Unveiling the diagnostic enigma of D‐dimer testing in cancer patients: Current evidence and areas of application

Author:

Gotta Jennifer1ORCID,Gruenewald Leon D.1,Eichler Katrin1,Martin Simon S.1,Mahmoudi Scherwin1,Booz Christian1,Biciusca Teodora1ORCID,Reschke Philipp1,Bernatz Simon1,Pinto Dos Santos Daniel1ORCID,Scholtz Jan‐Erik1,Alizadeh Leona S.1,Nour‐Eldin Nour‐Eldin A.1,Hammerstingl Renate M.1,Gruber‐Rouh Tatjana1,Mader Christoph1,Hardt Stefan E.2,Sommer Christof M.3,Bucolo Giuseppe4,D'Angelo Tommaso4ORCID,Onay Melis1,Finkelmeier Fabian1,Leistner David M.1,Vogl Thomas J.1,Giannitsis Evangelos2,Koch Vitali1ORCID

Affiliation:

1. Goethe University Hospital Frankfurt Frankfurt am Main Germany

2. Department of Cardiology, Angiology and Pulmonology Heidelberg University Hospital Heidelberg Germany

3. Clinic of Diagnostic and Interventional Radiology Heidelberg University Hospital Heidelberg Germany

4. Department of Biomedical Sciences and Morphological and Functional Imaging University of Messina Messina Italy

Abstract

AbstractBackgroundCancer is a well‐known risk factor for venous thromboembolism (VTE). A combined strategy of D‐dimer testing and clinical pre‐test probability is usually used to exclude VTE. However, its effectiveness is diminished in cancer patients due to reduced specificity, ultimately leading to a decreased clinical utility. This review article seeks to provide a comprehensive summary of how to interpret D‐dimer testing in cancer patients.MethodsIn accordance with PRISMA standards, literature pertaining to the diagnostic and prognostic significance of D‐dimer testing in cancer patients was carefully chosen from reputable sources such as PubMed and the Cochrane databases.ResultsD‐dimers have not only a diagnostic value in ruling out VTE but can also serve as an aid for rule‐in if their values exceed 10‐times the upper limit of normal. This threshold allows a diagnosis of VTE in cancer patients with a positive predictive value of more than 80%. Moreover, elevated D‐dimers carry important prognostic information and are associated with VTE reoccurrence. A gradual increase in risk for all‐cause death suggests that VTE is also an indicator of biologically more aggressive cancer types and advanced cancer stages. Considering the lack of standardization for D‐dimer assays, it is essential for clinicians to carefully consider the variations in assay performance and the specific test characteristics of their institution.ConclusionsStandardizing D‐dimer assays and developing modified pretest probability models specifically for cancer patients, along with adjusted cut‐off values for D‐dimer testing, could significantly enhance the accuracy and effectiveness of VTE diagnosis in this population.

Publisher

Wiley

Subject

Clinical Biochemistry,Biochemistry,General Medicine

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