Postoperative radiotherapy with concomitant temozolomide plus anlotinib for newly diagnosed glioblastoma: Study protocol for a multicenter, double-blind, randomized phase II trial

Glioma Pub Date : 2022-04-01 DOI:10.4103/glioma.glioma_17_22
Yuanyuan Chen, Baiqiang Dong, Guihong Liu, Pengfei Sun, Meihua Li, Xuejun Yang, Shiyu Feng, Liang-liang Wang, Y. Hua, Ming Zhao, Yanhui Liu, J. Ran, Lianlian Qiao, Xueguan Lu, Hao Jiang, Deqiang Mao, Junxin Wu, Xianming Li, Wei Zheng, Zhigang Liu, Song Lin, M. Deng, Qunying Yang, Chengcheng Guo, Jing Li, Zhongyan Chen
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引用次数: 0

Abstract

Background and Aim: Postoperative radiotherapy with concomitant temozolomide (TMZ) followed by ≤ six cycles of adjuvant TMZ chemotherapy (Stupp regimen) is the standard treatment for newly diagnosed glioblastoma (GBM); however, its effectiveness is limited. Anlotinib inhibits both tumor angiogenesis and tumor cell proliferation by targeting multiple kinases, and showing promising results in preclinical GBM models. We designed a Phase II trial to assess the efficacy and safety of the Stupp regimen plus anlotinib. Methods/Design: This is a multicenter, double-blind, randomized, placebo-controlled trial with an expected 150 patients randomly assigned 1:1 ratio to receive TMZ-based radiochemotherapy with anlotinib (Stupp regimen + anlotinib) or placebo (Stupp regimen + placebo). Postoperative patient recruitment will begin in July 2021, the analysis of primary outcome measures will be completed in July 2023, and the study will finish in July 2024. Major eligibility criteria include histologically confirmed newly diagnosed GBM and an Eastern Cooperative Oncology Group performance score ≤2. Other criteria for inclusion include age ≥18 years and lack of significant comorbidity. In this study, the primary endpoint will be the median progression-free survival (PFS). Secondary endpoints include 1-year overall survival rate, PFS at 6 months, overall response rate, duration of response, disease control rate, quality of life, and toxicity. The protocol has received approval from Sun Yat-sen University Cancer Center Ethics Committee (Approval No. B2021-073-01; approved on April 19, 2021). Discussion: Updated treatment modalities are required for newly diagnosed GBM. Our proposed treatment modality of the Stupp regimen combined with anlotinib therapy are waiting conclusion. Trial Registration: This study was registered with ClinicalTrials.gov under identifier NCT04959500 on July 13, 2021.
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术后放疗联合替莫唑胺加安洛替尼治疗新诊断的胶质母细胞瘤:一项多中心、双盲、随机II期试验的研究方案
背景和目的:术后放疗伴用替莫唑胺(TMZ),然后≤6个周期的TMZ辅助化疗(Stupp方案)是新诊断的胶质母细胞瘤(GBM)的标准治疗方法;然而,它的有效性是有限的。安洛替尼通过靶向多种激酶抑制肿瘤血管生成和肿瘤细胞增殖,并在临床前GBM模型中显示出有希望的结果。我们设计了一项II期试验来评估Stupp方案加安洛替尼的疗效和安全性。方法/设计:这是一项多中心、双盲、随机、安慰剂对照试验,预计150名患者按1:1的比例随机分配,接受基于TMZ的安洛替尼放射化疗(Stupp方案+安洛替尼)或安慰剂(Stupp方案+安慰剂)。术后患者招募将于2021年7月开始,主要结果指标的分析将于2023年7月完成,研究将于2024年7月结束。主要资格标准包括组织学确诊的新诊断GBM和东部肿瘤协作组绩效得分≤2。纳入的其他标准包括年龄≥18岁和无明显合并症。在这项研究中,主要终点将是中位无进展生存期(PFS)。次要终点包括1年总生存率、6个月PFS、总有效率、反应持续时间、疾病控制率、生活质量和毒性。该方案已获得中山大学癌症中心伦理委员会的批准(批准号B2021-073-01;于2021年4月19日批准)。讨论:新诊断的GBM需要更新治疗方式。我们提出的Stupp方案联合安洛替尼治疗模式尚待结论。试验注册:本研究于2021年7月13日在ClinicalTrials.gov注册,标识符为NCT04959500。
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