MIB1 staining index and scoring of histologic features in meningioma. Indicators for the prediction of biologic potential and postoperative management

Cancer. 1994 Dec 15;74(12):3176-89. doi: 10.1002/1097-0142(19941215)74:12<3176::aid-cncr2820741217>3.0.co;2-n.

Abstract

Background: The biology of brain tumors, including cell kinetics, has been studied. Recently, monoclonal antibody to Ki67 (MIB1), a nuclear protein related to cell proliferation, has been analyzed immunohistochemically using tissue prepared from paraffin embedded sections.

Methods: The authors assessed the prognostic usefulness of various histologic indicators of the biologic potential of meningiomas in patients who underwent total resection (Simpson's Grade I and II) by evaluating the time to recurrence as an end point. Forty-three patients with a total of 36 meningiomas and 7 hemangiopericytomas were investigated by immunohistochemical analysis using MIB1.

Results: MIB1 staining index (SI) and histologic score were well correlated with the recurrence-free interval (r = -0.6749, P = 0.002 and r = -0.4939, P = 0.027, respectively) and with each other (r = 0.7909, P < 0.001). The MIB1 SI and histologic score in the nonrecurrence group were significantly lower than those in the recurrence/metastasis group (P < 0.001 and P = 0.001, respectively). The values of these indicators showed that as the value increased, so did the recurrence rate.

Conclusions: Evaluation using the MIB1 SI and total histologic score of meningioma is useful in assessing the prognosis as well as postoperative management of these patients.

MeSH terms

  • Adolescent
  • Adult
  • Cell Cycle
  • Female
  • Humans
  • Immunohistochemistry
  • Ki-67 Antigen
  • Male
  • Meningeal Neoplasms / chemistry
  • Meningeal Neoplasms / pathology*
  • Meningeal Neoplasms / surgery
  • Meningioma / chemistry
  • Meningioma / pathology*
  • Meningioma / surgery
  • Middle Aged
  • Neoplasm Metastasis
  • Neoplasm Proteins / analysis*
  • Neoplasm Recurrence, Local
  • Nuclear Proteins / analysis*
  • Polymerase Chain Reaction
  • Prognosis
  • Transcription, Genetic

Substances

  • Ki-67 Antigen
  • Neoplasm Proteins
  • Nuclear Proteins