Diagnostic efficacy of serum microRNAs in predicting pathology of retroperitoneal lymph node dissection in patients with testicular germ cell tumors: a systematic review and meta-analysis
Jazyk angličtina Země Německo Médium electronic
Typ dokumentu časopisecké články, systematický přehled, metaanalýza, přehledy
PubMed
40146282
PubMed Central
PMC11950128
DOI
10.1007/s00345-025-05571-y
PII: 10.1007/s00345-025-05571-y
Knihovny.cz E-zdroje
- Klíčová slova
- Germ cell tumor, MicroRNA, MicroRNA-371a-3p, RPLND, Testicular cancer,
- MeSH
- germinální a embryonální nádory * krev patologie chirurgie sekundární MeSH
- lidé MeSH
- lymfadenektomie * MeSH
- mikro RNA * krev MeSH
- prediktivní hodnota testů MeSH
- retroperitoneální prostor MeSH
- testikulární nádory * patologie krev chirurgie MeSH
- Check Tag
- lidé MeSH
- mužské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- metaanalýza MeSH
- přehledy MeSH
- systematický přehled MeSH
- Názvy látek
- mikro RNA * MeSH
- MIRN371 microRNA, human MeSH Prohlížeč
PURPOSE: To evaluate the diagnostic efficacy of serum microRNAs in predicting pathologic findings of retroperitoneal lymph node dissection (RPLND) in patients with testicular germ cell tumors (TGCT). METHODS: PUBMED, SCOPUS, and Cochrane Library were searched in August 2024 to identify eligible studies according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA 2020) guidelines. RESULTS: Nine studies comprising 603 patients were selected in this review. The pooled sensitivity, specificity, and diagnostic odds ratio (DOR) of microRNA-371a-3p for predicting viable tumor other than pure teratoma in RPLND specimen were 0.76 (95% CI 0.49-0.90), 0.97 (95% CI 0.81-0.99) and 31.75 (95% CI 9.24-109.10), respectively. The pooled sensitivity for primary and post-chemotherapy RPLND (PC-RPLND), were 0.77 (95% CI 0.47-0.93) and 0.73 (95% CI 0.28-0.95), respectively. The pooled specificity for primary and PC-RPLND were 0.92 (95% CI 0.72-0.98) and 0.99 (95% CI 0.62-1.00), respectively. The pooled DOR for primary and PC-RPLND were 13.86 (95% CI 2.97-64.79) and 64.11 (95% CI 13.09-313.98), respectively. The major limitation is the lack of standardization of miR371 testing. CONCLUSION: miR-371a-3p is a relatively sensitive and highly specific marker for predicting viable tumors in RPLND pathologic findings. The DOR was particularly significant for patients who underwent PC-RPLND. While serum microRNAs may be useful in distinguishing viable germ cell tumors from necrosis, fibrosis, and teratomas, their ability to differentiate teratomas from necrosis is limited. Well-designed prospective studies are essential to enhance our understanding of the predictive performance of microRNAs.
Department of Urology 2nd Faculty of Medicine Charles University Prague Czech Republic
Department of Urology Faculty of Medicine Shimane University Shimane Japan
Department of Urology Jikei University School of Medicine Tokyo Japan
Department of Urology Shariati Hospital Tehran University of Medical Sciences Tehran Iran
Department of Urology University of California San Diego San Diego CA USA
Department of Urology University of Texas Southwestern Medical Center Dallas TX USA
Departments of Urology Weill Cornell Medical College New York NY USA
Division of Urology Department of Special Surgery The University of Jordan Amman Jordan
James Buchanan Brady Urological Institute Johns Hopkins University Baltimore MD USA
Karl Landsteiner Institute of Urology and Andrology Vienna Austria
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