Evidence map›Paper›PMID 29304828›Full record

ArticleRadiation oncology (London, England)2018

Oncogene addiction and radiation oncology: effect of radiotherapy with photons and carbon ions in ALK-EML4 translocated NSCLC.

Ying Dai, Quanxiang Wei, Christian Schwager, Janina Hanne, Cheng Zhou, Klaus Herfarth, Stefan Rieken, Kenneth E Lipson, Jürgen Debus, Amir Abdollahi

Open access · goldAbstract read
In one paragraph

Article in Radiation oncology (London, England), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
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

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 55 citations in OpenAlex.

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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

10 authors at 2 institutions in 3 countries.

Ying DaiGerman Cancer Consortium (DKTK), Heidelberg, Germany.
Quanxiang WeiGerman Cancer Consortium (DKTK), Heidelberg, Germany.
Christian SchwagerGerman Cancer Consortium (DKTK), Heidelberg, Germany.
Janina HanneGerman Cancer Consortium (DKTK), Heidelberg, Germany.
Cheng ZhouGerman Cancer Consortium (DKTK), Heidelberg, Germany.
Klaus HerfarthGerman Cancer Consortium (DKTK), Heidelberg, Germany.
Stefan RiekenGerman Cancer Consortium (DKTK), Heidelberg, Germany.
Kenneth E LipsonFibroGen, Inc., San Francisco, CA, 94158, USA.
Jürgen DebusGerman Cancer Consortium (DKTK), Heidelberg, Germany.
Amir AbdollahiGerman Cancer Consortium (DKTK), Heidelberg, Germany. a.amir@dkfz.de.
German Cancer Research Center · DEFibroGen (United States) · US

Funding

Deutsche Forschungsgemeinschaft (DE) KFO214
6 · The paper itself

Abstract

backgroundPatients with Echinoderm microtubule-associated protein-like 4 (EML4)-anaplastic lymphoma kinase (ALK) positive lung cancer are sensitive to ALK-kinase inhibitors. TAE684 is a potent second generation ALK inhibitor that overcomes Crizotinib resistance. Radiotherapy is an integral therapeutic component of locally advanced lung cancer. Therefore, we sought to investigate the effects of combined radiotherapy and ALK-inhibition via TAE684 in ALK-positive vs. wild type lung cancer cells.

methodsHuman non-small cell lung cancer (NSCLC) cell lines harboring wild-type ALK (A549), EML4-ALK translocation (H3122) and murine Lewis Lung Cancer (LLC) cells were investigated. Cells were irradiated with 1-4 Gy X-Rays (320 keV) and carbon ions (Spread-out Bragg Peak, SOBP (245.4-257.0 MeV/u)) at Heidelberg Ion Therapy center. TAE684 was administered at the dose range 0-100 nM. Clonogenic survival, proliferation and apoptosis via caspase 3/7 expression level were assessed in all three cell lines using time-lapse live microscopy.

resultsTAE684 inhibited the proliferation of H3122 cells in a dose-dependent manner with a half maximal inhibitory concentration (IC

conclusionsThis is the first report demonstrating synergistic effects of combined TAE684 and radiotherapy in EML4-ALK positive lung cancer cells. In addition to conventional photon radiotherapy, ALK-inhibition also enhanced the effects of particle irradiation using carbon ions. Our data indicate beneficial effects of combined ALK-inhibition and radiotherapy in treatment of this distinct subpopulation of NSCLC that warrant further evaluation.

Indexed as

Carcinoma, Non-Small-Cell LungLung NeoplasmsOncogene AddictionAnaplastic Lymphoma KinaseAnimalsAntineoplastic AgentsApoptosisCarcinoma, Lewis LungCell Cycle ProteinsCell Line, TumorCell ProliferationCell SurvivalChemoradiotherapyHeavy Ion RadiotherapyHumansMiceALK protein, humanAlk protein, mouseAnaplastic Lymphoma KinaseAntineoplastic AgentsCell Cycle ProteinsEML4 protein, humanMicrotubule-Associated ProteinsNVP-TAE684Protein Kinase InhibitorsPyrimidinesReceptor Protein-Tyrosine KinasesSerine EndopeptidasesALK inhibitorsCarbon ionsEML4-ALK-fusionNon-small-cell lung cancerRadiotherapy

Identifiers

PMID29304828
PMCPMC5756447
OpenAlexW2782108405

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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.