Evidence map›Paper›PMID 30767431›Full record

ArticleCancer medicine2019

Differences in the genomic profiles of cell-free DNA between plasma, sputum, urine, and tumor tissue in advanced NSCLC.

Zhen Wu, Zhen Yang, Chun Sun Li, Wei Zhao, Zhi Xin Liang, Yu Dai, Qiang Zhu, Kai Ling Miao, Dong Hua Cui, Liang An Chen

Registry-linked trialOpen access · goldAbstract readComparative Study
In one paragraph

Article in Cancer medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02778854 (Liquid Biopsy for Detection of Driver Mutation in Diagnostic and Prognostic of NSCLC), which is not on this map. Cited by 30 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 1 pooled it
2.9field-weighted citation impact, top 8% 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.

NCT02778854 unknown statusnot on this map

Liquid Biopsy for Detection of Driver Mutation in Diagnostic and Prognostic of NSCLC

Typeobservational_patient_registrySponsorChinese PLA General HospitalRan2015 to 2020Enrolled200ConditionsNon Small Cell Lung CancerArmsdetection of driver mutation
3 · Its place in the literature

Who cites it

30 citing papers in PubMed, 1 synthesis or guideline pooled it, 54 citations in OpenAlex.

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  20. Urinary Biomarkers for Early Diagnosis of Lung Cancer.Journal of clinical medicine · 2021
    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

10 authors at 1 institution in 1 country.

Zhen WuRespiratory Department of Chinese PLA General Hospital, Beijing, China.
Zhen YangRespiratory Department of Chinese PLA General Hospital, Beijing, China.
Chun Sun LiRespiratory Department of Chinese PLA General Hospital, Beijing, China.
Wei ZhaoRespiratory Department of Chinese PLA General Hospital, Beijing, China.
Zhi Xin LiangRespiratory Department of Chinese PLA General Hospital, Beijing, China.
Yu DaiRespiratory Department of Chinese PLA General Hospital, Beijing, China.
Qiang ZhuRespiratory Department of Chinese PLA General Hospital, Beijing, China.
Kai Ling MiaoRespiratory Department of Chinese PLA General Hospital, Beijing, China.
Dong Hua CuiRespiratory Department of Chinese PLA General Hospital, Beijing, China.
Liang An ChenRespiratory Department of Chinese PLA General Hospital, Beijing, China.ORCID 0000-0002-7373-0595
Chinese PLA General Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Liquid biopsy has provided an efficient way for detection of gene alterations in advanced non-small-cell lung cancer (NSCLC). However, the correlation between systematic determination of somatic genomic alterations in liquid biopsy and tumor biopsy still remained unclear, and the concordance rate between cell-free DNA (cfDNA) and matched tumor tissue DNA needs to be increased. A prospective study was performed to detect differences in genetic profiles of cfDNA in sputum, plasma, urine, and tumor tissue from 50 advanced NSCLC patients in parallel by the same next-generation sequencing (NGS) platform. Driver genes alterations were identified in cfDNA sample and matched tumor sample, with an overall concordance rate of 86% in plasma cfDNA, 74% in sputum cfDNA, 70% in urine cfDNA, and 90% in cfDNA of combination of plasma, sputum, and urine. And the concordant rate of cfDNA in sputum in patients with smoking history was higher than that in patients without history of smoking (89% vs. 66%, P = 0.033) and equal to that in plasma cfDNA of the smoking patients (89% vs. 89%). In conclusion, sputum cfDNA can be considered as an alternative medium to liquid biopsy, while the complementarity of genomic profiles in cfDNA among plasma, sputum, and urine was beneficial to detect more diver genes alterations and improve the utility of liquid biopsy in advanced NSCLC (Liquid Biopsy for Detection of Driver Mutation in NSCLC; NCT02778854).

Indexed as

AdultAgedAged, 80 and overBiomarkers, TumorCarcinoma, Non-Small-Cell LungCell-Free Nucleic AcidsFemaleHumansLung NeoplasmsMaleMiddle AgedMutationNeoplasm MetastasisProspective StudiesSputumUrinalysisBiomarkers, TumorCell-Free Nucleic Acidscell-free DNAliquid biopsylung cancernext-generation sequencingsputum

Identifiers

PMID30767431
PMCPMC6434190
OpenAlexW2914054477

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Registered trials

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.