seems a relevant tool to characterize the molecular profile and prognosis of NSCLC patients harboring EGFR mutations.

Indexed as

Biomarkers, TumorCarcinoma, Non-Small-Cell LungDNA Mutational AnalysisDrug Resistance, NeoplasmErbB ReceptorsFemaleFollow-Up StudiesHumansLung NeoplasmsMaleMiddle AgedMutationNeoplasm StagingPrognosisProtein Kinase InhibitorsReal-Time Polymerase Chain ReactionBiomarkers, TumorEGFR protein, humanErbB ReceptorsProtein Kinase InhibitorsCell-free DNADroplet digital PCREGFR mutationNon-small cell lung cancerPrognosisTumor heterogeneity

Identifiers

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.