4.6 Article

Intracerebral administration of CpG oligonucleotide for patients with recurrent glioblastoma: a phase II study

Journal

NEURO-ONCOLOGY
Volume 12, Issue 4, Pages 401-408

Publisher

OXFORD UNIV PRESS INC
DOI: 10.1093/neuonc/nop047

Keywords

CpG-ODN; convection-enhanced delivery; glioblastoma; phase II; TLR9

Funding

  1. Fondation pour la Recherche Medicale (FRM)
  2. Agence Nationale de la Recherche (ANR) [RIB 2006]
  3. Association Oligocyte
  4. Association pour la Recherche sur les Tumeurs Cerebrales (ARTC)
  5. Oligovax
  6. Assistance Publique-Hopitaux de Paris (AP/HP)

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Immunostimulating oligodeoxynucleotides containing CpG motifs (CpG-ODN) have shown promising efficacy in cancer models when injected locally. In a phase I clinical trial, intratumoral infusions of CpG-ODN in glioblastoma (GBM) patients were well tolerated at doses up to 20 mg. This phase II trial was designed to study the efficacy of a local treatment by CpG-ODN in patients with recurrent GBMs. Patients with recurrent GBM occurring at least 3 months after radiotherapy, and previously treated with 1 or 2 regimens of chemotherapy received 20 mg of CpG-ODN (CpG-28) by convection-enhanced delivery. The primary endpoint was the percentage of patients without tumor progression 6 months after inclusion. Secondary endpoints were tolerance, survival, and radiological response. Thirty-four patients were enrolled in two centers between November 2004 and March 2006. Thirty-one patients received CpG-ODN treatment. The progression-free survival (PFS) at 6 months was 19%. One partial response and 3 minor responses were observed. The median overall survival was 28 weeks. Eight patients (24%) were alive 1 year after inclusion and 5 patients (15%) were alive after 2 years. Treatment was usually well tolerated. As reported previously, the most common toxicities were lymphopenia, mild fever, seizures, and transient neurological worsening. Despite a few cases showing a radiological response, CpG-28 showed modest activity on the 6-month PFS in this patient population. The molecular or clinical characteristics of a subgroup of patients that could potentially benefit from such an approach remain to be defined.

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