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Diagnostic Value of Nonacid Nucleic Blood Tumor Marker Panels in Early Diagnosing Breast Cancer: A Systematic Review and Network Meta-Analysis Publisher Pubmed



Raja V1 ; Farajzadegan Z2 ; Mansourian M3 ; Ghasemi K4 ; Aboutalebi MS5 ; Nouri R6 ; Mokarian F7
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Authors Affiliations
  1. 1. Clinical Laboratory Sciences, Amin Hospital, Isfahan University of Medical Sciences, Isfahan, Iran
  2. 2. Community and Preventive Medicine, Isfahan University of Medical Sciences, Isfahan, Iran
  3. 3. Biostatistics, Department of Biostatistics and Epidemiology, School of Public Health, Isfahan, Iran
  4. 4. Department of Biostatistics and Epidemiology, School of Public Health, Isfahan University of Medical Sciences, Isfahan, Iran
  5. 5. Faculty of Nursing and Midwifery, Isfahan University of Medical Sciences, Isfahan, Iran
  6. 6. Department of Medical Library and Information Sciences, Isfahan University of Medical Sciences, Isfahan, Iran
  7. 7. Hematology and Oncology Department of Internal Medicine, Isfahan University of Medical Sciences, Isfahan, Iran

Source: Disease Markers Published:2022


Abstract

This study is aimed at determining the best nonacid nucleic blood tumor marker panels in terms of sensitivity, specificity, and accuracy in order to detect breast cancer in early stages (I, II, and III) among eligible women for breast cancer screening. PubMed, Web of Science, Embase, Scopus, and Cochrane were systematically reviewed to assess nonacid nucleic blood tumor marker panels' diagnostic value in women, both healthy and patient (before any anticancer treatment), for detecting breast cancer. A network meta-analysis was carried out using a Bayesian network meta-analysis to estimate combined odd ratio (OR) and 95% CI credible interval for presenting the results. Rankograms plot was drawn to rank the diagnostic value of different panels. Of the 2358 titles initially identified, 9 studies and 8 panels were included in the network meta-analysis. Panels A (MMP-9/TIMP-1) and K (TF1+TF2+TF3) had the highest sensitivity in early stages, as panel A with OR=11.61 and 95% CI (1.49-102.5) demonstrated a better function than mammography. Panels H (CA 15.3 + IL-18) and A (MMP-9/TIMP-1) had the highest specificity in early stages, but no significant difference with mammography. Panels A (MMP-9/TIMP-1) and H (CA 15.3 + IL-18) had the highest accuracy in early stages, as they significantly exhibited a higher function than mammography with OR=6.87 and 95% CI (2.07-31.35) as well as OR=3.44 and 95% CI (1.15-11.07), respectively. Panel A including MMP-9/TIMP-1 in early stages demonstrated a higher diagnostic value for breast cancer than the rest of the panels. © 2022 Vahid Raja et al.
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