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临床试验/NCT00083304
NCT00083304已完成3 期

A Phase 3 Randomized, Open-label Comparative Study of Standard Whole Brain Radiation Therapy With Supplemental Oxygen, With or Without Concurrent RSR13 (Efaproxiral), in Women With Brain Metastases From Breast Cancer

Spectrum Pharmaceuticals, Inc92 个研究点 分布在 5 个国家目标入组 368 人开始时间: 2004年2月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
已完成
入组人数
368
试验地点
92
主要终点
Overall Survival

研究概览

简要总结

RSR13 (efaproxiral) is a radiation sensitizer that has shown positive results in a Phase 3, randomized clinical trial of patients with brain metastases. Of 111 eligible breast cancer patients with brain metastases in that trial, 59 patients who received RSR13 prior to radiation therapy had a median survival time that was twice as long as the 52 patients who did not receive RSR13 prior to radiation therapy.

RSR13 (efaproxiral) is an experimental drug that increases the amount of oxygen released from blood into the tissues. It is well known that certain types of cancer tumors, including those in brain metastases, lack oxygen. Lack of oxygen in a tumor can reduce the effect of radiation therapy (RT). RSR13 may increase the oxygen level in brain tumors so that radiation therapy works better.

This study will enroll up to 360 women with brain metastases from breast cancer, and will evaluate if whole brain radiation therapy given with RSR13 will have a better treatment effect than whole brain radiation therapy alone. RSR13 will be infused intravenously (IV) through a central catheter placed in a central vein. Women randomized (assigned) to receive RSR13, therefore, will need to have a central catheter placed for treatment unless one is already in place.

详细描述

The screening process will include documentation of the cancer, which which will require a brain scan and may include a liver scan. Other screening measurements will include a Karnofsky Performance Status (KPS) assessment, measurement of the amount of oxygen in the blood, using a non-invasive device most often placed on the finger, lung function tests that will require blowing into a machine, and an electrocardiogram (ECG). About 2 teaspoons, or 10 mL, of blood will be taken for specific laboratory tests, and a pregnancy test will be done on the blood of women of childbearing potential.

All study patients will receive supplemental oxygen and whole brain radiation therapy (WBRT) (30 Gy, 3 Gy fractions) every weekday for 2 weeks. Half of the patients will be randomized (assigned) to receive RSR13 prior to WBRT, and will need to have a central catheter placed for treatment unless one is already in place. Patients who receive RSR13 will also need to continue to receive oxygen in the clinic until the amount of oxygen in their blood is near normal. This level has returned to near normal in most patients within 1 to 2 hours.

During treatment and follow-up visits, physical and neurological exam, KPS assessment, weight, height, and vital sign measurements, and about 2 teaspoons of blood may be required. Patients will need to return for follow-up visits 1 month after completion of treatment, 2 months later, and every 3 months thereafter until their doctor tells them otherwise.

研究设计

研究类型
Interventional
分配方式
Randomized
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
Female
接受健康志愿者

入选标准

  • Adult women with brain metastases from breast cancer
  • Minimum KPS of 70

排除标准

  • Previous treatment for brain metastases, including brain surgery and any form of radiation to the brain

研究组 & 干预措施

Efaproxiral + WBRT + Supplemental Oxygen

Experimental

干预措施: Efaproxiral (Drug)

Efaproxiral + WBRT + Supplemental Oxygen

Experimental

干预措施: Whole Brain Radiation Therapy (WBRT) (Radiation)

Efaproxiral + WBRT + Supplemental Oxygen

Experimental

干预措施: Supplemental Oxygen (Other)

WBRT + Supplemental Oxygen

Active Comparator

干预措施: Whole Brain Radiation Therapy (WBRT) (Radiation)

WBRT + Supplemental Oxygen

Active Comparator

干预措施: Supplemental Oxygen (Other)

结局指标

主要结局

Overall Survival

时间窗: Measured from randomization until death due to any cause.

次要结局

  • Response Rate in the Brain at 3 Months(Assessed at screening, 3 months after end of study treatment and at least 4 weeks after the 3-month scan.)
  • Karnofsky Performance Status & Neurological Signs & Symptoms(Assessed at baseline, 1 month follow-up (FU) visit, 3 month FU visit, and 6 month FU visit.)

研究者

申办方类型
Industry

研究点 (92)

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