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Occult cancer in patients with unprovoked venous thromboembolism: A nested case-control study.

Authors :
Sánchez-López, Verónica
Marín-Romero, Samira
Ferrer-Galván, Marta
Elías-Hernández, Teresa
Beristain, José Luis Lobo
Quincoces, Aitor Ballaz
Jara-Palomares, Luis
Martorell, Francisco Javier Rodríguez
Castro, María José
Hinojosa, Carmen Marín
López-Campos, José Luis
Otero-Candelera, Remedios
Source :
American Journal of Clinical Pathology; May2024, Vol. 161 Issue 5, p501-511, 11p
Publication Year :
2024

Abstract

Objectives Detecting occult cancer in patients with unprovoked venous thromboembolism (VTE) remains a significant challenge. Our objective was to investigate the potential predictive role of coagulation-related biomarkers in the diagnosis of occult malignancies. Methods We conducted a nested case-control study with a 1-year prospective cohort of 214 patients with unprovoked VTE, with a focus on identifying occult cancer. At the time of VTE diagnosis, we measured various biomarkers, including soluble P-selectin (sP-selectin), dimerized plasmin fragment D (D-dimer), platelets, leukocytes, hemoglobin, total extracellular vesicles (EVs), EVs expressing tissue factor on their surface (TF+EVs), and EVs expressing P-selectin on their surface (Psel+EVs) in all participants. Results We observed statistically significant increased levels of sP-selectin (P =.015) in patients with occult cancer. Despite an increase in Psel+EVs, TF+EVs, D-dimer, and platelets within this group, however, no significant differences were found. When sP-selectin exceeded 62 ng/mL and D-dimer surpassed 10,000 µg/L, the diagnosis of occult cancer demonstrated a specificity of up to 91% (95% CI, 79.9%-96.7%). Conclusions The combination of sP-selectin and D-dimer can be a valuable biomarker in detecting occult cancer in patients with unprovoked VTE. Further research is necessary to ascertain whether easily measurable biomarkers such as sP-selectin and D-dimer can effectively distinguish between patients who have VTE with and without hidden malignancies. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00029173
Volume :
161
Issue :
5
Database :
Complementary Index
Journal :
American Journal of Clinical Pathology
Publication Type :
Academic Journal
Accession number :
177084539
Full Text :
https://doi.org/10.1093/ajcp/aqad178