gms | German Medical Science

Joint-Meeting of the German Society for Neuropathology and Neuroanatomy (DGNN) and the Scandinavian Neuropathological Society (SNS)

Deutsche Gesellschaft für Neuropathologie und Neuroanatomie

22.09.-24.09.2016, Hamburg

PHH3 biomarker can improve the WHO classification of human meningiomas

Meeting Abstract

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  • presenting/speaker Theo L. Winther - NTNU, Dept. of Lab.Med., Children's and Women's Health, Trondheim, Norway
  • Magnus B. Arnli - NTNU, Dept. of Lab.Med., Children's and Women's Health, Trondheim, Norway
  • Øyvind Salvesen - NTNU, Dept. of Public Health and General Practice, Trondheim, Norway
  • Sverre H. Torp - St. Olav Hospital, Department of Pathology and Medical Genetics, Trondheim, Norway; NTNU, Dept. of Lab.Med., Children's and Women's Health, Trondheim, Norway

Deutsche Gesellschaft für Neuropathologie und Neuroanatomie. Scandinavian Neuropathological Society. Joint-Meeting of the German Society for Neuropathology and Neuroanatomy (DGNN) and the Scandinavian Neuropathological Society (SNS). Hamburg, 22.-24.09.2016. Düsseldorf: German Medical Science GMS Publishing House; 2016. Doc16dgnnP38

doi: 10.3205/16dgnn41, urn:nbn:de:0183-16dgnn418

Veröffentlicht: 14. September 2016

© 2016 Winther et al.
Dieser Artikel ist ein Open-Access-Artikel und steht unter den Lizenzbedingungen der Creative Commons Attribution 4.0 License (Namensnennung). Lizenz-Angaben siehe http://creativecommons.org/licenses/by/4.0/.


Gliederung

Text

The WHO classification of human meningiomas distinguishes between three histological malignancy grades related to risk of recurrence. Most tumors are graded based on mitotic index, a method of limited value due to substantial within-grade variation in recurrence risk, subjective assessment of grading criteria and poor reproducibility. To improve the diagnostics of human meningiomas this study investigated the prognostic value of phosphohistone-H3 (PHH3) proliferation index (PI) in 160 patients, and compared the reliability with the conventional mitotic index and the established biomarker MIB-1. Proliferative activity was determined by standardized immunohistochemistry on tissue microarrays and related to recurrence-free survival. All three proliferation assessment methods were significantly associated with WHO grade. The optimal cutoff values for recurrence prediction were 3% for the MIB-1 PI and 0.5% for the PHH3 PI. Increased PHH3 PI was significantly associated with recurrence-free survival in univariate Cox hazard analysis (P = 0.011) and remained an independent predictor in multivariate analysis (P = 0.005). Mitotic index and MIB-1 PI did not reach significance. PHH3 immunostaining allowed for the easiest, fastest and most objective assessment of proliferation, and proved to be the most accurate and reliable method for predicting recurrence in meningioma patients compared with the current established methods. For this reason, incorporating PHH3 PI into the diagnostics of meningiomas should be considered to ensure optimal treatment of these patients.