ArticleBrain tumor pathology2026
Rapid immunohistochemistry for intraoperative differentiation between high-grade gliomas and primary central nervous system lymphomas: a multicenter prospective study.
Article in Brain tumor pathology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
Rapid intraoperative differentiation between high-grade gliomas (HGGs) and primary central nervous system lymphomas (PCNSLs) is critical because surgical strategies and adjuvant therapies differ substantially. We conducted a multicenter prospective observational study to evaluate rapid immunohistochemistry (R-IHC) on frozen sections using alternating current electric field mixing. Forty-eight adults with newly suspected malignant intra-axial brain tumors underwent tumor resection or biopsy with intraoperative frozen section consultation. The prespecified primary endpoint was antibody level concordance between R-IHC and conventional immunohistochemistry on permanent formalin-fixed, paraffin-embedded sections. Intraoperative diagnostic performance using hematoxylin and eosin (HE) alone versus HE plus R-IHC was assessed descriptively. Final diagnoses were HGG in 37 patients, PCNSL in 8, and other lesions in 3. For HGG, HE-based intraoperative diagnosis showed 91.9% sensitivity and 90.9% specificity, whereas HE plus R-IHC showed 100% sensitivity in this cohort and unchanged specificity (90.9%). CD20 showed complete concordance between rapid and permanent staining. Ki-67 labeling indices were strongly correlated between the two methods (Spearman r = 0.821). Therefore, R-IHC provides reliable immunostaining results on frozen sections and may serve as a practical adjunct to HE-based intraoperative differentiation between HGGs and PCNSLs in this diagnostic setting.
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