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临床试验/NCT01674842
NCT01674842已完成1 期

A Phase I Dose-Escalation Study of Cisplatin and Radiation Therapy for Patients With Triple Negative Breast Cancer

Dana-Farber Cancer Institute5 个研究点 分布在 1 个国家目标入组 55 人开始时间: 2012年10月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
已完成
入组人数
55
试验地点
5
主要终点
Safety of Cisplatin w/ Radiation

研究概览

简要总结

This is a Phase I dose escalation study of cisplatin and concurrent radiation in patients with ER negative, PR negative and HER2 negative breast cancer who have undergone breast-conserving surgery or mastectomy.

Primary objective: To assess the safety, tolerability, and maximum tolerated dose (MTD) of cisplatin when given concurrently with radiation therapy for participants with Stage II or III breast cancer who have undergone breast conserving surgery or mastectomy

详细描述

This is a phase I dose escalation study of cisplatin and radiation to determine the toxicity of this combined treatment and establish an MTD.

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

  • Primary tumor is triple negative breast cancer
  • Breast-conserving surgery or mastectomy with surgical excision of all gross disease with negative surgical margins
  • Pathologic or clinical stage II or III disease
  • At least 3 week interval from last chemotherapy administration/breast surgery to radiation (no more than 8 weeks)

排除标准

  • Pregnant or breastfeeding
  • Prior radiation to breast or ipsilateral regional nodes
  • Ongoing therapy with other investigational agents
  • Hormonal therapy
  • Significant co-morbidity
  • Pathologic complete response following preoperative chemotherapy
  • Biopsy proven metastatic disease

研究组 & 干预措施

Cisplatin + Radiation Therapy

Experimental

Cisplatin concurrently with radiation therapy

干预措施: Radiation Therapy (Radiation)

Cisplatin + Radiation Therapy

Experimental

Cisplatin concurrently with radiation therapy

干预措施: Cisplatin (Drug)

结局指标

主要结局

Safety of Cisplatin w/ Radiation

时间窗: 2 years

To determine the maximum tolerated dose of cisplatin when given concurrently with radiation therapy for participants with Stage II or III breast cancer who have undergone breast conserving surgery or mastectomy.

次要结局

  • Local recurrence at 5 years(5 years)
  • Long term toxicity(2 years)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Jennifer Bellon

Principal Invstigator

Dana-Farber Cancer Institute

研究点 (5)

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