Rose Ella Burkhardt Brain Tumor Center, Cleveland Clinic, Cleveland, OH.
Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA.
J Clin Oncol. 2023 Mar 1;41(7):1453-1465. doi: 10.1200/JCO.22.00996. Epub 2022 Dec 15.
Despite intensive treatment with surgery, radiation therapy, temozolomide (TMZ) chemotherapy, and tumor-treating fields, mortality of newly diagnosed glioblastoma (nGBM) remains very high. SurVaxM is a peptide vaccine conjugate that has been shown to activate the immune system against its target molecule survivin, which is highly expressed by glioblastoma cells. We conducted a phase IIa, open-label, multicenter trial evaluating the safety, immunologic effects, and survival of patients with nGBM receiving SurVaxM plus adjuvant TMZ following surgery and chemoradiation (ClinicalTrials.gov identifier: NCT02455557).
Sixty-four patients with resected nGBM were enrolled including 38 men and 26 women, in the age range of 20-82 years. Following craniotomy and fractionated radiation therapy with concurrent TMZ, patients received four doses of SurVaxM (500 μg once every 2 weeks) in Montanide ISA-51 plus sargramostim (granulocyte macrophage colony-stimulating factor) subcutaneously. Patients subsequently received adjuvant TMZ and maintenance SurVaxM concurrently until progression. Progression-free survival (PFS) and overall survival (OS) were reported. Immunologic responses to SurVaxM were assessed.
SurVaxM plus TMZ was well tolerated with no serious adverse events attributable to SurVaxM. Of the 63 patients who were evaluable for outcome, 60 (95.2%) remained progression-free 6 months after diagnosis (prespecified primary end point). Median PFS was 11.4 months and median OS was 25.9 months measured from first dose of SurVaxM. SurVaxM produced survivin-specific CD8+ T cells and antibody/immunoglobulin G titers. Apparent clinical benefit of SurVaxM was observed in both methylated and unmethylated patients.
SurVaxM appeared to be safe and well tolerated. The combination represents a promising therapy for nGBM. For patients with nGBM treated in this manner, PFS may be an acceptable surrogate for OS. A large randomized clinical trial of SurVaxM for nGBM is in progress.
尽管进行了手术、放疗、替莫唑胺(TMZ)化疗和肿瘤治疗电场等强化治疗,新诊断的胶质母细胞瘤(nGBM)的死亡率仍然非常高。SurVaxM 是一种肽疫苗偶联物,已被证明能激活免疫系统对抗其靶分子存活素,该分子在胶质母细胞瘤细胞中高度表达。我们进行了一项 IIa 期、开放标签、多中心试验,评估了接受手术后和放化疗联合使用 SurVaxM 加辅助 TMZ 的 nGBM 患者的安全性、免疫效应和生存情况(ClinicalTrials.gov 标识符:NCT02455557)。
共纳入 64 例接受手术切除的 nGBM 患者,包括 38 名男性和 26 名女性,年龄 20-82 岁。在接受分次放疗和同步 TMZ 治疗后,患者接受 4 剂 500μg 的 SurVaxM(每 2 周一次),皮下给予 Montanide ISA-51 佐剂和沙格司亭(粒细胞巨噬细胞集落刺激因子)。随后,患者接受辅助 TMZ 和维持性 SurVaxM 联合治疗,直至疾病进展。报告无进展生存期(PFS)和总生存期(OS)。评估了对 SurVaxM 的免疫反应。
SurVaxM 加 TMZ 耐受性良好,无与 SurVaxM 相关的严重不良事件。在可评估结局的 63 例患者中,60 例(95.2%)在诊断后 6 个月时无疾病进展(主要预设终点)。中位 PFS 为 11.4 个月,从 SurVaxM 首次给药开始中位 OS 为 25.9 个月。SurVaxM 产生了存活素特异性 CD8+T 细胞和抗体/免疫球蛋白 G 滴度。在甲基化和非甲基化患者中均观察到 SurVaxM 的明显临床获益。
SurVaxM 似乎安全且耐受良好。该联合治疗代表了 nGBM 的一种有前途的治疗方法。对于采用这种方式治疗的 nGBM 患者,PFS 可能是 OS 的可接受替代指标。一项针对 nGBM 的 SurVaxM 大型随机临床试验正在进行中。