评估新辅助camrelizumab和apatinib在复发性高级别胶质瘤患者中的安全性和有效性的临床试验的初步报告:一项前瞻性II期单臂研究

Glioma Pub Date : 2022-01-01 DOI:10.4103/glioma.glioma_6_22
Fu-Hua Lin, C. Guo, Qunying Yang, Yinsheng Chen, Chao Ke, K. Sai, Ji Zhang, Xiaobing Jiang, Wanming Hu, S. Xi, Jian Zhou, Depei Li, Zhihuan Zhou, Qinqin Zhao, X. Cao, Zhongyan Chen
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引用次数: 0

摘要

背景与目的:高级别胶质瘤是中枢神经系统最常见的恶性原发性脑肿瘤。已经使用了多种策略,如手术、放疗和化疗,但高级别胶质瘤患者的预后仍然很差。复发性胶质瘤没有标准的治疗方法;然而,程序性细胞死亡蛋白1阻断剂与抗血管生成剂的联合治疗已在不同的实体瘤中显示出有希望的效果。因此,自2020年底以来,我们机构开展了一项临床试验,旨在评估卡雷珠单抗和阿帕替尼新辅助治疗复发性高级别胶质瘤患者的安全性和有效性。方法/设计:在这项前瞻性II期单臂研究中,复发性高级别胶质瘤患者将在肿瘤切除术再次手术前14天接受单剂量静脉注射卡雷珠单抗(200 mg)和每日口服阿帕替尼(250 mg/天,持续7天)。顺序治疗将在术后2周开始,每两周注射一次卡雷珠单抗,术后4周开始,每天给药阿帕替尼。卡雷利珠单抗和阿帕替尼的治疗将持续到疾病进展或不可接受的毒性或死亡。主要的结果衡量标准是中位总生存率。次要结果指标包括6个月和12个月的无进展生存率以及其他指标。该试验计划招募30名患者。本研究于2020年7月27日经中山大学癌症中心伦理委员会批准(中国广州;批准号:slB2020-149-01)。结果和结论:尽管仍无法进行评估,但截至2022年1月底,已有11名患者入选。一些患者已经显示出有希望的结果。这些初步数据表明,这项研究是值得的。我们希望这项研究能为更好地护理复发性高级别胶质瘤患者提供科学依据。试验注册:本研究于2020年10月19日在ClinicalTrials.gov注册,标识符为NCT04588987。
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Initial report of a clinical trial evaluating the safety and efficiency of neoadjuvant camrelizumab and apatinib in patients with recurrent high-grade gliomas: A prospective, phase II, single-arm study
Background and Aim: High-grade glioma is the most common malignant primary brain tumor in the central nervous system. Multiple strategies such as surgery, radiotherapy, and chemotherapy have been used, but the prognosis of patients with high-grade glioma remains poor. No standard treatment exists for recurrent gliomas; however, combination therapies of programmed cell death protein 1 blockades with antiangiogenic agents have demonstrated promising effects in different solid tumors. Therefore, since the end of 2020, a clinical trial designed to evaluate the safety and efficiency of neoadjuvant therapy using camrelizumab and apatinib in patients with recurrent high-grade gliomas has been carried out in our institution. Methods/Design: In this prospective, Phase II, single-arm study, patients with recurrent high-grade gliomas will receive single-dose intravenous injection of camrelizumab (200 mg) and daily oral administration of apatinib (250 mg/day for 7 days) 14 days before reoperation for tumor resection. Sequential therapy will begin 2 weeks after surgery with the biweekly injection of camrelizumab and 4 weeks after surgery with the daily administration of apatinib. Treatment of camrelizumab and apatinib will be continued until disease progression or unacceptable toxicity or death. The primary outcome measure will be the median overall survival rate. Secondary outcome measures will include progression-free survival rate at 6 months and at 12 months and other measures. The trial is planned to enroll 30 patients. This study was approved by the Ethics Committee of Sun Yat-sen University Cancer Center (Guangzhou, China; approval No. SL-B2020-149-01) on July 27, 2020. Results and Conclusions: Although an evaluation is still impossible to be conducted yet, 11 patients had been enrolled by the end of January 2022. Some patients have shown a promising outcome. These preliminary data suggest that this study would be worthwhile. We hope that this study will provide scientific evidence to better care of patients with recurrent high-grade glioma. Trial registration: This study was registered with ClinicalTrials.gov under identifier NCT04588987 on October 19, 2020.
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