Evidence map›Paper›PMID 41306356›Full record

ArticleMalawi medical journal : the journal of Medical Association of Malawi2025

Assessment of diagnostic efficacy: High fluorescent cells combined with CEA, NSE, and Cyfra21-1 in Malignant Pleural Effusion Identification.

Ning Zhang, Thomas Stuart Mughogho, Aubrey Nothale, Dokani Michael Ndovi, Rashid Kaseka, Zhonglin Wang, Jian Hu, Jie Zheng, Xiaoqin Wang

Abstract read
In one paragraph

Article in Malawi medical journal : the journal of Medical Association of Malawi, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. 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

9 authors.

Ning ZhangDepartment of Clinical Laboratory, The First Affiliated Hospital of Xi'an Jiaotong University, 277# West Yanta Road, Xi'an, 710061, Shaanxi Province, China.
Thomas Stuart MughoghoLaboratory Department, Mzuzu Central Hospital, Private Bag 209, Luwinga, Mzuzu 2, Malawi.
Aubrey NothaleLaboratory Department, Mzuzu Central Hospital, Private Bag 209, Luwinga, Mzuzu 2, Malawi.
Dokani Michael NdoviLaboratory Department, Mzuzu Central Hospital, Private Bag 209, Luwinga, Mzuzu 2, Malawi.
Rashid KasekaLaboratory Department, Mzuzu Central Hospital, Private Bag 209, Luwinga, Mzuzu 2, Malawi.
Zhonglin WangDepartment of Clinical Laboratory, The First Affiliated Hospital of Xi'an Jiaotong University, 277# West Yanta Road, Xi'an, 710061, Shaanxi Province, China.
Jian HuDepartment of Clinical Laboratory, The First Affiliated Hospital of Xi'an Jiaotong University, 277# West Yanta Road, Xi'an, 710061, Shaanxi Province, China.
Jie ZhengDepartment of Radiology, The First Affiliated Hospital of Xi'an Jiaotong University, 277# West Yanta Road, Xi'an, 710061, Shaanxi Province, China.
Xiaoqin WangDepartment of Clinical Laboratory, The First Affiliated Hospital of Xi'an Jiaotong University, 277# West Yanta Road, Xi'an, 710061, Shaanxi Province, China.

Funding

Science and Technology Program of Xi'an 24LLRHZDZX0028
6 · The paper itself

Abstract

Objective: To determine routine and biochemical parameters, as well as tumor markers, that are significantly different between malignant pleural effusion (MPE) and benign pleural effusion (BPE), and to evaluate the diagnostic efficacy of the combination of routine and biochemical parameters, along with carcinoembryonic antigen (CEA), neuron-specific enolase (NSE), and cytokeratin 19 fragment (Cyfra21-1) measurements in pleural effusion for identifying MPE. Methods: 1,238 patients with pleural effusion from the First Affiliated Hospital of Xi'an Jiaotong University were recruited and categorized into two groups: MPE (n = 397) and BPE (n = 841). Biomarker levels were compared, and receiver operating characteristic (ROC) curves were performed on the statistically significant indicators to assess the diagnostic efficacy for MPE. Results: High-Fluorescent cells (HFC), CEA, NSE, and Cyfra21-1 were significantly elevated in MPE (P < 0.001) and positively correlated with its presence (P < 0.001). The area under the curve (AUC), cutoff value, sensitivity, and specificity were: [0.726 (95% CI: 0.696-0.756), 17.5, 8.5%, 57.4%]; [0.894 (95% CI: 0.873-0.914), 5.78, 80.7%, 88.6%]; [0.703(95% CI: 0.672-0.735), 10.97, 59.3%, 71.9%] and [0.774 (95% CI: 0.746-0.802), 34.61, 74.7%, 67.9%], respectively. When focusing on multi-biomarker strategy, the combination of HFC and CEA offered the highest diagnostic efficiency (AUC: 0.868; 95% CI: 0.847-0.889), with a sensitivity of 88.4% and a specificity of 70.7%. Conclusion: HFC, CEA, NSE, and Cyfra21-1 are valuable diagnostic markers for MPE, with optimal cutoff values of 17.5 × 10

Indexed as

Antigens, NeoplasmBiomarkers, TumorCarcinoembryonic AntigenKeratin-19Phosphopyruvate HydratasePleural EffusionPleural Effusion, MalignantAdultAgedAged, 80 and overFemaleHumansMaleMiddle AgedROC CurveSensitivity and Specificityantigen CYFRA21.1Antigens, NeoplasmBiomarkers, TumorCarcinoembryonic AntigenKeratin-19Phosphopyruvate HydrataseCEACyfra21-1High-fluorescent cellsMalignant pleural effusionNSE

Identifiers

PMID41306356
PMCPMC12153219

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.