Key result
D-dimer levels in patients with various malignant tumors were significantly higher than in healthy controls, with concentrations depending on patient age, tumor primary site, and tumor stage.
Cross-Sectional (n=1,518)
Yes
D-dimer levels are significantly elevated in cancer patients compared to healthy controls and vary by tumor type and stage, suggesting that standard reference ranges may overestimate venous thromboembolism risk in this population.
May support cancer-specific D-dimer thresholds to refine VTE assessment; leaves open prospective validation by stage and site.
D-dimer level in cancer patients is associated with risk of venous thromboembolism and deep venous thrombosis. Most cancer patients have "abnormal" D-dimer levels based on the current normal reference range. To investigate tumor-specific D-dimer reference range, we compared D-dimer levels for nine different tumour types with healthy controls by using simultaneous quantile regression and constructing a median, 5th percentile, and 95th percentile model of normal tumour D-dimer concentration. Associations with tumour primary site, stage, pathological type, and treatment were also explored. Additionally, 190 patients were tracked to reveal the relevance of initial D-dimer levels to cancer prognosis. D-dimer ranges (median, 5th, 95th) in various cancers (mg/L) were: liver 1.12, 0.27, 5.25; pancreatic 0.96, 0.23, 4.81; breast 0.44, 0.2, 2.17; gastric 0.65, 0.22, 5.03; colorectal 0.73, 0.22, 4.45; lung 0.7, 0.25, 4.0; gynaecological 0.61, 0.22, 3.98; oesophageal 0.23, 0.7, 3.45; and head and neck 0.22, 0.44, 2.19. All were significantly higher than that of healthy controls (0.18, 0.07, 0.57). D-dimer peaked 1-2 days postoperatively but had decreased to the normal range by 1 week. Additionally, cancer patients with high initial D-dimer were shown a tendency of poor prognosis in survival rate. In conclusion, D-dimer levels in cancer depend on patient age, tumour primary site, and tumour stage. Thrombosis prevention is necessary if D-dimer has not decreased to the tumor-specific baseline a week after surgery.
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Yu et al. (2016) conducted a cross-sectional in Malignant tumors (n=1,518). Malignant tumors vs. Healthy controls was evaluated on D-dimer concentration (p=<0.001). D-dimer levels in patients with various malignant tumors were significantly higher than in healthy controls, with concentrations depending on patient age, tumor primary site, and tumor stage.
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