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临床试验/NCT04856852
NCT04856852Unknown不适用

Iodine-125 Brachytherapy Together With Chemotherapy Compared With Surgical Resection Followed by Concomitant Radiochemotherapy in Patients With Newly Diagnosed Glioblastoma,a Randomized, Open-label, Multi-center Clinical Trial

The Affiliated Hospital of Qingdao University0 个研究点目标入组 84 人开始时间: 2021年6月28日最近更新:
适应症

试验速览

阶段
不适用
入组人数
84
主要终点
Progression-free survival (PFS)

研究概览

简要总结

The purpose of this study is to evaluate the efficacy and safety of Iodine-125 brachytherapy together with chemotherapy compared with surgical resection followed by concomitant radiochemotherapy in patients with newly diagnosed glioblastoma.

详细描述

This is a prospective, multicentric open-label trial to evaluate the efficacy and safety of Iodine-125 brachytherapy together with chemotherapy compared with surgical resection followed by concomitant radiochemotherapy in patients with newly diagnosed glioblastoma.

The primary efficacy outcome was evaluated with progression-free survival (PFS).

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Diagnosis of glioblastoma confirmed by histology
  • Age: 18-75 years old
  • Single lesion located in one hemisphere with a diameter between 2 and 6 centimeters
  • No prior anticancer therapy for glioblastoma besides biopsy.
  • ECOG PS:0-2 point

排除标准

  • Infra-tentorial tumor or tumor involves the ependymal surface.
  • Nonmeasurable disease.
  • Evidence of uncontrolled intracranial pressure.
  • Severe heart, brain, and lung diseases.
  • 5.Severe hepatic or renal dysfunction.
  • Uncontrolled, active infection.
  • Severe clotting dysfunction.
  • Uncontrolled hypertension.
  • Participated in any other clinical treatment trial within 4 weeks before randomization.
  • Severe vascular diseases within 6 months before randomization.
  • Participants who received major surgical treatment within 4 weeks or were expected to be treated during the trial.

结局指标

主要结局

Progression-free survival (PFS)

时间窗: 2.5 years after randomization

PFS is defined as the time from randomization to progression or death from any causes. Progression is defined as the RANO Criteria indicated.

次要结局

  • Overall Survival (OS)(2.5 years after randomization)
  • Survival rates at 6 months and 1 year(at 6 months and 1 year after operation respectively)
  • EORTC QLQ-C30(2.5 year after randomization)
  • Complications(within 1 week after operation)
  • ECOG Performance Status(2.5 year after randomization)

研究者

申办方类型
Other
责任方
Sponsor

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