Evidence map›Paper›PMID 30642553›Full record

ArticleLung cancer (Amsterdam, Netherlands)2019

Feasibility of lung cancer RNA acquisition from a single transbronchial or transthoracic needle pass (FASTT trial).

Travis Dotson, Christina Bellinger, Jing Su, Kris Hansen, Graham E Parks, James O Cappellari, Lou Craddock, Hollins Clark, Clifford Howard, W Jeffrey Petty and 6 more

Abstract read
In one paragraph

Article in Lung cancer (Amsterdam, Netherlands), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.7field-weighted citation impact, top 25% 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

4 citing papers in PubMed, 9 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

16 authors at 2 institutions in 1 country.

Travis DotsonDepartment of Medicine, Pulmonary & Critical Care Medicine, Wake Forest School of Medicine, Winston-Salem, NC, United States.
Christina BellingerDepartment of Medicine, Pulmonary & Critical Care Medicine, Wake Forest School of Medicine, Winston-Salem, NC, United States.
Jing SuDepartment of Biostatistics Sciences, Wake Forest School of Medicine, Winston-Salem, NC, United States.
Kris HansenWake Forest Baptist Comprehensive Cancer Center, Winston-Salem, NC, United States.
Graham E ParksDepartment of Pathology, Wake Forest School of Medicine, Winston-Salem, NC, United States.
James O CappellariDepartment of Pathology, Wake Forest School of Medicine, Winston-Salem, NC, United States.
Lou CraddockDepartment of Cancer Biology, Wake Forest School of Medicine, Winston-Salem, NC, United States.
Hollins ClarkDepartment of Radiology, Wake Forest School of Medicine, Winston-Salem, NC, United States.
Clifford HowardDepartment of Radiology, Wake Forest School of Medicine, Winston-Salem, NC, United States.
W Jeffrey PettyWake Forest Baptist Comprehensive Cancer Center, Winston-Salem, NC, United States.
Bharat PrakashDepartment of Medicine, Pulmonary & Critical Care Medicine, Wake Forest School of Medicine, Winston-Salem, NC, United States.
Kounosuke WatabeDepartment of Cancer Biology, Wake Forest School of Medicine, Winston-Salem, NC, United States.
Michael ChanDepartment of Radiation Oncology, Wake Forest School of Medicine, Winston-Salem, NC, United States.
Jonathan HovdaDepartment of Medicine, Pulmonary & Critical Care Medicine, Wake Forest School of Medicine, Winston-Salem, NC, United States.
Lance D MillerDepartment of Cancer Biology, Wake Forest School of Medicine, Winston-Salem, NC, United States.
Jimmy RuizWake Forest Baptist Comprehensive Cancer Center, Winston-Salem, NC, United States; W.G. (Bill) Hefner VA Medical Center, Salisbury, NC, United States. Electronic address: jruiz@wakehealth.edu.
Wake Forest University · USAtrium Health Wake Forest Baptist · US

Funding

Tumor Tissue CoreP30CA012197 · NCI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI Ruben A. Mesa · 1985 to 2026
$55.4M
NCI NIH HHS P30 CA012197
6 · The paper itself

Abstract

introductionRNA isolation from tumor tissue is used for biomarker analyses and validation. Limited diagnostic material from small volume biopsies combined with an increasing demand for standard histologic, molecular characterization, and next generation sequencing applications often leads to limited material for research. We sought to evaluate small volume sampling of lung cancer tissue collected from a single needle pass during a diagnostic procedure and determine if it can provide RNA of acceptable quantity and quality.

methodsWe enrolled 140 patients with probable primary bronchogenic carcinoma and collected RNA from a dedicated FNA aspiration. Total RNA (ηg), RNA integrity number (RIN), and %Mass in base pairs were evaluated from each patient sample. A customized nanoString nCounter® 95-gene panel was used to profile the expression patterns of feature NSCLC genes. We compared gene expression patterns that distinguish lung adenocarcinoma (LUAD) and squamous cell carcinoma (LUSC) in our cohort with a corresponding Cancer Genome Atlas (TCGA) NSCLC datasets.

resultsOf the 149 patients consented. RNA-extraction was performed in 101 eligible patients. A satisfactory total RNA mass and RIN was quantified for all samples with a similar distribution among cellular subtypes. Mean %-Mass over 300 base pairs was noted for all specimens and 96% of samples met criteria to perform genetic evaluation with our commercialized gene expression assay. The FNA-derived transcriptomic results showed excellent consistency with the TCGA counterparts, and the differential expression pattern of LUAD vs LUSC subtypes were highly similar. DISCUSSION: In this study, RNA retrieval from a single-pass FNA regardless of procedural approach showed equivalence and suitability for gene expression assessments. RNA extraction from small volume samples has the potential to provide valuable material for genetic profiling.

Indexed as

AdultAgedAged, 80 and overBiomarkers, TumorBiopsy, Fine-NeedleCarcinoma, BronchogenicCohort StudiesFeasibility StudiesFemaleGene Expression Regulation, NeoplasticHumansLung NeoplasmsMaleMiddle AgedRNA, NeoplasmTranscriptomeBiomarkers, TumorRNA, NeoplasmFine needle aspiration biopsyGene-expressionNon-small cell lung cancerRibonucleic acid

Identifiers

PMID30642553
PMCPMC6386467
OpenAlexW2900831612

What OpenQuestion holds

Textmetadata
LicenceTDM
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.