Evidence map›Paper›PMID 37714814›Full record

ArticleMolecular oncology2023

A rapid, multiplex digital PCR assay to detect gene variants and fusions in non-small cell lung cancer.

Bryan Leatham, Katie McNall, Hari K K Subramanian, Lucien Jacky, John Alvarado, Dominic Yurk, Mimi Wang, Donald C Green, Gregory J Tsongalis, Aditya Rajagopal and 1 more

Open access · goldAbstract read
In one paragraph

Article in Molecular oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

10 citing papers in PubMed, 11 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

11 authors at 4 institutions in 1 country.

Bryan LeathamChromaCode Inc, Carlsbad, CA, USA.ORCID 0009-0005-0065-3057
Katie McNallChromaCode Inc, Carlsbad, CA, USA.
Hari K K SubramanianChromaCode Inc, Carlsbad, CA, USA.
Lucien JackyChromaCode Inc, Carlsbad, CA, USA.
John AlvaradoChromaCode Inc, Carlsbad, CA, USA.
Dominic YurkChromaCode Inc, Carlsbad, CA, USA.
Mimi WangChromaCode Inc, Carlsbad, CA, USA.
Donald C GreenDepartment of Pathology and Laboratory Medicine, Dartmouth Hitchcock Medical Center, Lebanon, NH, USA.
Gregory J TsongalisDepartment of Pathology and Laboratory Medicine, Dartmouth Hitchcock Medical Center, Lebanon, NH, USA.
Aditya RajagopalChromaCode Inc, Carlsbad, CA, USA.
Jerrod J SchwartzChromaCode Inc, Carlsbad, CA, USA.ORCID 0009-0001-4076-9178
Ionis Pharmaceuticals (United States) · USDartmouth–Hitchcock Medical Center · USCalifornia Institute of Technology · USUniversity of Southern California · US

Funding

Translational Engineering in Cancer (TEC)P30CA023108 · NCI · DARTMOUTH COLLEGE · PI Fred W Kolling IV · 1985 to 2026
$91.3M
NCI NIH HHS P30 CA023108
6 · The paper itself

Abstract

Digital PCR (dPCR) is emerging as an ideal platform for the detection and tracking of genomic variants in cancer due to its high sensitivity and simple workflow. The growing number of clinically actionable cancer biomarkers creates a need for fast, accessible methods that allow for dense information content and high accuracy. Here, we describe a proof-of-concept amplitude modulation-based multiplex dPCR assay capable of detecting 12 single-nucleotide and insertion/deletion (indel) variants in EGFR, KRAS, BRAF, and ERBB2, 14 gene fusions in ALK, RET, ROS1, and NTRK1, and MET exon 14 skipping present in non-small cell lung cancer (NSCLC). We also demonstrate the use of multi-spectral target-signal encoding to improve the specificity of variant detection by reducing background noise by up to an order of magnitude. The assay reported an overall 100% positive percent agreement (PPA) and 98.5% negative percent agreement (NPA) compared with a sequencing-based assay in a cohort of 62 human formalin-fixed paraffin-embedded (FFPE) samples. In addition, the dPCR assay rescued actionable information in 10 samples that failed to sequence, highlighting the utility of a multiplexed dPCR assay as a potential reflex solution for challenging NSCLC samples.

Indexed as

Carcinoma, Non-Small-Cell LungLung NeoplasmsHigh-Throughput Nucleotide SequencingHumansMutationPolymerase Chain ReactionProto-Oncogene ProteinsReceptor Protein-Tyrosine KinasesProto-Oncogene ProteinsReceptor Protein-Tyrosine Kinasesamplitude modulationdigital PCRmultiplexmulti-spectralnon-small cell lung cancer

Identifiers

PMID37714814
PMCPMC10620117
OpenAlexW4386759764

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.