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Cell-free DNA methylation analysis as a marker of malignancy in pleural fluid.
Bixby, Billie; Vrba, Lukas; Lenka, Jyoti; Oshiro, Marc M; Watts, George S; Hughes, Trina; Erickson, Heidi; Chopra, Madhav; Knepler, James L; Knox, Kenneth S; Jarnagin, Lisa; Alalawi, Raed; Kala, Mrinalini; Bernert, Richard; Routh, Joshua; Roe, Denise J; Garland, Linda L; Futscher, Bernard W; Nelson, Mark A.
Affiliation
  • Bixby B; Pulmonary, Critical Care, Allergy and Sleep Medicine, Department of Medicine, University of Arizona, Tucson, USA.
  • Vrba L; Precision Epigenomics, Tucson, AZ, USA.
  • Lenka J; Pulmonary, Critical Care, Allergy and Sleep Medicine, Department of Medicine, University of Arizona, Tucson, USA.
  • Oshiro MM; Boyer Liver Institute, Department of Medicine, University of Arizona, Tucson, USA.
  • Watts GS; Department of Pharmacology and Toxicology, University of Arizona, Tucson, USA.
  • Hughes T; Pulmonary, Critical Care, Allergy and Sleep Medicine, Department of Medicine, University of Arizona, Tucson, USA.
  • Erickson H; Pulmonary, Critical Care, Allergy and Sleep Medicine, Department of Medicine, University of Arizona, Tucson, USA.
  • Chopra M; Pulmonary, Critical Care, Allergy and Sleep Medicine, Department of Medicine, University of Arizona, Tucson, USA.
  • Knepler JL; Pulmonary, Critical Care, Allergy and Sleep Medicine, Department of Medicine, University of Arizona, Tucson, USA.
  • Knox KS; Pulmonary, Critical Care, Allergy and Sleep Medicine, Department of Medicine, University of Arizona, Phoenix, USA.
  • Jarnagin L; Pulmonary, Critical Care, Allergy and Sleep Medicine, Department of Medicine, University of Arizona, Phoenix, USA.
  • Alalawi R; Pulmonary, Critical Care, Allergy and Sleep Medicine, Department of Medicine, University of Arizona, Phoenix, USA.
  • Kala M; Department of Internal Medicine, University of Arizona, Phoenix, USA.
  • Bernert R; Precision Epigenomics, Tucson, AZ, USA.
  • Routh J; Midwestern University, Glendale, USA.
  • Roe DJ; Mel and Enid Zuckerman College of Public Health, University of Arizona, Tucson, USA.
  • Garland LL; Hematology Oncology, Department of Medicine, University of Arizona, Tucson, USA.
  • Futscher BW; Department of Pharmacology and Toxicology, University of Arizona, Tucson, USA.
  • Nelson MA; Department of Pathology, University of Arizona, Tucson, AZ, 85724, USA. manelson@arizona.edu.
Sci Rep ; 14(1): 2939, 2024 02 05.
Article in En | MEDLINE | ID: mdl-38316884
ABSTRACT
Diagnosis of malignant pleural effusion (MPE) is made by cytological examination of pleural fluid or histological examination of pleural tissue from biopsy. Unfortunately, detection of malignancy using cytology has an overall sensitivity of 50%, and is dependent upon tumor load, volume of fluid assessed, and cytopathologist experience. The diagnostic yield of pleural fluid cytology is also compromised by low abundance of tumor cells or when morphology is obscured by inflammation or reactive mesothelial cells. A reliable molecular marker that may complement fluid cytology for the diagnosis of malignant pleural effusion is needed. The purpose of this study was to establish a molecular diagnostic approach based on pleural effusion cell-free DNA methylation analysis for the differential diagnosis of malignant pleural effusion and benign pleural effusion. This was a blind, prospective case-control biomarker study. We recruited 104 patients with pleural effusion for the study. We collected pleural fluid from patients with MPE (n = 48), indeterminate pleural effusion in subjects with known malignancy or IPE (n = 28), and benign PE (n = 28), and performed the Sentinel-MPE liquid biopsy assay. The methylation level of Sentinel-MPE was markedly higher in the MPE samples compared to BPE control samples (p < 0.0001) and the same tendency was observed relative to IPE (p = 0.004). We also noted that the methylation signal was significantly higher in IPE relative to BPE (p < 0.001). We also assessed the diagnostic efficiency of the Sentinel-MPE test by performing receiver operating characteristic analysis (ROC). For the ROC analysis we combined the malignant and indeterminate pleural effusion groups (n = 76) and compared against the benign group (n = 28). The detection sensitivity and specificity of the Sentinel-MPE test was high (AUC = 0.912). The Sentinel-MPE appears to have better performance characteristics than cytology analysis. However, combining Sentinel-MPE with cytology analysis could be an even more effective approach for the diagnosis of MPE. The Sentinel-MPE test can discriminate between BPE and MPE. The Sentinel-MPE liquid biopsy test can detect aberrant DNA in several different tumor types. The Sentinel-MPE test can be a complementary tool to cytology in the diagnosis of MPE.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pleural Effusion / Pleural Effusion, Malignant / Cell-Free Nucleic Acids Type of study: Diagnostic_studies Limits: Humans Language: En Journal: Sci Rep Year: 2024 Document type: Article Affiliation country: Estados Unidos Publication country: ENGLAND / ESCOCIA / GB / GREAT BRITAIN / INGLATERRA / REINO UNIDO / SCOTLAND / UK / UNITED KINGDOM

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pleural Effusion / Pleural Effusion, Malignant / Cell-Free Nucleic Acids Type of study: Diagnostic_studies Limits: Humans Language: En Journal: Sci Rep Year: 2024 Document type: Article Affiliation country: Estados Unidos Publication country: ENGLAND / ESCOCIA / GB / GREAT BRITAIN / INGLATERRA / REINO UNIDO / SCOTLAND / UK / UNITED KINGDOM