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临床试验/NCT00328575
NCT00328575已完成1 期

Phase I Dose Escalation Trial in Patients With Brain Metastases Using IMRT

Sidney Kimmel Comprehensive Cancer Center at Thomas Jefferson University2 个研究点 分布在 1 个国家目标入组 10 人开始时间: 2005年10月1日最近更新:
适应症

试验速览

阶段
1 期
状态
已完成
入组人数
10
试验地点
2
主要终点
Unacceptable Acute CNS Toxicity

研究概览

简要总结

The purpose of this study is to determine if using intensity modulated radiation therapy for brain metastases is safe and will improve local control more than standard whole brain radiation therapy.

详细描述

Traditionally, whole brain radiation therapy (WBRT) has been the primary therapy for patients with brain metastases. Despite this therapy, patients still have poor survival of four to six months. Untreated patients have a median survival of one month. Up to one half of these patients die of causes related to the presence of brain metastases. In a Phase I/II RTOG trial, the efficacy and safety of delivering accelerated fractionation was investigated in patients with good prognostic factors. No toxicity was observed with escalating dose of irradiation up 70.40Gy in 1.6Gy twice daily treatments. However, in a randomized trial, the use of hyperfractionation did not appear to improve survival when compared to 30Gy whole brain irradiation delivered in 10 fractions.

Current therapeutic approach also includes stereotactic radiosurgery (SRS). Several retrospective studies have demonstrated improved local tumor control of 80% with addition of SRS to WBRT. These local control rates were comparable to surgery. In a recently published randomized trial by RTOG 95-08 (TJU accrued 42 patients to this trial), Andrews et al. demonstrated improved survival in patients with solitary brain lesion treated with SRS. Median survival was 6.5 months in patients treated with WBRT and SRS compared to 4.9 months in patients treated with WBRT alone. Also, these patients were more likely to have stable or improved performance status.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

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

入选标准

  • Histologically confirmed malignancy
  • 2-5 parenchymal brain metastases on magnetic resonance imaging (MRI) with a maximum size of 4 cm
  • Partial resection allowed. Complete resection allowed only in patients with more than 3 lesions.
  • Karnofsky Performance Status (KPS) equal to or greater than 60
  • Neurologic function equal to or greater than 2

排除标准

  • Recurrent brain tumors
  • Major medical or psychiatric illnesses
  • Metastases in brainstem, midbrain, pons, or medulla
  • Patients with leukemia or lymphoma

结局指标

主要结局

Unacceptable Acute CNS Toxicity

时间窗: 3 weeks

The primary endpoint is the frequency of patients developing unacceptable acute CNS toxicity.

次要结局

  • Dose-Limiting Toxicity (DLT)(30 days)

研究者

研究点 (2)

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