Evidence map›Paper›PMID 29130105›Full record

ArticleOncology reports2017

Tumor molecular profiling of NSCLC patients using next generation sequencing.

Nikolaos Tsoulos, Eirini Papadopoulou, Vasiliki Metaxa-Mariatou, Georgios Tsaousis, Chrisoula Efstathiadou, Georgia Tounta, Aikaterini Scapeti, Eugenia Bourkoula, Pavlos Zarogoulidis, George Pentheroudakis and 9 more

Abstract read
In one paragraph

Article in Oncology reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed, 1 pooled it
–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

44 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Observational
  3. [Advances in Targeted Therapy for Advanced Non-small Cell Lung Cancer 
with HER2 Mutation].Zhongguo fei ai za zhi = Chinese journal of lung cancer · 2025
    Review
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  19. Radial-EBUS: CryoBiopsy Versus Conventional Biopsy: Time-Sample and C-Arm.International journal of environmental research and public health · 2022
    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

19 authors.

Nikolaos TsoulosGeneKor Medical S.A., Athens 15344, Greece.
Eirini PapadopoulouGeneKor Medical S.A., Athens 15344, Greece.
Vasiliki Metaxa-MariatouGeneKor Medical S.A., Athens 15344, Greece.
Georgios TsaousisGeneKor Medical S.A., Athens 15344, Greece.
Chrisoula EfstathiadouGeneKor Medical S.A., Athens 15344, Greece.
Georgia TountaGeneKor Medical S.A., Athens 15344, Greece.
Aikaterini ScapetiGeneKor Medical S.A., Athens 15344, Greece.
Eugenia BourkoulaGeneKor Medical S.A., Athens 15344, Greece.
Pavlos ZarogoulidisPulmonary Department, Oncology Unit, 'G. Papanikolaou' General Hospital, Aristotle University of Thessaloniki, Thessaloniki 54124, Greece.
George PentheroudakisDepartment of Medical Oncology, University Hospital of Ioannina, Ioannina 45500, Greeece.
Stylianos KakolyrisDepartment of Medical Oncology, University General Hospital of Alexandroupoli, Alexandroupoli 68100, Greece.
Ioannis BoukovinasMedical Oncology, 'Bioclinic' of Thessaloniki, Thessaloniki 54622, Greece.
Pavlos PapakotoulasSecond Department of Medical Oncology, Theagenion Anticancer Hospital of Thessaloniki, Thessaloniki 54639, Greece.
Elias AthanasiadisDepartment of Medical Oncology, Mitera Hospital, Athens 15123, Greece.
Theofanis FlorosAthens Naval and Veterans Hospital, Athens 11521, Greece.
Anna KoumarianouHematology-Oncology Unit, Fourth Department of Internal Medicine, Attikon Hospital, National and Kapodistrian University of Athens, Athens 12462, Greece.
Vasileios BarbounisThird Medical Oncology Department, 'Metropolitan' Hospital, Pireas 18547, Greece.
Anca DinischiotuDepartment of Biochemistry and Molecular Biology, Faculty of Biology, University of Bucharest, Bucharest 0050095, Romania.
George NasioulasGeneKor Medical S.A., Athens 15344, Greece.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Non‑small cell lung cancer (NSCLC) is the most common type of lung cancer and a tumor with a broad spectrum of targeted therapies already available or in clinical trials. Thus, molecular characterization of the tumor using next generation sequencing (NGS) technology, has become a key tool for facilitating treatment decisions and the clinical management of NSCLC patients. The performance of a custom 23 gene multiplex amplification hot spot panel, based on Ion AmpliSeq™ technology, was evaluated for the analysis of tumor DNA extracted from formalin-fixed and paraffin-embedded (FFPE) tissues. Furthermore, the Ion AmpliSeq™ RNA Fusion Lung Cancer Research Panel was used for fusion RNA transcript analysis. The mutation spectrum of the tumors was determined in a cohort of 502 patients with NSCLC using the aforementioned targeted gene panels. The panel used for tumor DNA analysis in this study exhibited high rates (100%) of sensitivity, specificity and reproducibility at a mutation allelic frequency of 3%. At least one DNA mutation was detected in 374 patients (74.5%) and an RNA fusion was identified in 16 patients, (3.2%). In total, alterations in a cancer-driver gene were identified (including point mutations, gene rearrangements and MET amplifications) in 77.6% of the tumors tested. Among the NSCLC patients, 23% presented a mutation in a gene associated with approved or emerging targeted therapy. More specifically, 13.5% (68/502) presented a mutation in a gene with approved targeted therapy (EGFR, ALK, ROS1) and 9.4% (47/502) had an alteration in a gene related to emerging targeted therapies (ERBB2, BRAF, MET and RET). Furthermore, 51.6% of the patients had a mutation in a gene that could be related to an off label therapy or indicative for access to a clinical trial. Thus, the targeted NGS panel used in this study is a reliable approach for tumor molecular profiling and can be applied in personalized treatment decision making for NSCLC patients.

Indexed as

MutationCarcinoma, Non-Small-Cell LungFemaleGene Regulatory NetworksGenetic Predisposition to DiseaseHigh-Throughput Nucleotide SequencingHumansLung NeoplasmsMaleMolecular Targeted TherapySequence Analysis, DNA

Identifiers

PMID29130105
PMCPMC5783588

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.