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Comprehensive Analysis of Paraneoplastic Neurologic Syndrome and PNS-CARE Diagnostic Criteria in Clinical Practice. | LitMetric

Comprehensive Analysis of Paraneoplastic Neurologic Syndrome and PNS-CARE Diagnostic Criteria in Clinical Practice.

Neurol Neuroimmunol Neuroinflamm

From the Departments of Neurology (H.Z.-F., M.R., P.G., A.Z., E.P.F., S.J.P., A.M., D.D.) and Laboratory Medicine and Pathology (M.R., P.G., A.Z., E.P.F., S.J.P., A.M., D.D.), Mayo Clinic, Rochester, MN; and Department of Neurology (S.S.), Vanderbilt University, Nashville, TN.

Published: December 2024

AI Article Synopsis

  • The 2021 PNS-CARE score, an updated diagnostic tool for Paraneoplastic Neurologic Syndrome (PNS), was assessed for its effectiveness and application in a cohort of patients at the Mayo Clinic.
  • A retrospective study involving 484 patients suspected of having PNS found that 212 were confirmed to have the syndrome, with common autoantibodies including PCA1, KLHL11, and CRMP5.
  • The newer criteria showed high sensitivity and specificity (93% and 100% respectively), outperforming the previous criteria from 2004, which had lower sensitivity (67%) but similar specificity (99%).

Article Abstract

Background And Objectives: Paraneoplastic neurologic syndrome (PNS) diagnostic criteria were first proposed in 2004 and updated in 2021. The PNS-CARE score, derived from the updated criteria, is a composite model for assigning likelihood for patients with suspected PNS. In this study, we evaluated the utility and applicability of the 2021 PNS-CARE score and present our PNS cohort.

Methods: This is a retrospective study. We identified Mayo Clinic patients suspected to have PNS (1/2005-12/2020) and collected relevant information including demographics, PNS presentation, and clinical outcomes. Inclusion criteria were the following: (1) patients with a syndrome consistent with PNS and (2) patients with sufficient information available in charts. Exclusion criteria were the following: (1) evaluation only before 2005, (2) patients not evaluated by neurology, (3) presentation after immune checkpoint inhibitors, and (4) syndromes not included in 2021 criteria. All patients were evaluated for the 2021 and 2004 PNS criteria.

Results: We identified 484 patients suspected to have PNS at initial presentation, of whom 212 (44%) were considered to have PNS after completion of evaluation. Among these 212 patients, the most common autoantibodies were PCA1 (Yo)-IgG (17%), KLHL11-IgG (16%), and CRMP5-IgG (14%) and the most common phenotypes were rapidly progressive cerebellar syndrome (29%), brainstem encephalitis (14%), and limbic encephalitis (8%). The 2021 PNS criteria definite/probable categorization (PNS-CARE score ≥ 6) had a sensitivity and specificity of 93% and 100%, respectively, while the 2004 PNS criteria definite categorization had a sensitivity and specificity of 67% and 99%, respectively. We found 15 patients with a PNS-CARE score ≤5 who likely had PNS on our review. The most common presentation among these patients was KLHL11-IgG brainstem encephalitis (7/15, 47%) with likely burned-out testicular tumor.

Discussion: Our study validates the PNS-CARE score. A clearer understanding of typical PNS presentation and common underlying malignancies and autoantibodies can aid in earlier and more accurate diagnosis, which is crucial for downstream clinical decisions. Some patients with an intermediate-risk phenotype do not meet probable/definite criteria despite the presence of high-risk antibodies and/or underlying malignancy.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11443324PMC
http://dx.doi.org/10.1212/NXI.0000000000200316DOI Listing

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