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Classification of microvascular patterns via cluster analysis reveals their prognostic significance in glioblastoma.
Chen, Long; Lin, Zhi-Xiong; Lin, Guo-Shi; Zhou, Chang-Fu; Chen, Yu-Peng; Wang, Xing-Fu; Zheng, Zong-Qing.
Afiliação
  • Chen L; Tumor Invasion Microecological Laboratory, Fujian Medical University, Fuzhou 350005, China; Intensive Care Unit, the First Affiliated Hospital of Fujian Medical University, Fuzhou 350005, China.
  • Lin ZX; Department of Neurosurgery, the First Affiliated Hospital of Fujian Medical University, Fuzhou 350005, China. Electronic address: lzx1967@sina.com.
  • Lin GS; Department of Neurosurgery, the First Affiliated Hospital of Fujian Medical University, Fuzhou 350005, China.
  • Zhou CF; Department of Neurosurgery, the First Affiliated Hospital of Fujian Medical University, Fuzhou 350005, China.
  • Chen YP; Department of Pathology, the First Affiliated Hospital of Fujian Medical University, Fuzhou 350005, China.
  • Wang XF; Department of Pathology, the First Affiliated Hospital of Fujian Medical University, Fuzhou 350005, China.
  • Zheng ZQ; Department of Neurosurgery, the First Affiliated Hospital of Fujian Medical University, Fuzhou 350005, China.
Hum Pathol ; 46(1): 120-8, 2015 Jan.
Article em En | MEDLINE | ID: mdl-25455996
ABSTRACT
There are limited researches focusing on microvascular patterns (MVPs) in human glioblastoma and their prognostic impact. We evaluated MVPs of 78 glioblastomas by CD34/periodic acid-Schiff dual staining and by cluster analysis of the percentage of microvascular area for distinct microvascular formations. The distribution of 5 types of basic microvascular formations, that is, microvascular sprouting (MS), vascular cluster (VC), vascular garland (VG), glomeruloid vascular proliferation (GVP), and vasculogenic mimicry (VM), was variable. Accordingly, cluster analysis classified MVPs into 2 types type I MVP displayed prominent MSs and VCs, whereas type II MVP had numerous VGs, GVPs, and VMs. By analyzing the proportion of microvascular area for each type of formation, we determined that glioblastomas with few MSs and VCs had many GVPs and VMs, and vice versa. VG seemed to be a transitional type of formation. In case of type I MVP, expression of Ki-67 and p53 but not MGMT was significantly higher as compared with those of type II MVP (P < .05). Survival analysis showed that the type of MVPs presented as an independent prognostic factor of progression-free survival (PFS) and overall survival (OS) (both P < .001). Type II MVP had a more negative influence on PFS and OS than did type I MVP. We conclude that the heterogeneous MVPs in glioblastoma can be categorized properly by certain histopathologic and statistical analyses and may influence clinical outcome.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Encefálicas / Interpretação de Imagem Assistida por Computador / Análise por Conglomerados / Glioblastoma / Microvasos / Neovascularização Patológica Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Encefálicas / Interpretação de Imagem Assistida por Computador / Análise por Conglomerados / Glioblastoma / Microvasos / Neovascularização Patológica Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2015 Tipo de documento: Article