Evidence map›Paper›PMID 42130036›Full record

ArticlePulmonary medicine2026

Diagnostic Yield of Malignant Pleural Effusion in Various Primary and Metastatic Cancers: Insights Across Cancer Subtypes.

Santosh Basyal, Antony D Rawindraraj, Rahul Parajuli, Shardul Bhattarai, Laxman Wagle, Kritick Bhandari, Vikas Pathak

Abstract read
In one paragraph

Article in Pulmonary medicine, 2026. 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

7 authors.

Santosh BasyalDepartment of Internal Medicine, Nepal Medical College and Teaching Hospital, Kathmandu, Nepal.ORCID https://orcid.org/0009-0008-6898-9413
Antony D RawindrarajDepartment of Internal Medicine, University of Missouri, Columbia, Missouri, USA, missouri.edu.ORCID https://orcid.org/0000-0001-8802-5816
Rahul ParajuliDepartment of Pulmonology and Critical Care, Hospital for Advanced Medicine and Surgery (HAMS), Kathmandu, Nepal.ORCID https://orcid.org/0000-0003-0223-3185
Shardul BhattaraiDepartment of Internal Medicine, Nepal Medical College and Teaching Hospital, Kathmandu, Nepal.ORCID https://orcid.org/0009-0002-7191-2130
Laxman WagleDepartment of Internal Medicine, Ascension Saint Agnes Hospital, Baltimore, Maryland, USA.ORCID https://orcid.org/0009-0000-5651-1246
Kritick BhandariDepartment of Internal Medicine, Kist Medical College Teaching Hospital, Lalitpur, Nepal.ORCID https://orcid.org/0009-0006-7156-7604
Vikas PathakInterventional Pulmonology and Critical Care Medicine, Virginia Institute of Lung Diseases, Mechanicsville, Virginia, USA.ORCID https://orcid.org/0000-0002-7482-5908

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

OBJECTIVE/

backgroundPleural fluid cytology remains a cornerstone in diagnosing malignant pleural effusions (MPEs); however, its diagnostic yield varies considerably across cancer subtypes. This study is aimed at evaluating the diagnostic performance of cytology stratified by malignancy type.

methodsWe conducted a retrospective study at a tertiary referral center in Raleigh, North Carolina, enrolling patients aged 18-100 years who underwent thoracentesis for suspected MPE between January 2015 and August 2018. MPE was defined by positive pleural fluid cytology, VATS findings, or histopathological confirmation. Variables analyzed included demographics, cytology results, thoracoscopic findings, and pleural biopsy histopathology.

resultsOf the 779 pleural fluid samples, we included 667 patients (99 malignant and 482 benign); the remaining 86 samples included therapeutic thoracenteses, dry taps, and inadequate volume for cytology. Cytology diagnosed 86 cases of MPE (86.86%), while VATS identified additional eight cases. Overall cytology specificity was 99.8% (95% CI: 99.3%-100%). Adenocarcinoma demonstrated the highest cytologic sensitivity (90.24%), particularly in breast cancer-related MPE (67.44%). Among 482 cytology-negative cases, 130 had documented cancer histories, most frequently lung cancer (17.69%), hematological malignancies (12.30%), and breast cancer (10.76%). Skin and prostate cancers were more likely to yield false-negative cytology results. Malignant mesothelioma requires repeat cytology or VATS for definitive diagnosis in most cases.

conclusionPleural fluid cytology is highly specific and most sensitive for lung and breast adenocarcinomas. Combined cytology and VATS demonstrate superior diagnostic accuracy and should be the standard approach when initial cytology is negative and malignancy remains clinically suspected.

Indexed as

NeoplasmsPleural Effusion, MalignantAdolescentAdultAgedAged, 80 and overFemaleHumansLung NeoplasmsMaleMiddle AgedNorth CarolinaRetrospective StudiesSensitivity and SpecificityThoracentesisThoracic Surgery, Video-Assistedcytologymalignant pleural effusionmedical thoracoscopythoracoscopyvideo-assisted thoracoscopic surgery (VATS)

Identifiers

PMID42130036
PMCPMC13172289

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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.