Abstract

BackgroundDiagnosing primary central nervous system lymphoma (PCNSL) remains a challenge. MicroRNAs (miRNAs) are promising noninvasive markers for the identification of PCNSL. The present study aims to assess the diagnostic value of miRNAs for PCNSL patients as biomarkers.MethodsWe systematically searched PubMed, Embase, and the Cochrane library from inception to January 31, 2021. The pooled sensitivity, specificity, positive likelihood ratio (PLR), negative likelihood ratio (NLR), diagnostic odds ratio (DOR), together with the summary receiver operator characteristic (SROC) curve, and the area under the SROC curve (AUC) value were used to estimate the overall diagnostic performance. We used Q statistic and I2 to test heterogeneity and used subgroup analyses to investigate the source of heterogeneity. The statistical analyses were independently performed by two investigators using Stata 14.0 and Revman 5.3.ResultsIn total, 11 studies from 6 records were included in the current meta-analysis with 281 PCNSL patients and 367 controls. Our statistical analysis demonstrated that the pooled sensitivity, specificity, PLR, NLR, DOR, and AUC were 0.91 (95% CI 0.84–0.95), 0.88 (95% CI 0.84–0.91), 7.48 (95% CI 5.71–9.78), 0.11 (95% CI 0.06–0.19), 70 (95% CI 35–142), and 0.90 (95% CI 0.87–0.92), respectively. The studies had substantial heterogeneity (I2 = 54%, 95% CI 0–100). Two subgroup analyses were conducted based on the type of specimen and miRNAs profiled.ConclusionsThis meta-analysis indicated that miRNAs were suitable as noninvasive diagnostic biomarkers for PCNSL with high accuracy. In addition, both cerebrospinal fluid-based and blood-based miRNAs assays for PCNSL detection were considered reliable for clinical application. MicroRNA-21 assays also seemed to be more accurate in the diagnosis of PCNSL. Good quality studies with large samples should be conducted to verify our results.

Highlights

  • Primary central nervous system lymphoma (PCNSL) is a rare but aggressive form of extranodal non-Hodgkin lymphoma (NHL) solely affecting the central nervous system, including the brain, spinal cord, leptomeninges, and eyes [1]

  • The diagnostic performance of miRNAs was evaluated by calculating aggregate sensitivity, specificity, positive likelihood ratio (PLR), negative likelihood ratio (NLR), diagnostic odds ratio (DOR), together with the summary receiver operator characteristic (SROC) curve, and the area under the SROC curve (AUC) value [18]

  • Versus; PCNSL, primary central nervous system lymphoma; CSF, cerebrospinal fluid; qRT-PCR, quantitative real-time polymerase chain reaction; AUC, area under the curve; 95% CI, 95% confidence interval; \, not available

Read more

Summary

Introduction

Primary central nervous system lymphoma (PCNSL) is a rare but aggressive form of extranodal non-Hodgkin lymphoma (NHL) solely affecting the central nervous system, including the brain, spinal cord, leptomeninges, and eyes [1]. With an incidence of 0.44 per 100,000, PCNSL accounts for 1 to 2% of all NHLs and 2 to 7% of all primary central nervous system (CNS) tumors [2]. The histological examination of tumor specimens, preferably obtained through stereotactic needle biopsy, is the standard diagnostic procedure for PCNSL [5]. Less invasive liquid biopsy plays an important role in the diagnosis of PCNSL. The analysis of CSF includes cytomorphology, flow cytometry, and immunoglobulin gene rearrangement, but these methods have low diagnostic yield [6,7,8]. MicroRNAs (miRNAs) obtainability from blood or CSF have shown promising prospect as markers for the liquid biopsy analysis of PCNSL, for improving diagnostic yield and for monitoring therapy response [9, 10]. The present study aims to assess the diagnostic value of miRNAs for PCNSL patients as biomarkers

Objectives
Methods
Results
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call