Prognostic value of CD109+ circulating endothelial cells in recurrent glioblastomas treated with bevacizumab and irinotecan

PLoS One. 2013 Sep 12;8(9):e74345. doi: 10.1371/journal.pone.0074345. eCollection 2013.

Abstract

Background: Recent data suggest that circulating endothelial and progenitor cells (CECs and CEPs, respectively) may have predictive potential in cancer patients treated with bevacizumab, the antibody recognizing vascular endothelial growth factor (VEGF). Here we report on CECs and CEPs investigated in 68 patients affected by recurrent glioblastoma (rGBM) treated with bevacizumab and irinotecan and two Independent Datasets of rGBM patients respectively treated with bevacizumab alone (n=32, independent dataset A: IDA) and classical antiblastic chemotherapy (n=14, independent dataset B: IDB).

Methods: rGBM patients with KPS ≥50 were treated until progression, as defined by MRI with RANO criteria. CECs expressing CD109, a marker of tumor endothelial cells, as well as other CEC and CEP subtypes, were investigated by six-color flow cytometry.

Results: A baseline count of CD109+ CEC higher than 41.1/ml (1(st) quartile) was associated with increased progression free survival (PFS; 20 versus 9 weeks, P=0.008) and overall survival (OS; 32 versus 23 weeks, P=0.03). Longer PFS (25 versus 8 weeks, P=0.02) and OS (27 versus 17 weeks, P=0.03) were also confirmed in IDA with CD109+ CECs higher than 41.1/ml but not in IDB. Patients treated with bevacizumab with or without irinotecan that were free from MRI progression after two months of treatment had significant decrease of CD109+ CECs: median PFS was 19 weeks; median OS 29 weeks. The presence of two non-contiguous lesions (distant disease) at baseline was an independent predictor of shorter PFS and OS (P<0.001).

Conclusions: Data encourage further studies on the predictive potential of CD109+ CECs in GBM patients treated with bevacizumab.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Angiogenesis Inhibitors / administration & dosage
  • Antibodies, Monoclonal, Humanized / administration & dosage
  • Antigens, CD / metabolism*
  • Antineoplastic Agents / administration & dosage
  • Antineoplastic Combined Chemotherapy Protocols / adverse effects
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use
  • Bevacizumab
  • Camptothecin / administration & dosage
  • Camptothecin / analogs & derivatives
  • Disease Progression
  • Endothelial Cells / metabolism*
  • Female
  • GPI-Linked Proteins / metabolism
  • Glioblastoma / drug therapy
  • Glioblastoma / metabolism*
  • Glioblastoma / mortality
  • Glioblastoma / pathology*
  • Humans
  • Immunophenotyping
  • Irinotecan
  • Male
  • Middle Aged
  • Neoplasm Proteins / metabolism*
  • Neoplasm Recurrence, Local
  • Prognosis
  • Treatment Outcome
  • Young Adult

Substances

  • Angiogenesis Inhibitors
  • Antibodies, Monoclonal, Humanized
  • Antigens, CD
  • Antineoplastic Agents
  • CD109 protein, human
  • GPI-Linked Proteins
  • Neoplasm Proteins
  • Bevacizumab
  • Irinotecan
  • Camptothecin

Grants and funding

This work was partially supported by a grant from Italian Ministry of Health (http://www.salute.gov.it/ricercaSanitaria/paginaMenuRicercaSanitaria.jsp?menu=finalizzata&lingua=italiano ; http://ricerca.cbim.it/index.html) [RF-INN-2008-1142520 to GF, RF-2009-1524104 to FB]; Italian Association for Research on Cancer; (http://www.airc.it/) [IG 10249 to FB]; and Fondazione Umberto Veronesi (http://www.fondazioneveronesi.it/) [Call 2010 to FB]. Drugs were supplied by Roche S.p.A. (Monza, Italy) and Hospira (Napoli, Italy). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.