Evidence map›Paper›PMID 38269023›Full record

ArticleFrontiers in oncology2023

Cerebrospinal fluid ctDNA testing shows an advantage over plasma ctDNA testing in advanced non-small cell lung cancer patients with brain metastases.

Xiaocui Liu, Fengjun Mei, Mei Fang, Yaqiong Jia, Yazhu Zhou, Chenxi Li, Panpan Tian, Chufan Lu, Guangrui Li

Open access · goldAbstract read
In one paragraph

Article in Frontiers in oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

9 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
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  7. Leptomeningeal Disease: Current Approaches and Future Directions.Current neurology and neuroscience reports · 2025
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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

9 authors at 4 institutions in 1 country.

Xiaocui LiuDepartment of Neurology, The Fourth Hospital of Hebei Medical University, Shijiazhuang, Hebei, China.
Fengjun MeiDepartment of Neurology, The Fourth Hospital of Hebei Medical University, Shijiazhuang, Hebei, China.
Mei FangDepartment of Reproductive Medicine, The Fourth Hospital of Hebei Medical University, Shijiazhuang, Hebei, China.
Yaqiong JiaDepartment of Neurology, The Fourth Hospital of Hebei Medical University, Shijiazhuang, Hebei, China.
Yazhu ZhouDepartment of Neurology, The Fourth Hospital of Hebei Medical University, Shijiazhuang, Hebei, China.
Chenxi LiDepartment of Neurology, The Fourth Hospital of Hebei Medical University, Shijiazhuang, Hebei, China.
Panpan TianDepartment of Neurology, The Fourth Hospital of Hebei Medical University, Shijiazhuang, Hebei, China.
Chufan LuDepartment of Neurology, The Fourth Hospital of Hebei Medical University, Shijiazhuang, Hebei, China.
Guangrui LiDepartment of Neurology, The First Hospital of Hebei Medical University, Shijiazhuang, Hebei, China.
Hebei Medical University · CNFourth Hospital of Hebei Medical University · CNFirst Affiliated Hospital of Hebei Medical University · CNNorth China University of Science and Technology Affiliated Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Brain metastases (BM), including brain parenchyma metastases (BPM) and leptomeningeal metastases (LM), are devastating metastatic complications in advanced cancer patients. Next-generation sequencing (NGS) is emerging as a new promising tool for profiling cancer mutation, which could facilitate the diagnosis of cancer. This retrospective study aimed to investigate the molecular genetic characteristics of non-small cell lung cancer (NSCLC) patients with BPM and LM using NGS. Methods: Cerebrospinal fluid (CSF) samples and paired plasma samples were collected from 37 patients of NSCLC-BM. We profiled genetic mutation characteristics using NGS from NSCLC-BM by comparing CSF circulating tumour DNA (ctDNA) with plasma ctDNA and primary tumour tissues. Results: Among the 37 patients with NSCLC-BM, 28 patients had LM with or without BPM, while 9 patients only had BPM. Driver and drug-resistant mutations in primary tumours with LM included: Conclusion: Our study indicated that the CSF ctDNA detected by NGS may reflect the molecular characteristics and heterogeneity of NSCLC-LM. Timely screening of patients with NSCLC for CSF ctDNA, especially for patients with positive plasma ctDNA, may facilitate the early detection of LM. Furthermore, patients with the

Indexed as

brain parenchyma metastases (BPM)cerebrospinal fluid circulating tumour DNA (ctDNA)leptomeningeal metastases (LM)next generation sequencingnon-small cell lung cancer (NSCLC)

Identifiers

PMID38269023
PMCPMC10806520
OpenAlexW4390696614

What OpenQuestion holds

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Registered trials

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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.