Evidence map›Paper›PMID 27377626›Full record

ArticleEBioMedicine2016

Identification of Circulating Tumor DNA for the Early Detection of Small-cell Lung Cancer.

Lynnette Fernandez-Cuesta, Sandra Perdomo, Patrice H Avogbe, Noemie Leblay, Tiffany M Delhomme, Valerie Gaborieau, Behnoush Abedi-Ardekani, Estelle Chanudet, Magali Olivier, David Zaridze and 15 more

Open access · goldAbstract read
In one paragraph

Article in EBioMedicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 110 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
110citing papers in PubMed, 3 pooled it
11.0field-weighted citation impact, top 1% 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

110 citing papers in PubMed, 3 syntheses or guidelines pooled it, 184 citations in OpenAlex.

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  9. Current and future therapies for small cell lung carcinoma.Journal of hematology & oncology · 2025
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50 more citing papers are in PubMed but not listed here.

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

25 authors at 8 institutions in 6 countries.

Lynnette Fernandez-CuestaInternational Agency for Research on Cancer (IARC-WHO), 150 cours Albert Thomas, 69008 Lyons, France.
Sandra PerdomoInternational Agency for Research on Cancer (IARC-WHO), 150 cours Albert Thomas, 69008 Lyons, France; Institute of Nutrition, Genetics and Metabolism Research, Universidad El Bosque, Bogotá, Colombia.
Patrice H AvogbeInternational Agency for Research on Cancer (IARC-WHO), 150 cours Albert Thomas, 69008 Lyons, France.
Noemie LeblayInternational Agency for Research on Cancer (IARC-WHO), 150 cours Albert Thomas, 69008 Lyons, France.
Tiffany M DelhommeInternational Agency for Research on Cancer (IARC-WHO), 150 cours Albert Thomas, 69008 Lyons, France.
Valerie GaborieauInternational Agency for Research on Cancer (IARC-WHO), 150 cours Albert Thomas, 69008 Lyons, France.
Behnoush Abedi-ArdekaniInternational Agency for Research on Cancer (IARC-WHO), 150 cours Albert Thomas, 69008 Lyons, France.
Estelle ChanudetInternational Agency for Research on Cancer (IARC-WHO), 150 cours Albert Thomas, 69008 Lyons, France.
Magali OlivierInternational Agency for Research on Cancer (IARC-WHO), 150 cours Albert Thomas, 69008 Lyons, France.
David ZaridzeRussian N.N. Blokhin Cancer Research Centre, Moscow, Russian Federation.
Anush MukeriaRussian N.N. Blokhin Cancer Research Centre, Moscow, Russian Federation.
Marta VilenskyInstituto Angel Roffo, Buenos Aires, Argentina.
Ivana Holcatova1st Faculty of Medicine, Charles University, Prague, Czech Republic.
Jerry PoleselCRO Aviano National Cancer Institute, Aviano, Italy.
Lorenzo SimonatoDepartment of Molecular Medicine, University of Padova, Padova, Italy.
Cristina CanovaDepartment of Molecular Medicine, University of Padova, Padova, Italy.
Pagona LagiouUniversity of Athens Medical School, Greece.
Christian BrambillaCHU Grenoble, University Grenoble- Alpes, INSERM U823, Grenoble, France.
Elisabeth BrambillaCHU Grenoble, University Grenoble- Alpes, INSERM U823, Grenoble, France.
Graham ByrnesInternational Agency for Research on Cancer (IARC-WHO), 150 cours Albert Thomas, 69008 Lyons, France.
Ghislaine SceloInternational Agency for Research on Cancer (IARC-WHO), 150 cours Albert Thomas, 69008 Lyons, France.
Florence Le Calvez-KelmInternational Agency for Research on Cancer (IARC-WHO), 150 cours Albert Thomas, 69008 Lyons, France.
Matthieu FollInternational Agency for Research on Cancer (IARC-WHO), 150 cours Albert Thomas, 69008 Lyons, France.
James D McKayInternational Agency for Research on Cancer (IARC-WHO), 150 cours Albert Thomas, 69008 Lyons, France. Electronic address: MckayJ@iarc.fr.
Paul BrennanInternational Agency for Research on Cancer (IARC-WHO), 150 cours Albert Thomas, 69008 Lyons, France. Electronic address: BrennanP@iarc.fr.
Centre international de recherche sur le cancer · FRInserm · FRRussian Cancer Research Center NN Blokhin · RUUniversity of Padua · ITCentro di Riferimento Oncologico · ITCharles University · CZNational and Kapodistrian University of Athens · GRUniversidad El Bosque · CO

Funding

World Health Organization 001
6 · The paper itself

Abstract

Circulating tumor DNA (ctDNA) is emerging as a key potential biomarker for post-diagnosis surveillance but it may also play a crucial role in the detection of pre-clinical cancer. Small-cell lung cancer (SCLC) is an excellent candidate for early detection given there are no successful therapeutic options for late-stage disease, and it displays almost universal inactivation of TP53. We assessed the presence of TP53 mutations in the cell-free DNA (cfDNA) extracted from the plasma of 51 SCLC cases and 123 non-cancer controls. We identified mutations using a pipeline specifically designed to accurately detect variants at very low fractions. We detected TP53 mutations in the cfDNA of 49% SCLC patients and 11.4% of non-cancer controls. When stratifying the 51 initial SCLC cases by stage, TP53 mutations were detected in the cfDNA of 35.7% early-stage and 54.1% late-stage SCLC patients. The results in the controls were further replicated in 10.8% of an independent series of 102 non-cancer controls. The detection of TP53 mutations in 11% of the 225 non-cancer controls suggests that somatic mutations in cfDNA among individuals without any cancer diagnosis is a common occurrence, and poses serious challenges for the development of ctDNA screening tests.

Indexed as

Biomarkers, TumorDNA, NeoplasmCase-Control StudiesEarly Detection of CancerFemaleHumansLeukocytesLung NeoplasmsMaleMutationNeoplasm StagingSmall Cell Lung CarcinomaTumor Suppressor Protein p53Biomarkers, TumorDNA, NeoplasmTumor Suppressor Protein p53cfDNActDNAEarly detectionScreeningSmall-cell lung cancerTP53 mutations

Identifiers

PMID27377626
PMCPMC5036515
OpenAlexW2464329385

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

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.