Department of Neurosurgery, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
National Clinical Research Center for Neurological Diseases, Center of Brain Tumor, Beijing Institute for Brain Disorders and Beijing Key Laboratory of Brain Tumor, Beijing, China.
Front Immunol. 2021 May 7;12:632547. doi: 10.3389/fimmu.2021.632547. eCollection 2021.
World Health Organization (WHO) grade IV glioma remains one of the most lethal tumors with a dismal prognosis and inevitable recurrence. We evaluated the safety and efficacy of immunotherapy with radiotherapy in this population of patients.
This study was a single-arm, open-label, phase I trial based on patients with recurrent WHO grade IV glioma. Patients were treated with intracranial and systemic immunoadjuvants in combination with low-dose reirradiation. The primary endpoint of the present trial was safety. Secondary endpoints were overall survival (OS) and progression-free survival (PFS). This trial is registered at ClinicalTrials.gov, NCT03392545.
Thirty patients were enrolled. The most common adverse events (AEs) were fever (66.7%), vomiting (33.3%), headache (30.0%), and fatigue (23.3%). Only a single patient experienced grade 3 fever, and no grade 4 AEs or deaths related to treatment were observed. Of the 30 patients, 1 (3.3%) had a complete response, 5 (16.7%) had a partial response, 9 (30.0%) had stable disease, and 15 (50.0%) had progressive disease, resulting in an objective response rate of 20.0%. The median PFS of the entire cohort was 88.0 (61.0-254.0) days, and the median OS was 362.0 (197.0-601.0) days. Patients could be divided into responders and non-responders, and these groups exhibited a significant difference in terms of survival time, T lymphocyte subsets, frequency of cell division cycle 27 (CDC27) mutation status, and CD15 and CD68 expression (<0.05).
The combination of immunotherapy and radiotherapy is well tolerated and may provide clinical benefit for patients with recurrent WHO grade IV glioma. A prospective phase II study is needed to further validate the efficacy of our therapeutic regimen.
世界卫生组织(WHO)四级胶质瘤仍然是最致命的肿瘤之一,预后极差,不可避免地会复发。我们评估了免疫疗法联合放疗在这一人群中的安全性和疗效。
这是一项基于复发性 WHO 四级胶质瘤患者的单臂、开放标签、I 期试验。患者接受颅内和全身免疫佐剂联合低剂量再放疗。本试验的主要终点是安全性。次要终点是总生存期(OS)和无进展生存期(PFS)。该试验在 ClinicalTrials.gov 上注册,NCT03392545。
共纳入 30 例患者。最常见的不良事件(AE)为发热(66.7%)、呕吐(33.3%)、头痛(30.0%)和疲劳(23.3%)。仅有 1 例患者出现 3 级发热,无 4 级 AE 或与治疗相关的死亡。30 例患者中,1 例(3.3%)完全缓解,5 例(16.7%)部分缓解,9 例(30.0%)病情稳定,15 例(50.0%)病情进展,客观缓解率为 20.0%。全队列的中位 PFS 为 88.0(61.0-254.0)天,中位 OS 为 362.0(197.0-601.0)天。患者可分为应答者和无应答者,这两组在生存时间、T 淋巴细胞亚群、细胞周期蛋白 27(CDC27)突变状态、CD15 和 CD68 表达频率方面存在显著差异(<0.05)。
免疫治疗联合放疗耐受性良好,可能为复发性 WHO 四级胶质瘤患者带来临床获益。需要进行前瞻性 II 期研究进一步验证我们治疗方案的疗效。