跳至主要内容
临床试验/NCT03567135
NCT03567135Unknown不适用

A Retrospective Clinical Study of Postoperative Concurrent Chemoradiotherapy Combined With Anti-angiogenic Drugs in the Treatment of Glioblastoma.

Fuzhou General Hospital1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2017年10月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
入组人数
60
试验地点
1
主要终点
Progression-Free-Survival(PFS)

研究概览

简要总结

Temozolomide (TMZ) is an oral chemotherapy drug. It is an alkylating agent used as a first-line treatment for glioblastoma. This methylation damages the DNA and triggers the death of tumor cells. According to the results of several clinical studies, TMZ synchronous plus radiotherapy and subsequent as adjuvant therapy can significantly improve the survival rate of newly diagnosed glioblastoma patients.

详细描述

Glioma is the highest incidence of the central nervous system tumor. Surgical treatment is one of the most important therapeutic methods in patients with glioblastoma. But since malignant glioma is a highly invasive tumor, the rate of surgery failure is . So the postoperative therapy shall be accompanied by radiotherapy. Since 1998, the clinical application of Temozolomide(TMZ) has brought hope for malignant glioma patients with its definite curative effect. According to the results of several clinical studies, TMZ synchronous plus radiotherapy and subsequent as adjuvant therapy can significantly improve the survival rate of newly diagnosed GBM patients and break the survival limit of malignant glioma patients. Besides, antiangiogenic therapy is also a choice for the treatment of glioblastoma patients. Vascular endothelial growth factor receptors (VEGFRs) inhibitors block the new formation around the tumor and cut down the supply of oxygen, nutrients and metabolic waste, so that the tumor is hard to proliferate and metastases.

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Retrospective

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

Experimental 1

concurrent chemoradiotherapy(Temozolomide+apatinib) maintenance therapy(Temozolomide)

干预措施: Apatinib (Drug)

Experimental 1

concurrent chemoradiotherapy(Temozolomide+apatinib) maintenance therapy(Temozolomide)

干预措施: Temozolomide(TMZ) (Drug)

control

concurrent chemoradiotherapy(Temozolomide) maintenance therapy(Temozolomide)

干预措施: Temozolomide(TMZ) (Drug)

Experimental 2

concurrent chemoradiotherapy(Temozolomide+apatinib) maintenance therapy(Temozolomide+apatinib)

干预措施: Apatinib (Drug)

Experimental 2

concurrent chemoradiotherapy(Temozolomide+apatinib) maintenance therapy(Temozolomide+apatinib)

干预措施: Temozolomide(TMZ) (Drug)

结局指标

主要结局

Progression-Free-Survival(PFS)

时间窗: From date of randomization until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 36 months.

in this Survival Duration neither Progression nor death occurs in the subjects.

Assessment of brain edema

时间窗: From date of randomization until the date of end of the trial, assessed up to 36 months

The average score of edema grading in patients before and after treatment was calculated separately.

Number of participants with treatment-related adverse events as assessed by CTCAE v4.0

时间窗: From date of randomization until the date of end of the trial, assessed up to 36 months

To observe any adverse events that occurred during the clinical study.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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