Literature DB >> 23249106

Bevacizumab-based therapy in relapsed glioblastoma: rationale and clinical experience to date.

Olivier L Chinot1.   

Abstract

Relapsed glioblastoma (GBM) has an extremely poor prognosis and remains an invariably fatal disease, with a median overall survival of 6-7 months. Despite numerous clinical trials over the past 20-30 years, treatment options for relapsed GBM remain limited. In recent years, significant research efforts have focused on the use of antiangiogenic therapies for the treatment of GBM. Bevacizumab is a humanized monoclonal antibody that specifically inhibits the proangiogenic VEGF, with well-established clinical efficacy in a number of solid malignancies, which is now under investigation for the treatment of GBM. In this review, we discuss the available data regarding bevacizumab-based therapy in relapsed GBM, highlighting its potential and ongoing challenges in this difficult-to-treat disease.

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Year:  2012        PMID: 23249106     DOI: 10.1586/era.12.128

Source DB:  PubMed          Journal:  Expert Rev Anticancer Ther        ISSN: 1473-7140            Impact factor:   4.512


  6 in total

1.  Cerebral Blood Flow Changes in Glioblastoma Patients Undergoing Bevacizumab Treatment Are Seen in Both Tumor and Normal Brain.

Authors:  Jalal B Andre; Seema Nagpal; Daniel S Hippe; Ali C Ravanpay; Heiko Schmiedeskamp; Roland Bammer; Gerald J Palagallo; Lawrence Recht; Greg Zaharchuk
Journal:  Neuroradiol J       Date:  2015-04-28

2.  Dynamic Susceptibility Contrast-Enhanced MR Perfusion Imaging in Assessing Recurrent Glioblastoma Response to Superselective Intra-Arterial Bevacizumab Therapy.

Authors:  R Singh; K Kesavabhotla; S A Kishore; Z Zhou; A J Tsiouris; C G Filippi; J A Boockvar; I Kovanlikaya
Journal:  AJNR Am J Neuroradiol       Date:  2016-05-26       Impact factor: 3.825

3.  Limited impact of prognostic factors in patients with recurrent glioblastoma multiforme treated with a bevacizumab-based regimen.

Authors:  E Tabouret; M Barrie; A Thiebaut; M Matta; C Boucard; D Autran; A Loundou; O Chinot
Journal:  J Neurooncol       Date:  2013-06-12       Impact factor: 4.130

4.  Recurrence of glioblastoma after radio-chemotherapy is associated with an angiogenic switch to the CXCL12-CXCR4 pathway.

Authors:  Emeline Tabouret; Aurelie Tchoghandjian; Emilie Denicolai; Christine Delfino; Philippe Metellus; Thomas Graillon; Celine Boucard; Isabelle Nanni; Laetitia Padovani; L'Houcine Ouafik; Dominique Figarella-Branger; Olivier Chinot
Journal:  Oncotarget       Date:  2015-05-10

5.  Increased Antiangiogenic Effect by Blocking CCL2-dependent Macrophages in a Rodent Glioblastoma Model: Correlation Study with Dynamic Susceptibility Contrast Perfusion MRI.

Authors:  Hye Rim Cho; Nisha Kumari; Hien Thi Vu; Hyeonjin Kim; Chul-Kee Park; Seung Hong Choi
Journal:  Sci Rep       Date:  2019-07-31       Impact factor: 4.379

6.  Talin1 targeting potentiates anti-angiogenic therapy by attenuating invasion and stem-like features of glioblastoma multiforme.

Authors:  Wonyoung Kang; Sung Heon Kim; Hee Jin Cho; Juyoun Jin; Jeongwu Lee; Kyeung Min Joo; Do-Hyun Nam
Journal:  Oncotarget       Date:  2015-09-29
  6 in total

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