Evidence map›Paper›PMID 34257540›Full record

ArticlePathology oncology research : POR2021

Landscape of Biomarkers in Non-small Cell Lung Cancer Using Comprehensive Genomic Profiling and PD-L1 Immunohistochemistry.

Richard S P Huang, Eric Severson, James Haberberger, Daniel L Duncan, Amanda Hemmerich, Claire Edgerly, N Lynn Ferguson, Garrett Frampton, Clarence Owens, Erik Williams and 18 more

Open access · goldAbstract read
In one paragraph

Article in Pathology oncology research : POR, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

13 citing papers in PubMed, 20 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

28 authors at 2 institutions in 1 country.

Richard S P HuangFoundation Medicine, Inc., Morrisville, NC, United States.
Eric SeversonFoundation Medicine, Inc., Morrisville, NC, United States.
James HaberbergerFoundation Medicine, Inc., Morrisville, NC, United States.
Daniel L DuncanFoundation Medicine, Inc., Morrisville, NC, United States.
Amanda HemmerichFoundation Medicine, Inc., Morrisville, NC, United States.
Claire EdgerlyFoundation Medicine, Inc., Morrisville, NC, United States.
N Lynn FergusonFoundation Medicine, Inc., Morrisville, NC, United States.
Garrett FramptonFoundation Medicine, Inc., Cambridge, MA, United States.
Clarence OwensFoundation Medicine, Inc., Morrisville, NC, United States.
Erik WilliamsFoundation Medicine, Inc., Cambridge, MA, United States.
Julia ElvinFoundation Medicine, Inc., Cambridge, MA, United States.
Jo-Anne VergilioFoundation Medicine, Inc., Cambridge, MA, United States.
Jonathan Keith KillianFoundation Medicine, Inc., Cambridge, MA, United States.
Douglas LinFoundation Medicine, Inc., Cambridge, MA, United States.
Samantha MorleyFoundation Medicine, Inc., Cambridge, MA, United States.
Deborah McEwanFoundation Medicine, Inc., Cambridge, MA, United States.
Oliver HolmesFoundation Medicine, Inc., Cambridge, MA, United States.
Natalie DanzigerFoundation Medicine, Inc., Cambridge, MA, United States.
Michael B CohenWake Forest Comprehensive Cancer Center, Wake Forest School of Medicine, Winston-Salem, NC, United States.
Pratheesh SathyanFoundation Medicine, Inc., Cambridge, MA, United States.
Kimberly McGregorFoundation Medicine, Inc., Cambridge, MA, United States.
Prasanth ReddyFoundation Medicine, Inc., Cambridge, MA, United States.
Jeffrey VenstromFoundation Medicine, Inc., Cambridge, MA, United States.
Rachel AnhornFoundation Medicine, Inc., Cambridge, MA, United States.
Brian AlexanderFoundation Medicine, Inc., Cambridge, MA, United States.
Charlotte BrownFoundation Medicine, Inc., Morrisville, NC, United States.
Jeffrey S RossFoundation Medicine, Inc., Morrisville, NC, United States.
Shakti H RamkissoonFoundation Medicine, Inc., Morrisville, NC, United States.
Foundation Medicine (United States)Wake Forest University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Comprehensive genomic profiling (CGP) and immunohistochemistry (IHC) are important biomarker tools used for patients with non-small cell lung cancer (NSCLC) given the expanding number of standard-of-care therapies that require companion diagnostic testing. We examined 9450 NSCLC real-world patient samples that underwent both CGP and programmed death-ligand 1 (PD-L1) IHC to understand the biomarker landscape in this patient cohort. By assessing National Comprehensive Cancer Network (NCCN)-recommended biomarkers including genomic alterations, tumor mutational burden (≥10 mutations/Mb cut-off), and PD-L1 expression (Tumor Proportion Score (TPS) ≥ 50% cut-off), we show that CGP + PD-L1 IHC yielded potentially actionable results for 70.5% of the 9,450 patients with NSCLC. Among the remaining 29.5% (2,789/9,450) of patients, 86.7% (2,419/2,789) were potentially eligible for another biomarker-associated therapy and/or clinical trial based on their genomic profile. In addition, in the PD-L1

Indexed as

AgedB7-H1 AntigenBiomarkers, TumorCarcinoma, Non-Small-Cell LungFemaleGenomicsHumansImmunohistochemistryImmunotherapyLung NeoplasmsMaleMutationB7-H1 AntigenBiomarkers, TumorCD274 protein, humanbiomarkerscomprehensive genomic profilingimmunohistochemistrynon-small cell lung cancerPD-L1

Identifiers

PMID34257540
PMCPMC8262230
OpenAlexW3136709261

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.