Diagnostic and prognostic value of plasma D-dimer levels for metastasis and survival in gastric cancer: A systematic review and meta-analysis.

Y Yashaswi Guntupalli (Sri Venkateswara Institute of Medical Sciences - SPMCW, Tirupati, Andhra Pradesh, India) R Rithish Nimmagadda (5One Brooklyn Health, Department of Internal Medicine, New York City, United States) S Satwik Kuppili (Konaseema Institute of Medical Sciences and Research Foundation, Amalapuram, India) A Amruth Akhil Alluri (American University of the Caribbean School of Medicine, Cupecoy, Sint Maarten (Dutch part)) S Sameer Krishna Prasad Garlapati (Howard University, Washington D.C, District of Columbia, United States) N Nayanika Chowdary Tummala (NYMC at St. Mary’s General Hospital and Saint Clare’s Health, Denville, NJ) A Ayesha Mubeen Farooq (1Gandhi Medical College, Secunderabad, India) E Eshika Madala (Apollo Institute of Medical Sciences and Research, Hyderabad, India) T Tejaswi Mangalagiri (6Meenakshi Medical College Hospital and Research Institute, Department of Medicine, Kanchipuram, India) V Vineeth Potluri (7Cleveland Clinic, Department of Internal Medicine, Cleveland, United States)

Abstract

e16089 Background: Gastric cancer (GC) is frequently associated with hypercoagulability, yet the clinical utility of D-dimer as a biomarker remains inconsistent. While elevated D-dimer is linked to venous thromboembolism, its potential to predict distant metastasis and long-term survival in GC is debated. We performed a systematic review and meta-analysis to evaluate the diagnostic accuracy of pretreatment D-dimer for detecting metastasis and its prognostic value for overall survival (OS). Methods: We searched PubMed, Embase, and Cochrane Library databases through January 2026 for observational studies evaluating D-dimer in histologically confirmed GC. Inclusion criteria were studies reporting diagnostic performance (sensitivity/specificity) for metastasis or hazard ratios (HR) for survival. Quality was assessed using QUADAS-2 and NOS. A bivariate random-effects model was used to pool diagnostic metrics. Due to heterogeneous reporting of survival outcomes, prognostic data were synthesized qualitatively. Results: Eight studies comprising 6,189 patients were included. Four studies (n = 5,008) provided extractable data for diagnostic meta-analysis of metastasis (hematogenous, lymph node, or bone). The pooled sensitivity and specificity of elevated D-dimer for detecting metastasis were 0.67 (95% CI, 0.66-0.69) and 0.78 (95% CI, 0.77-0.79), respectively. The diagnostic odds ratio (DOR) was 7.40, indicating patients with metastasis had 7-fold higher odds of elevated D-dimer. The area under the summary receiver operating characteristic curve (SROC AUC) was 0.81, indicating moderate-to-high diagnostic accuracy. Regarding prognosis, 5 studies assessed survival outcomes. Elevated pretreatment D-dimer was universally associated with shorter OS in univariate analyses (P < 0.001). However, multivariate results were mixed: two studies confirmed D-dimer as an independent prognostic factor for 1-year mortality and OS, whereas two others found it dependent on tumor stage. D-dimer levels consistently correlated with tumor load, TNM stage, and vascular invasion. Conclusions: Pretreatment plasma D-dimer demonstrates high specificity and moderate sensitivity for detecting metastasis in gastric cancer, making it a viable, cost-effective initial screening tool. While consistently associated with poor survival, its independent prognostic value varies by study population. Routine D-dimer assessment may aid in risk stratification for occult metastasis. Diagnostic performance of d-dimer for gastric cancer metastasis. Study N Cut-off (mg/L) Sensitivity (%) Specificity (%) AUC (95% CI) Zhang X et al. 2022 3,447 0.91 68.2 76.3 0.77 (0.76–0.79) Wang et al. 2023 454 1.03 69.0 72.8 0.76 (0.71–0.80) Yan et al. 2025 65 1.63 87.1 94.1 0.91 (0.83–0.99) Diao et al. 2014 1,042 1.50 61.9 86.6 0.80 (0.76–0.83)

Article Details

Volume / Issue Vol. 44, Issue 16_suppl
Published June 01, 2026
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (10)

Y

Yashaswi Guntupalli

Sri Venkateswara Institute of Medical Sciences - SPMCW, Tirupati, Andhra Pradesh, India

R

Rithish Nimmagadda

5One Brooklyn Health, Department of Internal Medicine, New York City, United States

S

Satwik Kuppili

Konaseema Institute of Medical Sciences and Research Foundation, Amalapuram, India

A

Amruth Akhil Alluri

American University of the Caribbean School of Medicine, Cupecoy, Sint Maarten (Dutch part)

S

Sameer Krishna Prasad Garlapati

Howard University, Washington D.C, District of Columbia, United States

N

Nayanika Chowdary Tummala

NYMC at St. Mary’s General Hospital and Saint Clare’s Health, Denville, NJ

A

Ayesha Mubeen Farooq

1Gandhi Medical College, Secunderabad, India

E

Eshika Madala

Apollo Institute of Medical Sciences and Research, Hyderabad, India

T

Tejaswi Mangalagiri

6Meenakshi Medical College Hospital and Research Institute, Department of Medicine, Kanchipuram, India

V

Vineeth Potluri

7Cleveland Clinic, Department of Internal Medicine, Cleveland, United States