Department of Neurosurgery, Hôpital Lariboisiére, Paris, France.
Neuro Oncol. 2010 Apr;12(4):401-8. doi: 10.1093/neuonc/nop047. Epub 2010 Jan 25.
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.
含有 CpG 基序的免疫刺激寡脱氧核苷酸(CpG-ODN)在局部注射时已显示出在癌症模型中具有良好的疗效。在一项 I 期临床试验中,胶质母细胞瘤(GBM)患者瘤内注射 CpG-ODN 的剂量高达 20mg 时,耐受性良好。这项 II 期临床试验旨在研究 CpG-ODN 局部治疗复发性 GBM 患者的疗效。在放疗后至少 3 个月发生复发且之前接受过 1 或 2 种化疗方案治疗的复发性 GBM 患者,接受 20mg 的 CpG-ODN(CpG-28)通过增强递送进行治疗。主要终点是纳入后 6 个月无肿瘤进展的患者比例。次要终点为耐受性、生存和影像学反应。2004 年 11 月至 2006 年 3 月,两个中心共招募了 34 名患者。31 名患者接受了 CpG-ODN 治疗。6 个月时的无进展生存期(PFS)为 19%。观察到 1 例部分缓解和 3 例轻微缓解。中位总生存期为 28 周。8 名患者(24%)在纳入后 1 年存活,5 名患者(15%)在纳入后 2 年存活。治疗通常耐受性良好。与之前报道的一样,最常见的毒性是淋巴细胞减少、轻度发热、癫痫发作和短暂的神经恶化。尽管有少数病例显示出影像学反应,但 CpG-28 在该患者人群中 6 个月 PFS 上显示出适度的活性。仍需确定能够从这种治疗方法中获益的亚组患者的分子或临床特征。