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临床试验/NCT02581670
NCT02581670Unknown不适用

Prospective Non-randomized Phase II Study on Stereotactic Body Radiation Therapy for Medically Inoperable Lung and Liver Oligometastases From Breast Cancer

Istituto Clinico Humanitas2 个研究点 分布在 1 个国家目标入组 65 人开始时间: 2015年11月4日最近更新:
适应症

试验速览

阶段
不适用
发起方
入组人数
65
试验地点
2
主要终点
Local control of disease after SBRT according to EORTC questionnaire

研究概览

简要总结

Investigators designed a phase II study to evaluate safety and efficacy of lung and liver stereotactic radiation therapy (SRT) in oligometastatic breast cancer patients unsuitable for surgery, using VMAT RapidArc approach.

详细描述

Investigators designed a prospective phase II study to evaluate safety and efficacy of lung and liver stereotactic radiation therapy (SRT) scheduled for oligometastatic breast cancer patients unsuitable for surgery with age major than 18 years old and with adequate performance status (ECOG), using VMAT RapidArc approach. The potential advantage of this technique is the ability to deliver a more selective irradiation to tumour's target while reducing doses to normal tissue, optimizing the therapeutic window.

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
Female
接受健康志愿者

入选标准

  • Patients aged >18 years with ECOG 0-2
  • Diagnosis of Breast Cancer
  • DFI (Disease-free interval) > 1 year
  • No extrapulmonary and/or extrahepatic disease or other metastatic sites stable or responding after chemotherapy
  • No life threatening conditions
  • Lung and liver lesions < 5 (with maximum diameter < 5 cm)
  • Chemotherapy completed at least 3 weeks before treatment
  • Chemotherapy started at least 2 weeks after treatment allowed
  • Systemic therapies other than chemotherapy allowed (i.e hormonal therapies and/or immunotherapy)
  • Written informed consent

排除标准

  • ECOG > 2
  • Pregnant women
  • Patients with inability to consent

结局指标

主要结局

Local control of disease after SBRT according to EORTC questionnaire

时间窗: 2 years

Toxicity in oligometastatic breast cancer patients monitoring using CTCAE v.4

时间窗: 3 years

次要结局

  • Overall survival using Kaplan-Meyer statistical curves(2 months)
  • Progression free survival using Kaplan-Meyer statistical curves(2 months)
  • Quality of life at the end of the treatment with questionnaire EORTC QLQ C30(2 months)

研究者

发起方
Istituto Clinico Humanitas
申办方类型
Other
责任方
Principal Investigator
主要研究者

Michele Tedeschi

MD

Istituto Clinico Humanitas

研究点 (2)

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