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PMID: 23009708 Published · epublish English Journal Article Research Support, Non-U.S. Gov't

Pleural fluid cell-free DNA integrity index to identify cytologically negative malignant pleural effusions including mesotheliomas.

BMC cancer ·Vol. 12 ·2012-09-25 ·Pages 428

Sriram KB, Relan V, Clarke BE, Duhig EE, Windsor MN, Matar KS, Naidoo R, Passmore L, McCaul E, Courtney D, Yang IA, Bowman RV, Fong KM

Abstract

The diagnosis of malignant pleural effusions (MPE) is often clinically challenging, especially if the cytology is negative for malignancy. DNA integrity index has been reported to be a marker of malignancy. The aim of this study was to evaluate the utility of pleural fluid DNA integrity index in the diagnosis of MPE. We studied 75 pleural fluid and matched serum samples from consecutive subjects. Pleural fluid and serum ALU DNA repeats [115bp, 247bp and 247bp/115bp ratio (DNA integrity index)] were assessed by real-time quantitative PCR. Pleural fluid and serum mesothelin levels were quantified using ELISA. Based on clinico-pathological evaluation, 52 subjects had MPE (including 16 mesotheliomas) and 23 had benign effusions. Pleural fluid DNA integrity index was higher in MPE compared with benign effusions (1.2 vs. 0.8; p<0.001). Cytology had a sensitivity of 55% in diagnosing MPE. If cytology and pleural fluid DNA integrity index were considered together, they exhibited 81% sensitivity and 87% specificity in distinguishing benign and malignant effusions. In cytology-negative pleural effusions (35 MPE and 28 benign effusions), elevated pleural fluid DNA integrity index had an 81% positive predictive value in detecting MPEs. In the detection of mesothelioma, at a specificity of 90%, pleural fluid DNA integrity index had similar sensitivity to pleural fluid and serum mesothelin (75% each respectively). Pleural fluid DNA integrity index is a promising diagnostic biomarker for identification of MPEs, including mesothelioma. This biomarker may be particularly useful in cases of MPE where pleural aspirate cytology is negative, and could guide the decision to undertake more invasive definitive testing. A prospective validation study is being undertaken to validate our findings and test the clinical utility of this biomarker for altering clinical practice.

MeSH Terms
Adult Aged Aged, 80 and over Biomarkers, Tumor/analysis,genetics DNA, Neoplasm/analysis,blood,genetics Female GPI-Linked Proteins/analysis,genetics Humans Male Mesothelin Mesothelioma/chemistry,genetics,pathology Middle Aged Neoplasms/chemistry,genetics,pathology Pleural Effusion/genetics,pathology Pleural Effusion, Malignant/chemistry,genetics,pathology ROC Curve Sensitivity and Specificity Statistics, Nonparametric Transition Temperature
Chemicals
Biomarkers, Tumor DNA, Neoplasm GPI-Linked Proteins Mesothelin
Authors & Affiliations
13 authors, click to expand affiliations / ORCID
Sriram Krishna B
UQ Thoracic Research Centre, School of Medicine, The University of Queensland, Queensland, Australia. [email protected]
Relan Vandana
Clarke Belinda E
Duhig Edwina E
Windsor Morgan N
Matar Kevin S
Naidoo Rishendran
Passmore Linda
McCaul Elizabeth
Courtney Deborah
Yang Ian A
Bowman Rayleen V
Fong Kwun M
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Article Info
Journal
BMC cancer
Abbr.
BMC Cancer
ISSN
1471-2407
Published
2012-09-25
Epub
2012-00-25
Pages
428
Language
English
Region
England
NLM ID
100967800
PMCID
PMC3495778
Subset
IM
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