Evidence map›Paper›PMID 30979741›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2019

Profiling the Mutational Landscape in Known Driver Genes and Novel Genes in African American Non-Small Cell Lung Cancer Patients.

Christine M Lusk, Donovan Watza, Greg Dyson, Douglas Craig, Valerie Ratliff, Angela S Wenzlaff, Fulvio Lonardo, Aliccia Bollig-Fischer, Gerold Bepler, Kristen Purrington and 2 more

Open access · greenAbstract read
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 1 pooled it
2.4field-weighted citation impact, top 10% 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

19 citing papers in PubMed, 1 synthesis or guideline pooled it, 26 citations in OpenAlex.

  1. Pooled it
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  14. If Virchow and Ehrlich Had Dreamt Together: What the Future Holds forInternational journal of molecular sciences · 2021
    Review
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  17. Whole-Exome Profiling of NSCLC Among African Americans.Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer · 2020
    Article
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  19. 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

12 authors at 1 institution in 1 country.

Christine M Lusk *Karmanos Cancer Institute, Detroit, Michigan.
Donovan Watza *Karmanos Cancer Institute, Detroit, Michigan.
Greg DysonKarmanos Cancer Institute, Detroit, Michigan.
Douglas CraigKarmanos Cancer Institute, Detroit, Michigan.
Valerie RatliffKarmanos Cancer Institute, Detroit, Michigan.
Angela S WenzlaffKarmanos Cancer Institute, Detroit, Michigan.ORCID 0000-0001-8669-8240
Fulvio LonardoKarmanos Cancer Institute, Detroit, Michigan.
Aliccia Bollig-FischerKarmanos Cancer Institute, Detroit, Michigan.
Gerold BeplerKarmanos Cancer Institute, Detroit, Michigan.
Kristen PurringtonKarmanos Cancer Institute, Detroit, Michigan.
Shirish GadgeelKarmanos Cancer Institute, Detroit, Michigan.
Ann G SchwartzKarmanos Cancer Institute, Detroit, Michigan. schwarta@karmanos.org.ORCID 0000-0002-9525-1157
Wayne State University · US

Funding

Tumor Biology and Microenvironment (Program 1)P30CA022453 · NCI · WAYNE STATE UNIVERSITY · PI Julie Lynn Boerner · 1985 to 2026
$68.4M
Inflammation Pathways and COPD in the Development of Lung CancerR01CA141769 · NCI · WAYNE STATE UNIVERSITY · PI SCHWARTZ, ANN G. · 2011 to 2016
$8.7M
TRAINING PROGRAM IN THE BIOLOGY OF CANCERT32CA009531 · NCI · WAYNE STATE UNIVERSITY · PI Larry H Matherly · 1985 to 2026
$5.3M
SURVEILLANCE, EPIDEMIOLOGY, AND END RESULTS--SEERN01PC065064 · PC · WAYNE STATE UNIVERSITY · PI SCHWARTZ, ANN G · 1996 to 2000
$4.5M
Profiling Genetic Alterations in NSCLC in African AmericansR21CA184778 · NCI · WAYNE STATE UNIVERSITY · PI GADGEEL, SHIRISH, SCHWARTZ, ANN G. · 2014 to 2015
$364k
CCR NIH HHS HHSN261201300011CNCI NIH HHS N01 PC065064NCI NIH HHS P30 CA022453NCI NIH HHS R01 CA141769NCI NIH HHS R21 CA184778NCI NIH HHS T32 CA009531
6 · The paper itself

Abstract

purposeIdentifying novel driver genes and mutations in African American non-small cell lung cancer (NSCLC) cases can inform targeted therapy and improve outcomes for this traditionally underrepresented population. EXPERIMENTAL

designTumor DNA, RNA, and germline DNA were collected from African American NSCLC patients who participated in research conducted at the Karmanos Cancer Institute (KCI) in Detroit, Michigan. Known mutations were ascertained through the Sequenom LungCarta panel of 214 mutations in 26 genes,

resultsOf the 193 tumors tested, 77 known driver mutations were identified in 66 patients (34.2%). Sixty-seven of the 127 patients without a known driver mutation were sequenced. In 54 of these patients, 50 nonsynonymous mutations were predicted to have damaging effects among the 26 panel genes, 47 of which are not found in The Cancer Genome Atlas NSCLC white or African American samples. Analyzing the whole-exome sequence data using MutSig2CV identified a total of 88 genes significantly mutated at FDR

conclusionsThese findings suggest that broader mutation profiling including both known and novel driver genes in African Americans with NSCLC will identify additional mutations that may be useful in treatment decision-making.

Indexed as

Genes, NeoplasmMutationBlack or African AmericanCarcinoma, Non-Small-Cell LungDNA Mutational AnalysisGene Expression ProfilingHigh-Throughput Nucleotide SequencingHumansLung NeoplasmsMaleMiddle AgedMolecular Targeted TherapyPrognosisSurvival Rate

Identifiers

PMID30979741
PMCPMC6635071
OpenAlexW2938552338

What OpenQuestion holds

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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.