跳至主要内容
临床试验/NCT03530605
NCT03530605撤回不适用

Use of Optune TTF With Radiation as an Alternative for Elderly Patients With Primary CNS Lymphoma

Saint Luke's Health System0 个研究点开始时间: 2020年8月31日最近更新:
适应症

试验速览

阶段
不适用
状态
撤回
主要终点
Overall Survival Time

研究概览

简要总结

This study will compare the overall survival (OS) time of elderly patients who would not tolerate standard chemotherapy for PCNSL treated with WBXRT together with Optune-TTF to those treated with whole-brain radiotherapy alone.

Standard treatment of primary central nervous system lymphoma (PCNSL) for patients with good performance status involves high-dose methotrexate-based chemotherapy regimens and whole-brain radiation therapy (WBXRT). Although up to 20% of patients with PCNSL are 80 years of age or older, little data exist with regard to optimal treatment of this patient population and they often do not qualify for clinical trials. In addition, elderly patients have a poorer rate of complete and partial response and increased risk of toxicity when treated with standard chemotherapy regimens. Though a consensus does not exist, radiotherapy alone is often used in these patients to minimize toxic effects of more aggressive chemotherapies.

The Optune TTF device has proven effective in treating high-grade gliomas and is currently being investigated to treat meningiomas and metastatic lesions in the brain as well as other tumor types elsewhere in the body. It is generally well tolerated with no known systemic side effects, producing only an occasional local skin reaction. The mechanism of action is independent of tumor type and therefore may be effective in treating lymphoma as well.

研究设计

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

入排标准

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

入选标准

  • Histological de novo diagnosis of PCNSL
  • Tumor located in the supra-tentorial brain region
  • Karnofsky performance score of 70 or above
  • Ineligible for chemotherapy due to age or other co-morbidities
  • Life expectancy of at least 3 months
  • Patient has a caretaker willing to assist with study compliance
  • Patient is able to provide written consent on their own behalf

排除标准

  • Second or subsequent recurrence of PCNSL
  • Patient wishes to receive systemic treatment
  • Implanted electronic medical device in the brain (deep brain stimulator, vagus nerve stimulator, programmable shunt, etc.)
  • Skull defect without replacement
  • Prior radiation, surgery, or chemotherapy for PCNSL within the 4 weeks prior to enrollment
  • Patient unable to comply with Optune device treatment or the study follow- up schedule
  • Active participation in another therapeutic clinical trial
  • Patient unable to provide written consent on their own behalf

结局指标

主要结局

Overall Survival Time

时间窗: 4 years

Overall survival time

次要结局

  • Steroid & Antiepileptic Use(2 years)
  • Progression-Free Survival Time(2 years)
  • One-Year Survival Rate(1 year)
  • Radiographic Response Rate(2 years)

研究者

申办方类型
Other
责任方
Sponsor

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